Patent Application
20230040324
The present invention provides novel negatively charged fluorescent dyes with aromatic amino groups, low mass-to-charge (m/z) ratios and demonstrates their use as fluorescent tags facilitating separation of the analytes and their sensitive detection by fluorescence. The novel dyes contain polycyclic aromatic systems (acridine, pyrene), anionic groups (e.g., primary phosphate, N-cyanosulfonamide) and are applied within carbohydrate analysis, in particular, as reagents for reductive amination of glycans, followed by separation and fluorescence detection of the carbohydrate derivatives. Their emission wavelengths are finely tunable over a wide range including green and red regions. The separation techniques applicable for the dyes of the present invention (e.g., hydrophilic interaction chromatography (HILIC), reversed phase liquid chromatography (HPLC), electrophoresis, in particular, capillary (gel) electrophoresis with laser-induced fluorescence detection) can be coupled to mass-spectrometry, which can be used alone (as a detection method) or in addition to fluorescence detection.
Glycosylation reactions are defined as enzymatically driven and highly diverse transformations of proteins, lipids or other noncarbohydrates in eukaryotic cells. Glycosylation creates a new chemical bond between a carbohydrate (the glycone; donor) and another (noncarbohydrate) molecule (the aglycon; acceptor). The term “carbohydrate(s)” as used herein is the collective term for monosaccharide(s), like xylose arabinose, glucose, galactose, mannose, fructose, fucose, N-acetylglucosamine, homo or hetero sialic acids; disaccharide(s), like lactose, sucrose, maltose, cellobiose; glycans (e.g. N- and O-glycans), homo- or hetero oligosaccharide(s), galactooligosaccharides (GOS), fructooligosaccharides (FOS), milk oligosaccharides (MOS), or even glycomoieties of glycolipids; and, in particular, polysaccharide(s), like amylose, amylopektin, cellulose, glycogen, glycosaminoglycan, or chitin. Oligo- and polysaccharides can be linear, branched or multiply branched. Typically, the aglycone is either a protein (“glycoprotein”) or a lipid (“glycolipid”). In a more general sense, “glycoconjugate” means a carbohydrate covalently linked to any other chemical entity such as protein, peptide, lipid, or even saccharide.
Glycoconjugates represent the most structurally and functionally diverse entities in nature (
Glycoconjugates range in complexity from the relatively simple glycolipids to extraordinarily complex and multiple glycosylated proteins. Although the carbohydrate moiety is commonly composed of only a few monosaccharides, including N-acetylglucosamine, N-acetylgalactosamine, mannose, galactose, fucose, glucose, and sialic acids, their structural diversity (not yet fully revealed) is much larger than that of proteins or DNA. The reasons for this diversity are the presence of the anomers and the ability of monosaccharides to branch and build different (glycosidic) linkages. Accordingly, an oligosaccharide with a relatively small chain length may have an enormous number of structural isomers. Moreover, unlike protein biosynthesis, which is based on RNA as a template, the information flow from the genome to the glycome is a complex and no longer a template-driven process. The co- and post-translational modifications of proteins in glycan biosynthesis are caused by enzymatic reactions. This leads to a drastic increase of complexity and structural diversity of glycans (as depicted in
In order to elucidate the structural features of glycome (the complete set of glycoconjugates that cells produce under specified conditions) and to understand its functions and interaction with the DNA and protein “machinery”, rapid, robust and high resolution bioanalytic techniques must be available.
Many analytic techniques have been utilized to analyze carbohydrates. Complex samples containing a variety of different oligosaccharides can be separated by chromatographic or electrokinetic techniques. The chromatographic techniques include size exclusion chromatography (SEC), hydrophilic interaction chromatography (HILIC), high-performance liquid chromatography (HPLC), reversed-phase ion-pairing chromatography (RPIPC), and porous graphitized carbon chromatography (PGC). Mass spectrometry (MS) and nuclear magnetic resonance (NMR) allow de novo structural characterization of complex oligosaccharides. A combination of several techniques is often applied, e.g. HPLC-NMR, HPLC-MS (also called LC-MS; LC=liquid chromatography) or capillary electrophoresis coupled with mass-spectrometry (CE-MS). As soon as the structure of a particular glycan is determined, its characteristic properties, such as constitution, net charge, the exact molecular mass, retention or migration times, are tabulated. By comparing the data obtained for unknown samples with tabulated parameters, the rapid screening and evaluation of unknown samples can be performed.
Carbohydrates do not absorb visible light; for the sensitive fluorescence detection they must be labeled with fluorescent tags. Thus, for analysis via chromatographic or electrokinetic separation followed by fluorescence detection, it is necessary to label the oligosaccharides with fluorescent dyes prior to the analysis. Consequently, besides providing proper excitation and emission wavelengths (and additional electric charges required for electrophoretic separation; see below), these dyes must have a reactive group.
The most common and straightforward method for labeling carbohydrates with fluorescent dyes is the reductive amination (
The electrokinetic separation is based on the motion of charged particles under the influence of an applied electric field and includes various electrophoretic techniques. The most important electrokinetic separation methods for glycoanalysis are capillary zone electrophoresis (CZE) and capillary (gel) electrophoresis (C(G)E). These techniques provide high resolution, fast separation, and allow for quantification. Capillary electrophoresis (CE) is a family of electrokinetic separation methods defined by the IUPAC as “separation techniques carried out in capillaries based solely on the differences in the electrophoretic mobilities of charged species (analytes) either in aqueous or non-aqueous background electrolyte solution” (see also M.-L. Riekkola, J. A. Jönsson, R. M. Smith, Pure Appl. Chem. 2004, 76, 443-451). In other words, CE terms the separation of ions by electrophoresis within a thin capillary. CGE is defined by the IUPAC as “a special case of capillary sieving electrophoresis when the capillary is filled with a cross-linked gel” (see also M.-L. Riekkola et al., above). The net electrical charge is required for separation of the analytes by C(G)E. The electrophoretic mobility of a compound depends on the mass to charge ratio, and when employing CGE—due to the gels sieving effect—it depends additionally on the molecular shape. The native carbohydrates, except sialic or glucuronic acids, sulphated or phosphorylated derivatives, are electroneutral and cannot be separated by their mass to charge ratio (electrophoresis). Since the size of a molecule is strongly related to the mass, and the size is rather difficult to evaluate, it is reasonable to use the mass to charge ratio as an approximation for predicting the electrophoretic mobility.
Remarkably, the mass to charge (or size to charge) ratio of many macromolecules such as DNA is virtually constant because each nucleotide adds practically the same mass and charge to the macromolecule keeping the mass to charge ratio nearly constant on average [D. N. Heiger, High performance capillary electrophoresis. An introduction: a primer, Agilent Technologies, Germany, 2000, pp. 19-24, 70]. This regularity may limit the separation ability of electrophoresis. However, the limitation can be overcome by using capillary gel electrophoresis. The capillary is filled with gel, and the separation works like in traditional gel electrophoresis, but using 10 to 100 times higher electric fields without the negative effects of Joule heating [due to efficient heat dissipation; H. H. Lauer, G. P. Rozing, High Performance Capillary Electrophoresis. A Primer. Agilent Technologies, 2009, pp. 17, 60-65, 157-159]. Since small molecules are likely to pass more pores than large molecules, small molecules move faster through the gel matrix. Due to this sieving effect, not only the mass to charge ratio but also the size and shape of a sample ion are affecting the electrophoretic mobility. The factor of molecular size is important, as it enables to use DNA-ladder (mixture of DNA oligomers of various lengths labeled with a fluorescent dye) as an internal standards for calibration of the migration times (see below). The factors of molecular size and shapes predict that the fluorescent tags providing fast-moving derivatives of glycans must have compact structures (one of the aims of the present application).
Capillary gel electrophoresis (CGE) emerged as a particularly important method for analyzing glycoconjugates including glycoproteins, glycopeptides and “released” (enzymatically cleaved from the acceptors) N- or O-glycans ((a) Novotny, M. V.; Alley, W. R., Recent trends in analytical and structural glycobiology. Curr. Opin. Chem. Biol. 2013, 17 (5), 832-840. (b) Lu, G.; Crihfield, C. L.; Gattu, S.; Veltri, L. M.; Holland, L. A. Chem. Rev. 2018, 118, 7867-7885. (c) Ruhaak, L. R.; Xu, G.; Li, Q.; Goonatilleke, E.; Lebrilla, C. B. Chem. Rev. 2018, 118, 7886-7930.) Combined with laser induced fluorescence detection (LIF), this method (CGE-LIF) allows fast and very fine resolution of analytes according to their charge-to-size ratio (G. Lu, C. L. Crihfield, S. Gattu, L. M. Veltri, L. A. Holland, Chem. Rev. 2018, 118, 7867-7885). Since the hydrodynamic radius is difficult to evaluate, the mass-to-charge ratio (m/z) is used as an estimate of the electrophoretic mobility. The main reason for using CGE-LIF is the sensitivity of detection provided by fluorescence (measuring the emission intensity) and the possibility to improve separation of the analytes by labeling them with fluorescent markers having additional electrical charges.
The procedure of glycan analysis can be divided into the following steps: sample preparation (e.g. deglycosylation), glycan labeling, sample purification, chromatographic or electrokinetic separation with detection by emission and the data analysis. The present invention introduces the negatively charged organic dyes with an amino group for glycan labeling, followed by electrophoretic separation of the derivatives obtained upon labeling and, finally, their detection by fluorescence (with an additional option of quantification). In another embodiment, the present invention introduces the negatively charged and red-emitting organic dyes with an amino group for reductive amination of carbohydrates and preparation of internal standards—mixtures of oligosaccharides labeled with a fluorescent dye detectable independently from the analytes (e.g., in a separate “color channel” of a fluorescence detector). The internal standards' mixture is injected together with an analytical sample. The components of an internal standard must have retention times covering the whole range of the analytically relevant compounds. This aspect of the present application will be discussed in detail below.
Importantly, the features of an “ideal” fluorescent tag intended for modification of glycans followed by the electrophoretic separation and detection of the derivatives—the reactive group, electrical charge and emissive properties—can be incorporated into one structure with (multiple) charges and the amino group reacting with aldehyde residues in reducing sugars. After derivatization (reductive amination) and purification (to remove proteins, excess electrolytes, excess dye, labeling reagents, etc.), the labeled sample is injected into the chromatographic column, or the electrokinetic capillary, and the separation is carried out. Due to different properties (structure, polarity, mass/charge ratio, shape, etc.), the carbohydrates are separated and reach the detector according to their characteristic retention, or migration times. When the labeled carbohydrates reach the fluorescence detector, the fluorescent markers are excited (most often with 488 nm (argon) laser or 505 nm solid state laser), and the emission signal is detected.
The first step of the reductive amination (
Thus, the applicability of the reaction sequence depicted in
Therefore, the applied amine (fluorescent dye R3NH2) has to be a weak base, because the full protonation of amine R3NH2 in
The aromatic amines are negatively charged (or potentially charged) groups. These compounds can be used for reductive amination of carbohydrates. Emission colors of conjugates (obtained according
APTS is a routinely used fluorescent marker for labelling of glycans (R. A. Evangelista, M.-S. Liu, F.-T. A. Chen, Anal. Chem. 1995, 67, 2239-2245.). The main spectral properties of APTS and its conjugates with glycans are given in
1-Aminopyrene dyes other than APTS have been disclosed as fluorescent tags for carbohydrates. WO 2012/027717 A1 describes systems comprising functionally substituted 1,6,8-trisulfonamido-3-aminopyrenes (APTS derivatives), an analyte-reactive group, a cleavable anchor as well as a porous solid phase. WO 2010/116142 A2 describes a large variety of fluorophores and fluorescent sensor compounds which also encompass aminopyrene-based dyes. However, these documents do not disclose negatively charged 1,6,8-tris-[(3-hydroxy-azetidinyl)sulfonyl]-3-aminopyrenes or 1,6,8-tris-[(3-hydroxycyclobutyl)sulfonyl]-3-aminopyrenes according to the present invention.
Previously, the use of 7-aminoacridone-2-sulfonamides with multiple negatively charged groups and orange emission (for example VBDP in
U.S. Pat. No. 9,127,164B2 (Fluorescent dyes and uses thereof) describes 9-aminoacridine dyes and peptides obtained from them. This document anticipates 9-aminoacridines independently substituted with amino or alkylamino groups, and electron-withdrawing groups such as halogen, amide, cyano, nitro, carbonyl, carboxyl, sulphonic acid etc. WO 2013/093481 A1 (Fluorescent dyes based on acridine and acridinium derivatives) describes acridine dyes and peptides obtained from them. This document anticipates acridines independently substituted with amino or alkylamino groups, and electron-withdrawing groups such as halogen, amide, cyano, nitro, carbonyl, carboxyl, sulphonic acid etc. US20120220537A1 (9-Aminoacridine derivatives, their preparation and uses) describes the synthesis of N-substituted 9-aminoacridines with electron-withdrawing groups or electron-donating groups. WO2011127406A2 (Acridines as inhibitors of haspin and dyrk kinases) describes N-substituted 9-aminoacridines as inhibitors of haspin and dyrk kinases. This document anticipates acridines independently substituted in 2-, 6- and 7-positions with —CN, —C(O)NRARB, —S(O)2RA, —S(O)2NRARB, or —NRARB etc.
Though the documents mentioned above represent the closest prior art, they are irrelevant to the subject matter of the present application, because here are claimed specific compounds with multiple negative charges localized on primary phosphate (—OP(O)(OH)2 with two negative charges at pH 8 and above) or N-cyanosulfonamide (—SO2NHCN with one negative charge at pH>5-6) groups which are covered by the general formula C.
None of these dyes has been previously shown or suggested to have superior spectral and electrophoretic properties, in particular as conjugates with carbohydrates, in comparison with APTS. APTS is a unique dye for reductive amination of oligosaccharides (Pabst, M.; Kolarich D.; Poltl, G.; Dalik, T.; Lubec, G.; Hofinger, A.; Altmann, F. Anal. Biochem. 2009, 384, 263-273), but its performance as a fluorescent tag providing only one emission color, moderate brightness and three negative charges, is limited. The fluorescence of APTS labeled glycans is captured in the “green” color channel of the standard LIF detectors of DNA sequencers. APTS and its structural analogs—Teal™ and Turquoise™ dyes—are excitable with an argon laser (emission lines 488 nm and 514 nm) (H.-T. Feng, P. Li, G. Rui, J. Stray, S. Khan, S.-M. Chen, S. F. Y Li, Electrophoresis 2017, 38, 1788-1799). In this context, “the superior spectral and electrophoretic properties” would mean higher brightness (product of the absorbance at the excitation wavelength and fluorescence quantum yield), red-shifted emission, and higher electrophoretic mobility (to reveal “heavy” and slowly moving glycans, yet undetectable as APTS conjugates). The higher brightness is required not only upon excitation with 488 nm light (or Argon laser), but also with 505 nm light (solid state laser in new DNA sequencers).
The red-shifted emission of the new dyes would mean fluorescent tags having minimal interference with the APTS detection window (and different migration profile due to different structure and net electrical charge). The new dyes are needed to cross-validate or increase the precision of glycan identification. The use of a “second dye” complementary to APTS is expected to provide different selectivity profile for complex mixtures of carbohydrates. The new set of migration times based on a new fluorescent tag will enable to create new databases for glycan identification.
Labelled glycans are identified by comparison of their migration times with a standard, the so-called “LIZ 600 DNA Ladder”, which is added to the glycan sample (H.-T. Feng, P. Li, G. Rui, J. Stray, S. Khan, S.-M. Chen, S. F. Y Li, Electrophoresis 2017, 38, 1788-1799). The standard consists of several (ten to twenty) DNA oligomers labeled with a red-emitting fluorescent dye of unknown structure (FRET pair of dyes with a donor absorbing at 488 nm, and an acceptor emitting at about 600 nm). The oligomers have variable migration times covering the region where all “analytically important” APTS conjugates appear in the course of CGE-LIF. The standard DNA Ladder is detected in the red region of the emission spectrum, whereas the labeled glycan samples are detected in the green region. Both samples—mixture of labeled glycans and LIZ 600 DNA Ladder—are excited by the same laser source, thus enabling their simultaneous detection within the same run (without any cross-talk in the detection channel). However, the DNA-based standard is not an ideal marker (US20170369431A1, EP2112506 A1). The structures and shapes of DNA molecules are very different from the structures and shapes of natural glycans. Therefore, the migration parameters of the DNA-based standards “drift” (change in time) differently than these of APTS-labeled glycans. In this context, “drift” means the (long-term) changes of the migration times caused by various factors, e.g., ageing of the gel in capillaries, fluctuations in temperature, buffer concentration, etc. Therefore, up to now, the usability and reproducibility of CGE-LIF for glycan analysis is compromised (limited) by improper and imprecise alignment of migration times of the analytes. The peak of each analyte is positioned between two peaks of the standard, and if the positions of these three peaks drift not uniformly, identification becomes difficult. New fluorescent dyes capable of reductive amination are highly needed to create better internal standards based on glycan oligomers of various lengths decorated with a fluorescent tag (a red-emitting and negatively charged dye detected separately from APTS-glycan conjugates). Maltodextrin oligomers are commercially available and represent the so-called “dextran ladder” consisting of glucose (monomer, M=180), maltose (dimer, M=342), maltotriose (trimer, M=504), etc. For an “n-mer”, the molecular mass will be 180n-18(n−1)=162n+18. Dextran oligomers with average molecular masses of 1000, 5000 (ca. “31-mer”), 9000-11000 and 12000 Da are available from Sigma-Aldrich (Merck). These oligosaccharides can be labeled with APTS dye and provide the so-called “APTS-dextran ladder”. Analogously, labeling of a “dextran ladder” with another (red-emitting and negatively charged) dye will result in a new “dye-dextran ladder” usable as an internal standard for calibration of the migration times. The main challenge is to design and prepare a compact fluorescent dye (with an aromatic amino group and multiple negative charges) excitable with 488 nm or 505 nm light and emitting red light (ca. 600 nm), far away from the band-edge emission of APTS conjugates (520 nm). This would mean the dye with a large Stokes shift (separation between the absorption and emission maxima) of ca. 100 nm. These dyes are rare and have low quantum yields.
In view of the drawbacks of the fluorescent dyes of the prior art, the main objective of the present invention was to provide novel fluorescent dyes with improved properties, such as even higher electrophoretic mobility and/or higher brightness or other favorable spectroscopic characteristics, as compared to APTS. These properties are highly demanded from fluorescent tags for carbohydrate analysis based on electrokinetic separation with fluorescence detection.
This objective has been achieved according to the present invention by providing novel 9-aminoacridine and 1-aminopyrene dyes with multiple negatively charged groups according to claims 1-10, as well as by providing the carbohydrate-dye conjugates comprising these dyes according to claim 14-15. Further aspects and more specific embodiments of the invention are the subject of further claims.
The structures of the novel fluorescent dyes of the invention are selected from the group consisting of compounds of the following general Formulae A-E or protonated forms or salts thereof:
Specifically, the structures of the novel 9-aminoacridine fluorescent dyes with an additional amino group (at C-7) are selected from compounds having the following Formulae A (7,9-diaminoacridine-2-sulfonamides), B (7,9-diaminoacridine-2-sulfones) or salts (protonated forms) thereof:
The structures of the novel 1-aminopyrene fluorescent dyes are selected from compounds having either three cyanamidosulfonyl (C), or (3-hydroxyazetidinyl)sulfonamido (D), or (3-hydroxycyclobutyl)sulfonyl (E) groups in positions 3, 6 and 9, or salts (protonated forms) thereof:
The term “substituted” as used herein, generally refers to the presence of one or more substituents, in particular substituents selected from the group comprising straight or branched alkyl, in particular C1-C4 alkyl, e.g. methyl, ethyl, propyl, butyl; isoalkyl, e.g. isopropyl, isobutyl (2-methylpropyl); secondary alkyl group, e.g. sec-butyl (but-2-yl); tert-alkyl group, e.g. tert-butyl (2-methylpropyl). Additionally, the term “substituted” may refer here to alkyl groups having at least one deuterium-, fluoro-, chloro- or bromo substituent instead of hydrogen atoms, or methoxy, ethoxy, 2-(alkyloxy)ethyloxy groups (alk-OCH2CH2O), and, in a more general case, oligo(ethylenglycol) residues of the art alk(OCH2CH2)nOCH2CH2—, where alk=CH3, C2H5, C3H7, C4H10, and n=1-12.
The term “linker” as used herein, generally refers to a single covalent bond (“zero-linker”) or any divalent residue incorporating 1-20 nonhydrogen atoms selected from the group consisting of C, N, O, S and P that covalently attaches the fluorescent compounds to another entity, such as solubilizing and/or ionizable anion-providing group or a chemically reactive group. Exemplary linkers include any divalent moiety derived from an alkyl, heteroalkyl, in particular, alkyloxy group, and represented, for example, by CH2OCH2, CH2CH2O, CH2CH2OCH2CH2. Further, linkers may include any divalent moiety derived from alkylamino or dialkylamino groups; particularly derived from the structures of diethanolamine or N-alkylmonoethanolamine, such as N(CH3)CH2CH2O— and N(CH2CH2O—)2. Linkers may include in their structures difluoromethyl (CF2), alkene or alkyne moieties in any combinations, at any occurrence, linear or branched, with the length ranging from C1 to C12.
A “cleavable linker” is a linker comprises one or more “cleavable groups” that may be broken by irradiation with light (a “photocleavable linker”) or in the course of a chemical transformation, including enzymatic reaction. Exemplary enzymatically cleavable groups include natural amino acids or peptide sequences that end with a natural amino acid. Cleavage of a linker breaks at least one chemical bond and releases a (fluorescent) dye or any other “active” part of the initial assembly; e.g., a physiologically active drug, catalyst, inhibitor, acidic or basic component, quencher of the fluorescence signal.
The term “alkyl” refers to any alkyl group selected from the group comprising straight or branched alkyl, more specifically C1-C20 alkyl, C1-C12 alkyl, or C1-C6 alkyl, e.g. methyl, ethyl, propyl, butyl; isoalkyl, e.g. isopropyl, isobutyl (2-methylpropyl); secondary alkyl group, e.g. sec-butyl (but-2-yl); tert-alkyl group, e.g. tert-butyl (2-methylpropyl) etc.
The terms “aromatic heterocyclic group” or “heteroaromatic group”, as used herein, generally refer to an unsubstituted or substituted cyclic aromatic radical (residue) having from 5 to 10 ring atoms of which at least one ring atom is selected from S, O and N; the radical being joined to the rest of the molecule via any of the ring atoms. Representative, but not limiting examples are furyl, thienyl, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, quinolinyl and isoquinolinyl.
The term “groups capable of forming an active ester”, as used herein, generally refers to groups which activate a carboxyl group, making it more reactive with nucleophiles such as, but not limited to, free amino groups of peptides, polyaminoacids, polysaccharides, or analytes under such conditions that no interfering side reactions with other reactive groups of the nucleophile-carrying substance can usefully occur. Examples of such groups that form active esters include N-succinimidyl, sulfo-N-succinimidyl, 1-benzotriazolyl, and the like.
In some specific embodiments of the novel fluorescent dyes according to the present invention, the analyte-reactive group at variable positions R1, R2, R3, R4, R5, R6 in Formula A or the analyte-reactive group at variable positions R1, R2, R3, R4 in Formula B may be represented by an aromatic or heterocyclic amine, carboxylic acid, ester of the carboxylic acid (e.g., N-hydroxysuccinimidyl or another amino reactive ester); or represented by alkyl azide (CH2)nN3, alkyne (e. g., propargyl), strained cyclic alkene, strained cyclic alkyne, amino (NH2), amino-oxyalkyl (CH2)mONH2, maleimido (C4H3NO2 with a nucleophile-reactive double bond) or halogeno ketone function (COCH2X; X═Cl, Br and I), as well as halogeno amide group (NRCOCH2X, R═H, C1-C6-alkyl, X═Cl, Br, I) connected either directly or indirectly via alkandiyl —(CH2)p—, carbonyl (>CO), amido (—CONRa—), nitrogen (—NRb—), oxygen (—O—) or sulfur-containing linkers (—S—, >SO, >SO2). R, Ra, Rb are independent from each other and represent H, lower alkyl group (C1-C6), or (functionally substituted) lower alkyl group (C1-C6); n, m, p=1-8 (independent from each other).
In some other specific embodiments the aryl amino groups (NR1R2 and/or NR3R4) in Formula A or B are connected to an analyte-reactive group via (poly)methylene, poly(ethylene glycol), carbonyl, nitrogen or sulfur-containing linear or branched linkers, particularly (CH2)nCONR (R═H, low (substituted) alkyl), CO(CH2)mNR (R═H, low (substituted) alkyl), CO(CH2)pS(CH2)n, (CH2)qS(CH2)nCO, CO(CH2)rSO2(CH2)s, (CH2)tSO2(CH2)uCO, their combinations, or linked as a part of nitrogen-containing non-aromatic heterocycles (e.g., piperazines, pipecolines, oxazolines, azetidines); m, n, p, q, r, s, t, u are independent integers ranging from 0 to 12 or 1 to 12; or alternatively the aryl amino groups (NR1R2 and/or NR3R4) in Formula A or B are connected to an acyl hydrazine or alkyl hydrazine moiety indirectly, via linkers, thus comprising hydrazides (ZCONHNH2) or hydrazines (ZNHNH2), respectively, wherein Z denotes the dye residue of Formula A or B that includes aryl amino groups and linkers;
in particular, R1 and R3 may be represented by: (CH2)mCONR, CO(CH2)nNR (R═H, low (substituted) alkyl), CO(CH2)pS(CH2)n, (CH2)qS(CH2)rCO, CO(CH2)sSO2(CH2)t, (CH2)uSO2(CH2)wCO and their combinations; m, n, p, q, r, s, t, u, w are independent integers ranging from 0 to 12;
linkers may also be represented by non-aromatic O, N and S-containing heterocycles, e. g., piperazines, pipecolines, azetidines.
A further specific embodiment of the invention relates to a fluorescent dye or dye salt according to formulae A or B above, wherein carbohydrate-reactive groups, particularly hydrazine —N(R)NH2, hydroxylamine —N(R)OH or aminooxy —ONH2 groups with R being H, lower alkyl (C1-C6), heteroalkyl (e.g. CH3O(CH2CH2)nO(CH2CH2)m; n, m=1-6), alkenyl (e.g., allyl), or (per)fluoroalkyl (C1-C6) are connected to the nitrogen site N(R1)R2 in the dye of formulae A or B via all types of linkers (groups R1, R2, R3, R4, R5 or R6 in structures A and B), or linkers L in formula B.
Some further specific and preferred embodiments of the present invention are described below.
In Formula A above, NR1R2 and/or NR3R4 typically comprise or represent carbonyl-reactive groups. Preferably, R1, R2, R3 and R4 are represented by hydrogen, a primary amino group (NH2) or secondary amino group (NHR10); R10=alkyl C1-C6 or (functionally) substituted alkyl (C1-C6); linear or branched alkyl, hydroxyalkyl or perfluoroalkyl groups. Substituents R3, R4, R5 and R6 preferably comprise solubilizing and/or anion-providing groups, particularly hydroxyalkyl ((CH2)nOH), thioalkyl ((CH2)nSH), carboxyalkyl ((CH2)nCO2H), alkyl sulfonate ((CH2)nSO3H), alkyl sulfate ((CH2)nOSO3H), alkyl phosphate ((CH2)nOP(O)(OH)2) or alkyl phosphonate ((CH2)nP(O)(OH)2), wherein n is an integer ranging from 1 to 12.
Alternatively, substituents R1, R2, R3, R4, R5 and R6 may be represented by carboxylic acid residues (CH2)nCOOH, where n=1-12, and their reactive esters (CH2)nCOOR7 as nucleophile-reactive groups. R7 can be alkyl (including tert-butyl), benzyl, 9-fluorenylmethyl, polyhalogenoalkyl, CH2CN, polyhalogenophenyl (e. g., tetra- or pentafluorophenyl, pentachlorophenyl), 2- and 4-nitrophenyl, N-succinimidyl, sulfo-N-succinimidyl, 1-benzotriazolyl or other groups forming an “active” ester of a carboxylic acid. The alkyl chains (or backbones) (CH2)n may be linear or branched.
Further, the aryl amino groups (NR1R2 and/or NR3R4) in Formula A can be connected to an analyte-reactive group via (poly)methylene, polyethylene glycol, carbonyl, nitrogen or sulfur-containing linear or branched linkers, particularly (CH2)mCONR (R═H, low (substituted) alkyl), CO(CH2)mNR (R═H, low (substituted) alkyl), CO(CH2)mS(CH2)n, (CH2)mS(CH2)nCO, CO(CH2)mSO2(CH2)n, (CH2)mSO2(CH2)nCO, their combinations, or linked as a part of nitrogen-containing non-aromatic heterocycles (e.g., piperazines, pipecolines, oxazolines, azetidines); m and n are integers ranging from 0 to 12 or 1 to 12.
Alternatively, aryl amino groups (NR1R2 and/or NR3R4) in Formula A can be connected to an acyl hydrazine or alkyl hydrazine moiety indirectly, via linkers, thus comprising hydrazides (ZCONHNH2) or hydrazines (ZNHNH2), respectively. Here Z denotes the dye residue of Formula A that includes aryl amino groups and linkers. In particular, R1 and R3 may be represented by: (CH2)mCONR, CO(CH2)mNR (R═H, low (substituted) alkyl), CO(CH2)mS(CH2)n, (CH2)mS(CH2)nCO, CO(CH2)mSO2(CH2)n, (CH2)mSO2(CH2)nCO and their combinations; m and n are integers ranging from 0 to 12. Linkers may also be represented by non-aromatic O, N and S-containing heterocycles (e. g., piperazines, pipecolines, azetidines).
Further, R1, R2, R3, R4 may be represented by CH2—C6H4—NH2, COC6H4—NH2, CONHC6H4—NH2 or CSNHC6H4—NH2 with C6H4 being a 1,2-, 1,3- or 1,4-phenylene, COC5H3N—NH2 or CH2—C5H3N—NH2, with C5H3N being pyridine-2,4-diyl, pyridine-2,5-diyl, pyridine-2,6-diyl, pyridine-3,5-diyl.
The analyte-reactive group at variable positions R1, R2, R3, R4, R5, R6 may be represented by an aromatic or heterocyclic amine, carboxylic acid, ester of the carboxylic acid (e.g., N-hydroxysuccinimidyl or another amino reactive ester); or represented by alkyl azide (CH2)nN3, alkyne (propargyl), amino-oxyalkyl (CH2)nONH2, maleimido (C4H3NO2 with a nucleophile-reactive double bond) or halogeno ketone function (COCH2X; X═Cl, Br and I), as well as halogeno amide group (NRCOCH2X, R═H, C1-C6-alkyl, X═Cl, Br, I) connected either directly or indirectly via carbonyl, amido, nitrogen, oxygen or sulfur-containing linkers listed for hydrazine derivatives where n=1-12.
One especially preferred embodiment of the present invention relates to compounds of Formula A above, where the negative charges are provided by several primary phosphate groups, in particular, triple O-phosphorylated 7,9-diaminoacridine-2-sulfonamide (compound 13).
Further specific and preferred embodiments of the present invention are described by Formula B, where:
L is a divalent linker (CH2)m (m=2-6) connecting the dye core with one or more solubilizing and/or ionizable moieties X, and the moieties L and X are combined according to the formulae (CH2)mOP(O)(OH)2 and (CH2)mOH;
NR1R2 and/or NR3R4 comprise carbonyl-reactive groups. Preferably, R1, R2, R3 and R4 are represented by hydrogen, linear or branched alkyl, hydroxyalkyl or perfluoroalkyl groups. Substituents R3, R4 preferably comprise solubilizing and/or anion-providing groups, particularly hydroxyalkyl ((CH2)nOH), thioalkyl ((CH2)nSH), carboxyalkyl ((CH2)n CO2H), alkyl sulfonate ((CH2)nSO3H), alkyl sulfate ((CH2)nOSO3H), alkyl phosphate ((CH2)nOP(O)(OH)2) or alkyl phosphonate ((CH2)nP(O)(OH)2), wherein n is an integer ranging from 1 to 12.
Alternatively, substituents R1, R2, R3, R4 may be represented by carboxylic acid residues (CH2)nCOOH, where n=1-12, and their reactive esters (CH2)nCOOR7 as nucleophile-reactive groups. R7 can be alkyl (including tert-butyl), benzyl, 9-fluorenylmethyl, polyhalogenoalkyl, CH2CN, polyhalogenophenyl (e. g., tetra- or pentafluorophenyl, pentachlorophenyl), 2- and 4-nitrophenyl, N-succinimidyl, sulfo-N-succinimidyl, 1-benzotriazolyl or other groups forming an “active” ester of a carboxylic acid. The alkyl chains (CH2)n may be linear or branched.
Further, the aryl amino groups (NR1R2 and/or NR3R4) in Formula B can be connected to an analyte-reactive group via (poly)methylene, polyethylene glycol, carbonyl, nitrogen or sulfur-containing linear or branched linkers, particularly (CH2)nCONR, (CH2)mCONR (R═H, low (substituted) alkyl), CO(CH2)mS(CH2)n, (CH2)mS(CH2)nCO, CO(CH2)mSO2(CH2)n, (CH2)mSO2(CH2)nCO, their combinations, or linked as a part of nitrogen-containing non-aromatic heterocycles (e.g., azetidines, piperazines, pipecolines, oxazolines); m and n are integers ranging from 0 to 12 or 1 to 12.
Substituents R1, R2, R3, R4 in Formula B may be also represented by a primary amino group, thus comprising carbonyl-reactive aryl hydrazines, unsubstituted or substituted with solubilizing and/or anion-providing moieties, particularly: hydroxyalkyl (CH2)nOH, thioalkyl ((CH2)nSH), carboxyalkyl ((CH2)nCO2H), alkyl sulfonate ((CH2)nSO3H), alkyl sulfate ((CH2)nOSO3H), alkyl phosphate ((CH2)nOP(O)(OH)2) or phosphonate ((CH2)nP(O)(OH)2), wherein n is an integer ranging from 0 to 12 or 1 to 12.
Alternatively, aryl amino groups (NR1R2 and/or NR3R4) in Formula B can be connected to an acyl hydrazine or alkyl hydrazine moiety indirectly, via linkers, thus comprising hydrazides (ZCONHNH2) or hydrazines (ZNHNH2), respectively. Here Z denotes the dye residue of Formula B that includes aryl amino groups and linkers. In particular, R1 and R3 may be represented by: (CH2)mCONR, CO(CH2)mNR (R═H, low (substituted) alkyl), CO(CH2)mS(CH2)n, (CH2)mS(CH2)nCO, CO(CH2)mSO2(CH2)n, (CH2)mSO2(CH2)nCO and their combinations; m and n are integers ranging from 0 to 12. Linkers may also be represented by non-aromatic O, N and S-containing heterocycles (e. g., piperazines, pipecolines, azetidines).
Further, R1, R2, R3, R4 may be represented by CH2—C6H4—NH2, COC6H4—NH2, CONHC6H4—NH2 or CSNHC6H4—NH2 with C6H4 being a 1,2-, 1,3- or 1,4-phenylene, COC5H3N—NH2 or CH2—C5H3N—NH2, with C5H3N being pyridine-2,4-diyl, pyridine-2,5-diyl, pyridine-2,6-diyl, pyridine-3,5-diyl.
The analyte-reactive group at variable positions R1, R2, R3, R4 may be represented by an aromatic or heterocyclic amine, carboxylic acid, ester of the carboxylic acid (e.g., N-hydroxysuccinimidyl or another amino reactive ester); or represented by alkyl azide (CH2)nN3, alkyne (propargyl), amino-oxyalkyl (CH2)nONH2, maleimido (C4H3NO2 with a nucleophile-reactive double bond) or halogeno ketone function (COCH2X; X═Cl, Br and I), as well as halogeno amide group (NRCOCH2X, R═H, C1-C6-alkyl, X═Cl, Br, I) connected either directly or indirectly via carbonyl, amido, nitrogen, oxygen or sulfur-containing linkers listed for hydrazine derivatives where n=1-12.
In preferred embodiments, the fluorescent dye according to claim 1 of Formulae A or B above has a negative net charge q of −1; preferably −3, −5, or higher; the fluorescent dye of Formula C has a net charge z of −3, the fluorescent dye of Formulae D or E above has a net charge z of 0, −3, or −6, preferably −6; in particular in an aqueous medium at pH ranging from 7 to 13. Compounds of Formulae A-E can exist and be applied in the form of salts that involve all possible types of cations, preferably Na+, K+, Li+, NH4+, organic ammonium (e.g. tetraalkylammonium) or organic phosphonium cations.
In more specific embodiments, a fluorescent dye salt according to the present invention may comprise negatively charged N-cyanamidosulfonate and/or phosphate groups and counterions selected from inorganic or organic cations, preferably alkaline metal cations, preferably Na+, K+, Li+, ammonium cations or cations of organic ammonium and phosphonium compounds cations (such as tetraalkylammonium cations), and/or comprising a positively charged group or a charge-transfer complex formed at the nitrogen site N(R1)R2 (with R1 and R2 as defined for formulae A-E above) in the dye of formulae A-E with a counterion selected from anions of a strong mineral, organic or a Lewis acid (such as BF3).
In an especially preferred embodiment, the fluorescent dye of the general Formula A as defined above has one of the following formulae, including salts or protonated forms thereof:
In another especially preferred embodiment, the fluorescent dye of the general Formula B as defined above has one of the following formulae, including salts or protonated forms thereof:
In another especially preferred embodiment, the fluorescent dye of the general Formulae C-E as defined above has one of the following formulae, including salts or protonated forms thereof:
The novel fluorescent dyes of the present invention exhibit favorable properties justifying their use as fluorescent tags (derivatization reagents) facilitating separation of the analytes and their sensitive detection by fluorescence:
they possess either aromatic amino group (ArNH2), or hydrazine group (NRNH2, R═H, (substituted) alkyl), hydrazide (CONRNH2, R═H, (substituted) alkyl), alkoxyamino group (R′ONH2, R′=substituted alkyl, or L-linker as defined below) for efficient and “clean” (with minimal side products) reductive amination at pH˜2-5 or direct condensation with aldehydes (carbohydrates);
preferably, the aromatic amino group is primary (ArNH2), but it can also be a secondary one (ArNHR; R=(substituted) alkyl C2-C6);
multiple net electrical charges in conjugates (derivatives obtained from biomolecules and reactive dyes)—in the range of −3 to −6 at pH=7-10;
high solubility in aqueous (buffered) solutions at pH 3-10;
high molar absorptivity (extinction coefficient) providing efficient excitation with an argon ion laser (emitting at 488 and 514 nm), 488 nm laser, or 505 nm solid state laser; high brightness (the product of the fluorescence quantum yield and molar absorptivity at the excitation wavelength; e.g., 488 nm or 505 nm);
chemical stability of the dye core against reduction with reducing agents, in particular, borane-based reagents (e.g., sodium cyanoborohydride, 2-picoline borane) at pH=2-6; reactivity towards aldehydes, in particular, reducing carbohydrates and their mixtures (i.e. dextran ladder) under reductive amination conditions;
low emission at ca. 520 nm of their conjugates with aldehydes (carbohydrates) enabling to avoid spectral cross-talk, i.e. simultaneous detection, with APTS-labeled glycans;
high electrophoretic mobility of their conjugates with aldehydes (carbohydrates), outperforming corresponding APTS-labeled glycans;
easy purification resulting in high purity (>99%), as controlled by HPLC and/or electrophoresis.
Summarizing, the present invention provides new 9-aminoacridine dyes with an additional amino group (at C-2), multiple negative charges and red emission. The acridine dyes feature (functionally substituted) sulfonamide or alkylsulfone residues, as strong electron-acceptor groups. The present invention further provides yellow-emitting 1-aminopyrene dyes with six negative charges, as well as 1-aminopyrene dyes with three negatively charged N-cyanosulfonamide residues, which also have sulfonamide or alkylsulfone residues, as electron-acceptor groups providing bathochromic and bathofluoric shifts.
The usefulness of all new dyes for reductive amination and fluorescence detection of glycans is demonstrated by preparation of conjugates with carbohydrates, electrophoresis and fluorescence detection. The spectral properties of dyes and their conjugates (absorption and emission spectra, brightness, stability, reductive amination capacities, electrophoretic mobilities) have been exemplified as shown below.
The novel compounds of the present invention have small molecular size and, in preferred embodiments, a low (negative) net charge (z) at pH>7: such as z=−3 for phosphorylated 7,9-diaminoacridine-2-sulfones (Formula B), z=−3 for pyrene dyes of Formula C, z=−5 for phosphorylated 7,9-diaminoacridine-2-sulfonamides (Formula A), as well as −6 for phosphorylated pyrene dyes of the Formulae D, E. These properties (small molecular size and high negative charge) are equivalent to low mass to charge ratios (m/z), typically in the range from 130 to 199, and a small hydrodynamic radius. As a result, high electrophoretic mobilities and fast separation times can be achieved for these compounds and their conjugates with carbohydrates.
The negative charges are provided by acidic groups which can be deprotonated in basic or even neutral media. Phosphate groups are preferred for this purpose, because primary alkyl phosphates (R—OPO3H2) have pKa values for the first and the second acidic protons in the range of 1-2 and 6-7, respectively. As a consequence, one single phosphate group can introduce two negative charges in buffer solutions under basic conditions (e.g., at pH 8 and above, when one group R—OPO32— is present), provided that no other basic (proton-acceptor) group is present in the structure. To achieve the negative charge of −4, the attachment of two phosphate groups is necessary, etc. Other acidic groups, for example, N-cyanosulfonamide residues SO2NHCN are suitable for providing one negative charge.
In a broader scope, compounds of Formulae A-E decorated with additional reactive groups (see text below) are suitable for the use as fluorescent labels for natural products: amino acids, peptides, proteins, including primary and secondary antibodies, single-domain antibodies, taxanes (docetaxel, cabazitaxel, larotaxel), avidin, streptavidin and their modifications, aptamers, nucleotides, nucleic acids, toxins, lipids, carbohydrates, including 2-deoxy-2-aminoglucose and other 2-deoxy-2-aminoaminopyranosides, glycans, biotin, and other so-called “small molecules”, i.e. chemical entities having well-defined known structures with molecular masses of less than 1500 Da, e.g., jasplakinolide and its modifications.
A further aspect of the present invention relates to compounds of formulae A-E and salts thereof for use as a fluorescent label for natural products; e.g., amino acids, peptides, proteins, including primary and secondary antibodies, single-domain antibodies, avidin, streptavidin and their modifications, aptamers, nucleotides, nucleic acids, toxins, lipids, carbohydrates, including 2-deoxy-2-amino glucose and other 2-deoxy-2-aminoaminopyranosides, glycans, biotin, and other small molecules, i.e. having molecular masses of less than 1500 Da, e.g., docetaxel, cabazitaxel, larotaxel, aminophalloidin, jasplakinolide and their modifications.
The claimed compounds are suitable for and may be used as fluorescent reagents for conjugation to analytes, wherein the conjugation comprises formation of at least one covalent chemical bond or at least one molecular complex with a chemical entity or substance, such as amine, carboxylic acid, aldehyde, alcohol, aromatic compound, heterocycle, dye, amino acid, peptide, protein, carbohydrate, nucleic acid, toxin and lipid, followed by fluorescence detection, which can be used alone or combined with any other detection method (e.g., mass-spectrometric detection).
The claimed compounds are in particular suitable for use in the reductive amination and in the conjugation with reducing sugars, i.e. monomeric, oligomeric or polymeric carbohydrates possessing an aldehyde group in a free form or as hemiacetal, including glycans.
Consequently, closely related aspects of the present invention relate to this use and methods for the reductive amination of and/or conjugation with reducing sugars.
In one embodiment, a method for obtaining of dyes' conjugates with reducing sugars, in particular with a mixture of reducing mono-, di- and oligosaccharides with incremental addition of monomeric units and stepwise increasing molecular masses, (so called fluorescent “sugar ladders”) is based on a two-step procedure: 1) formation (and optionally isolation) of the (protonated) imine intermediate (Schiff's base) prepared from the fluorescent dye (8-aminopyrene-1,3,6-trisulfonic acid (APTS), the salt thereof, or any dye according to Formulae A-E and an unlabeled mixture of reducing mono-, di- and oligosaccharides with incremental addition of monomeric units and stepwise increasing molecular masses (unlabeled “sugar ladder”), 2) reduction of the said intermediate.
More specifically, said method for obtaining of dyes' conjugates with reducing sugars comprises a step 1), in which the formation of the (protonated) imine intermediate (Schiff's base) is facilitated by removal of water and high-boiling solvent from the reaction solution containing: a) APTS, the salt thereof, or any dye according to Formulae A-E, b) a reducing sugar of a mixture of reducing sugars; c) acid with pKa=2-6.
In another specific embodiment of the claimed method for obtaining of dyes' conjugates with reducing sugars a dye (APTS, the salt thereof, or any dye according to Formulae A-E), an individual reducing sugar (e.g. glucose or its oligomers) or a “sugar ladder” as defined above are dissolved in water, combined with an organic acid (e.g., 5-20 equiv. of citric, malonic, or malic acid) dissolved in DMSO, incubated at elevated temperature (25-70° C. for 0.5-2 h), followed by removal of solvents under reduced pressure (p<0.2 mbar).
In a still more specific embodiment of the above method, a dye (10 μL of 0.1 M solution in water) is mixed with a dextran ladder (1.0 mg, maltodextrin oligosaccharides—DP2 to DP15, Carbosynth) and malonic acid (10 equiv., 10 μL of 1 M solution in DMSO) followed by incubation at 40° C. for 1 h, removal of the solvents under reduced pressure (p<0.2 mbar), addition of a solution of 2-picoline-borane complex (10 equiv., 10 μL of 1 M solution in DMSO), incubation at 40° C. for 16 h and, finally, isolation of the products.
A further important aspect of the present invention relates to carbohydrate-dye conjugates comprising fluorescent dyes according to Formulae A-E, for example obtainable by the methods described above.
Typically, in said carbohydrate-dye conjugates the carbohydrate moiety is selected from the group comprising or consisting of reducing glycans, such as mannose, N-acetylglucosamine and N-acetylgalactosamine residues, galactose, fucose, glucose, maltose and its oligomers (e.g. maltotriose, maltotetraose, maltopentaose, maltohexaose, maltoheptaose, higher maltose oligomers), as well as sialic acids in various possible combinations.
In a more specific embodiment, the carbohydrate-dye conjugate is selected from the following structures:
wherein the carbohydrate moiety is selected from the group comprising or consisting of reducing glycans, such as mannose, N-acetylglucosamine and N-acetylgalactosamine residues, galactose, fucose, glucose, maltose and their oligomers (e.g. maltotriose, maltotetraose, maltopentaose, maltohexaose, maltoheptaose, higher maltose oligomers), as well as sialic acids in various possible combinations.
One preferred embodiment of this aspect of the present invention relates to compounds of Formula A above, where the negative charges are provided by several primary phosphate groups, in particular, triple O-phosphorylated 7,9-diaminoacridine-2-sulfonamide. i.e. compound 13. Their glycoconjugates emit red light and have high electrophoretic mobilities. This preferred embodiment of the present invention is in particular represented by the compounds below, where “carbohydrate” denotes reducing glycans (e.g., containing mannose, N-acetylglucosamine and N-acetylgalactosamine residues, galactose, fucose, glucose, maltose and its oligomers (e.g. maltotriose, maltotetraose, maltopentaose, maltohexaose, maltoheptaose, higher maltose oligomers), as well as sialic acids in various possible combinations).
A still further aspect of the present invention relates to a kit or composition comprising one or more of the dyes of Formulae A-E and/or one or more carbohydrate conjugates as disclosed above.
According to the state of the art, glycans may be identified by comparison of their migration times (on the electrophoretogram) against a dextran ladder standard (i.e., fluorescently labeled dextran carbohydrate oligomers differing by one glucose molecule). The dextran ladder may be run in parallel with the glycan samples, and specific glycans may then be identified by locating the time point at which they elute relative to the dextran ladder. Known retention times for specific glycan structures and molecular weights may previously be recorded in an empirically-derived database, which may then be searched. An analysis software may then compare retention times (relative to the dextran ladder) of peaks from an electrophoretogram of unknown glycans with the retention time database to identify the glycans.
Thus, a further aspect of the invention relates to a method of characterizing a sample containing one or more glycans, the method comprising:
a) providing a sample containing one or more glycans (conjugated with a fluorescent dye “A”) as analytes of unknown structure and quantity (concentration) and a known quantity of a fluorescent reference glycan standard, wherein the reference glycan standard is labeled with a dye (“B”) according to Formulae A-E above;
b) contacting (e.g., mixing, co-injecting, etc.) the sample with a dye “B” according to Formulae A-E above conjugated with known (reference) glycans that is different from the dye “A” (fluorescent dye conjugated with one or more unknown glycans) used in step (a);
c) separating the sample by electrophoresis or HPLC;
d) selective (separate) detection of the analytes and reference glycans due to different emission signatures of dyes “A” and “B” and
e) quantifying at least one glycan in the sample relative to the reference glycan standard.
The fluorescent dye “A” may be any dye suitable for conjugation with glycans, in particular any fluorescent dye commonly used for this purpose including ATPS, and may also include a compound of formulae A-E above, provided it is not identical with the compound used as dye “B” of the reference standard used in this method.
A still further aspect of the present invention relates to the compounds according to Formulae A-E or the carbohydrate-dye conjugates comprising the same for the use for spectral calibration of a fluorescence detector, in particular a detector for detection of laser induced fluorescence (LIF) or capillary gel electrophoresis with detection by laser induced fluorescence (CGE-LIF).
The present invention further relates to a method for spectral calibration of a fluorescence detector which comprises injecting a solution containing 2 or more fluorescent dyes according to Formulae A-E above or carbohydrate-dye conjugates comprising the same into an electrophoresis device followed by separation and detection, in particular multichannel detection, of light emitted by each component of the dye mixture by a CCD camera, diodes array detector or similar device providing the spectral resolution and separate detection of the emitted light.
General synthesis and characterization of the novel 7,9-aminoacridine dyes of the invention and their precursors
The generic structure of 7,9-diaminoacridines with electron-withdrawing group (EWG) in 2-position exemplified by sulfonamides (Formula A) and sulfones (Formula B) are shown above. Model 7,9-diaminoacridines (6-11) with a strong electron withdrawing group (EWG) in 2-position and ω-hydroxyalkyl substituents were prepared and applied in reductive amination of glucose (
After establishing the applicability of 2,9-diaminoacridines for labeling and fluorescence detection of reducing sugars, we decorated compounds 7 and 9 with two and three primary phosphate groups, respectively (see structures 12 and 13 in
The key features required for the superior fluorescent tags applicable in the reductive amination and C(G)E-LIF of glycans can be summarized as follows: an amino group with relatively low basicity (e.g., aromatic, RONH2) providing efficient reductive amination at pH˜ 3; the net charge in the range of −3 . . . -6 at pH˜8 (pH of the buffer solution in CE) enabling high electrophoretic mobility; solubility in aqueous buffers and stability against reduction with boranes or borohydrides within a wide range of pH (3-8); efficient “green” excitation (high absorption at 488 nm, ε488, or 505 nm, ε505); brightness (product of the fluorescence quantum yield and ε488 or ε505); minimal cross-talk with the “APTS channel” in the detector (low emission of conjugates at 520 nm). These properties follow from the conditions of the reductive amination (
Previously, yellow-orange emitting 7-aminoacridone-2-sulfonamides for fluorescence detection of glycans were reported ((PCT/EP2019/051396; e.g.VBDP in
The principles of molecular design outlined above are based on the combination of at least one electron-donor residue (e.g., an amino group) and one electron-acceptor group (e.g., sulfonamide) attached to the acridone system and interacting with each other (and the acridone scaffold) in a “push-pull” fashion. These principles can be applied to 9-aminoacridines to obtain dyes with red shifts in absorption and emission bands. Skripkina et al. reported that absorption bands of 9-aminoacridine-2-sulfonamides with electron-donating methoxy group in 7-position are red-shifted in comparison to the corresponding acridone (V. T. Skripkina, N. N. Dykhanov, V. P. Maksimets, L. D. Shcherbak, Chem. Heterocycl. Compd. 1971, 7, 107-109). A. Szymanska et al. compared 9-aminoacridine and acridone chromophores and reported the emission of acridines to be red-shifted (A. Szymanska, W. Wiczk, L. Lankiewicz, Chem. Heterocycl. Compd. 2000, 36, 801-808). P. Yang et al. described a chromophore based on 9-aminoacridine which showed longer absorption and fluorescence wavelengths than the corresponding acridone (P. Yang, Q. Yang, X. Qian, L. Tong, X. Li, J. Photochem. Photobiol. B, Biol. 2006, 84, 221-226).
The amino group at C-9 in acridine can participate in reductive amination (G. Gellerman, V. Gaisin, T. Brider, Tetrahedron Lett. 2010, 51, 836-839), though it is less reactive than the amino group attached to C-7. In order to exclude any competition between two amino groups (at C-7 and C-9), we decided to shield the amino group in 9-position by alkylation (see E. W. Baxter, A. B. Reitz, in Organic Reactions, 2002, pp. 1-125, doi:10.1002/0471264180.or059.01). The monoalkylation is preferred, since 9-(monoalkylamino)acridines were reported to be more hydrolytically stable than tertiary amines with a 9-(dialkylamino) group (J. R. Goodell, B. Svensson, D. M. Ferguson, J. Chem. Inf Model. 2006, 46, 876-883). The spectral properties of an acridine system and the reactivity of an amino group at C-7 are sensitive to the nature of an acceptor group in 2-position. The electron-acceptor properties of the substituents can be assessed and compared on the basis of their σ-constants in the Hammett equation (Table 1). The present inventors incorporated the strong electron-acceptor groups—cyano, sulfone and sulfonamide—into 7,9-diaminoacridine scaffold. The sulfone and sulfonamide groups are preferred, as they allow to introduce a hydroxyl-substituted side chain, which can be easily phosphorylated. As it was already mentioned above, first acridines 6-11 without phosphate groups (see
Synthesis of Model Compounds
The universal acridine precursor 18 was prepared in four steps in a good overall yield starting from 5-nitro-N-phenylanthranilic acid 14 (
2-Amino-7-cyano-9-(6-hydroxyhexyl)aminoacridine (6) with a cyano group at 7-position was synthesized in three steps to evaluate the suitability of 2-aminoacridines with a strong acceptor at C-7 for fluorescent labelling of reducing saccharides (
Acridine 7 with an electron-withdrawing sulfone substituent at C-7 was prepared in four steps (
Next, the synthesis of acridine-7-sulfonamides 8 and 9 bearing a primary and a secondary amino group in 9-position, respectively, was explored (
The inventors used tertiary sulfonamides as acceptor groups. Primary and secondary sulfonamides were avoided, because the acidity of SO2NH2 and SO2NHR groups in acridines might be high enough, which would lead to partial deprotonation at pH˜ 8, and this could broaden the peaks (bands) in electrophoresis. In an attempt to prepare 3-hyrdoxyazetidine derivative 31 (
Compounds 7-11 have a free amine group intended for the reductive amination of glycans (see next section). Before performing this reaction, the inventors measured the absorption and fluorescent spectra of the free dyes in aqueous buffer (25 mM HEPES, pH 8) and methanol. The aqueous buffer (pH 8) is highly relevant for the analysis of glycan conjugates using gel electrophoresis. The emission was observed from all dyes 7-11, and the spectral properties are given in Table 2. The absorption spectra of compounds 7-11 in aqueous buffer feature a broad band centered at λ=455-460 nm. When excited in this low-energy absorption band, an intense fluorescence centered at λ=603-626 nm was observed with quantum yields of 2-5%. Dyes 7-11 have particularly large Stokes shifts (156-166 nm) in aqueous buffer, and large Stokes shifts are associated with low emission efficiencies. Changing the solvent to methanol resulted in smaller Stokes shifts of 111-120 nm and larger quantum yields of 17-25%. Comparing sulfonamides (9, 10) with the structurally related alkyl sulfone 7, no significant difference in the position of absorption and emission bands was observed. The bathochromic shift was observed in absorption and fluorescence spectra, when the degree of alkylation of the amino group at C-9 increased. Compared to APTS (emission maximum at 503 nm in aqueous solutions), a remarkable red-shift of 100-113 nm was achieved. The solubility in aqueous media, orange-red emission, and a free amine group on their core structure are important features enabling the use of compounds 7-11 as fluorescent tags for labeling of glycans.
a25 mM HEPES pH 8.0;
bMeOH with 0.1% TEA;
cabsolute values of the fluorescence quantum yields.
Synthesis of Glucose Conjugates
To study the reaction of the dyes (6-7, 9-11) with glycans under conditions of reductive amination, the labeling of glucose was explored (
Spectroscopic Properties of Glucose Conjugates
The photophysical properties (absorption/emission maxima and quantum yields) of glucose conjugates are summarized in Table 3. In aqueous buffer, their absorption maxima are found at about 470 nm and provide a good match to 488 nm laser. They conjugates with glucose emit orange-red light (with emission maxima at 610-630 nm). The absolute values of the fluorescence quantum yields are 3-4%. Conjugation with glucose results in bathochromic and/or bathofluoric shifts. For example, the absorption and emission maxima of glycosylated sulfone 7-Glc are red-shifted by 18 nm and 12 nm, respectively (in aqueous solutions). In the case of sulfonamides (9-Glc to 11-Glc), glycosylation does not shift the emission maximum to the red region, but results in a bathochromic shift of 11-13 nm. The observed bathochromic shifts can be explained by the stronger electron-donor effect of N-alkyl groups vs. the primary amino group (Table 1). The orange-red emission of the acridine dyes conjugated with glucose is a remarkable feature, as their glycan conjugates (with emission maxima well beyond 600 nm) would have no-cross-talk with the APTS detection window of the standard DNA sequencing equipment (due to negligible emission at 520 nm). Acridines 7 and 9, as stable and more synthetically available compounds, were chosen for further development (phosphorylation).
a25 mM HEPES pH 8.0;
bMeOH with 0.1% TEA;
cabsolute values of the fluorescence quantum yields.
Synthesis and Properties of Phosphorylated Acridines
The residues with terminal hydroxyl groups, in particular 3-hydroxypropyl substituents, enable further modifications of dyes 6-11. For example, decoration with a primary phosphate group increases polarity, makes the dye hydrophilic and water-soluble, and brings a double negative charge (q=−2) in the range of pH (8.0-8.3) recommended for electrophoresis. At pH>8, fluorescent dyes with primary phosphate groups exist in fully ionized forms and move in electric field as sharp single bands.
The phosphorylated analog of diol 7 was prepared according to the route given in
In a similar fashion, acridine 30 with N,N-di(2-hydroxyethyl)sulfonamido group (see
To prove the applicability of phosphorylated acridines 12 and 13 as new reagents and fluorescent tags for reductive amination and electrophoretic detection of glycans, the inventors prepared their conjugates with glucose, maltotriose and maltoheptaose (
a25 mM HEPES pH 8.0;
bMeOH with 0.1% TEA;
cabsolute values of the fluorescence quantum yields.
The structures (
aRelative mobility units (RMU) were calculated from the cathodal edge of APTS band in the gel.
bAssuming protonation of acridine moiety at pH 8.3.
Compound 13 was tested with a partially hydrolyzed dextran ladder to demonstrate its feasibility in complex carbohydrate analysis (
General synthesis and characterization of the novel 1-aminopyrene dyes of the invention and precursors
The present invention provides novel aminopyrenes of general formulae C, D and E above as fluorescent dyes decorated with the negatively charged (−1) cyanamidosulfonyl groups (C) or (functionally substituted) hydroxyl groups attached to four-membered rings—azetidinyl (D) or cyclobutyl (E). The dyes emit yellow (C) or orange light (D, E). The hydroxyl groups in structures D and E (if R12═H) may be transformed into various functional derivatives, in particular, to primary phosphate residues. As an example of compounds represented by structure C, the inventors obtained 8-amino-1,3,6-tris[(cyanamido)sulfonyl]pyrene (40,
aabsolute values of the fluorescence quantum yields (if not stated otherwise);
bdata from ref. [Sharett, Z.; Gamsey, S.; Hirayama, L.; Vilozny, B.; Suri, J. T.; Wessling, R. A.; Singaram; B. Org. Biomol. Chem. 2009, 7, 1461-1470], abs. measured in HO, emission—in aq. phosphate buffer at pH =7.4;
cconjugate with maltohexaose, data from ref. [Evangelista, R. A.; Liu, M.-S.; Chen, F.-T. A. Anal. Chern. 1995, 67, 2239 - 2245];
dan absolute value measured for APTS-glucose conjugate in this study;
eas tris-triethylammonium salt;
faqueous EtN—H2CO3 buffer, pH 8.
Except higher brightness and detection sensitivity, 8-(R-amino)-1,3,6-tri[(cyanamido)sulfonyl]pyrenes (R═H, or carbohydrate residues, as in the left lane of
In order to increase the bathofluoric shift even further, and improve separation between the emission spectra of APTS and new dyes, the inventors designed 1,6,8-tris[(3-hydroxy-trans cis-cyclobutyl)sulfonyl]-pyrene-3-amines (
This indicates that they are much more powerful acceptors than (ionized) sulfonic acid residues with σm=0.05 and σp=0.09 according to H. Zollinger and C. Wittwer, Helv. Chim. Acta. 1953, 36, 1711-1722. The larger values for SO3− (σm=0.30 and σp=0.35) are mentioned by C. Hansch, A. Leo, R. W. Taft, Chem. Rev. 1991, 91, 165-195, but these are solely based on a private communication of Viktor Palm.
1-Aminopyrenes of general formulae E possess (functionally substituted) cis- or trans-(3-hydroxycyclobutyl)sulfonyl residues. Their synthesis is exemplified in
The dyes in Table 6 form two groups. The first group includes compounds with a primary amino group: APTS, 8-amino-1,3,6-tri[(cyanamido)sulfonyl]pyrene (40), sulfonamide 51, and O-phosphorylated sulfonamide 52. The second group includes dyes with N-alkylamino groups: APTS-G6, 40-G, and 52-G. Compounds of the second group are represented by the products formed in the course of reductive amination (
The following Examples illustrate the present invention in more detail.
General Materials and Methods
All commercially available chemicals (Acros, Aldrich, Fluka, Merck, Alfa Aesar, TCI) were used as received. The solvents had the purity “pro analysis”. For photophysical measurements solvents of spectrophotometric grade were used. Anhydrous solvents were stored over molecular sieves. Deuterated solvents were purchased from Deutero GmbH (CDCl3, CD3OD, D2O, DMF-d7, DMSO-d6, TFA-d). Reactions at “0° C.” were carried out using an ice-bath.
TLC. Normal phase TLC was performed on silica gel 60 F254 (Merck Millipore). Compounds were detected by exposing TLC plates to UV-light (254 or 366 nm).
Analytical HPLC. Analytical HPLC was performed on a Knauer Azura liquid chromatography system with a binary P 6.1 L pump (Article No. EPH35, Knauer), UV diode array detector DAD 6.1 L (Article No. ADC11, Knauer), an injection valve with a 20 μL loop and two electrical switching valves V 2.1 S with 6-port multiposition valve head (Article No. EWA10, Knauer). The UV detection was carried out with double wavelength pattern at wavelength channel 1 of 254 nm and wavelength channel 2 of 350 nm. The column temperature was not standardized, but remained at around 25° C.
Analytical columns: Knauer Eurospher II 100-5 C18, 5 m, 150×4 mm (if not stated otherwise), or Knauer Eurospher II 100-5 C18A, 5 m, 150×4 mm, or Knauer Eurospher II 100-10 C18A, m, 150×4 mm, or Interchim Uptisphere Strategy C18-HQ, 10 μm, 250×4.6 mm.
Flow rate: 1.2 mL/min.
Phase A: water+0.1% v/v trifluoroacetic acid (TFA).
Phase B: MeCN+0.1% v/v TFA.
Method 20-100: 20B (3 min); 20-100B (12 min).
Method 5-50: 5B (3 min); 5-50B (12 min); 50-100B (3 min).
For isolation and purification of phosphorylated dyes, acetonitrile (phase B)—aqueous systems containing 0.05 M of TEAB buffer (phase A, pH=8; self-prepared from 1 M aq. Et3N and CO2 gas obtained by evaporation of solid CO2).
Method TEAB-0-25: OB (3 min); 0-25B (12 min); 25-100B (3 min).
Method TEAB-0-40: OB (3 min); 0-40B (12 min); 40-100B (3 min).
FC. Flash chromatography was performed on an automated Biotage Isolera One or Interchim puriFlash™ flash purification system using the cartridges and solvent gradients indicated in the text.
MS. Mass spectra with ESI Ion source were recorded by J. Bienert (Chemical Facility, Max Planck Institute for Biophysical Chemistry, Göttingen) using a Varian 500 MS (Agilent). High resolution mass spectra were obtained on a Bruker maXis (ESI-QTOF-HRMS) or Bruker Autoflex Speed (MALDI-TOF HRMS) spectrometer by the team of Dr. H. Frauendorf (Facility of Mass Spectrometry, Georg-August-Universitat Gottingen).
NMR. NMR spectra were recorded on an Agilent 400MR DD2 spectrometer. All spectra are referenced to tetrametylsilane as an internal standard (6=0.00 ppm) using the signals of the residual protons of CHCl3 (7.26 ppm) in CDCl3, CHD2OD (3.31 ppm) in CD3OD, CHD2COCD3 (2.05 ppm) in (CD3)2CO or DMSO-d5 in DMSO-d6. Multiplicities of the signals are described as follows: s=singlet, br. s=broad singlet, d=doublet, t=triplet, q=quartet, m=multiplet. Coupling constants J are given in Hz. For 13C-signals, which were revealed by indirect detection by HSQC, only resonances of the carbon atoms linked to H-atoms were recorded.
UV-Vis and fluorescence. Absorption spectra was recorded on a double-beam UV-Vis spectrophotometer (Varian, series 4000). Measurements were performed in 1-cm quartz cells or UV-Vis disposable cuvettes (BRAND semi-micro), and in air-equilibrated solutions at ambient temperature (24-25° C.). Emission spectra and fluorescence quantum yield were obtained on a Quantaurus-QY Absolute PL quantum yield spectrometer C11347 (Quantaurus QY) or on a Cary Eclipse fluorescence spectrometer (Varian). Emission and UV-Vis scan spectra were recorded using following parameters: average time 0.1 s; data interval 1 nm; scan rate 600 nm/min; with base line correction.
Gel electrophoresis. The gel contained 50 mL of 20% of acrylamide, which was made up in the standard TBE buffer (89 mM Tris, 89 mM borate, 2 mM EDTA) containing 7 M urea. Polymerization was catalyzed by the addition of 162.5 μL of a ammoniumpersulfate (APS, 25 wt. % solution in water) and 43.8 μL of N,N,N′,N′-tetramethylethyleendiamine (TEMED). The gels were of the 8- or 17-well format (width 20 cm) with 30 cm well-to-read length and 0.75 mm thickness. The running buffer was 89 mM Tris-borate pH 8.3 containing 2 mM EDTA. Electrophoresis was performed at a constant power of 35 W (Consort EV3330) at ambient temperature with forced air cooling, the front glass plate was equipped with an external aluminium plate. After pre-running the gel for 30 min, the wells were thoroughly rinsed with the TBE buffer, and appropriate volumes (30-50 μL, ca. 50% formamide) of the samples were loaded. Usually one gel lane was skipped between each two samples, to avoid cross-contamination and to ease the lane tracking process. The electrophoresis voltage during separation was 1700-2200 V and the analysis was run until APTS reached the bottom of the gel (1.5-2 h). The fluorescence of APTS- and acridine derivatized carbohydrates was readily resolved in a UV viewing cabinet (254/365 nm) equipped with a digital camera or using Amersham Imager 600.
2-Nitroacridone was synthesized according to the literature (P. Graves and J. A. Smith. “Fluorogenic peptides and their method of production.” US 2011/0039289 A1, Mar. 14, 2008). 1H NMR (400 MHz, DMSO-d6): δ=12.33 (s, 1H), 8.95 (d, J=2.7 Hz, 1H), 8.45 (dd, J=9.4, 2.7 Hz, 1H), 8.22 (dd, J=8.2, 1.2 Hz, 1H), 7.80 (ddd, J=8.2, 7.0, 1.6 Hz, 1H), 7.65 (d, J=9.4 Hz, 1H), 7.58 (d, J=8.2 Hz, 1H), 7.36 (ddd, J=8.2, 7.0, 0.8 Hz, 1H) ppm.
2-Bromo-7-nitroacridone was synthesized according to the literature (A. Kliegl, L. Schaible, Chem. Ber. 1957, 90, 60-65.). 1H NMR (400 MHz, DMSO-d6): δ=12.47 (s, 1H), 8.92 (d, J=2.7 Hz, 1H), 8.46 (dd, J=9.2, 2.7 Hz, 1H), 8.27 (d, J=2.3 Hz, 1H), 7.93 (dd, J=8.6, 2.3 Hz, 1H), 7.65 (d, J=9.2 Hz, 1H), 7.54 (d, J=8.6 Hz, 1H) ppm.
2-Bromo-9-chloro-7-nitroacridine was synthesized according to the literature (K. Singh, G. Singh, Indian J. Pharm. 1952, 14, 47-49.). TLC (SiO2): Rf=0.4 (DCM/MeOH 20:0.05). 1H NMR (400 MHz, CDCl3): δ=9.41 (d, J=2.7 Hz, 1H), 8.64 (d, J=2.0 Hz, 1H), 8.53 (dd, J=9.4, 2.7 Hz, 1H), 8.33 (d, J=9.4 Hz, 1H), 8.13 (d, J=9.0 Hz, 1H), 7.96 (dd, J=9.0, 2.0 Hz, 1H) ppm.
A mixture of 7-bromo-9-chloro-2-nitroacridine (76 mg, 225 μmol) and phenol (1 g) was stirred at 100° C. for 1.5 hours under Ar. The reaction mixture was allowed to cool down to rt, diluted with DCM and washed with 0.1 M NaOH to remove phenol. The organic phase was further washed with brine (until pH became neutral), dried (Na2SO4), and the solvent was removed in vacuo to give a yellow solid (85 mg, 95%). TLC (SiO2): Rf=0.35 (DCM/MeOH 20:0.05). 1H NMR (400 MHz, CDCl3): δ=9.05 (d, J=2.0 Hz, 1H), 8.50 (dd, J=9.4, 2.3 Hz, 1H), 8.34 (dd, J=9.4, 0.8 Hz, 1H), 8.27 (d, J=1.6 Hz, 1H), 8.15 (d, J=9.4 Hz, 1H), 7.92 (dd, J=9.4, 2.3 Hz, 1H), 7.32-7.38 (m, 2H), 7.12-7.19 (m, 1H), 6.86-6.91 (m, 2H) ppm. 11C NMR (101 MHz, CDCl3): δ=159.2, 157.3, 151.0, 150.9, 145.2, 136.3, 131.9, 131.7, 130.4, 124.9, 123.8, 123.7, 121.6, 121.6, 120.8, 118.9, 115.7 ppm. HRMS: m/z 395.0022 ([M+H]+) calculated for C19H12BrN2O3+: 395.0026 (Δ1.0 ppm).
A mixture of 7-bromo-2-nitro-9-phenoxyacridine (85 mg, 215 μmol) and 6-amino-1-hexanol (50 mg, 430 μmol) in dry DMF (5 mL) was stirred at rt for 1 hour under Ar. The reaction mixture was diluted with DCM (50 mL) and washed with 0.1 M NaOH to remove phenol. The organic phase was further washed with brine (until pH became neutral), dried (Na2SO4), and the solvent was removed in vacuo to give a red-orange powder (85 mg, 95%). TLC (SiO2): Rf=0.19 (DCM/MeOH 20:1), Rf=0.39 (DCM/MeOH 20:2). HPLC (20-100, Knauer Eurospher II 100-10 C18A): tR=8.7 min. ESI-MS: m/z 418.2 [M+H]+. 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.22-9.72 (m, 1H), 8.60-8.84 (m, 1H), 8.71 (dd, J=9.4, 2.3 Hz, 1H), 8.15 (dd, J=9.0, 2.0 Hz, 1H), 7.91 (d, J=9.4 Hz, 1H), 7.77 (d, J=9.0 Hz, 1H), 4.14-4.20 (m, 2H), 3.56-3.61 (m, 2H), 1.99-2.18 (m, 2H), 1.57-1.67 (m, 4H), 1.47-1.57 (m, 2H) ppm.
Compound 19 (127 mg, 304 μmol), Zn(CN)2 (71 mg, 608 μmol) and Pd(PPh3)4 (35 mg, 30 μmol) were placed in a heat dried Schlenk tube filled with Ar, which was evacuated-backfilled with Ar (3×). DMF (2.5 mL) was added and the reaction mixture was immediately heated up to 100° C. After 30 min of stirring at the same temperature, the reaction mixture was allowed to cool down to rt, diluted with DCM, washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM/MeOH with 0.5-5% MeOH gradient) to give a red solid (96 mg, 87%). TLC (SiO2): Rf=0.42 (DCM/MeOH 10:1). HPLC (20-100, Knauer Eurospher II 100-10 C18A): tR=7.0 min. ESI-MS: m/z 365.2 [M+H]+. 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.26-9.72 (m, 1H), 8.81-9.08 (m, 1H), 8.75 (dd, J=9.4, 2.0 Hz, 1H), 8.23 (dd, J=9.0, 1.6 Hz, 1H), 7.85-7.98 (m, 2H), 4.16-4.26 (m, 2H), 3.54-3.63 (m, 2H), 1.98-2.22 (m, 2H), 1.57-1.72 (m, 4H), 1.48-1.56 (m, 2H) ppm.
Compound 20 (64 mg, 176 μmol) and SnCl2×2 H2O (199 mg, 880 μmol) were placed in a Schlenk flask, which was evacuated-backfilled with Ar. Absolute EtOH (0.5 mL) was added and the reaction mixture was immediately heated up to 70° C. After 15 min of stirring at the same temperature, the reaction mixture was allowed to cool down to rt, diluted with 18 mL of 0.1% aq. TFA and purified by FC (C18, 30C18AQ-F0025 cartridge, H2O/ACN (with 0.1% TFA) with 0-50% ACN gradient). Good fractions were pooled, concentrated in vacuo, and the excess of TFA was removed by filtration through C18 column using H2O-ACN as eluents. The resulting orange filtrate was diluted with H2O and lyophilized to give a red-orange powder (48 mg, 48%, TFA salt). HPLC (Knauer Eurospher II 100-10 C18A): tR=4.8 min (20-100); tR=10.7 min (5-50). ESI-MS: m/z 335.4 [M+H]+. HRMS: m/z 335.1867 ([M+H]+) calculated for C20H23N4O+: 335.1866 (Δ0.3 ppm). 1H NMR (400 MHz, D2O): δ=8.29 (s, 1H), 7.82 (br d, J=8.6 Hz, 1H), 7.47 (d, J=9.0 Hz, 1H), 7.32-7.42 (m, 2H), 7.10 (s, 1H), 3.81 (br dd, J=7.4, 7.0 Hz, 2H), 3.56 (dd, J=6.7, 6.3 Hz, 2H), 1.69-1.89 (m, 2H), 1.46-1.60 (m, 2H), 1.28-1.45 (m, 4H) ppm. The following signals were visible in the 13C NMR (100 MHz, D2O/ACN-d3, HSQC) spectra of 6: 6=134.3 (CH), 124.8, 120.1 (CH), 119.7 (CH), 118.7, 61.6 (CH2), 48.9 (CH2), 31.3 (CH2), 29.0 (CH2), 25.8 (CH2), 24.8 (CH2) ppm. 19F NMR (376 MHz, D2O): δ=−75.53 ppm.
A mixture of 7-bromo-2-nitro-9-phenoxyacridine (500 mg, 1.27 mmol) and 3-amino-1-propanol (191 mg, 2.54 mmol) in dry DMF (15 mL) was stirred at rt for 1 hour under Ar. The reaction mixture was diluted with DCM-MeOH (10:1, 500 mL) and washed with 0.1 M NaOH to remove phenol. MeOH was added to the organic phase whenever precipitates were formed. The organic phase was further washed with brine (until pH became neutral), dried (Na2SO4), and the solvent was removed in vacuo to give a red powder (440 mg, 92%). TLC (SiO2): Rf=0.18 (DCM/MeOH 20:1); Rf=0.46 (DCM/MeOH 10:1); Rf=0.55 (DCM/MeOH/H2O 90:10:1). HPLC (20-100): tR=7.2 min; λmax=442, 423, 363, 313, 271, 251 nm. ESI-MS: m/z 376.0 [M+H]+. HRMS: m/z 376.0291 ([M+H]+) calculated for C16H15BrN3O3: 376.0291 (Δ0.0 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.45 (d, J=2.0 Hz, 1H), 8.64-8.75 (m, 2H), 8.13 (dd, J=9.0, 2.0 Hz, 1H), 7.92 (d, J=9.0 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H), 4.39 (t, J=6.6 Hz, 2H), 3.91 (t, J=5.9, 5.5 Hz, 2H), 2.23 (quin., J=6.6, 5.9, 5.5 Hz, 2H) ppm.
Compound 21 (50 mg, 133 μmol), Pd2(dba)3 (7.4 mg, 8 μmol) and Xantphos (8.9 mg, 15 μmol) were placed in a heat dried Schlenk tube filled with Ar, which was evacuated-backfilled with Ar (3×). DMF (1.3 mL), DIPEA (46 μL, 266 μmol) and 3-mercapto-1-propanol (15 mg, 160 μmol) were added and the reaction mixture was immediately heated up to 100° C. After 1 h of stirring at the same temperature, the reaction mixture was allowed to cool down to rt, diluted with DCM-MeOH (10:1), washed with 10% aq. Na2SO3— aq. sat. NaHCO3 (1:1) and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM/MeOH with 0-15% MeOH gradient) to give a dark-red solid (46 mg, 89%). TLC (SiO2): Rf=0.24 (DCM/MeOH 10:1); Rf=0.3 (DCM/MeOH/H2O 90:10:1). HPLC: tR=7.0 min (20-100); tR=12.1 min (5-50); λmax=442, 345, 273 nm. ESI-MS: m/z 388.0 [M+H]+. HRMS: m/z 388.1327 ([M+H]+) calculated for C19H22N3O4S+: 388.1326 (Δ0.3 ppm). 1H NMR (400 MHz, CDCl3/MeOD-d3 7:3): δ=9.29 (d, J=2.3 Hz, 1H), 8.26 (dd, J=9.4, 2.3 Hz, 1H), 7.99 (d, J=2.0 Hz, 1H), 7.80 (d, J=9.4 Hz, 1H), 7.76 (d, J=9.0 Hz, 1H), 7.61 (dd, J=9.0, 2.0 Hz, 1H), 4.19 (t, J=6.3, 5.9 Hz, 2H), 3.93 (t, J=5.5, 5.1 Hz, 2H), 3.69 (t, J=5.9 Hz, 2H), 3.10 (t, J=7.4, 7.0 Hz, 2H), 2.04-2.11 (m, 2H), 1.82-1.97 (m, 2H) ppm.
Compound 22 (110 mg, 284 μmol) was suspended in H2O (6 mL). Oxone (166 mg, 270 μmol) was added in small portions. The suspension changed from red to yellow color. After 30 min of stirring at rt, the reaction mixture was diluted with 10% aq. Na2SO3— aq. sat. NaHCO3 (1:1), and the product was extracted into EtOAc (containing small amounts of MeOH). The organic phase was washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, DCM/MeOH/H2O 90:10:1) to give a light-orange solid (60 mg, 50%). TLC (SiO2): Rf=0.3 (DCM/MeOH/H2O 90:10:1); Rf=0.1 (DCM/MeOH 20:1). HPLC: tR=10.3 min (5-50); λmax=426, 408, 357, 303, 266 nm. ESI-MS: m/z 420.2 [M+H]+. HRMS: m/z 420.1227 ([M+H]+) calculated for C19H22N3O6S+: 420.1224 (Δ0.7 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.39-9.57 (m, 1H), 9.04 (d, J=1.6 Hz, 1H), 8.76 (dd, J=9.4, 1.6 Hz, 1H), 8.43 (dd, J=9.0, 1.6 Hz, 1H), 7.99 (d, J=9.0 Hz, 1H), 7.95 (d, J=9.4 Hz, 1H), 4.33-4.53 (m, 2H), 3.86-3.99 (m, 2H), 3.63 (t, J=6.3 Hz, 2H), 3.39-3.47 (m, 2H), 2.26 (quin., J=6.7, 6.3, 5.9, 5.5 Hz, 2H), 1.88-1.98 (m, 2H) ppm.
Compound 23 (15 mg, 36 μmol) was dissolved in MeOH (10 mL) and AcOH (10 μL) under Ar. A 10% Pd/C catalyst (7 mg) was added, and hydrogen atmosphere was applied. After 1 hour of stirring at rt, orange fluorescent solution was filtered through a pad of Celite, and concentrated in vacuo. The residue was dissolved in 10 mL of H2O and purified by FC (C18, 30C18AQ-F0025 cartridge, ACN/10 mM TEAAc pH 7.0) to give a red solid (3.4 mg, 22%, AcOH salt). HPLC: tR=9.0 min (5-50); λmax=428, 408, 301, 273, 227 nm. HRMS: m/z 390.1488 ([M+H]+) calculated for C19H24N3O4S+: 390.1482 (Δ1.5 ppm). 1H NMR (400 MHz, D2O/MeCN-d3 6:1): δ=8.69 (d, J=2.0 Hz, 1H), 8.07 (dd, J=9.0, 1.6 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H), 7.56 (d, J=9.0 Hz, 1H), 7.45 (dd, J=9.0, 2.0 Hz, 1H), 7.24 (d, J=1.6 Hz, 1H), 4.09 (t, J=7.0 Hz, 2H), 3.91 (t, J=5.9 Hz, 2H), 3.73 (t, J=6.3 Hz, 2H), 3.51-3.63 (m, 2H), 2.17 (quin, J=6.3 Hz, 2H), 2.00-2.07 (m, 2H), 1.99 (s, AcOH) ppm.
A mixture of 2-bromo-7-nitro-9-phenoxyacridine (100 mg, 253 μmol) and 25% aq. NH3 (75 μL, 1 mmol) in DMF (5 mL) was stirred at rt for 1 hour. The reaction mixture was diluted with DCM-MeOH (10:1) and washed with brine (until pH became neutral, MeOH was added to the organic phase whenever precipitates were formed), dried (Na2SO4) and concentrated in vacuo. The red residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM—DCM/MeOH/H2O 90:10:1) to give a red solid (67 mg, 83%). HPLC: tR=7.2 min (20-100); λmax=435, 415, 357, 311, 265, 250 nm. ESI-MS: m/z 318.1 [M+H]+. 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.64 (d, J=2.3 Hz, 1H), 8.82 (d, J=2.0 Hz, 1H), 8.72 (dd, J=9.4, 2.3 Hz, 1H), 8.17 (dd, J=9.0, 2.0 Hz, 1H), 7.96 (d, J=9.4 Hz, 1H), 7.81 (d, J=9.0 Hz, 1H) ppm. 3C NMR (101 MHz, MeOD-d3 with TFA-d): δ=159.4, 143.5, 142.2, 139.6, 138.8, 129.0, 126.8, 122.1, 120.8, 120.2, 118.2, 113.7, 111.0 ppm.
Compound 24 (24 mg, 75 μmol), Pd2(dba)3 (4 mg, 4 μmol) and Xantphos (5 mg, 8 μmol) were placed in a heat dried Schlenk tube filled with Ar, which was evacuated-backfilled with Ar (3×). DMF (1 mL), DIPEA (26 μL, 150 μmol) and p-methoxybenzylmercaptane (15 mg, 90 μmol) were added and the reaction mixture was immediately heated up to 100° C. After 2 h of stirring at the same temperature, the reaction mixture was allowed to cool down to rt, diluted with DCM-MeOH (10:1), washed with 10% aq. Na2SO3— aq. sat. NaHCO3 (1:1) and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM—DCM/MeOH/H2O 90:10:1) to give a red solid (23 mg, 79%). HPLC: tR=9.5 min (20-100); λmax=434, 341, 273 nm. ESI-MS: m/z 392.3 [M+H]+. 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.66 (d, J=2.3 Hz, 1H), 8.71 (dd, J=9.4, 2.3 Hz, 1H), 8.46 (d, J=2.0 Hz, 1H), 8.01 (dd, J=9.0, 2.0 Hz, 1H), 7.93 (d, J=9.4 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H), 7.24-7.30 (m, 2H), 6.79-6.85 (m, 2H), 4.32 (s, 2H), 3.74 (s, 3H) ppm.
Compound 21 (290 mg, 0.77 mmol), Pd2(dba)3 (37 mg, 0.04 mmol) and Xantphos (46 mg, 0.08 mmol) were placed in a heat dried Schlenk tube filled with Ar, which was evacuated-backfilled with Ar (3×). DMF (7.7 mL), DIPEA (268 μL, 1.54 mmol) and PMBSH (142 μg, 0.92 mmol) were added and the reaction mixture was immediately heated up to 100° C. After 2 h of stirring at the same temperature, the reaction mixture was allowed to cool down to rt, diluted with DCM-MeOH (10:1), washed with 10% aq. Na2SO3— aq. sat. NaHCO3 (1:1) and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM—DCM/MeOH/H2O 90:10:1) to give a red solid (325 mg, 94%). TLC (SiO2): Rf=0.35 (DCM/MeOH/H2O 90:10:1). HPLC: tR=9.6 min (20-100); λmax=441, 348, 274 nm. ESI-MS: m/z 450.3 [M+H]+. HRMS: m/z 450.1491 ([M+H]+) calculated for C24H24N3O4S+: 450.1482 (Δ2.0 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.43 (d, J=2.0 Hz, 1H), 8.67 (dd, J=9.4, 2.3 Hz, 1H), 8.24 (br s, 1H), 7.92-8.05 (m, 1H), 7.88 (d, J=9.4 Hz, 1H), 7.75 (d, J=9.0 Hz, 1H), 7.26 (d, J=8.6 Hz, 2H), 6.76-6.88 (m, 2H), 4.28 (s, 2H), 4.00-4.63 (m, 2H), 3.82-3.99 (m, 2H), 3.74 (s, 3H), 1.93-2.31 (m, 2H) ppm.
Compound 29 was synthesized from a corresponding sulfide 25 through a sulfonyl chloride intermediate 27 generated as described in Y-M. Pu, A. Christesen, Y.-Y. Ku, Tetrahedron Lett. 2010, 51, 418-421. Compound 25 (10 mg, 25 μmol) was suspended in the mixture of MeCN (500 μL), AcOH (20 μL) and H2O (12 μL) at 0° C., further 100 μL of DCM was added. DCDMH (10 mg, 50 μmol) was added in portions. The color changed to yellow. The formation of the sulfonyl chloride intermediate was monitored by HPLC (tR=7.3 min; λmax=416 sh., 401, 357, 300, 261 nm; method 20-100). After 40 min of stirring at 0° C., the educt was fully converted. Mixture of DEA (10 mg, 100 μmol), DIPEA (100 μL) and ACN (100 μL) was added, and the reaction mixture was allowed to warm to rt. The reaction mixture became a clear orange solution. After 15 min of stirring at rt, the reaction mixture was concentrated in vacuo. The residue was dissolved in 10 mL of 0.1% aq. TFA and purified by FC (C18, 30C18AQ-F0012 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled, basified with sat. NaHCO3, and the product was extracted into EtOAc-MeOH (10:1). The combined organic phase was washed with brine, dried (Na2SO4) and concentrated in vacuo to give a light orange solid (1 mg, 10%). TLC (SiO2): Rf=0.2 (DCM/MeOH/H2O 90:10:1). HPLC: tR=10.3 min (5-50); λmax=424, 404, 356, 305, 260 nm. ESI-MS: m/z 407.3 [M+H]+.
Compound 30 was synthesized from a corresponding sulfide 26 through a sulfonyl chloride intermediate 28 generated as described in Y-M. Pu, A. Christesen, Y.-Y. Ku, Tetrahedron Lett. 2010, 51, 418-421. Compound 26 (61 mg, 136 μmol) was suspended in 3 mL of MeCN/AcOH/H2O (20:0.75:0.5) at 0° C. DCDMH (75 mg, 381 μmol) was added portionwise. The color of suspension changed to yellow. The reaction mixture was stirred at 0° C. for 30 min, then 30 min at rt. The formation of the sulfonyl chloride intermediate was assessed by HPLC (tR=7.7 min, λmax=423, 406, 360, 302, 265 nm, method 20-100), the educt was fully converted. The solvent was removed in vacuo (35° C., <20 mbar). DEA (75 mg) in ACN (15 mL) was added. The color changed immediately to orange-brown. After 1 h of stirring at rt, the reaction mixture was diluted with EtOAc-MeOH (10:1), washed with sat. NaHCO3 and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, RediSep Rf 24 g cartridge, dry-load, DCM—DCM/MeOH/H2O 90:10:1) to give a light orange solid (52 mg, 82%). TLC (SiO2): Rf=0.2 (DCM/MeOH/H2O 90:10:1). HPLC: tR=10.5 min (5-50); λmax=428, 410, 360, 307, 267 nm. HRMS: m/z 465.1441 ([M+H]+) calculated for C20H25N407S+: 465.1438 (Δ0.6 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.33-9.63 (m, 1H), 8.95 (s, 1H), 8.73 (br dd, J=9.0, 0.8 Hz, 1H), 8.35 (br d, J=9.0 Hz, 1H), 7.95 (d, J=9.0 Hz, 2H), 4.31-4.55 (m, 2H), 3.83-4.04 (m, 2H), 3.74 (t, J=5.9, 5.5 Hz, 4H), 3.42 (t, J=5.5 Hz, 4H), 2.25 (quin, J=6.7, 6.3, 5.9, 5.5 Hz, 2H) ppm.
Compound 29 (1 mg, 2.5 μmol) was dissolved in MeOH (1 mL), containing AcOH (10 μL), under Ar. A 10% Pd/C catalyst (2 mg) was added, and hydrogen atmosphere was applied. After 1 hour of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of H2O (with 0.1% TFA) and purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a red solid (0.8 mg, TFA salt). HPLC: tR=9.0 min (5-50); λmax=453 sh., 422, 401, 302 sh., 270 nm. ESI-MS: m/z 377.3 [M+H]+.
Compound 30 (5 mg, 11 μmol) was dissolved in MeOH (10 mL), containing AcOH (10 μL), under Ar. A 10% Pd/C catalyst (1 mg) was added, and hydrogen atmosphere was applied. After 1 hour of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of H2O (with 0.1% TFA) and purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized (2×) to give a red solid (4.94 mg, 84%, TFA salt). HPLC: tR=9.0 min (5-50); λmax=430, 410, 272 nm. HRMS: m/z 435.1693 ([M+H]+) calculated for C20H27N4O5S+: 435.1697 (Δ0.9 ppm). 1H NMR (400 MHz, D2O): δ=8.35 (d, J=2.0 Hz, 1H), 7.95 (dd, J=9.0, 2.0 Hz, 1H), 7.48 (d, J=9.0 Hz, 1H), 7.25-7.38 (m, 2H), 7.07 (br s, 1H), 3.97 (t, J=7.0, 6.7 Hz, 2H), 3.81 (t, J=5.9, 5.5 Hz, 2H), 3.70 (t, J=5.9, 5.5 Hz, 4H), 3.37 (t, J=5.9, 5.5 Hz, 4H), 2.04 (quin, J=6.7, 6.3, 5.9 Hz, 2H) ppm. 19F NMR (376 MHz, D2O): δ=−75.53 ppm.
Reaction of sulfide 26 with 3-hydroxyazetidine through a sulfonyl chloride intermediate.
Compound 26 (22 mg, 50 μmol) was suspended in 1 mL of MeCN/AcOH/H2O (20:0.75:0.5) at 0° C. DCDMH (25 mg, 125 μmol) was added portionwise. The color of suspension changed to yellow. The reaction mixture was stirred at 0° C. for 30 min, then 30 min at rt. The formation of the sulfonyl chloride intermediate 26-SO2Cl was assessed by HPLC (tR=7.5 min, λmax=423, 406, 360, 302, 265 nm, method 20-100), the educt was fully converted. The solvent was removed in vacuo (35° C., <20 mbar). MeCN (10 mL), 3-hydroxyazetidine hydrochloride (50 mg, 456 μmol) and DIPEA (15 mL) were added. The color changed immediately to orange-brown. After 1 h of stirring at rt, the reaction mixture was stored at −20° C. overnight. The reaction mixture was diluted with EtOAc-MeOH (10:1), washed with sat. NaHCO3 and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, SNAP Ultra 10 g cartridge, dry-load, DCM—DCM/MeOH/H2O 90:10:1) to give the desired product 31 (3 mg, 14%) as a brown solid and side-product 32 (6 mg, 28%) as a light orange solid.
HPLC: tR=11.0 min (5-50); λmax=428, 410, 359, 305, 267 nm. ESI-MS: m/z 433.2 [M+H]+. HRMS: m/z 433.1177 ([M+H]+) calculated for C19H21N4O6S+: 433.1176 (Δ0.2 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.48 (br s, 1H), 8.94 (d, J=1.6 Hz, 1H), 8.76 (dd, J=9.4, 2.0 Hz, 1H), 8.35 (dd, J=9.0, 1.6 Hz, 1H), 8.02 (d, J=9.0 Hz, 1H), 7.96 (d, J=9.4 Hz, 1H), 4.43 (quin, J=6.3, 5.9, 5.5 Hz, 1H), 4.31-4.55 (m, 2H), 4.02-4.15 (m, 2H), 3.82-4.01 (m, 2H), 3.59 (dd, J=8.6, 5.5 Hz, 2H), 2.26 (quin, J=6.3, 5.9, 5.5 Hz, 2H) ppm.
HPLC: tR=10.5 min (5-50); λmax=425, 410, 361, 305, 269 nm. ESI-MS: m/z 431.3 [M+H]+. HRMS: m/z 431.1022 ([M+H]+) calculated for C19H19N4O6S−: 431.1020 (Δ0.5 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.00 (d, J=2.3 Hz, 1H), 8.68 (dd, J=9.4, 2.3 Hz, 1H), 8.51 (d, J=2.0 Hz, 1H), 8.25 (dd, J=9.0, 2.0 Hz, 1H), 7.95 (d, J=9.0 Hz, 1H), 7.91 (d, J=9.4 Hz, 1H), 5.27-5.38 (m, 2H), 5.15-5.26 (m, 2H), 4.88 (dddd, J=6.6, 4.4 Hz, 1H), 4.45 (dddd, J=6.6, 5.5 Hz, 1H), 4.02-4.12 (m, 2H), 3.54-3.63 (m, 2H) ppm.
Compound 31 (3 mg, 7 μmol) was dissolved in MeOH (10 mL), containing AcOH (10 μL), under Ar. A 10% Pd/C catalyst (1 mg) was added, and hydrogen atmosphere was applied. After 1 hour of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of H2O (with 0.1% TFA) and purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a red powder (2.26 mg, 63%, TFA salt). HPLC: tR=9.7 min (5-50); λmax=431, 410, 303, 273 nm. HRMS: m/z 403.1439 ([M+H]+) calculated for C19H23N4O4S+: 403.1435 (Δ1.0 ppm). 1H NMR (400 MHz, D2O): δ=8.45 (d, J=1.6 Hz, 1H), 8.00 (dd, J=9.0, 1.6 Hz, 1H), 7.64 (d, J=9.4 Hz, 1H), 7.37-7.48 (m, 2H), 7.25 (br s, 1H), 4.45 (quin, J=6.7, 6.3, 5.5, 5.1 Hz, 1H), 4.01-4.13 (m, 4H), 3.82 (t, J=5.9, 5.5 Hz, 2H), 3.60 (d, J=5.1 Hz, 1H), 3.57 (d, J=5.1 Hz, 1H), 2.07 (quin, J=6.7, 6.3, 5.9 Hz, 2H) ppm.
Compound 32 (6 mg, 14 μmol) was dissolved in MeOH (10 mL), containing AcOH (10 μL), under Ar. A 10% Pd/C catalyst (1 mg) was added, and hydrogen atmosphere was applied. After 1 hour of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of H2O (with 0.1% TFA) and purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a red powder (6 mg, 86%, TFA salt). HPLC: tR=8.6 min (5-50); λmax=430, 410, 277 nm. HRMS: m/z 401.1281 ([M+H]+) calculated for Cl9H21N4O4S+: 401.1278 (Δ0.7 ppm). 1H NMR (400 MHz, MeOD-d3): δ=8.47 (d, J=1.6 Hz, 1H), 8.08 (dd, J=9.0, 1.6 Hz, 1H), 7.85 (d, J=9.0 Hz, 1H), 7.64 (d, J=9.0 Hz, 1H), 7.47 (dd, J=9.0, 2.0 Hz, 1H), 7.32 (d, J=2.0 Hz, 1H), 5.17-5.43 (m, 2H), 4.98-5.16 (m, 2H), 4.83-4.91 (m, 1H), 4.45 (dq, J=6.3, 5.9 Hz, 1H), 4.06 (t, J=7.8 Hz, 2H), 3.57 (dd, J=8.6, 5.5 Hz, 2H) ppm. 13C NMR (101 MHz, MeOD-d3, HSQC): δ=158.4, 146.0, 142.4, 134.5, 132.4 (CH), 129.7 (CH), 127.9 (CH), 127.8, 120.5 (2×CH), 115.5, 111.3, 107.3 (CH), 72.6 (2×CH2), 63.4 (CH), 61.6 (2×CH2), 60.8 (CH) ppm. 19F NMR (376 MHz, MeOD-d3): δ=−76.71 ppm.
Compound 6 (20 mg, 36 μmol), glucose (32 mg, 178 μmol) and AcOH (4 mg, 71 μmol) were mixed in 1 mL of water. NaBH3CN (22 mg, 356 μmol) in 0.5 mL of MeOH was added. The reaction mixture was heated to 60° C. The reaction progress was monitored by HPLC. After 5 h of stirring at 60° C., the reaction mixture was cooled to rt, diluted with 10 mL of 0.1% aq. TFA and purified by FC (C18, 30C18AQ-F0025 cartridge, ACN—0.1% aq. TFA). The good fractions were pooled and lyophilized to give the title product 6-Glc (10 mg, TFA salt) as a red-purple solid. HPLC: tR=10.9 min (5-50). ESI-MS: m/z 499.4 [M+H]+. HRMS: m/z 499.2553 ([M+H]+) calculated for C26H34N4O6+: 499.2551 (Δ0.4 ppm). 1H NMR (400 MHz, D2O): 6=8.12 (s, 1H), 7.76 (dd, J=9.0, 1.6 Hz, 1H), 7.39 (d, J=9.0 Hz, 1H), 7.30 (dd, J=9.0, 2.0 Hz, 1H), 7.25 (d, J=9.0 Hz, 1H), 6.62 (d, J=2.0 Hz, 1H), 4.06 (ddtd, J=5.1, 4.3, 3.9, 0.9 Hz, 1H), 3.91 (dd, J=5.3, 2.2 Hz, 1H), 3.86 (dd, J=15.7, 2.7 Hz, 1H), 3.80-3.89 (m, 1H), 3.66-3.78 (m, 4H), 3.57 (t, J=6.7 Hz, 2H), 3.33 (dd, J=13.3, 3.9 Hz, 1H), 3.18 (dd, J=13.3, 8.2 Hz, 1H), 1.76 (quin, J=7.0 Hz, 2H), 1.54 (quin, J=6.7 Hz, 2H), 1.30-1.45 (m, 4H) ppm. 19F NMR (376 MHz, D2O): δ=−75.50 ppm.
General method for labelling of glucose with model compounds (7, 9-11). 1.5 mL Brand® micro tube with screw cap was charged with dye (1 equiv., 0.1 M solution in water), glucose (1 equiv., 0.1 M solution in water), malonic acid (10 equiv., 1 M solution in DMSO) and 2-picoline-borane complex (10 equiv., 1 M solution in DMSO). After vortexing for 10 s, the reaction mixture was incubated in an Eppendorf ThermoMixer® with shaking (400-600 rpm) at 40° C. for 18 h. The reaction mixture was cooled to rt, diluted with 10 mL of 0.1% aq. TFA and purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. TFA). The good fractions were pooled and lyophilized.
The title compound 7-Glc (0.8 μmol, TFA salt) was obtained as an orange-red solid from dye 7 (1.3 μmol) according to the general method for labelling of glucose. HPLC: tR=9.1 min (5-50); λmax=482, 319, 275 nm. ESI-MS: m/z 554.3 [M+H]+. HRMS: m/z 554.2160 ([M+H]+) calculated for C25H36N3O9S+: 554.2167 (Δ1.3 ppm). 1H NMR (400 MHz, D2O): δ=8.63 (d, J=1.0 Hz, 1H), 8.06 (d, J=9.0 Hz, 1H), 7.69 (dd, J=9.0, 0.4 Hz, 1H), 7.46 (d, J=9.0 Hz, 1H), 7.38-7.44 (m, 1H), 6.91 (s, 1H), 4.03-4.20 (m, 3H), 3.91 (dd, J=5.5, 2.2 Hz, 1H), 3.78-3.88 (m, 4H), 3.75 (dd, J=8.2, 2.2 Hz, 1H), 3.64-3.71 (m, 1H), 3.62 (t, J=6.3 Hz, 2H), 3.46-3.53 (m, 2H), 3.43 (dd, J=13.3, 3.5 Hz, 1H), 3.26 (dd, J=13.3, 8.2 Hz, 1H), 2.04-2.17 (m, 2H), 1.85-1.97 (m, 2H) ppm. 19F NMR (376 MHz, D2O): δ=−75.53 ppm.
The title compound 9-Glc (0.7 μmol, TFA salt) was obtained as an orange-red solid from dye 9 (1.6 μmol) according to the general method for labelling of glucose. HPLC: tR=9.1 min (5-50); λmax=480, 319, 276 nm. ESI-MS: m/z 599.3 [M+H]+. HRMS: m/z 599.2381 ([M+H]+) calculated for C26H39N4O10S+: 599.2381 (Δ0.0 ppm). 1H NMR (400 MHz, D2O): δ=8.53 (s, 1H), 8.01 (dd, J=9.0, 1.0 Hz, 1H), 7.61 (d, J=9.0 Hz, 1H), 7.36-7.47 (m, 2H), 6.88 (s, 1H), 4.01-4.17 (m, 3H), 3.93 (dd, J=5.5, 2.0 Hz, 1H), 3.80-3.89 (m, 4H), 3.75-3.80 (m, 1H), 3.62-3.75 (m, 5H), 3.33-3.48 (m, 5H), 3.27 (dd, J=13.1, 8.4 Hz, 1H), 2.04-2.17 (m, 2H) ppm. 19F NMR (376 MHz, D2O): δ=−75.52 ppm.
The title compound 10-Glc (0.6 μmol, TFA salt) was obtained as an orange-red solid from dye 10 (1.5 μmol) according to the general method for labelling of glucose. HPLC: tR=9.6 min (5-50); λmax=482, 320, 276 nm. ESI-MS: m/z 567.3 [M+H]+. HRMS: m/z 567.2120 ([M+H]+) calculated for C25H35N4O9S+: 567.2119 (Δ0.2 ppm). 1H NMR (400 MHz, D2O): δ=8.53 (s, 1H), 7.95-8.12 (m, 1H), 7.60-7.82 (m, 1H), 7.33-7.57 (m, 2H), 6.82-7.00 (m, 1H), 4.39-4.56 (m, 1H), 4.00-4.25 (m, 5H), 3.90-3.97 (m, 1H), 3.80-3.89 (m, 4H), 3.74-3.80 (m, 1H), 3.66-3.74 (m, 1H), 3.56-3.65 (m, 2H), 3.37-3.51 (m, 1H), 3.20-3.32 (m, 1H), 2.07-2.18 (m, 2H) ppm. 19F NMR (376 MHz, D2O): δ=−75.52 ppm.
The title compound 11-Glc (1.3 μmol, AcOH salt) was obtained as a red solid from dye 11 (5.1 μmol) according to the general method for labelling of glucose. The material was further purified by FC (C18, 15C18HP-F0012 cartridge, ACN—0.1% aq. AcOH). The product appeared to be unstable in the presence of TFA (by HPLC). HPLC: tR=8.8 min (5-50); λmax=485, 431, 320, 277 nm. HRMS: m/z 565.1959 ([M+H]+) calculated for C25H33N4O9S+: 565.1963 (Δ0.7 ppm). 1H NMR (400 MHz, D2O): δ=8.12 (d, J=1.2 Hz, 1H), 7.96 (dd, J=9.0, 1.2 Hz, 1H), 7.54 (br d, J=9.0 Hz, 1H), 7.37-7.48 (m, 2H), 6.87 (s, 1H), 5.04-5.25 (m, 2H), 4.87-5.01 (m, 2H), 4.78-4.82 (m, 1H), 4.47 (dt, J=11.7, 5.9 Hz, 1H), 4.00-4.16 (m, 3H), 3.91 (dd, J=5.5, 2.3 Hz, 1H), 3.78-3.86 (m, 2H), 3.75 (dd, J=8.0, 2.2 Hz, 1H), 3.64-3.71 (m, 1H), 3.61 (dd, J=9.2, 5.3 Hz, 2H), 3.47 (dd, J=13.5, 4.1 Hz, 1H), 3.29 (dd, J=13.5, 8.0 Hz, 1H), 1.88 (s, 2H, AcOH) ppm.
Compound 22 (330 mg, 0.79 mmol) and 1H-terazole (330 mg, 4.72 mmol) were placed in Ar-filled flask, which was evacuated-backfilled with Ar (3×). DMF (8 mL) and (t-BuO)2PNi-Pr2 (994 μL, 3.15 mmol) were added, and the reaction mixture was stirred 1 h at rt. Formation of the phosphite intermediate was monitored by HPLC (tR=14.3 min, 5-50). Then 50% aq. H2O2 (358 μL, 7.3 mmol) was added in one portion. After 30 min of stirring at rt, the reaction mixture was diluted with DCM (200 mL), washed with 10% aq. Na2SO3— aq. sat. NaHCO3 (100 mL, 1:1) and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, 15SIHP-F0040 cartridge, DCM/MeOH with 2-5% MeOH gradient) to give a light orange solid (260 mg, 41%). TLC (SiO2): Rf=0.3 (DCM/MeOH 20:1). HPLC: tR=10.9 min (20-100); tR=17.6 min (5-50); λmax=427, 410, 357, 303, 267 nm. ESI-MS: m/z 804.5 [M+H]+.
HRMS: m/z 804.3056 ([M+H]+) calculated for C35H56N3O12P2S+: 804.3054 (Δ0.2 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.29-9.75 (m, 1H), 8.89-9.28 (m, 1H), 8.75 (dd, J=9.4, 2.3 Hz, 1H), 8.42 (dd, J=9.0, 1.6 Hz, 1H), 8.00 (d, J=9.0 Hz, 1H), 7.95 (d, J=9.4 Hz, 1H), 4.36 (t, J=6.7 Hz, 2H), 4.19 (q, J=6.7, 6.3, 5.9 Hz, 2H), 4.06 (q, J=7.4, 6.3 Hz, 2H), 3.42-3.52 (m, 2H), 2.44 (quin, J=6.3 Hz, 2H), 2.04-2.17 (m, 2H), 1.44 (s, 9H), 1.44 (s, 9H), 1.42 (s, 18H) ppm. 31P NMR (162 MHz, CDCl3): δ=−7.99 (br s, 1P), −10.13 (s, 1P) ppm.
Compound 33 (50 mg, 62 μmol) was dissolved in MeOH (4 mL), containing AcOH (20 μL), under Ar. A 10% Pd/C catalyst (5 mg) was added, and hydrogen atmosphere was applied. After 1 h of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of ACN/0.1% aq. TFA (1:5) and purified by FC (C18, 30C18AQ-F0025 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a red powder (42 mg, 76%, TFA salt). HPLC: tR=10.3 min (20-100). ESI-MS: m/z 774.6 [M+H]+. HRMS: m/z 774.3315 ([M+H]+) calculated for C35H58N3O10P2S+: 774.3313 (Δ0.3 ppm). 1H NMR (400 MHz, MeOD-d3): δ=9.02 (d, J=1.6 Hz, 1H), 8.21 (dd, J=9.0, 1.6 Hz, 1H), 7.91 (d, J=9.0 Hz, 1H), 7.69 (dd, J=7.4, 2.3 Hz, 1H), 7.53 (s, 1H), 7.54 (dd, J=7.4, 2.3 Hz, 1H), 4.32 (t, J=7.0, 6.7 Hz, 2H), 4.20 (q, J=6.3, 5.9 Hz, 2H), 4.06 (q, J=7.8, 6.3, 5.9 Hz, 2H), 3.45 (m, J=7.8, 7.4, 2.3, 2.0 Hz, 2H), 2.38 (quin, J=6.3, 5.9 Hz, 2H), 2.05-2.16 (m, 2H), 1.45 (s, 18H), 1.44 (s, 18H) ppm. 31P NMR (162 MHz, MeOD-D3): δ=−10.61 (s, 1P), −10.62 (s, 1P) ppm.
Compound 34 (43 mg, 48 μmol) was stirred in 5% TFA in DCM (4 mL) for 4 h at rt under Ar. The reaction mixture was then concentrated in vacuo (without heating bath). The residue was dissolved in 10 mL of TEAAc buffer (1.0 M, pH 7) and purified by FC (C18, 30C18AQ-F0025, ACN—10 mM TEAAc pH 7). Good fractions were pooled and lyophilized to give a red powder (20 mg, 65%, TEA salt). HPLC (Knauer Eurospher II 100-5 C18A): tR=9.3 min (TEAB-O-25); λmax=455, 303, 273 nm. ESI-MS: m/z 548.2 [M−H]−. HRMS: m/z 550.0805 ([M+H]+) calculated for C19H26N3O10P2S+: 550.0809 (Δ0.7 ppm). 1H NMR (400 MHz, D2O): δ=8.35 (s, 1H), 7.94 (dd, J=9.0, 1.6 Hz, 1H), 7.49 (d, J=9.0 Hz, 1H), 6.94-7.13 (m, 2H), 6.83 (s, 1H), 4.06-4.22 (m, 2H), 3.85-3.98 (m, 4H), 3.46-3.59 (m, 2H), 3.18 (q, J=7.2 Hz, 6H, TEA), 2.09-2.20 (m, 2H), 1.98-2.08 (m, 2H), 1.26 (t, J=7.2 Hz, 9H, TEA) ppm. 31P NMR (162 MHz, D2O): δ=0.35 (s, 1P), 0.25 (s, 1P) ppm.
Reaction of 30 with di-tert-butyl N,N-diisopropylphosphoramidite with H2O2 as oxidant.
Compound 30 (57 mg, 0.12 mmol) and 1H-terazole (78 mg, 1.11 mmol) were placed in Ar-filled flask, which was evacuated-backfilled with Ar (3×). DMF (1.25 mL) and (t-BuO)2PNi-Pr2 (233 μL, 0.74 mmol) were added, and the reaction mixture was stirred 1 h at rt. Formation of the phosphite intermediate was monitored by HPLC (tR=9.2 min, 20-100). Then 50% aq. H2O2 (278 μL, 4.9 mmol) was added in one portion. After 30 min of stirring at rt, the reaction mixture was diluted with DCM (200 mL), washed with 10% aq. Na2SO3— aq. sat. NaHCO3 (100 mL, 1:1) and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by FC (SiO2, 30SIHP-F0025 cartridge, DCM/MeOH with 1-5% MeOH gradient) to give the desired product 35 (58 mg, 47%) as an orange oil and a side-product 36 (12 mg, 13%) as a yellow powder.
HPLC: tR=12.3 min (20-100); λmax=429, 412, 358, 307, 268 nm. HRMS: m/z 1041.4168 ([M+H]+) calculated for C44H76N4O16P3S+: 1041.4184 (Δ1.5 ppm). 1H NMR (400 MHz, MeOD-d3 with TFA-d): δ=9.29-9.80 (m, 1H), 8.83-9.23 (m, 1H), 8.76 (dd, J=9.4, 2.3 Hz, 1H), 8.40 (dd, J=9.0, 2.0 Hz, 1H), 7.97 (d, J=9.0 Hz, 1H), 7.96 (d, J=9.4 Hz, 1H), 4.37 (t, J=7.0, 6.7 Hz, 2H), 4.21 (q, J=6.7, 5.9 Hz, 2H), 4.13 (q, J=6.3, 5.9, 5.5 Hz, 4H), 3.66 (t, J=5.5 Hz, 4H), 2.47 (quin, J=6.3, 5.9 Hz, 2H), 1.46 (s, 36H), 1.45 (s, 18H) ppm. 31P NMR (162 MHz, MeOD-d3 with TFA-d): δ=−10.23 (s, 1P), −10.90 (s, 2P) ppm.
HPLC: tR=12.6 min (20-100); λmax=354, 298, 249 nm. ESI-MS: m/z 790.4 [M−H]−. HRMS: m/z 814.2515 ([M+Na]+) calculated for C33H51N3NaO13P2S+: 814.2510 (Δ0.6 ppm). 1H NMR (400 MHz, CDCl3): δ=12.05 (s, 1H), 9.08 (d, J=2.3 Hz, 1H), 8.82 (d, J=2.3 Hz, 1H), 8.29 (dd, J=9.0, 2.7 Hz, 1H), 7.98 (dd, J=8.6, 2.3 Hz, 1H), 7.57 (d, J=9.0 Hz, 1H), 7.43 (d, J=9.0 Hz, 1H), 4.19 (q, J=7.4, 6.3, 5.9 Hz, 4H), 3.64 (t, J=6.3, 5.9 Hz, 4H), 1.51 (s, 36H) ppm. 13C NMR (101 MHz, CDCl3, HSQC): δ=176.6, 144.4, 143.2, 142.0, 133.2, 131.3 (CH), 127.6 (CH), 127.2 (CH), 123.9 (CH), 120.8, 120.4, 119.0 (CH), 118.4 (CH), 83.4 (d, 4×C, JCP=7.6 Hz), 65.3 (d, 2×CH2, JCP=6.9 Hz), 48.9 (d, CH2, JCP=8.4 Hz), 29.9 (d, 12×CH3, JCP=3.8 Hz) ppm. 31P NMR (162 MHz, CDCl3): δ=−11.19 (s, 2P) ppm.
Compound 35 (58 mg, 56 μmol) was dissolved in MeOH (5 mL), containing AcOH (100 μL), under Ar. A 10% Pd/C catalyst (5 mg) was added, and hydrogen atmosphere was applied. After 1 h of stirring at rt, orange fluorescent solution was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of ACN/0.1% aq. TFA (1:5) and purified by FC (C18, 30C18AQ-F0025 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a red powder (27 mg, 43%, TFA salt). HPLC: tR=11.8 min (20-100); λmax=475, 312, 275 nm. HRMS: m/z 1011.4449 ([M+H]+) calculated for C44H78N4O14P3S+: 1011.4443 (A 0.6 ppm). 1H NMR (400 MHz, MeOD-d3): δ=8.95 (d, J=2.0 Hz, 1H), 8.17 (dd, J=9.0, 2.0 Hz, 1H), 7.86 (d, J=9.0 Hz, 1H), 7.66 (dd, J=8.2, 1.6 Hz, 1H), 7.51 (s, 1H), 7.49 (dd, J=9.0, 2.3 Hz, 1H), 4.30 (t, J=7.0, 6.7 Hz, 2H), 4.18 (q, J=6.3, 5.9 Hz, 2H), 4.10 (q, J=6.7, 5.9 Hz, 4H), 3.62 (t, J=5.9 Hz, 4H), 2.35 (quin, J=6.3, 5.9 Hz, 2H), 1.44 (s, 36H), 1.42 (s, 18H) ppm. 31P NMR (162 MHz, CDCl3): δ=−10.02 (s, 2P), −10.86 (s, 1P) ppm.
Compound 36 (12 mg, 15 μmol) was dissolved in MeOH (1 mL), containing AcOH (25 μL), under Ar. A 10% Pd/C catalyst (1 mg) was added, and hydrogen atmosphere was applied. After 1 h of stirring at rt, the reaction mixture was filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in 10 mL of ACN/0.1% aq. TFA (1:5) and purified by FC (C18, 30C18AQ-F0025 cartridge, ACN—0.1% aq. TFA). Good fractions were pooled and lyophilized to give a light yellow powder (6.3 mg, 77%, TFA salt). HPLC: tR=9.6 min (20-100); λmax=397, 380, 318, 306, 280, 256 nm. ESI-MS: m/z 762.4 [M+H]+. HRMS: m/z 762.2945 ([M+H]+) calculated for C33H54N3O11P2S+: 762.2949 (Δ0.5 ppm). 1H NMR (400 MHz, MeOD-d3): δ=8.78 (d, J=2.0 Hz, 1H), 8.07-8.13 (m, 2H), 7.66 (d, J=8.6 Hz, 1H), 7.62 (d, J=1.6 Hz, 2H), 4.09 (q, J=7.0, 6.3, 5.9 Hz, 4H), 3.56 (t, J=5.9 Hz, 4H), 1.45 (s, 36H) ppm. 13C NMR (100 MHz, MeOD-d3, HSQC): δ=177.2, 143.1, 138.6, 132.1, 131.2, 130.9 (CH), 127.5 (CH), 126.8 (CH), 121.6, 119.3 (CH), 119.2, 118.8 (CH), 116.2 (CH), 83.3 (d, 2×C, JCP=7.6 Hz), 65.3 (d, 2×CH2, JCP=6.9 Hz), 48.7 (d, 2×CH2, JCP=8.4 Hz), 28.7 (d, 12×CH3, JCP=3.8 Hz) ppm. 31P NMR (162 MHz, MeOD-d3): δ=−10.79 (s) ppm.
Compound 37 (11 mg, 10 μmol) was stirred in 5% TFA in DCM (0.75 mL) for 2 h at rt under Ar. The reaction mixture was then cooled to 0° C., and 5 mL of TEAAc buffer (1.0 M, pH 7) was added. The resulting emulsion was concentrated in vacuo (without heating bath) to obtain clear aqueous solution, which was purified by FC (C18, 30C18AQ-F0025, ACN—10 mM TEAAc pH 7). Good fractions were pooled and lyophilized (3×) to give a dark red solid (8 mg, 72%, TEA salt). HPLC (Knauer Eurospher II 100-5 C18A): tR=8.7 min (TEAB-0-25); tR=7.0 min (TEAB-0-40); λmax=458, 305, 273 nm. ESI-MS: m/z 673.2 [M−H]−. HRMS: m/z 673.0532 ([M−H]−) calculated for C20H28N4O14P3S−: 673.0541 (Δ1.3 ppm). 1H NMR (400 MHz, D2O): 6=8.46 (s, 1H), 8.05 (d, J=9.0 Hz, 1H), 7.63 (d, J=9.4 Hz, 1H), 7.30 (d, J=8.6 Hz, 1H), 7.25 (d, J=9.0 Hz, 1H), 7.16 (s, 1H), 4.08-4.20 (m, 2H), 4.04 (t, J=6.3, 5.9 Hz, 2H), 3.98 (q, J=5.9, 5.5, 5.1 Hz, 4H), 3.58 (t, J=5.5, 5.1 Hz, 4H), 3.19 (q, J=7.4 Hz, 26H, TEA), 2.12-2.26 (m, 2H), 1.26 (t, J=7.4 Hz, 38H, TEA) ppm. 31P NMR (162 MHz, D2O): δ=1.32 (s, 1P), 0.72 (s, 2P) ppm.
Compound 38 (6.3 mg, 7 μmol) was stirred in 5% TFA in DCM (0.75 mL) for 2 h at rt under Ar. The reaction mixture was then cooled to 0° C., and 5 mL of TEAAc buffer (1.0 M, pH 7) was added. The resulting emulsion was concentrated in vacuo (without heating bath) to obtain clear aqueous solution, which was purified by FC (C18, 30C18AQ-F0025, ACN—10 mM TEAAc pH 7). Good fractions were pooled and lyophilized (3×) to give a yellow-brown solid (4 mg, 79%, TEA salt). HPLC (Knauer Eurospher II 100-5 C18A): tR=8.6 min (TEAB-0-40); λmax=425, 297, 260 nm. ESI-MS: m/z 536.1 [M−H]−. HRMS: m/z 536.0298 ([M−H]−) calculated for C17H20N3O11P2S 536.0299 (Δ0.2 ppm). 1H NMR (400 MHz, D2O): δ=8.32 (d, J=2.0 Hz, 1H), 7.84 (dd, J=9.0, 1.2 Hz, 1H), 7.27 (d, J=9.0 Hz, 1H), 7.23 (s, 1H), 7.18 (dd, J=8.6, 0.8 Hz, 1H), 7.06 (d, J=9.0 Hz, 1H), 4.00 (q, J=5.9, 5.5 Hz, 4H), 3.51 (t, J=5.5, 5.1 Hz, 4H), 3.17 (q, J=7.4 Hz, TEA), 1.25 (t, J=7.4 Hz, TEA) ppm. 13C NMR (101 MHz, D2O, HSQC): 6=177.5, 141.7, 139.1, 135.2, 130.0 (CH), 129.6, 126.8 (CH), 126.6 (CH), 120.6, 119.1 (CH), 119.0 (CH), 117.4, 110.1 (CH), 63.5 (d, 2×CH2, JCP=4.6 Hz), 49.1 (d, 2×CH2, JCP=6.9 Hz), 46.7 (CH2, TEA), 8.3 (CH3, TEA) ppm. 31P NMR (162 MHz, D2O): δ=0.28 (s) ppm.
General method for labelling of carbohydrates with negatively charged amino-dyes for electrophoresis. 1.5 mL Brand® micro tube with a screw cap was charged with dye (1 equiv., 0.1 M solution in water), carbohydrate (1 equiv., 0.1 M solution in water), malonic acid (10 equiv., 1 M solution in DMSO) and 2-picoline-borane complex (10 equiv., 1 M solution in DMSO). After vortexing for 10 s, the reaction mixture was incubated in an Eppendorf ThermoMixer® with shaking (400-600 rpm) at 40° C. for 18 h. The reaction mixture was cooled to rt, diluted with 5 mL of TEAB buffer (1.0 M, pH 8) and purified by flash chromatography (RP C18, 15C18AQ-F0025 cartridge, ACN—20 mM TEAB, pH 8, 0-5% ACN, 10 column volumes). The appropriate fractions were pooled and lyophilized.
Removal of buffer at reduced pressure and prolonged drying gave the conjugation products of dye 13 as red powders. These compounds did not dissolve any more in water, methanol, ethanol, DMSO, or DMF even on heating.
General method for labelling of dextran ladder with negatively charged amino-dyes for electrophoresis. 1.5 mL Brand® micro tube with a screw cap was charged with a dextran ladder (0.4 mg, maltodextrin oligosaccharides—DP2 to DP15, Carbosynth), dye (5 μL, 0.1 M solution in water or DMSO), malonic acid (5 μL, 1 M solution in DMSO) and 2-picoline-borane complex (5 μL, 1 M solution in DMSO). After vortexing for 10 s, the reaction mixture was incubated in an Eppendorf ThermoMixer® with shaking (400-600 rpm) at 40° C. for 18 h. The reaction mixture was cooled to rt, diluted with 5 mL of TEAB buffer (1.0 M, pH 8) and purified by flash chromatography (RP C18, 15C18AQ-F0025 cartridge, ACN—20 mM TEAB, pH 8, 0-5% ACN, 10 column volumes). The appropriate fractions were pooled and concentrated in vacuo (rotary evaporator, then speedvac).
HPLC (Knauer Eurospher II 100-5 C18A): tR=9.5 min (TEAB-0-25); λmax=469, 317, 276 nm. ESI-MS: m/z 712.4 [M−H]−. HRMS: m/z 712.1339 ([M−H]−) calculated for C25H36N3O15P2S−: 712.1348 (Δ1.3 ppm). 1H NMR (400 MHz, D2O): δ=8.60 (s, 1H), 8.04 (d, J=8.6 Hz, 1H), 7.69 (d, J=9.4 Hz, 1H), 7.39 (d, J=9.0 Hz, 1H), 7.16-7.35 (m, 1H), 6.91 (s, 1H), 4.06-4.17 (m, 4H), 4.04 (quin, J=5.5, 4.3, 3.5 Hz, 1H), 3.86-3.96 (m, 3H), 3.78-3.86 (m, 2H), 3.74-3.79 (m, 1H), 3.64-3.73 (m, 1H), 3.49-3.61 (m, 2H), 3.40 (dd, J=13.5, 3.7 Hz, 1H), 3.23 (dd, J=13.7, 8.2 Hz, 1H), 3.18 (q, J=7.4 Hz, TEA), 2.17-2.29 (m, 2H), 1.97-2.08 (m, 2H), 1.25 (t, J=7.4 Hz, TEA) ppm. 31P NMR (162 MHz, D2O): δ=0.69 (s, 1P), 0.33 (s, 1P) ppm.
HPLC (Knauer Eurospher II 100-5 C18A): tR=8.8 min (TEAB-0-25). ESI-MS: m/z 1036.6 [M−H]−.
HPLC (Knauer Eurospher II 100-5 C18A): tR=8.8 min (TEAB-0-25). ESI-MS: m/z 1685.6 [M−H]−.
HPLC (Knauer Eurospher II 100-5 C18A): tR=8.8 min (TEAB-0-25); λmax=473, 318, 276 nm. ESI-MS: m/z 836.9 [M−H]−. HRMS: m/z 418.0568 ([M−2H]2−) calculated for C26H39N4O19P3S2: 418.0577 (z 2.2 ppm).
HPLC (Knauer Eurospher II 100-5 C18A): tR=9.0 min (TEAB-0-25). ESI-MS: m/z 1161.1 [M−H]−.
HPLC (Knauer Eurospher II 100-5 C18A): tR=8.8 min (TEAB-0-25). ESI-MS: m/z 904.1 [M−2H]2−.
HPLC (Knauer Eurospher 11100-5 C18A): tR=10.6 min (TEAB-0-25); λmax=439, 306, 254 nm. ESI-MS: m/z 714.2 [M−H]−. HRMS: m/z 356.5533 ([M−2H]2−) calculated for C24H33N3O16P2S2−: 356.5534 (Δ0.3 ppm).
HPLC (Knauer Eurospher II 100-5 C18A): tR=10.2 min (TEAB-0-25). ESI-MS: m/z 1038.4 [M−H]−.
HPLC (Knauer Eurospher II 100-5 C18A): tR=10.3 min (TEAB-0-25). ESI-MS: m/z 1686.6 [M−H]−.
a) Anhydrous trisodium salt of 8-aminopyrene-1,3,6-trisulfonic acid (52 mg, 0.10 mmol) was introduced into a 10 mL flask, cooled down to 0° C. (ice bath), and chlorosulfonic acid (356 mg, 204 μL, 3 mmol) was added dropwise with stirring. The reaction mixture was stirred at r. t. for 4 h. After cooling down to 0° C., the reaction mixture was carefully transferred onto crushed ice (50 g). The red precipitate of trisulfonyl chloride was isolated by centrifugation and washed with ice water (3×50 mL; with centrifugation). The crude compound was lyophilized to afford 42 mg of 1,3,6-tri(chlorosulfonyl)-8-aminopyrene (49) (82% yield). The flask was purged with Ar and kept in the freezer (−20° C.).
b) To a stirred and ice-cooled solution of cyanamide (50 mg, 1.2 mmol) and triethylamine (122 mg, 176 μL, 1.2 mmol) in aqueous MeCN (1:1, 1.5 mL), the solid sulfonylchloride (21 mg, 0.04 mmol) was added in portions. The reaction mixture turned orange. When the addition was complete, the reaction mixture was stirred for 10 min, diluted with aq. TEAB (Et3N*H2CO3, 2 mL, pH=8), frozen and lyophilized. Analytical HPLC: Kinetex, 5 μm C18 100, 250 mm, 4.6 mm, ACN/0.05 M TEAB: 5/95-60/40 in 20 min, 1.2 mL/min; tR=9.4 min. The title compound was isolated by preparative IPLC with UV-VIS detection (MeCN/TEAB 0.05 M in water, 5:95→30:70 in 20 min detected at 500 nm)
1H NMR (400 MHz, D2O) δ 9.14 (s, 1H), 8.84 (d, J=9.7 Hz, 1H), 8.57 (d, J=9.6 Hz, 1H), 8.52 (d, J=9.7 Hz, 1H), 8.03 (d, J=9.6 Hz, 1H), 7.99 (s, 1H), 3.20 (d, J=7.2 Hz, 1H), 2.82 (q, J=7.3 Hz, 18H, CH2 in Et3N), 0.99 (t, J=7.3 Hz, 27H, CH3 in Et3N). 13C NMR (101 MHz, D2O) δ 144.8, 138.2, 131.3, 131.1, 130.8, 130.4, 128.2, 126.4, 125.5, 124.8, 124.7, 122.5, 120.1, 116.6, 116.0, 115.4, 46.4, 8.0.
HR-MS: C19H11N7O6S3 found 527.9850 [M−H]−; calculated 527.9860.
λmax (absorption)=454 nm (H2O), F=23 900 M−1 cm−1, λmax (emission)=531 nm (excitation at 440 nm); Stocks shift 75 nm, fluorescence lifetime 5.6 ns (H2O; excitation at 440 nm); fluorescence quantum yield: 0.93 (H2O). See
A 1.5 mL Eppendorf vial was charged with dye 40 (100 μL of 0.02 M solution in water), glucose (5 equiv., 10 μmol, 2 mg), and malonic acid (10 equiv., 20 μL of 1 M solution in DMSO). The closed vial shaken at 40° C. for 1 h (Eppendorf ThermoMixer®), and then the solvents (water and DMSO) were removed by lyophilization (p<0.2 mbar). A solution of 2-picoline-borane complex (10 equiv., 20 μL of 1 M solution in DMSO) was added, and the sample was shaken at 40° C. for 16 hours (Eppendorf ThermoMixer®). The product was isolated by preparative HPLC with UV-VIS detection (MeCN/TEAB 0.05 M in water, 5:95→30:70 in 20 min, detected at 500 nm). The product was characterized by ESI-HRMS, UV-Vis and fluorescence spectroscopy.
HR-MS: C25H23N7O11S3 found 692.9850 [M−H]−; calculated 692.9860.
λmax (absorption)=483 nm (H2O), λmax (emission)=544 nm (excitation at 460 nm); Stocks shift 61 nm, fluorescence lifetime 5.34 ns (H2O; excitation at 440 nm); fluorescence quantum yield: 0.92 (H2O). See
N-enzyloxycarbonylazetidini-3-ol was synthesized according to the literature (T. A. Davis, M. W. Danneman, J. N. Johnston. Chem. Comm. 2012, 48, 5578-5580).
1H NMR (400 MHz, Acetone-d6) δ 7.47-7.24 (m, 5H), 5.06 (d, J=0.7 Hz, 2H), 4.62-4.53 (m, 1H), 4.15 (s, 2H), 3.84-3.68 (m, 2H).
1H-Tetrazole (840 mg, 12 mmol) and di-t-butyl N,N-diisopropylphosphoramidite (2.8 g, 3.18 mL, 9.6 mmol) were added to a solution of N-benzyloxycarbonylazetidin-3-ol (1.0 g, 4.8 mmol) in DMF (8 mL) under Ar, and the mixture was stirred at r.t. for 1 h. The course of the reaction was monitored by HPLC. After the starting compound disappeared, the mixture was cooled to 0° C., and H2O2 (70% aqueous solution, 1.5 mL) was added. After 15 min the cooling bath was removed, the reaction mixture analyzed by HPLC, and then aqueous Na2SO3 (10%, 30 mL) was added (with cooling of the reaction mixture in an ice bath). After 30 min, the reaction mixture was extracted with EtOAc (30 mL×3). The combined solutions were washed with brine, dried over MgSO4, and evaporated. The residue was submitted to flash chromatography (SNAP Ultra cartridge with 50 g SiO2, hexane/EtOAc with 20-65% EtOAc-gradient over 15 CV) to provide a white solid (1.2 g, 62% yield).
HR-MS: C19H30NO6P found 400.1882 [M+H]+, calculated 400.1884; found 422.1703 [M+Na]+, calculated 422.1703.
1H NMR (400 MHz, Acetone-d6) δ 7.41-7.28 (m, 5H), 5.08 (s, 2H), 5.06-4.98 (m, 1H), 4.33-4.23 (m, 2H), 4.06-3.97 (m, 2H), 1.47 (d, J=0.7 Hz, 18H).
13C NMR (101 MHz, Acetone-d6) δ 138.0, 129.2, 128.7, 128.6, 83.2, 83.1, 66.9, 66.0, 65.9, 30.0. 31P NMR (162 MHz, Acetone-d6) δ−10.93.
A solution of N-benzyloxycarbonylazetidin-3-yl di(t-butyl)phosphate (46) (640 mg, 1.6 mmol) in MeOH (10 mL) was added to a Schlenk-flask charged with Pd/C (10% Pd in an oxidized form, 160 mg) in THE (3 mL), which was pre-reduced with H2. The reaction mixture was stirred overnight at r.t. under hydrogen. The reaction mixture was flushed with argon, transferred into centrifuge tubes, the catalyst removed, and washed with THF. The supernatant was evaporated to give a colorless oil (390 mg, 92% yield).
HR-MS: C11H24NO4P, found 266.1504 [M+H]+, calculated 266.1516; found 288.1346 [M+Na]+, calculated 288.1335.
1H NMR (400 MHz, Acetonitrile-d3) δ 5.03-4.94 (m, 1H), 4.26-4.18 (m, 2H), 4.11-4.01 (m, 2H), 1.41 (d, J=0.7 Hz, 18H).
13C NMR (101 MHz, Acetonitrile-d3) δ 85.6, 85.5, 67.2, 65.2, 55.3, 54.6, 30.0, 29.9, 1.9, 1.7.
31P NMR (162 MHz, Acetonitrile-d3) δ −12.02.
A solid sulfonyl chloride 49 (0.02 mmol, 11 mg) was added in portions to a stirred and cooled (0° C.) solution of azetidin-3-yl di(t-butyl)phosphate 48 (0.2 mmol, 53 mg) and Et3N (52 μL, 0.4 mmol) in MeCN (2 mL). After stirring for 10 min, the reaction mixture was analyzed by TLC (DCM/MeOH, 10/1), and a spot with Rf=0.5 was detected. The reaction mixture was lyophilized, and the residue was submitted to flash chromatography (SNAP Ultra cartridge with 10 g SiO2, gradient of DCM/MeOH with 2-15% MeOH over 15 CV) to provide an orange solid (2.0 mg, 8% yield).
HR-MS: C49H77N4O18P3S3, found 1199.3645 [M+H]+, calculated 1199.3681; found 1221.3505 [M+Na]+, calculated 1221.3500
1H NMR (400 MHz, Acetonitrile-d3) δ 9.24 (d, J=9.8, 0.6 Hz, 1H), 9.09 (d, J=0.6 Hz, 1H), 9.05 (d, J=9.7, 0.6 Hz, 1H), 8.89 (d, J=9.8, 0.6 Hz, 1H), 8.60 (d, J=9.7 Hz, 1H), 8.24 (d, J=0.6 Hz, 1H), 6.18 (s, 2H), 4.84-4.72 (m, 3H), 4.26-4.10 (m, 6H), 4.01-3.84 (m, 6H), 1.29 (s, 18H), 1.29 (s, 18H), 1.24 (s, 18H).
31P NMR (162 MHz, Acetonitrile-d3) 6-11.63 (“d”, J=4.3 Hz), −11.75.
A solution of sulfonyl chloride 49 (0.2 mmol, 110 mg) in 3.0 mL of ACN was added dropwise to a stirred and cooled (0° C.) solution of 3-(tet-butyldimethylsilyloxy)azetidine (1.35 mmol, 253 mg) and Et3N (176 μL, 1.35 mmol) in MeCN (1 mL). After stirring for 1 h, the reaction mixture was analyzed by TLC (DCM/MeOH, 10/1), and a spot with Rf=0.98 was detected. The reaction mixture was lyophilized, the residue submitted to flash chromatography (SNAP Ultra cartridge with 25 g SiO2, gradient of DCM/MeOH with 1-10% MeOH over 15 CV) to provide an orange solid (48 mg, 25% yield).
HR-MS: C43H68N4O9S3Si3, found 965.3522 [M+H]+, calculated 965.3529; found 987.3341 [M+Na]+, calculated 987.3348
1H NMR (400 MHz, Acetonitrile-d3) δ 9.24 (d, J=9.8 Hz, 1H), 9.08 (s, 1H), 9.06 (d, J=9.6 Hz, 1H), 8.90 (d, J=9.7 Hz, 1H), 8.57 (d, J=9.7 Hz, 1H), 8.22 (s, 1H), 6.11 (s, 2H), 4.55-4.43 (m, 3H), 4.11-4.01 (m, 6H), 3.75-3.62 (m, 6H), 0.67 (d, J=0.7 Hz, 18H), 0.61 (s, 10H), −0.09 (d, J=0.5 Hz, 12H), −0.13 (s, 6H).
13C NMR (126 MHz, Acetonitrile-d3) δ 147.7, 135.4, 134.4, 131.9, 130.3, 128.0, 127.3, 127.2, 127.1, 126.6, 124.2, 121.4, 119.5, 61.5, 61.4, 61.3, 61.2, 25.8, 25.7, 18.3, −5.0, −5.05, −5.1.
The reaction was carried out in a plastic test-tube (with a screw-cap) used for centrifugation. To a stirred solution of TBDMS-pyrene (44 mg, 0.45 mmol) in MeCN, 50-55% aq. HF (74 μL, 2.33 mmol) was added at 0° C. After stirring for 4 h, an additional amount of HF was added (74 μL, 2.33 mmol), and the reaction mixture was stirred overnight at r.t. The reaction mixture was analyzed by TLC (DCM/MeOH, 10/1), a new spot with Rf=0.25 was detected. The reaction was “quenched” by addition of an aqueous sodium bicarbonate solution (5%, 10 mL) and brine. The product was extracted with DCM/iPrOH (1:1; 3×100 mL). The combined organic solutions were dried over MgSO4 and concentrated in vacuo. The residue was submitted to flash chromatography (SNAP Ultra cartridge with 25 g SiO2, gradient of DCM/MeOH with 2-20% MeOH over 15 CV) to provide an orange solid (27 mg, 96%).
HR-MS: C25H26N4O9S3, found 623.0913 [M+H]+, calculated 623.0935; found 621.0773 [M−H]−, calculated 624.0789.
1H NMR (400 MHz, DMSO-d6) δ 9.06 (d, J=9.7 Hz, 1H), 8.91 (s, 1H), 8.87 (d, J=9.7 Hz, 1H), 8.83 (d, J=9.7 Hz, 1H), 8.70 (d, J=9.8 Hz, 1H), 8.16 (s, 1H), 7.70 (s, 2H), 5.72-5.59 (m, 3H), 4.38-4.24 (m, 3H), 4.07-3.91 (m, 6H), 3.65-3.45 (m, 6H).
13C NMR (101 MHz, DMSO-d6) δ 148.2, 134.3, 133.3, 133.1, 130.6, 129.1, 127.1, 126.6, 125.9, 125.0, 124.0, 121.9, 119.1, 117.1, 116.7, 115.8, 60.2, 60.0, 58.6, 58.5, 40.4.
λmax (absorption)=483 nm (ε=19000 M−1 cm−1, MeOH), λmax (emission)=534 nm (MeOH; excitation at 450 nm); Stocks shift 51 nm, fluorescence lifetime 5.6 ns (MeOH), fluorescence quantum yield: 0.77 (absolute value in MeOH). See
Ester 50 (2.0 mg, 1.67 μmol) was dissolved in dichloromethane (0.5 mL), the solution cooled to +5° C. in an ice bath, and then a solution of TFA in DCM (5% v/v, 0.5 mL) was added slowly with stirring. The reaction mixture was allowed to warm-up to r. t. and stirred for 2 h. The volatile materials were removed in vacuo. The residue was treated with 1 M aq. Et3N*H2CO3 buffer (TEAB; pH=8-9) and stirred, until the pH stabilized at 8-9. The title compound was isolated by preparative HPLC (Kinetex 5 μm EVO C18 100A 250×21 mm column, MeCN/water+0.05 M TEAB, 10 mL/min, 5-30% MeCN over 20 min) to afford 2 mg of dye 52 as red solid (88% yield of pentakis triethylammonium salt, according to 1H-NMR).
HR-MS: C25H29N4O18P3S3, found 860.9760 [M−H]−, calculated 860.9779.
1H NMR (400 MHz, D2O) δ 9.05 (s, 1H), 8.97 (d, J=9.8 Hz, 1H), 8.72 (d, 1H), 8.63 (d, J=7.0 Hz, 1H), 8.44 (d, J=16.6 Hz, 1H), 8.14 (s, 1H), 4.23-4.13 (m, 6H), 4.04-3.89 (m, 6H), 3.17 (q, 30H), 1.26 (t, J=7.3, 0.6 Hz, 45H).
λmax (absorption)=476 nm (H2O), λmax (emission)=543 nm (H2O; excitation at 450 nm); Stocks shift 67 nm, fluorescence lifetime 5.9 ns (H2O), fluorescence quantum yield: 0.8 (absolute value in H2O). See
A 1.5 mL Eppendorf vial was charged with dye 52 (2 mg, 1.5 μmol), glucose (5 equiv., 7.5 μmol, 1.5 mg) and malonic acid (10 equiv., 15 μL of 1 M solution in DMSO). The sample was stirred at 40° C. for 1 h (Eppendorf ThermoMixer®), and then water and DMSO were removed under reduced pressure (p<0.2 mbar) in lyophilizer. A solution of 2-picoline-borane complex (10 equiv., 15 μL of 1 M solution in DMSO) was added to the residue, and the samples were shaken at 40° C. for 16 h (Eppendorf ThermoMixer®). The product was isolated by preparative HPLC with UV-VIS detection (MeCN/TEAB 0.05 M in water, 5:95→30:70 in 20 min, detected at 500 nm).
HR-MS: C31H41N4O23P3S3, found 1025.3522 [M−H]−, calculated 1025.3529.
λmax (absorption)=505 nm (H2O), λmax (emission)=565 nm (H2O; excitation at 485 nm); Stocks shift 60 nm, fluorescence lifetime 5.8 ns (H2O), fluorescence quantum yield: 0.85 (absolute value in H2O). See
General Procedure:
1.5 mL Eppendorf vial was charged with a dye (compound 40 or APTS, 10 μL of 0.1 M solution in water), a dextran ladder (1.0 mg, maltodextrin oligosaccharides—DP2 to DP15, Carbosynth), and malonic acid (10 equiv., 10 μL of 1 M solution in DMSO). The samples were shaken at 40° C. for 1 h (Eppendorf ThermoMixer®), and then solvents were removed under reduced pressure (p<0.2 mbar) in lyophilizer. A solution of 2-picoline-borane complex (10 equiv., 10 μL of 1 M solution in DMSO) was added, and the samples were shaken at 40° C. for 16 h (Eppendorf ThermoMixer®). The products were isolated by preparative HPLC with UV-VIS detection (MeCN/aq. TEAB 5:95→30:70 in 20 min detected at 500 nm) or FC (C18, 15C18AQ-F0025 multi-use cartridge, MeCN/aq. TEAB 5:95→30:70).
Analytical HPLC: Kinetex, 5 μm C18 100, 25 cm×4.6 mm, MeCN/aq. TEAB 5:95→30:70 in 20 min detected at 500 nm, 1.2 mL/min;
Preparative HPLC: Kinetex, 5 μm C18 100, 25 cm×10 mm, MeCN/aq. TEAB 5:95→30:70 in 20 min detected at 500 nm, 4 mL/min;
Flash chromatography: RP (C18) cartridge, 15C18AQ-F0025 (Interchim), MeCN/aq. TEAB 5:95→30:70
This application is a U.S. National Phase Application of PCT/EP2019/084067, filed Dec. 6, 2019, the contents of which are incorporated herein by reference in their entireties for all purposes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/084067 | 12/6/2019 | WO |
