Patent Application
20170267726
Human Immunodeficiency Virus 1 (HIV-1) is thought to have infected up to 60 million people since its discovery over 20 years ago. Of those infected, more than 20 million have died, with the vast majority of individuals affected being from developing countries. There exists a need for more effective treatments for HIV-1 infections.
HIV-1 is able to replicate in primary human macrophages without stimulating a innate immune response, despite reverse transcription of genomic RNA into double stranded DNA, an activity that might be expected to trigger innate pattern recognition receptors (PRRs). HIV-1 replication is thus cloaked in human macrophages, so that it is invisible to the cell autonomous innate immune system. Very little is known of the mechanism behind the cloaking of HIV-1 replication. However, interference with this cloaking mechanism should result in activation of PRRs and a corresponding innate immune response via interferon secretion. Disruption of the HIV-1 cloaking mechanism could therefore provide an effective treatment for patients infected with HIV-1, by activation of their innate immune response.
The present inventors have surprisingly found that certain derivatives of cyclosporin are able to disrupt the HIV-1 cloaking mechanism, which means that PRRs are activated and interferons are secreted. The innate immune response is thus activated. It has also surprisingly been found that a similar anti-viral effect is observed, via activation of PRRs, with other viruses, such as human cytomegalovirus (hCMV).
Furthermore, it has surprisingly been found that these derivatives of cyclosporin are non-immunosuppressive, unlike cyclosporin itself. The compounds of the invention are therefore suitable for administration to patients infected with viruses, such as HIV-1, who will often have compromised immunity.
The combined properties of high anti-viral activity and low immunosuppressivity associated with the cyclosporin derivatives of the invention, as compared to unmodified cyclosporin or other cyclosporin derivatives, make these compounds promising therapeutic agents in the treatment or prevention of viral infections.
Thus, the present invention provides a cyclosporin derivative which is a compound of formula (I) or a pharmaceutically acceptable salt thereof, for use in the
wherein:
A represents
B represents methyl or ethyl,
R2 represents ethyl or isopropyl,
R4 represents —CH2CH(CH3)CH3, —CH2CH(CH3)CH2CH3, —CH(CH3)CH3 or —CH(CH3)CH2CH3, and
either (a) one of R1 and R1* represents hydrogen and the other represents methyl, and R3 represents -L3-G3, or (b) one of R1 and R1* represents hydrogen and the other represents -L1-G1, and R3 represents H, wherein
L1 and L3 represent a direct bond, a C1-C6 alkylene group or a C2-C6 alkenylene group, and
G1 and G3 represent a hydrogen atom, a —COOR′ group, or a phenyl moiety which is unsubstituted or substituted by one, two or three substituents selected from a halogen atom, a —COOR′ group, a —CONR′R″ group, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group, wherein R′ and R″ are the same or different and represent hydrogen or a C1-C6 alkyl group, provided that (a) G1 does not represent a hydrogen atom when L1 represents a direct bond or methylene, and (b) G3 does not represent a hydrogen atom when L3 represents a direct bond or methylene.
The invention further provides a cyclosporin derivative which is a compound of formula (I*), or a pharmaceutically acceptable salt thereof:
wherein:
A represents
B represents methyl or ethyl,
R2 represents ethyl or isopropyl,
R4 represents —CH2CH(CH3)CH3, —CH2CH(CH3)CH2CH3, —CH(CH3)CH3 or —CH(CH3)CH2CH3, and
either (a) one of R1 and R1* represents hydrogen and the other represents methyl, and R3 represents -L3-G3, or (b) one of R1 and R1* represents hydrogen and the other represents -L1-G1, and R3 represents H, wherein
L1 and L3 represent a direct bond, a C1-C6 alkylene group or a C2-C6 alkenylene group, and
G1 and G3 represent a hydrogen atom, a —COOR′ group, or a phenyl moiety which is substituted by one, two or three substituents selected from a halogen atom, a —COOR′ group, a —CONR′R″ group, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group, wherein R′ and R″ are the same or different and represent hydrogen or a C1-C6 alkyl group, provided that (a) G1 does not represent a hydrogen atom when L1 represents a direct bond or methylene, and (b) G3 does not represent a hydrogen atom when L3 represents a direct bond or methylene.
The invention further provides a pharmaceutical composition comprising a cyclosporin derivative which is a compound of formula (I*) or a or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient, diluent or carrier.
The invention further provides a cyclosporin derivative which is a compound of formula (I*) or a pharmaceutically acceptable salt thereof, for use in the treatment of the human or animal body.
The invention further provides use of a cyclosporin derivative which is a compound of formula (I) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in the treatment or prevention of a viral infection.
The invention further provides a method of treating or preventing a viral infection in a patient, which method comprises administering to said patient a cyclosporin derivative which is a compound of formula (I) or a pharmaceutically acceptable salt thereof.
In the compounds of the present invention, G1 does not represent a hydrogen atom when L1 represents a direct bond or methylene, and G3 does not represent a hydrogen atom when L3 represents a direct bond or methylene.
Compounds of formula (I*) in which G1 and G3 do not represents an unsubstituted phenyl moiety have not been described previously. It is therefore preferred that G1 and G3 represent a hydrogen atom, a —COOR′ group, or a phenyl moiety which is substituted by one, two or three substituents selected from a halogen atom, a —COOR′ group, a —CONR′R″ group, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group, wherein R′ and R″ are the same or different and represent hydrogen or a C1-C6 alkyl group.
Preferably, G1 and G3 represent a hydrogen atom, a —COOR′ group or phenyl moiety which is substituted by one or two, preferably one, substituents selected from a —COOR′ group, a hydroxyl group and a C1-C6 alkoxy group, wherein R′ represents hydrogen or a C1-C6 alkyl group.
More preferably, G1 and G3 represent hydrogen atom, a —COOH group or a phenyl moiety which is substituted by one substituent which is a —COOR′, more preferably a —COOH group. The substituent of the phenyl ring is preferably in the meta or para position, more preferably the para position. Thus, G1 and G3 most preferably represent a hydrogen atom, a —COOH group or a phenyl group which is substituted by one —COOH moiety in the para position.
Typically, L1 and L3 represent a C1-3 alkylene moiety or a C3-C5 alkenylene group.
It is particularly preferred that L1 and L3 represent a C1-3 alkylene moiety and G1 and G3 represent a phenyl moiety which is substituted by one substituent which is a —COOR′ group, more preferably a —COOH group. The substituent of the phenyl ring is preferably in the meta or para position, more preferably the para position.
It is also particularly preferred that L1 and L3 represent a C3-C5 alkenylene group and G1 and G3 represent a hydrogen atom or a —COOR′ group, more preferably a —COOH group.
It is further particularly preferred that L1 and L3 represent a C1-3 alkylene moiety and G1 and G3 represent a —COOR′ group, more preferably a —COOH group.
Typically, R′ and R″ are the same or different and represent hydrogen or methyl group.
Typically, R3 represents -L3-G3. Thus, the cyclosporin derivative is typically a compound of formula (I′) or a pharmaceutically acceptable salt thereof:
Preferably, the compound of formula (I′) has (R) stereochemistry at the 3′ position, that is the position where the -L3-G3 moiety is attached.
Preferably, in the compound of formula (I′), R1 represents methyl and R1* represents hydrogen.
In formula (I′), L typically represents a direct bond or a C1-C6 alkylene group; and G represents a phenyl moiety which is unsubstituted or substituted by one, two or three substituents selected from a halogen atom, a —COOR′ group, a —CONR′R″ group, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group, wherein R′ and R″ are the same or different and represent hydrogen or a C1-C6 alkyl group. Preferably L3 represents a C1-3 alkylene moiety, more preferably a methylene moiety. Preferably G3 represents a phenyl moiety which is substituted by one or two, preferably one, substituents selected from a —COOR′ group, a hydroxyl group and a C1-C6 alkoxy group, wherein R′ represents hydrogen or a C1-C6 alkyl group. G3 more preferably represents a phenyl moiety which is substituted by one substituent which is a —COOR′, more preferably a —COOH group. The substituent is preferably in the meta or para position, more preferably the para position. Thus, in formula (I′), G3 most preferably represents a phenyl group which is substituted by one —COOH or one —COOMe moiety in the para position. Preferred examples are the compounds of formulae (I′A) and (I′B) or a pharmaceutically acceptable salt thereof:
It is preferable that the compounds have (R) stereochemistry, and thus are formulae (I′C) or (I′D) or a pharmaceutically acceptable salt thereof:
It is also particularly preferred in formula (I′) that L3 represents a C3-C5 alkenylene group and G3 represents a hydrogen atom or a —COOR′ group, more preferably a —COOH group. Preferred examples are the compound of formulae (I′E), (I′F) and (I′G) or pharmaceutically acceptable salts thereof:
Alternatively, R3 may represent hydrogen, in which case the cyclosporin derivative is a compound of formula (I″) or a pharmaceutically acceptable salt thereof:
Typically, in formula (I″) R1* represents hydrogen and R1 represents -L1-G1.
It is particularly preferred in formula (I″) that L1 represent a C1-3 alkylene moiety and G1 represent a —COOR′ group, more preferably a —COOH group. A preferred example is the compound of formula (I″H) or a pharmaceutically acceptable salt thereof:
The residue at the 1 position of the cyclosporin derivatives of formula (I), (I′) and (I″) and (I*) contains either a hydroxyl group or a ketone, depending on the identity of A. Thus, the residue at the 1 position is of formula (II) if A represents
and of formula (II′) if A represents
Typically, A represents
Typically, B represents methyl.
Typically, R2 represents ethyl.
Typically, R4 represents —CH2CH(CH3)CH3.
Preferably, A represents
B represents methyl, R2 represents ethyl and R4 represents —CH2CH(CH3)CH3.
As used herein, a C1-C6 alkyl group may be straight or branched and is typically a C1-C3 alkyl group. Preferred C1-C6 alkyl groups include, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl and hexyl.
As used herein, a C1-C6 alkylene group is a said C1-C6 alkyl group which is divalent.
As used herein, a C2-C6 alkenylene group is a divalent moiety which may be straight or branched and is typically a C3-C5 alkenylene group. A C2-C6 alkenylene group typically contains one carbon-carbon double bond. The carbon-carbon double bond can have cis or trans configuration, with trans preferred.
As used herein, a C1-C6 alkoxy group is a said C1-C6 alkyl group which is attached to an oxygen atom. The alkoxy group is typically C1-C3 alkoxy group.
Particularly preferred alkoxy groups include, for example, methyoxy, ethyoxy, propoxy, isopropoxy, butoxy, isobutoxy, tert-butoxy, pentoxy and hexoxy.
As used herein, a halogen is typically chlorine, fluorine, bromine or iodine and is preferably chlorine, bromine or fluorine.
As used herein, a pharmaceutically acceptable salt is typically a salt with a pharmaceutically acceptable base. Pharmaceutically acceptable bases include alkali metal (e.g. sodium or potassium) and alkali earth metal (e.g. calcium or magnesium) hydroxides and organic bases such as alkyl amines, aralkyl amines or heterocyclic amines.
The cyclosporin derivatives of the invention may be prepared by standard methods known in the art, typically starting from commercially available cyclosporin A.
The cyclosporin derivatives of the invention are useful in the treatment or prevention of a viral infection in a patient. The treatment or prevention of the viral infection is typically mediated by activation of innate pattern recognition receptors. Typically, the cyclosporin derivatives of the invention are useful in the treatment of a viral infection in a patient. Typically, the patient is a mammal, such as a human or a cat, preferably a human.
Typically, the viral infection is human immunodeficiency virus-1 (HIV-1), influenza virus, human cytomegalovirus (hCMV), hepatitis C virus (HCV), dengue virus, a vaccinia virus (such as Small Pox), feline immunodeficiency virus (FIV) or a corona virus (such as SARs). Preferably, the viral infection is human immunodeficiency virus-1 (HIV-1), influenza virus, human cytomegalovirus (hCMV) or hepatitis C virus (HCV), more preferably human immunodeficiency virus-1 (HIV-1).
It is particularly preferred that, the cyclosporin derivatives of the invention are for use in the treatment human immunodeficiency virus-1 (HIV-1), influenza virus, human cytomegalovirus (hCMV) or hepatitis C virus (HCV), more preferably human immunodeficiency virus-1 (HIV-1), in patients, typically human patients.
The cyclosporin derivatives of the invention may be administered to humans in various manners such as oral, rectal, vaginal, parenteral, intramuscular, intraperitoneal, intraarterial, intrathecal, intrabronchial, subcutaneous, intradermal, intravenous, nasal, buccal or sublingual routes of administration. The particular mode of administration and dosage regimen will be selected by the attending physician, taking into account a number of factors including the age, weight and condition of the patient.
The compound may be given to prevent viral (HIV) infection and administered via a medical device inserted into the vagina or rectum such that the device allows a slow release of the compound over a period of weeks or months such that the patient is protected from infection during the period that the device is in place.
The cyclosporin derivative is typically administered as a pharmaceutical composition, which generally comprises a derivative of the invention and a pharmaceutically acceptable excipient, diluent or carrier. Thus, pharmaceutical compositions that contain the cyclosporin derivatives of the invention will normally be formulated with an appropriate pharmaceutically acceptable excipient, carrier or diluent depending upon the particular mode of administration being used. For instance, parenteral formulations are usually injectable fluids that use pharmaceutically and physiologically acceptable fluids such as physiological saline, balanced salt solutions, or the like as a vehicle. Oral formulations, on the other hand, may be solids, e.g. tablets or capsules, or liquid solutions or suspensions.
Compositions may be formulated in unit dosage form, i.e., in the form of discrete portions containing a unit dose, or a multiple or sub-unit of a unit dose.
The amount of the cyclosporin derivative of the invention that is given to a patient will depend upon on the activity of the particular compound in question. Further factors include the condition being treated, the nature of the patient under treatment and the severity of the condition under treatment. The timing of administration of the compound should be determined by medical personnel. As a skilled physician will appreciate, and as with any drug, the compound may be toxic at very high doses. For example, the compound may be administered at a dose of from 0.01 to 30 mg/kg body weight, such as from 0.1 to 10 mg/kg, more preferably from 0.1 to 5 mg/kg body weight.
The cyclosporin derivatives of the invention may be given alone or in combination with one or more additional anti-viral agents, preferably one or more agents useful for treating human immunodeficiency virus-1 (HIV-1), influenza virus, human cytomegalovirus (hCMV), hepatitis C virus (HCV), dengue virus, vaccinia virus, feline immunodeficiency virus (FIV) or corona virus.
Anti-viral agents useful for treating HIV-1 include non-nucleoside reverse transcriptase inhibitors (NNRTIs), nucleoside analogue reverse transcriptase inhibitor (NRTIs) and nucleotide analog reverse-transcriptase inhibitors (NtRTIs). Preferred NRTIs include Zidovudine, Didanosine, Zalcitabine, Stavudine, Lamivudine, Abacavir, Emtricitabine, Entecavir and Apricitabine, Preferred NNRTIs include Efavirenz, Nevirapine, Delavirdine, Etravirine and Rilpivirine. Preferred NtRTIs include Tenofovir and Adefovir.
Anti-viral agents useful for treating influenza virus include (a) neuraminidase inhibitors such as oseltamivir and zanamivir, and (b) M2 protein inhibitors such as amantadine and rimantadine.
Anti-viral agents useful for treating human cytomegalovirus (hCMV) include human cytomegalovirus antibodies and antiviral agents such as Ganciclovir, Valganciclovir, Foscarnet and cidofovir.
Anti-viral agents useful for treating hepatitis C virus (HCV) include pegylated interferon alpha and ribavirin.
Anti-viral agents useful for treating vaccinia virus include cidofovir.
Anti-viral agents useful for treating feline immunodeficiency virus (FIV) include Lymphocyte T-Cell Immunomodulator.
The active ingredients are typically administered as a combined preparation.
Accordingly, the present invention also provides a combination comprising a cyclosporin derivative of the invention and one or more said additional anti-viral agents. The combination is typically for use in the treatment or prevention of said viral infection in a patient.
The invention further provides a cyclosporin derivative of the invention for use in the treatment or prevention of a viral infection in a patient, by co-administration with one or more said additional anti-viral agents. Co-administration can be simultaneous, concurrent, separate or sequential.
The invention further provides one or more additional said anti-viral agents, for use in the treatment or prevention of a said viral infection in a patient, by co-administration with a cyclosporin derivative of the invention. Co-administration can be simultaneous, concurrent, separate or sequential.
The present invention further provides a product comprising a cyclosporin derivative of the invention and one or more said additional anti-viral agents, as a combined preparation for simultaneous, concurrent, separate or sequential use in the treatment or prevention of a said viral infection in a patient.
The following Examples illustrate the invention.
All commercially available solvents and reagents were used without further treatment as received unless otherwise noted. NMR spectra were measured with a Bruker DRX 500 or 600 MHz spectrometer; chemical shifts are expressed in ppm relative to TMS as an internal standard and coupling constants (J) in Hz. LC-MS spectra were obtained using a Waters ZQ2000 single quadrupole mass spectrometer with electrospray ionisation (ESI), using an analytical C4 column (Phenomenex Gemini, 50×3.6 mm, 5 μm) and an AB gradient of 50-95% for B at a flow rate of 1 mL/minute, where eluent A was 0.1:5:95 formic acid/methanol/water and eluent B was 0:5:95 formic acid/water/methanol. High resolution mass spectra were acquired on a Waters LCT time of flight mass spectrometer with electrospray ionisation (ESI) or chemical ionization (CI).
To LDA [1.8 M in hexane/ethylheptane] (39 mL, 70 mmol) in THF (40 mL) at −15° C. was added LiCl solid and the solution stirred for 10 minutes (brown colour). Enantiomerically pure cyclosporin A (CsA) (6.0 g, 5 mmol) in THF (25 mL) was added drop-wise keeping the temperature at −15 to −20° C. The reaction was stirred 30 minutes at −20° C. (brown colour). 4-bromomethylmethylbenzoate (2.0 g, 8.7 mmol) in THF (4 mL) was added dropwise keeping the temperature at −20° C. to −15° C. The reaction was stirred at this temperature for 30 minutes (red colour). The temperature allowed to rise to −5° C. then the reaction stopped by addition of 5% AcOH/methanol (100 mL). The reaction was stirred overnight then a rotary evaporator used to remove THF and methanol. DCM (200 mL) and water (100 mL) were added. The DCM layer was separated. The water layer was extracted with DCM (2×50 mL). The combined DCM extracts were dried (Na2SO4). This gave 7.54 g of crude CsA methyl ester. The product was purified using silica gel chromatography employing acetone/DCM to obtain a product of approximately 90% purity, 710 mg.
The CsA methyl ester (700 mg, 0.52 mmol) was dissolved in THF (7 mL) and methanol (2 mL) and lithium hydroxide solution (LiOH. H2O, 210 mg, 5 mmol) dissolved in 5 mL water added. The reaction was stirred for 48 hours at room temperature and monitored by liquid chromatography-mass spectrometry (LCMS). A further equivalent of LiOH was added to drive the hydrolysis to completion. Compound 1 was isolated using ion exchange chromatography eluting with acetic acid/methanol/DCM. Yield 170 mg.
FAB+ve; Calc. m/z C70H117N11O14 (M+Na) 1358.86787. Found (M+Na) 1358.86447.
CypA was expressed in Escherichia coli C41(DE3) cells (Lucigen) from tagless expression vector pOPT. Cells were grown overnight at 18° C. before being harvested, sonicated and purified by SP ion-exchange chromatography (GE Healthcare) followed by gel filtration. Crystals of Compound 1 in complex with CypA were grown at 17° C. in sitting drops. Protein solution (1 mM each of CypA and Compound 1 in 20 mM Tris pH 8, 50 mM NaCl, 1 mM DTT, 1% DMSO) was mixed with reservoir solution (1 M LiCl, 0.1 M MES pH 6, 30% w/v PEG 6000) in a 1:1 mix, producing 0.15 mm×0.10 mm×0.10 mm crystals within 24 h.
Crystals were flash-frozen in liquid nitrogen before data collection using a Mar-345 detector. Crystal data and diffraction statistics are provided in Table 1 below.
Crystallographic analysis was performed using programs from the CCP4 suite13. Data were indexed and scaled in MOSFLM and SCALA, respectively. The structure of CsA:CypA (pdb 1CWA14) was used as a search model. Structures were refined in REFMAC and Coot13. Structureswere created using PyMol.
The crystal structure of Compound 1 in complex with CypA is shown in
Primary monocyte-derived macrophages (MDM) were prepared from fresh blood from healthy volunteers. Peripheral blood mononuclear cells were isolated by Ficoll-Hypaque (Axis-Shield) density centrifugation. The isolated cells were washed with PBS and plated in RPMI (Invitrogen) supplemented with 10% heat-inactivated autologous human serum (HS) and 40 ng/ml macrophage colony stimulating factor (M-CSF) (R&D systems). The medium was then refreshed after 3 days (RPMI 1640 with 10% HS), removing any remaining non-adherent cells. After 6 days, media was replenished with RPMI containing 5% type AB HS (Sigma-Aldrich-Aldrich). Replicate experiments were performed with cells derived from different donors.
Virus particles were produced by transient transfection of HEK293T cells. 3.5 g of molecular clone DNA; NL4.3Bal was transfected using Fugene 6 transfection reagent (Promega). Virus supernatants were harvested 48 hr, 72 hr and 96 hr post transfection. All virus suspensions were filtered and ultracentrifuged through a 20% sucrose buffer and resuspended in RPMI 1640 with 5% HS, for subsequent infection of MDM. All virus preparations were quantified by reverse transcriptase (RT) enzyme linked immunosorbant assay (ELISA) (Roche).
MDM were infected with 100 pg RT/well (MOI 0.2) in 48-well plates and subsequently fixed and stained using CA specific antibodies (EVA365 & 366 National Institute of Biological Standards AIDS Reagents Programme) and a secondary antibody linked to beta galactosidase. Infection was performed in DMSO in the presence or absence of 10 μM Compound 1. Cells were stained for Gag p24 at specific time points after infection and infected colonies counted. During the time course, supernatants were collected for IFN-β ELISA (PBL Interferon Source) according to manufacturer's instructions.
Human cytomegalovirus (hCMV, strain Towne RC256) was used to infect primary human foreskin fibroblasts (HFF) at a multiplicity of 0.01 particle forming units per cell in the presence of either 5 μM Compound 1 in DMSO or DMSO vehicle as a control. The infected cells were then incubated for time points as shown in
Progeny virus was detected by plaque assay of supernatants on fresh HFF. 7 days later, HCMV plaques were revealed by immunocytochemical staining using the cytomegalovirus early antigen specific primary mouse monoclonal antibody HCMV3, and goat anti mouse antibody conjugated to alkaline phosphatase, with the colorimetric substrate fast red. Plaque forming units of HCMV are plotted against time in
Feline immunodeficiency virus (FIV) is used to infect a feline T cell line or a feline fibroblast line at a multiplicity of 0.01 particle forming units per cell in the presence of either 5 μM of the test compound of the invention in DMSO or DMSO vehicle as a control. The infected cells are then incubated for various time points before fixation with paraformaldehyde and enumeration of the infected cells.
To detect infected cells the cells are stained with anti-FIV antibody and secondary antibody labeled with a fluorescent marker. Fluorescent cells are then measured by flow cytometry. The number of infected cells are plotted against time.
Human influenza A virus (IAV) was used to infect human A549 cells at a multiplicity of 0.01 infectious unit per cell in the presence of either 5 μM of the test compound of the invention in DMSO or DMSO vehicle as a control. The infected cells are then incubated for various time points before collection of the supernatants. Progeny virus are detected by plaque assay of supernatants on fresh A549 cells. IAV plaques are revealed by immunocytochemical staining using IAV specific primary antibody, and secondary antibody conjugated to alkaline phosphatase, with the colorimetric substrate fast red. Plaque forming units of IAV are plotted against time.
To assess the impact of compounds of the invention on vaccinia virus (VACV) infection, primary human foreskin fibroblasts (HFFs) are infected at an MOI of 1 with recombinant VACV expressing EGFP under the control of an early/late viral promoter in the presence of increasing concentrations of the compound of the invention. At six hours post infection cells are harvested and scored for EGFP by flow cytometry. In order to determine if the compound impacted VACV production, HFFs are infected with wildtype virus at an MOI of 1. Twenty-four hours post infection cells are harvested and virus released by three cycles of freeze/thawing. Virus production is quantified by plaque assay on BSC40 green monkey kidney cells. For all experiments samples treated with vehicle alone (DMSO) are used as controls.
Inhibition of HCV by the compounds of the invention is tested using subgenomic replicons derived from HCV. The subgenomic replicons encode all proteins required for RNA replication and a marker gene such as luciferase or green fluorescent protein (GFP). Cells expressing the subgenomic replicon are treated with the test compounds for various time points between 4 and 48 hours. At these time points replication are assessed by measurement of the marker (luciferase or GFP).
Inhibition of Dengue virus by the compounds of the invention is tested using subgenomic replicons derived from Dengue virus. The subgenomic replicons encode all proteins required for RNA replication and a marker gene such as luciferase or green fluorescent protein (GFP). Cells expressing the subgenomic replicon are treated with the test compounds for various time points between 4 and 48 hours. At these time points replication are assessed by measurement of the marker (luciferase or GFP).
To a stirred solution of 1.8M lithium diisopropylamide (39 mL, 70 mmol) in anhydrous THF at −10° C. was added dropwise a cooled solution of Cyclosporin A (6 g, 5 mmol) and lithium chloride (3.81 g, 89 mmol) in THF. The mixture was stirred at this temperature for an hour before the dropwise addition of a solution of allyl bromide (0.755 ml, 8.7 mmol) in THF. After a further 3 hours stirring at −5° C. the reaction was quenched by the addition of 5% acetic acid in methanol solution.
The mixture was concentrated under reduced pressure before dissolution in DCM and water. The DCM layer was separated and the aqueous layer was extracted twice with DCM. The organic fractions were combined, dried over magnesium sulphate and concentrated under reduced pressure. The product was purified by flash silica chromatography (0-20% acetone:DCM gradient) to give Compound 2 as an off-white solid (1.144 g, 18%).
HRMS (m/z): [MH]+ calcd. for C65H115N11O12, 1242.88. found 1242.89.
To a solution of Compound 2 (3-allyl Cyclosporin A) (75 mg, 0.06 mmol) in DCM (2 mL) was added acrylic acid (5 μl, 0.072 mmol) and Hoveyda-Grubbs 2nd generation catalyst (7 mg, 0.01 mmol, 17 mol %). The reaction was stirred in the microwave at 90° C. for 30 minutes and then allowed to cool. Triethylamine was added to the mixture and then stirred overnight with excess P(CH2OH)3 to coordinate the ruthenium catalyst. This was then washed away with brine and water before the mixture was then passed through a Stratospheres SPE, PL Thiol MP SPE cartridge (polymer Lab, Varian Inc) to remove any remaining catalyst. The crude product was purified by flash silica chromatography (40:8:1 DCM:MeOH:NH3) to give Compound 3 as an off-white solid (45 mg, 53%).
HRMS (m/z): [MH]+ calcd. for C66H115N11O14, 1286.68 found 1286.94.
To a solution of cyclosporin A (500 mg, 0.415 mmol) in DCM (2 mL) was added 4-pentenoic acid acid (128 μl, 1.245 mmol) and Hoveyda-Grubbs 2nd generation catalyst (44 mg, 0.07 mmol, 17 mol %). The reaction was stirred in the microwave at 90° C. for 30 minutes and then allowed to cool. Triethylamine was added to the mixture and then stirred overnight with excess P(CH2OH)3 to coordinate the ruthenium catalyst. This was then washed away with brine and water before the mixture was then passed through a Stratospheres SPE, PL Thiol MP SPE cartridge (polymer Lab, Varian Inc) to remove any remaining catalyst. The crude product was purified by flash silica chromatography (5% MeOH in DCM) to give Compound 4 as an off-white powder (322 mg, 62%).
HRMS (m/z): [MH]+ calcd. for C64H133N11O14, 1260.65. found 1260.84.
To a solution of the benzoic acid derivative (25 mg, 0.019 mmol) in methanol (2 mL) was added a catalytic amount of concentrated sulphuric acid. The reaction was heated to reflux for an hour and then allowed to cool before neutralising with 10% NaHCO3 solution. The product was extracted with DCM, washed with water and concentrated under reduced pressure. The crude product was purified by preparative HPLC chromatography (MeOH:H20:formic acid) to give Compound 5 as a white solid (5 mg, 20%).
LC-MS [MH]+ calcd. for C71H119N11O14, 1350.77. found 1350.50.
To a stirred solution of 2M lithium diisopropylamide in heptane/THF (3.75 mL, 7.5 mmol) in anhydrous THF at −10° C. was added dropwise a cooled solution of Cyclosporin A (0.6 g, 0.5 mmol) in THF. The mixture was stirred at this temperature for an hour before the dropwise addition of a solution of 5-bromopent-1-ene (0.190 ml, 1.25 mmol) in THF. After a further 3 hours stirring at −5° C. the reaction was quenched by the addition of 5% acetic acid in methanol solution.
The mixture was concentrated under reduced pressure before dissolution in DCM and water. The DCM layer was separated and the aqueous layer was extracted twice with DCM. The organic fractions were combined, dried over magnesium sulphate and concentrated under reduced pressure. The product was purified by flash silica chromatography (0-20% acetone:DCM gradient) to give Compound 6 as an off-white solid (0.065 g, 10%).
LC-MS [MH]+ calcd. for C67H119N11O12, 1270.73. found 1270.60.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1303681.9 | Mar 2013 | GB | national |
| 1303685.0 | Mar 2013 | GB | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14768684 | Aug 2015 | US |
| Child | 15608840 | US |
