Patent Application
20050148768
1. Field of the Invention
The present invention relates generally to cobalt-porphyrin complexes which are useful as anti-obesity agents, as well as to compounds, compositions and methods related to the same.
2. Description of the Related Art
Porphine i is the parent substance of porphyrins, a group of compounds found in all living matter and which are the basis of respiratory pigments in animals and plants. Porphyrins constitute a class of compounds wherein the hydrogen atoms of porphine's pyrrole rings are substituted with various side chains. Porphyrins have received extensive study, much of which is presented in a multi-volume treatise entitled The Porphyrins, D. Dolphin, Ed., Academic Press, N.Y., 1978.
An exemplary porphyrin is protoporphyrin IX ii. Protoporphyrin IX is the immediate precursor of heme, which is the complex formed upon chelation of iron by protophorphryin. In addition to iron, protoporphryin IX readily chelates with other metals.
When chelated to cobalt, the resulting complex is cobalt-protoporphyrin iii (including salts and/or ligand complexes thereof).
A related analogue of protoporphyrin IX ii is mesoporphyrin iv, which differs from protoporphyrin to the extent that the two ethylene side chains are fully saturated. When chelated to cobalt, cobalt mesoporphyrin v results (including salts and/or ligand complexes thereof).
Cobalt protoporphyrin (“Co-PP”) has been reported to regulate food intake and body weight in rats (Galbraith and Kappas, Proc. Natl. Acad. Sci. U.S.A. 86: 7653-7657, 1989), as well as in other animals such as rats, dogs and monkeys. A single subcutaneous injection of Co-PP produces a prompt dose-dependent decrease in food intake in Sprague Dawley rats. This result is accompanied by a sustained decrease in body weight, that is characterized by decreases in carcass fat content without changes in protein content. Smaller doses of Co-PP delivered by intracerebroventricular administration has also been found to elicit the same effect.
The regulatory effect of Co-PP has also been extended to animals that are genetically destined to become markedly obese. Thus, subcutaneous administration of Co-PP to Zucker rats whose obesity is conferred by homozygosity of the fa gene (fa/fa) produces long-sustained reduction in body weight (Galbraith and Kappas, Pharmacology 41: 292-298, 1990). The effect of Co-PP is profound and believed to be caused by the phenotype of gene expression in the fa/fa animal to revert to a phenotype similar to that of the heterozygous lean animal. Whereas cobalt mesoporphyrin (“Co-MP”) has a comparable biological profile, the same effect is not found upon administration of inorganic cobalt, or a number of other metal chelates of porphyrins. The mechanism of action of Co-PP for regulation of body weight is unknown, and it has been shown that the weight loss in rats is not mediated by the neuropeptide Y system (Choi et al, Brain Research 729: 223-227, 1996; Turner et al, Physiology and Behavior 56: 10009-1014, 1994).
Administration of Co-PP and/or Co-MP for regulation of body weight is not without drawbacks. For example, oxidative stress has been associated with administration of high doses of Co-PP (see Tomaro et al., Arch. Biochem. Biophys. 286: 610-617, 1991). Accordingly, there is a need in the art for compounds which have the beneficial properties associated with Co-PP and/or Co-MP, such as the ability to regulate body weight, but which not possess the unwanted side-effects presently encountered with administration of the same. The present invention fulfills these needs and provides other related advantages.
Briefly stated, the present invention is directed to cobalt-porphyrin (Co-P″) complexes which are useful as an anti-obesity agents, as well as to compositions and methods related to the same. Cobalt-porphyrins of this invention are referred to as a “complex” since the porphyrin ring serves as a tetradentate ligand which complexes (i.e., chelates) the central cobalt ion. The Co-P complexes of this invention have activity over a wide range of therapeutic application, including (but not limited to) use as anti-obesity agents.
More specifically, the cobalt-porphyrin (Co-P) complexes of this invention have the following structure (I):
including salts thereof, wherein:
In one embodiment, reduced redox activity is achieved by conjugating Co-P, at the R1 and/or R2 positions, with a reactive oxygen species (ROS) modulating agent. In an alternative embodiment, reduced redox activity is imparted by coordination of Co-P with an appropriate L1 and/or L2 ligand.
It should be understood that structure (I) above is intended to encompass both cobalt (II) and cobalt (III), as well as any coordination complex thereof. For example, when chelated by the tetradentate porphyrin ligand, cobalt typically has an oxidation number of (II) or (III)— that is, Co+2 or Co+3, respectively—and has a coordination number of 4 (square planer) or 6 (octahedral). Thus, when in a tetrahedral form, two additional ligands (designated as L1 and L2 in structure (I) above) are coordinated with the cobalt ion. On the other hand, when in the tetrahedral form, L1 and L2 are not present. For this reasons, L1 and L2 are referred to as “optional” in structure (I) above and, when present, may be the same or different.
These and other aspects of the present invention will become evident upon reference to the following detailed description and attached drawings. To that end, various references are set forth herein which describe in more detail certain aspects of this invention, and are each incorporated by reference in their entirety.
The present invention is generally directed to cobalt-porphyrin (Co-P) complexes, as well as to compositions and methods related to the same. As noted above, a Co-P complex of this invention has the following structure (I):
R1 and R2 are the same or different and independently —(CH2)n-A-R5, wherein A is —C(═O)O—, —OC(═O)—, —C(═O)N(R)—, —N(R)C(═O)—, —C(═O)—, —N(R)—, —O— or —S—, R is hydrogen, alkyl, substituted alkyl, arylalkyl or substituted arylalkyl, and n is 2 or 3;
As used herein, the terms used above have the following meaning:
“Alkyl” means a straight chain or branched, saturated or unsaturated, cyclic or non-cyclic hydrocarbon having from 1 to 10 carbon atoms, while “lower alkyl” has the same meaning but only has from 1 to 6 carbon atoms. Representative saturated straight chain alkyls include methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, and the like; while saturated branched alkyls include isopropyl, sec-butyl, isobutyl, tert-butyl, isopentyl, and the like. Unsaturated alkyls contain at least one double or triple bond between adjacent carbon atoms (also referred to as an “alkenyl” or “alkynyl”, respectively). Representative straight chain and branched alkenyls include ethylenyl, propylenyl, 1-butenyl, 2-butenyl, isobutylenyl, 1-pentenyl, 2-pentenyl, 3-methyl-1-butenyl, 2-methyl-2-butenyl, 2,3-dimethyl-2-butenyl, and the like; while representative straight chain and branched alkynyls include acetylenyl, propynyl, 1-butynyl, 2-butynyl, 1-pentynyl, 2-pentynyl, 3-methyl-1 butynyl, and the like. Representative saturated cyclic alkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, (cyclohexyl)CH2—, and the like; while unsaturated cyclic alkyls include cyclopentenyl and cyclohexenyl, and the like. Cycloalkyls are also referred to herein as “carbocyclic” rings systems, and include bi- and tri-cyclic ring systems having from 8 to 14 carbon atoms such as a cycloalkyl (such as cyclo pentane or cyclohexane) fused to one or more aromatic (such as phenyl) or non-aromatic (such as cyclohexane) carbocyclic rings.
“Halogen” means fluorine, chlorine, bromine or iodine.
“Oxo” means a carbonyl group (i.e., “═O”).
“Aryl” means an aromatic carbocyclic moiety such as phenyl or naphthyl.
“Arylalkyl” means an alkyl having at least one alkyl hydrogen atom replaced with an aryl moiety, such as benzyl, —(CH2)2phenyl, —(CH2)3phenyl, —CH(phenyl)2, and the like.
“Heteroaryl” means an aromatic heterocycle ring of 5- to 10 members and having at least one heteroatom selected from nitrogen, oxygen and sulfur, and containing at least 1 carbon atom, including both mono- and bicyclic ring systems. Representative heteroaryls are pyridyl, furyl, benzofuranyl, thiophenyl, benzothiophenyl, quinolinyl, pyrrolyl, indolyl, oxazolyl, benzoxazolyl, imidazolyl, benzimidazolyl, thiazolyl, benzothiazolyl, isoxazolyl, pyrazolyl, isothiazolyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, cinnolinyl, phthalazinyl, and quinazolinyl.
“Heteroarylalkyl” means an alkyl having at least one alkyl hydrogen atom replaced with a heteroaryl moiety, such as —CH2pyridinyl, —CH2pyrimidinyl, and the like.
“Heterocycle” means a 5- to 7-membered monocyclic, or 7- to 10-membered bicyclic, heterocyclic ring which is either saturated, unsaturated, or aromatic, and which contains from 1 to 4 heteroatoms independently selected from nitrogen, oxygen and sulfur, and wherein the nitrogen and sulfur heteroatoms may be optionally oxidized, and the nitrogen heteroatom may be optionally quaternized, including bicyclic rings in which any of the above heterocycles are fused to a benzene ring. The heterocycle may be attached via any heteroatom or carbon atom. Heterocycles include heteroaryls as defined above. Thus, in addition to the heteroaryls listed above, heterocycles also include morpholinyl, pyrrolidinonyl, pyrrolidinyl, piperidinyl, piperazinyl, hydantoinyl, valerolactamyl, oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydroprimidinyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, and the like.
“Heterocyclealkyl” means an alkyl having at least one alkyl hydrogen atom replaced with a heterocycle, such as —CH2morpholinyl, and the like.
The term “substituted” as used herein means any of the above groups (i.e., aryl, arylalkyl, heterocycle and heterocyclealkyl) wherein at least one hydrogen atom is replaced with a substituent. In the case of an oxo substituent (“═O”) two hydrogen atoms are replaced. Substituents include halogen, hydroxy, alkyl, substituted alkyl (such as haloalkyl, mono- or di-substituted aminoalkyl, alkyloxyalkyl, and the like), aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocycle, substituted heterocycle, heterocyclealkyl, substituted heterocyclealkyl, —NRaRb, —NRaC(═O)Rb, —NRaC(═O)NRaRb, —NRaC(═O)Rb —NRaSO2Rb, —ORa, —C(═O)Ra —C(═O)ORa —C(═O)NRaRb, —OC(═O)Ra, —OC(═O)ORa, —OC(═O)NRaRb, —NRaSO2Rb, or a radical of the formula —Y-Z-Ra where Y is alkanediyl, substitute alkanediyl, or a direct bond, Z is —O—, —S—, —S(═O)—, —S(═O)2—, —N(Rb)—, —C(═O)—, —C(═O)O—, —OC(═O)—, —N(Rb)C(═O)—, —C(═O)N(Rb)— or a direct bond, wherein Ra and Rb are the same or different and independently hydrogen, amino, alkyl, substituted alkyl (including halogenated alkyl), aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocycle, substituted heterocycle, heterocylealkyl or substituted heterocyclealkyl, or wherein Ra and Rb taken together with the nitrogen atom to which they are attached form a heterocycle or substituted heterocycle.
In one embodiment, both of R3 and R4 are —CH═CH2 and a Co-P complex of this invention has the following structure (II):
In another embodiment, both R3 and R4 are —CH2CH3 and a Co-P complex of this invention has the following structure (III):
In still a further embodiment, R1 and R2 are both —(CH2)n-A-R5 wherein A is —C(═O)O—, and a Co-P complex of this invention has the following structure (IV):
In still other embodiments, R1 and R2 are both (CH2)n-A-R5 wherein A is —OC(═O)—, —C(═O)N(R)—, —N(R)C(═O)—, —C(═O)—, —N(R)—, —O— or —S—, and a Co-P complex of this invention has the following structure (V), (VI), (VII), (VIII), (IX), (X) or (XI), respectively:
In the context of this invention, it has been found that a Co-P complex of structure (I) above retains many of the beneficial properties associated with Co-PP and/or Co-MP, such as the ability to regulate body weight, but reduces and/or eliminates many of the unwanted side-effects presently encountered upon administration of the same. Although not intending to be limited by the following theory, it is believed that administration of Co-PP and/or Co-MP triggers significant production of reactive oxygen species at the site of injection, particularly hydrogen peroxide, which have deleterious consequences to tissue. For example, such reactive oxygen species result in free radical damage to DNA, protein and membrane components, and increased intracellular levels of reactive oxygen species lead to increased vulnerability to apoptotic and necrotic cell death. Indeed, administration of high doses of Co-PP results in induction of heme oxygenase, and such induction is preceded by oxidative stress that is triggered by depletion of reduced glutathione levels (see Tomao et al. Arch. Biochem. Biophys. 286: 610-617, 1991).
In the practice of this invention, generation of reactive oxygen species is modulated by conjugating Co-P with a reactive oxygen species (ROS) modulating agent, and/or by coordinating Co-P with a ligand. In the first case, one or both of the R1/R2 moieties serves as a ROS modulating agent. Linking R5 via linker A may be achieved by chemistry known in this field, such as, for example, starting with the corresponding carboxylic acid (i.e., wherein A is —C(═O)O— and R5 is hydrogen). In the second case, Co-P is complexed with one or more ligands, L1 and L2. Again, formation of such complexes is know to one skilled in this field, and is accomplished by appropriate selection and coordination of the L1 and/or L2 ligands. As used herein, a “ROS modulating agent” means a moiety which can be covalently joined to Co-P (through linker A), and which serves to modulate generation of ROS normally induced by administration of Co-PP and/or Co-MP. In this regard, a “ligand” means any molecule or ion that has at least one electron pair that can be donated. In general, the ability of such a moiety or ligand to modulate generation of ROS can be identified by its ability, when bound to Co-P of structure (I), to prevent generation of reactive oxygen species in the assays disclosed in Examples 15 and/or 16.
In one embodiment of this invention, the ROS modulating agent is thioctic acid or ebelsen, as depicted below, joined to Co-P via linker A of structure (I):
Thioctic acid is a cyclic disulfide that is interconvertible with dihydrothioctic acid. Ebelsen is a selenoorganic compound that is an effective mimic of glutathione peroxidase, an enzyme that catalyses the reduction of hydroperoxides at the expense of thiol reducing equivalents (Sies, H, Free Radical Biology & Medicine 14: 313-323, 1993). The substrate specificity of ebselen ranges from hydrogen peroxide to smaller organic hydroperoxides to membrane-bound phospholipids and cholesterol hydroperoxides. Both thioctic acid and ebelsen are endogenous cofactors of mitochondrial pyruvate dihydrogenase and α-ketoglutarate dehydrogenase complexes, help maintain glutathione and α-tocopherol in their reduced states, and possess intrinsic free-radical scavenging properties.
In generally, ROS modulating agents may be joined to Co-P by formation of a suitable covalent bond. For example, if an amide bond is to be utilized, the carboxylic acid of thioctic acid may be converted to the corresponding amide by well-known organic chemistry techniques, or an amine-substituted derivative of ebselen may be utilized. The amine may then be reacted with the carboxylic acid of Co-PP (or Co-MP), again using well-known techniques, to yield representative compounds (Va) and (Vb). (Note: In the following structures (Va) and (Vb) optional ligands L1 and L2 are not depicted):
In another embodiment, an as mentioned above, the generation of ROS are modulated by coordinating Co-P with a ligand. Formation of such complexes is generally known to one skilled in this field, and is accomplished by appropriate selection and coordination of the L1 and/or L2 ligands. In this regard, suitable ligands include any ligand capable of donating electrons to the electron-deficient metal ion, which, in this case, is cobalt. Such ligands are capable of occupying one position in the inner coordination sphere and forming at least one coordinate bond to cobalt, and are typically unidentate ligands. Representative ligands include, but are not limited to, halo (fluoro, chloro, bromo or iodo), cyano, amino, mono- or di-substituted amino wherein the substituent(s) is(are) as defined above for Ra and Rb, amino groups of amino acid such as glycinate, and substituted or unsubstituted heterocycles containing one or more nitrogen, oxygen and/or sulfur heteroatoms as defined above, including substituted or unsubstituted heteroaryls such as piperidine and imidazole.
As noted above, Co-P compounds of structure (I) must have reduced redox activity compared to cobalt mesoporphyrin (Co-MP). Such activity can be readily determined by, for example, the assay disclosed in Example 16. In that assay, redox activity is measured by oxygen consumption catalyzed by a Co-P test compound in the presence of ascorbate and TMPD. This same assay is also performed on Co-MP, and a comparison is made to determine whether the test compound exhibits reduced redox activity compared to Co-MP.
In the context of novel Co-P complexes of this invention, the Co-P complex of structure (I) has reduced redox activity compared to Co-MP. Such comparison is made by assigning a value of 100% to the redox activity of Co-MP. A novel Co-P complex of this invention has 5% (or less) the redox activity of Co-MP. Preferably, the Co-P complex has a redox activity of 4% (or less), more preferably of 3% (or less), even more preferably of 2% (or less), and most preferably of 1% (or less) the redox activity of Co-MP. In even a more specific and preferred embodiment, the redox activity of the novel Co-P complex of this invention is not detectable by the assay disclosed in Example 16 (i.e., 0% the redox activity of Co-MP).
In the context of the methods of this invention, such as methods for treating obesity, the Co-P complex of structure (I) has 50% (or less) the redox activity of Co-MP. Preferably, the Co-P complex has 20% (or less), more preferably 10% (or less), even more preferably of 5% (or less), and most preferably of 1% (or less) the redox activity of Co-MP. In even a more specific and preferred embodiment, the redox activity of the Co-P complex administered to a patient within a method of this invention is not detectable by the assay disclosed in Example 16.
Such redox activity measurements are illustrated in Table 3 of Example 18, wherein Co-MP was assigned a value of 1 (ie., 100%). In that example, Co-PP was found to have a higher redox activity than Co-MP (2.2 times higher), while the representative Co—P complexes identified in Table 3 all had reduced redox activity (with some having no detectible activity) compared to Co-MP.
A Co-P complex of this invention, or a pharmaceutically acceptable salt thereof, is administered to a patient in a therapeutically effective amount. A therapeutically effective amount is an amount calculated to achieve the desired effect. It will be apparent to one skilled in the art that the route of administration may vary with the particular treatment. Routes of administration may be either non-invasive or invasive. Non-invasive routes of administration include oral, buccal/sublingual, rectal, nasal, topical (including transdermal and ophthalmic), vaginal, intravesical, and pulmonary. Invasive routes of administration include intraarterial, intravenous, intradermal, intramuscular, subcutaneous, intraperitoneal, intrathecal and intraocular. In a typical embodiment, administration is by injection.
The required dosage may vary with the particular treatment and route of administration. In general, dosages for Co-P complex will be from about 1 to about 5 milligrams of the compound per kilogram of the body weight of the host animal per day; frequently it will be between about 100 μg and about 5 mg but may vary up to about 50 mg of compound per kg of body weight per day. Therapeutic administration is generally performed under the guidance of a physician, and pharmaceutical compositions contain the mitochondria protecting agent in a pharmaceutically acceptable carrier. These carriers are well known in the art and typically contain non-toxic salts and buffers. Such carriers may comprise buffers like physiologically-buffered saline, phosphate-buffered saline, carbohydrates such as glucose, mannose, sucrose, mannitol or dextrans, amino acids such as glycine, antioxidants, chelating agents such as EDTA or glutathione, adjuvants and preservatives. Acceptable nontoxic salts include acid addition salts or metal complexes, e.g., with zinc, iron, calcium, barium, magnesium, aluminum or the like (which are considered as addition salts for purposes of this application). Illustrative of such acid addition salts are hydrochloride, hydrobromide, sulphate, phosphate, tannate, oxalate, fumarate, gluconate, alginate, maleate, acetate, citrate, benzoate, succinate, malate, ascorbate, tartrate and the like. If the active ingredient is to be administered in tablet form, the tablet may contain a binder, such as tragacanth, cornstarch or gelatin; a disintegrating agent, such as alginic acid; and a lubricant, such as magnesium stearate. If administration in liquid form is desired, sweetening and/or flavoring may be used, and intravenous administration in isotonic saline, phosphate buffer solutions or the like may be effected.
The following examples are offered by way of illustration, and not by way of limitation.
Cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (329.5 mg, 0.500 mmol) was slurried in dry alcohol (10 mL). The mixture was cooled on an ice-bath and while stirred, H2SO4 (0.500 ml) was added dropwise over ca 30 sec. The reaction flask was tightly stoppered and the mixture was stirred overnight (ca 16 h) at ambient temperature. The reaction mixture was partitioned between CH2Cl2 (40 ml) and 1.0 M HCl (20 ml), the organic layer was dried over anhydrous Na2SO4. The solvent was removed by rotary evaporation to provide a deep red glassy material. Further purification was achieved by silica gel flash chromatography using CH2Cl2/MeOH (9/1 and 85/15) as eluents. Appropriate fractions were pooled and evaporated, furnishing the desired diester as its putative chloride salt.
Conversion to the respective bisglycinate complexes was performed as follows. The putative chloride salt was dissolved in EtOH at a concentration of 10 mM. To this solution was added a methanolic solution of sodium glycinate (0.10 M, 3.0 eq.). After 10 min of stirring, the reaction solution was evaporated to dryness and redissolved in dioxane:H2O (2:3, 25 ml), frozen, and lyophilized to a fluffy red solid. 1H-NMR spectroscopy confirmed the presence of axially coordinated glycinate ligands and the presence of close to one equivalent of un-coordinated sodium glycinate. High resolution MALDI-FTMS analysis provided composition data for the un-coordinated cobalt mesoporphyrin diesters.
By the above procedures, the following compounds were made and characterized:
(1-1) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Dimethyl Ester
Yield: 84%; 1H-NMR. (d3-MeOD): 10.56 (s, 1H), 10.52 (s, 1H), 10.50 (s, 1H), 10.49 (s, 1H), 4.55 (t, 3H), 4.24 (m, 4H), 3.79-3.77 (4s, 12H), 3.62 (s, 6H), 3.40 (m, 4H), 1.96 (m, 6H), −4.08 (m, 4H), −5.45 (m, exchangeable); MALDI-FTMS: calc. for C36H40CoN4O4+—651.2376, found—651.2355.
(1-2) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Dibutyl Ester
Yield: 87%; 1H-NMR (d3-MeOD): 10.58 (s, 1H), 10.52 (s, 1H), 10.50 (s, 1H), 10.49 (s, 1H), 4.55 (t, 3H), 4.24 (m, 4H), 4.14 (m, 4H) 3.79-3.77 (4s, 12H), 3.40 (m, 4H), 1.96 (m, 6H), 1.59 (m, 4H), 1.36 (m, 4H), 0.90 (m, 6H), −4.08 (m, 4H), −5.46 (m, exchangeable); MALDI-FTMS: calc. for C42H52CoN4O4+—735.3315, found—735.3285.
(1-3) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Diisobutyl Ester
Yield: 86%; 1H-NMR (d3-MeOD): 10.59 (s, 1H), 10.52 (s, 1H), 10.50 (s, 1H), 10.49 (s, 1H), 4.55 (t, 3H), 4.24 (m, 4H), 3.95 (m, 4H), 3.81-3.76 (4s, 12H), 3.42 (m, 4H), 1.96 (m, 6H), 1.93 (m, 2H), 0.96-0.86 (m, 12H), −4.08 (m, 4H), −5.47 (m, exchangeable); MALDI-FTMS: calc. for C42H52CoN4O4+—735.3315, found —735.3300.
(1-4) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Diisoamyl Ester
Yield: 91%; 1H-NMR (d3-MeOD): 10.57 (s, 1H), 10.52 (s, 1H), 10.49 (s, 1H), 10.48 (s, 1H), 4.54 (t, 3H), 4.23 (m, 4H), 4.18 (t, 2H), 4.03 (t, 2H), 3.79-3.76 (4s, 12H), 3.39 (m, 4H), 1.96 (m, 6H), 1.69 (m, 2H), 1.52 (m, 4H), 0.94-0.89 (m, 12H), 4.09 (m, 4H), −5.47 (m, exchangeable); MALDI-FTMS: calc. for C44H56CoN4O4+—763.3628, found—763.3651.
(1-5) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Diethyl Ester
Yield: 86%; 1H-NMR (d3-MeOD): 10.58 (s, 1H), 10.52 (s, 1H), 10.50 (s, 1H), 10.49 (s, 1H), 4.55 (t, 3H), 4.24 (m, 4H), 4.15 (m, 4H), 3.79-3.77 (4s, 12H), 3.40 (m, 4H), 1.96 (m, 6H), 1.18 (m, 4H), −4.09 (m, 4H), −5.46 (m, exchangeable); MALDI-FTMS: calc. for C39H44CoN4O4+—679.2689, found—679.2678.
(1-6) Cobalt (III) Mesoporphyrin IX Bisglycinate Monosodium Salt, Diisopropyl Ester
Yield: 66%; 1H-NMR (d3-MeOD): 10.59 (s, 1H), 10.52 (s, 1H), 10.50 (s, 1H), 10.49 (s, 1H), 5.08 (m, 2H), 4.54 (t, 3H), 4.24 (m, 4H), 3.79-3.77 (4s, 12H), 3.37 (m, 4H), 1.96 (m, 6H), 1.16 (m, 12H), −4.09 (m, 4H), −5.48 (m, exchangeable); MALDI-FTMS: calc. for C40H48CoN4O4+—707.3002, found—707.2995.
Cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (329.5 mg, 0.500 mmol) was dried by evaporation of its solution in anhydrous DMF (10 ml). The residue was dissolved in dry DMF (25 ml). Carbonylbis(2-methylimdazole) (380 mg, 2.00 mmol) was added in one portion, the flask stoppered and the contents stirred at ambient temperature for 60 min. Dry methanol (0.405 ml, 10.0 mmol) was added and stirring continued for 3 h. The DMF was removed by rotary evaporation and the residue thus formed further purified by silica gel flash chromatography using CH2Cl2/MeOH (9/1 and 85/15) as eluents. Appropriate fractions were pooled and evaporated, furnishing 332 mg of the desired dimethyl ester as its putative chloride salt.
Removal of the axial nitrogenous ligands was accomplished by partitioning the crude bis(2-methylimidazole) complex between CH2Cl2 (40 ml) and 6 M HCl (20 ml). The organic layer was dried over Na2SO4 and evaporated to give 139 mg of the putatively uncomplexed dimethyl ester.
This material was dissolved in EtOH (20.2 ml) and the resulting solution treated with a methanolic solution of sodium glycinate (0.10 M, 6.1 ml, 3.0 eq.). After 10 min stirring the reaction solution was evaporated to dryness and redissolved in dioxane:H2O (2:3, 25 ml), frozen, and lyophilized to give a powdery red solid, 203 mg (41%). 1H-NMR data was in essence identical to the data obtained for material prepared via direct acidic esterification and confirmed the presence of axially coordinated glycinate ligands and the presence of close to one equivalent of un-coordinated sodium glycinate.
Cobalt (III) protoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (327.5 mg, 0.500 mmol) was slurried in dry methanol (10 ml). The mixture was cooled on an EtOH/dry ice cooling bath and while stirred, H2SO4 (0.500 ml) was added dropwise over ca 30 sec. The reaction flask was tightly stoppered and the mixture placed in a freezer kept at −20° C. During the first hour of reaction, the contents of the flask were shaken periodically to avoid deposition of starting material. After being kept cold overnight (ca 16 h), the reaction mixture was partitioned between CH2Cl2 (40 ml) and 1.0 M HCl (20 ml). The organic layer was dried over anhydrous Na2SO4, and solvent removed by rotary evaporation. The crude product was further purified by flash silica gel chromatography using CH2Cl2/MeOH (9/1 and 85/15) as eluents. Appropriate fractions were pooled and evaporated, furnishing the desired dimethyl ester as its putative chloride salt, 257 mg.
This material was dissolved in EtOH (37.6 ml) and the resulting solution treated with a methanolic solution of sodium glycinate (0.10 M, 11.3 ml, 3.0 eq.). After 10 min of stirring, the reaction solution was evaporated to dryness and redissolved in dioxane:H2O (2:3, 25 ml), frozen, and lyophilized to give a powdery red solid. 1H-NMR spectroscopy confirmed the presence of axially coordinated glycinate ligands and the presence of close to one equivalent of un-coordinated sodium glycinate. High resolution MALDI-FTMS analysis provided composition data for the un-coordinated cobalt protopoporphyrin dimethyl ester.
By the above procedures, the following compound was made and characterized:
(3-1) Cobalt (III) Protoporphyrin IX bisglycinate monosodium salt, dimethyl ester
Yield: 72%; 1H-NMR (d3-MeOD): 10.66 (s, 1H), 10.59 (s, 1H), 10.57 (s, 1H), 10.54 (s, 1H), 8.52 (m, 2H), 6.42 (dd, 2H), 6.26 (dd, 2H), 4.53 (t, 3H), 3.87 (s, 3H), 3.85 (s, 3H), 3.79 (s, 3H), 3.76 (s, 3H), 3.65 (s, 3H), 3.59 (s, 3H), 3.40 (m, 4H), −4.00 (m, 4H), −5.22 (m, exchangeable); MALDI-FTMS: calc. for C36H36CoN4O4+—647.2068, found—647.2055.
Cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (33.0 mg, 50 μmol) was dissolved in dry DMF (2.5 ml). To the dark red solution was added 1,1′-carbonyldiimidazole (32.4 mg, 200 μmol) and the reaction mixture stirred at ambient temperature for 30 min. Benzylamine (27.3 μl, 250 μmol) was added to the reaction mixture and stirring was continued for 16 hr with exclusion of moisture and light. Water (100 μl) was added to hydrolyze excess reagents and the solvent was removed by rotary evaporation. The resulting dark red residue was purified by silica gel flash chromatography using portions of CH2Cl2:MeOH (90/10 and 85/15, respectively) to elute the corresponding diamide of Co-MP IX. Appropriate fractions were pooled, evaporated and dried to furnish a dark red solid. 1H-NMR analysis of the crude target molecule revealed the presence of free as well as coordinated imidazole. In a post-synthetic step aimed at removing excess imidazole, a solution of the crude target molecule in CH2Cl2 (20 ml) was washed with 1/2-saturated NaCl(aq): 1 M HCl(aq) (21 ml, 20:1). The organic layer was slowly filtered through a pad of Na2SO4 and evaporated to afford the bis amide derivative as a red solid. 1H-NMR spectroscopy confirmed the presence of axially coordinated imidazole ligands. Yields are based on the molecular weights of the corresponding chloride salt. High resolution MALDI-FTMS analysis provided composition data for the un-coordinated cobalt mesoporphyrin diamides.
By the above procedures, the following compounds were made and characterized:
(4-1) Cobalt (III) mesoporphyrin IX bisimidazole, dibenzyl amide
Yield: 51%; 1H-NMR (d3-MeOD): 10.43 (s, 1H), 10.28 (s, 1H), 10.17 (s, 1H), 10.13 (s, 1H), 9.23 (b, 2H), 8.34 (m, 2H), 6.54 (t, 1H), 6.41 (t, 1H), 5.99 (d, 2H), 5.91 (m, 4H), 5.77 (t, 2H), 4.24 (q, 2H), 4.18 (q, 2H), 4.07 (s, 2H), 4.05 (m, 2H), 3.96 (m, 2H), 3.81 (s, 3H), 3.80 (m, 4H), 3.74 (s, 3H), ), 3.06 (m, 4H), 3.06 (s, 3H), 3.01 (s, 3H), 1.99 (t, 3H), 1.95 (t, 3H), 0.60 (s, 2H), −0.22 (s, 2H); MALDI-FTMS: calc. for C48H50CoN6O2+—801.3322, found—801.3345.
(4-2) Cobalt (III) mesoporphyrin IX bisimidazole, di(4-methoxybenzyl)amide
Yield: 27%; 1H-NMR (d3-MeOD): 10.43 (s, 1H), 10.29 (s, 1H), 10.20 (s, 1H), 10.18 (s, 1H), 9.11 (b, 2H), 8.21 (m, 2H), 5.85 (d, 2H), 5.82 (d, 2H), 5.21 (d, 2H), 5.18 (d, 2H), 4.22 (q, 2H), 4.16 (q, 2H), 4.09 (m, 2H), 4.02 (m, 2H), 4.02 (s, 2H), 3.76 (s, 3H), 3.73 (m, 4H), 3.72 (s, 3H), 3.16 (s, 3H), 3.13 (s, 3H), 3.07 (m, 4H), 3.03 (s, 3H), 2.99 (s, 3H), 1.96 (m, 6H), 0.49 (s, 2H), −0.28 (s, 2H); MALDI-FTMS: calc. for C50H54CoN6O4+—861.3533, found—861.3559.
(4-3) Cobalt (III) mesoporphyrin IX bisimidazole, bis(3,4-dimethoxybenzyl)amide
Yield: 40%; 1H-NMR (d3-MeOD): 10.49 (s, 1H), 10.36 (s, 1H), 10.24 (s, 1H), 10.24 (s, 1H), 9.16 (b, 2H), 8.36 (m, 2H), 5.94 (s, 1H), 5.92 (s, 1H), 5.19 (d, 1H), 5.08 (d, 1H), 4.44 (d, 1H), 4.25 (q, 2H), 4.19 (q, 2H), 4.11 (s, 2H), 4.07 (m, 2H), 4.00 (m, 2H), 3.81 (s, 3H), 3.79 (m, 4H), 3.76 (s, 3H), 3.14 (m, 4H), 3.12 (s, 3H), 3.11 (s, 3H), 3.07 (s, 3H), 3.03 (s, 3H), 2.92 (s, 3H), 2.91 (s, 3H), 1.99 (t, 6H), 0.61 (s, 2H), −0.23 (s, 2H); MALDI-FTMS: calc. for C52H58CoN6O6+—921.3744, found—921.3749.
(4-4) Cobalt (III) mesoporphrin IX bisglycinate, di-(N-isopropyl)amide
To a solution of cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (659 mg, 1.0 mmole) in anhydrous DMF (25 ml) was added carbonyldimethylimidazole (CDMI) (761 mg, 4.0 mmole). The mixture was stirred at room temperature for 1 hour followed by addition of isopropylamine (0.043 ml, 5.0 mmole). The mixture was stirred at room temperature for 17 hours. The reaction was quenched with water (1.0 ml). The solvent was removed under vacuum and the residue was filtrated through a silica gel pluge using DCM/MeOH (90/10) then DCM/MeOH (85/15) as eluents to give the cobalt (III) mesoporphyrin IX bis(methylimidazole), di-(N-isopropyl)amide as a red solid (510 mg). This red solid was dissolved in DCM (40 ml) washed with 6 N aqueous HCl (2×40 ml) and dried over anhydrous sodium sulfate to furnish the cobalt (III) mesoporphyrin IX chloride salt, di-(N-isopropyl)amide as a red solid (80 mg). This material was dissolved in ethanol (11 ml) and treated with a solution of sodium glycinate in methanol (0.10 M×3.24 ml) for 30 minutes. The solvent was removed under vacuum and the residue was lyophilized from water/dioxane (2/3, 15 ml) to give the title compound as a red powder (116 mg). 1H NMR (500 MHz, CD3OD) d 10.57(s, 1H), 10.51(s, 1H), 10.50(s, 1H), 10.49(s, 1H), 4.56(m, 2H), 4.24(m, 6H), 3.99(m, 4H), 3.77(s, 12H), 3.17(m, 4H), 1.95(m, 6H), 0.80(s, 12H), −4.05(m, 4H), −5.51(m, 4H).
Cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (0.25 g, 0.37 mmol) was dissolved in anhydrous methanol (6 ml), sulphuric acid (100 μL) and the homogeneous mixture was heated at 60° C. After 7 hrs, methanol was removed under vacuum and the residue was diluted with ethyl acetate (20 ml). The organic layer was washed with water (20 ml×1), brine (20 ml×1), dried over Na2SO4 and concentrated. The crude product (5-1) was obtained as a red solid (0.26 g, 98% yield and >90% purity by LCMS). LCMS. Calc'd for C36H40ClCoN4O4: 686; found 651 [M-Cl]+.
Cobalt (III) mesoporphyrin IX dimethylester, chloride salt (Porphyrin Products, Inc., Logan, Utah) (0.15 g, 0.22 mmol) was dissolved in dry THF (4 ml) under argon atmosphere and cooled to 0° C. Lithium aluminum hydride (0.017 g, 0.43 mmol) was added and heated at 60° C. After 4 hrs, the reaction mixture was cooled to 0° C., quenched with aq. NH4Cl solution and stirred for 15 min. The solid was removed by filtration over celite and the residue was washed with ethyl acetate. The organic layer was separated, washed with brine (20 ml×1), dried over Na2SO4 and concentrated. The crude product (6-1) was obtained as a red solid (0.13 g, 100% yield and >85% purity by LCMS). LCMS. Calc'd for C34H40ClCoN4O2: 630; found 595 [M-Cl]+.
Cobalt mesoporphyrin diol (6-1) (0.025 g, 0.04 mmol) was dissolved in dry CH2Cl2 (2 ml) under argon atmosphere, cooled to 0° C., pyridine (52 μL, 0.63 mmol) and acetic anhydride (33 μL, 0.32 mmol) were added. The mixture was stirred at 0° C. for 3 hrs. The reaction was quenched with water (20 ml) and diluted with CH2Cl2 (10 ml). The organic layer was separated, washed with brine (25 ml×1), dried over Na2SO4, concentrated and dried. The crude product (7-1) was obtained as a red solid (0.028 g, 100% yield, >95% purity by LCMS). LCMS. Calc'd for C38H44ClCoN4O4: 714; found 679 [M-Cl]+.
To a suspension of sodium hydride (0.006 g, 0.25 mmol) in dry THF (2 ml) at 0° C. under argon atmosphere was added dropwise a solution of cobalt mesoporphyrin diol (6-1) (0.04 g, 0.064 mmol) in THF (0.5 ml). After 30 min, a solution of benzyl bromide (15 μL) in dry THF (0.5 ml) was added and the mixture was stirred at 0° C. for 2 hrs. The reaction was quenched with water (20 ml) and diluted with ethyl acetate (30 ml). The organic layer was separated and washed with water (30 ml×1), brine (30 ml×1), dried over Na2SO4 and concentrated. The crude product (8-1) was obtained as a red solid (0.053 g). LCMS. Calc'd for C48H52ClCoN4O2: 810; found 775 [M-Cl]+.
To a solution of cobalt mesoporphyrin diol (6-1) (0.15 g, 0.24 mmol) in dry CH2Cl2 (4 ml) at 0° C. under argon was added Et3N (190 μL, 1.43 mmol) and DMAP (0.003 g, 0.024 mmol). A solution of MsCl (74 μL, 0.95 mmol) in dry CH2Cl2 (0.5 ml) was added (very slowly for 15 min) and stirred for 2 hrs. The reaction was quenched with water (20 ml) and diluted with CH2Cl2 (10 ml). The organic layer was separated and washed with sat. NaHCO3 (10 ml×1), water (20 ml×1), brine (30 ml×1), dried over Na2SO4, and concentrated. The crude product (9-1) was obtained as a red solid (0.18 g, 96% yield, >95% pure by LCMS). LCMS. Calc'd for C38H44ClCoN4O4: 786; found 751 [M-Cl]+.
To a suspension of sodium hydride (0.01 g, 0.38 mmol) in dry THF (2 ml) at 0° C. under argon was added a solution of benzyl mercaptan (32 μL, 0.25 mmol) in THF (0.5 ml) slowly. After 30 min, a solution of cobalt mesoporphyrin dimesylate (9-1) (0.05 g, 0.063 mmol) in dry THF (0.5 ml) was added slowly and the reaction mixture was stirred at 0° C. for 2 hrs. The reaction was quenched with water (20 ml) and diluted with ethyl acetate (30 ml). The organic layer was separated and washed with water (20 ml×1), brine 20 ml×1), dried over Na2SO4 and concentrated. The crude product (10-1) was obtained as a red solid (0.058 g, 110% yield). LCMS. Calc'd for C49H52ClCoN4S2: 842; found 807 [M-Cl]+.
Cobalt (III) mesoporphyrin IX, chloride salt (Porphyrin Products, Inc., Logan, Utah) (0.05 g, 0.078 mmol) was dissolved in dry THF (2 ml) and cooled to 0° C. under argon atmosphere. Phenyl lithium (879 μL, 1.8 M in hexanes, 1.5 mmol) in THF (1 ml) was slowly added over 5 min. After 2 hrs, TMSCl (400 μL, 3 mmol) was quickly added and stirred for an additional 1 hr and allowed to warm to room temperature. The mixture was diluted with 1N HCl (30 ml) and extracted with ethyl acetate (20 ml×3). The combined organic layer was washed with water (20 ml×1), brine (20 ml×1), dried over Na2SO4, and concentrated. The crude product (11-1) was obtained as a red solid (0.058 g, 98% yield, >75% pure by LCMS).
To a solution of cobalt mesoporphyrin dimesylate (9-1) (0.03 g, 0.038 mmol) in methanol (1 ml) was added a solution of methylamine (380 μL, 2 M in methanol, 0.76 mmol) and the reaction mixture was stirred at 60° C. for 12 hrs. The solvent was removed under vacuum, residue was dissolved in CH2Cl2 (30 ml), washed with water (20 ml×1), brine (20 ml×1), dried over Na2SO4 and concentrated. The crude product (12-1) was obtained as a red solid (0.023 g). LCMS. Calc'd for C36H46ClCoN6: 656; found 621 [M-Cl]+.
To a solution of cobalt mesoporphyrin (12-1) (0.025 g, 0.038 mmol, ca. 50% pure) in dry CH2Cl2 (3 ml) at 0° C. under argon atmosphere was added Et3N (78 μL, 0.61 mmol) and acetic anhydride (31 μL, 0.3 mmol). The mixture was stirred at 0° C. for 3 hrs and quenched with water (20 ml) and diluted with CH2Cl2 (10 ml). The organic layer was separated, washed with brine (30 ml×1), dried over Na2SO4 and concentrated. The crude product (12-2) was obtained as a red solid (0.023 g). LCMS. Calc'd for C40H52ClCoN6O2: 740; found 705 [M-Cl]+.
To a solution of cobalt mesoporphyrin dimesylate (9-1) (0.03 g, 0.038 mmol) in methanol (1 ml) was added ammonium hydroxide (90 μL, 30% in water, 0.76 mmol) and stirred at 60° C. for 12 hrs. The solvent was removed under vacuum, residue was dissolved in CH2Cl2 (30 ml), washed with water (20 ml×1), brine (20 ml×1), dried over Na2SO4 and concentrated. The crude product (13-1) was obtained as a red solid (0.023 g). LCMS. Calc'd for C34H42ClCoN6: 628; found 593 [M-Cl]+.
To a solution of the crude cobalt mesoporphyrin (13-1) (0.020 g, 0.032 mmol, ca. 10% pure) in dry CH2Cl2 (2 ml) at 0° C. under argon atmosphere was added Et3N (33 μL, 0.25 mmol) and acetic anhydride (13 μL, 0.13 mmol). The mixture was stirred for 3 hrs and was quenched with water (30 ml) and diluted with CH2Cl2 (30 ml). The organic layer was separated, washed with brine (20 ml×1), dried over Na2SO4 and concentrated. The crude product (14-1) was obtained as a red solid (0.020 g). LCMS. Calc'd for C38H46ClCoN6O2: 712; found 677 [M-Cl]+.
All cell culture reagents were incubated in a water bath at 37° C. for approximately 30 minutes. Existing media from a near confluent tissue culture flask containing SH-SY5Y neuroblastoma cells was aspirated using a flame sterilized glass transfer pipette attached to a trapped vacuum apparatus. Calcium free PBS buffer was pipetted into the tissue culture flask (2 ml for a 75 cm2 flask, 3 ml for a 175 cm2 flask). The flask was tipped slightly to ensure that the buffer covers the cell culture and then the buffer was removed by aspiration. Trypsin media was pipetted into the tissue culture flask (2 ml for a 75 cm2 flask, 3 ml for a 175 cm2 flask) and evenly spread to ensure that the trypsin covered the cell culture. The cell culture was incubated with trypsin media for 4-6 minutes at room temperature. After cells were released from the flask, the flask was tilted to one corner. Using the existing media within the flask, the aggregated cells were collected towards one corner and repeatedly pipetted to obtain a single cell suspension. The cell suspension was transferred with a pipette into a 15 ml conical shaped centrifuge tube then cell culture media was added to the suspension up to a total volume of 14 ml. Ten μl aliquots were withdrawn and the cells were counted using a hemocytometer. The suspension was centrifuged at 200×g for 10 minutes, the supernatant was aspirated off, and the cell pellet was resuspended at 3.75×105 cells/ml in cell culture medium. Two hundred μl of cell suspension were aliquoted per well in the 96 well dish to obtain a final cell number of 75,000 cells per well. The plates were incubated overnight at 37° C. and 5% CO2 in a humidified cell incubator.
The medium was carefully removed from the wells by aspiration with an 18 g needle. The wells were gently rinsed once with 200 μl of warm Hanks balanced saline solution (HBSS, Gibco-BRL). 200 μl of 30 μM dichlorofluorescin-diacetate (DCFC-DA) was added to each well and the cells were incubated for 1 hour at 37° C. under 5% CO2 in a humidified cell incubator. The excess DCFC-DA was removed by needle aspiration and each well was gently rinsed twice with 200 μl of warm Hank's Balanced Salt Solution (HBSS).
Stock solutions of test compound, such as Co-PP, Co-MP, or a Co-P of this invention, and of an H2O2 scavenger such as ebselen, were typically prepared in dimethylformamide or dimethylsulfoxide and diluted further into working concentrations using HBSS. The final concentration of the organic solvents were kept at or below 0.1% when on cells. Eighty μl of HBSS was aliquoted into the well and 20 μl of test compound solution in HBSS. The plate was read immediately in Cytofluor model 2350 system (Millipore; excitation wavelength: 485 nm; emission wavelength: 530 nm) for a 0 min timepoint reading. The cells were incubated for 30 minutes at room temperature with test compound following which a 30 min reading was taken. The change in RMF over the 30 minutes period was calculated for each well. The well media was removed by needle aspiration and 15.6 μl of 37% formaldehyde was added to each well. The cells were incubated for 2-10 min and washed with 200 μl of H2O. Then 100 μl of a 10 μg/ml aqueous solution of Hoechst 33342 was added to each well and the plate was kept in the dark for 10 min. The plate was then read in the Cytofluor (excitation wavelength: 360 nm; emission wavelength: 460 nm) and the Hoechst fluorescence values were used to normalize the DCFC-DA RMF data.
As illustrated in
Ten mM stock solutions of a Co-P of this invention (i.e., test compound) were prepared using ethanol as solvent. KCl media consists of 125 mM KCl, 2 mM K2HPO4, 20 mM HEPES, pH 7.0. Oxygen consumption measurements were carried out using a Clark type oxygen electrode (Rank Brothers Ltd., Cambridge, UK) and assay solutions were magnetically stirred during the course of the experiments. To 500 μof assay solution (KCl media supplemented with 2 mM sodium ascorbate and 40 μM N,N,N′,N′-1,4-tetramethylenediamine (TMPD)) is added 2 ill of a stock solution of test compound (40 μM final concentration) and the oxygen consumption rate is followed for 2-4 min. Subsequently, a 511 aliquot of a freshly made catalase solution (100 mg/ml solution in KCl media) is added to determine if H2O2 is generated via redox cycling of the test compound.
Referring to
Reduced cytochrome c was prepared by the addition of an excess of ascorbic acid to a solution of cytochrome c and allowing the solution to stand for 5 to 10 minutes. The reduced protein was purified over a Sephadex G50 column and checked spectrophotometrically by measuring absorbance at 550 nm, followed by the addition of a few grains of dithionite and measuring absorbance again at 550 nm. The extinction coefficient for fully reduced cytochrome c is 29 mM−1. Initial rates of oxidation of reduced cytochrome c at three concentrations (5.3 μM, 10.5 μM and 26 μM) were followed in the presence of 0, 5, 10, 20 and 100 μM CoPP. Assays were conducted in 1 ml of assay buffer (20 mM potassium phosphate, pH 7.0, 0.2 mg/ml dodecyl-β-maltoside) and initiated by the addition of desired concentration of reduced cytochrome c and monitoring the change in absorbance at 550 nm for 90 seconds. The fully oxidized absorbance value was determined by the addition of a few grains of ferricyanide to the cuvette.
Representative Co-P compounds of this invention were prepared by the procedures disclosed above, and assayed by the procedure of Example 16 to measure oxygen consumption catalyzed by the test compound in the presence of ascorbate/TMPD. As shown in
Male Sprague Dawley rats (approximately 200 g) were purchased from Charles River Canada, Inc. and were shipped to the Animal Care Facility at the University of Vermont. Upon arrival they were housed in separate cages with corncob bedding and ad lib access to tap water and purina rat chow. The animal facility is maintained at a temperature of 71° F.+/−1° F. with a 12-hour light/dark cycle, lights on at 6:00 am and off at 6:00 pm. Two days later (Day—3) all rats were shaved in the nuchal area and baseline color photographs of the nuchal area were taken (light halothane anesthesia was utilized to facilitate the shaving). Three days later (Day 0) experimental compounds were made up at 12 mM concentrations in vehicle (i.e., saline:PEG400:EtOH (5:4:1), pH 7.4). Animals were injected subcutaneously in the nuchal area with the various stock solutions at a dose of 400 μl per 100 grams body weight. Typical injection volumes, therefore, range from 1 to 1.5 ml per animal. Animals were injected using a modified Z-track technique to try and minimize outflow of injected compounds due to the high volume utilized. Each animal was weighed prior to injection and all injections were accomplished in an approximately two-hour period. No anesthesia was utilized for injections.
Animals subsequently underwent daily weighing with a Mettler 6 second integrating balance and had ad lib access to tap water and purina rat chow. At various intervals after injections, the nuchal area of rats was again photographed. In addition to the photographic record, from the second experiment on, all rats had a daily assessment of the severity of any lesions in the nuchal area. The scale used was 0 for no lesions, 5 for the worst lesions with breakdown of the skin and open flow of exudates. Grades in-between were estimated by the operator based on the size and severity of the lesion. In those cases where animals had a grade 5 lesion, either individuals animals were euthanized or the experiment was terminated rapidly after the appearance of such lesions. After 8 days, final photographs were taken and all animals were euthanized, marking the end of the experiment.
Means of body weights for each group were calculated and plotted over time (
From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.
| Number | Date | Country | |
|---|---|---|---|
| 60255960 | Dec 2000 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10020867 | Dec 2001 | US |
| Child | 10984557 | Nov 2004 | US |
