WO2002062777A2 - Amino ceramide-like compounds and therapeutic methods of use - Google Patents
Amino ceramide-like compounds and therapeutic methods of use Download PDFInfo
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- WO2002062777A2 WO2002062777A2 PCT/US2002/000808 US0200808W WO02062777A2 WO 2002062777 A2 WO2002062777 A2 WO 2002062777A2 US 0200808 W US0200808 W US 0200808W WO 02062777 A2 WO02062777 A2 WO 02062777A2
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- 0 CC(C)c1cccc(C(C(C*)NC(*)=O)O)c1 Chemical compound CC(C)c1cccc(C(C(C*)NC(*)=O)O)c1 0.000 description 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Definitions
- the present invention relates generally to ceramide-like compounds and, more particularly, to prodrugs of ceramide-like compounds that inhibit glucosylceramide formation.
- glycosphingolipids are derived from glucosylceramide (GlcCer), which is enzymatically formed from ceramide and UDP-glucose.
- the enzyme involved in GlcCer formation is UDP-glucose:N-acylsphingosine glucosyltransferase (GlcCer synthase).
- the rate of GlcCer formation under physiological conditions may depend on the tissue level of UDP-glucose, which in turn depends oh the level of glucose in a particular tissue (Zador, I.Z.
- GSLs controls a variety of cell functions, such as growth, differentiation, adhesion between cells or between cells and matrix proteins, binding of microorganisms and viruses to cells, and metastasis of tumor cells.
- the GlcCer precursor, ceramide may cause differentiation or inhibition of cell growth (Bielawska, A. et al., "Modulation of Cell Growth and Differentiation by
- GSL function Another example of the importance of GSL function is seen in a mechanism by which blood cells, whose surfaces contain selectins, can, under certain conditions, bind to GSLs in the blood vessel walls and produce acute, life- threatening inflammation (Alon, R. et al., "Glycolipid Ligands for Selectins Support Leukocyte Tethering & Rolling Under Physiologic Flow Conditions.” J. Immunol., 154:5356-5366 (1995)).
- Gaucher disease wherein the normal enzyme which has been isolated from normal human tissues or cultured cells is administered to the patient.
- great care is needed to prevent contamination with a virus or other dangerous substances.
- Treatment for an individual patient is extremely expensive, costing hundreds of thousands, or even millions of dollars, over a patient's lifetime. It would thus be desirable to provide a treatment which includes administration of a compound that is readily available and/or producible from common materials by simple reactions.
- glucolipids Possibly of even greater clinical relevance is the role of glucolipids in cancer.
- certain GSLs occur only in tumors; certain GSLs occur at abnormally high concentrations in tumors; certain GSLs, added to tumor cells in culture media, exert marked stimulatory or inhibitory actions on tumor growth; antibodies to certain GSLs inhibit the growth of tumors; the GSLs that are shed by tumors into the surrounding extracellular fluid inhibit the body's normal immunodefense system; the composition of a tumor's GSLs changes as the tumors become increasingly malignant; and, in certain kinds of cancer, the level of a GSL circulating in the blood gives useful information regarding the patient's response to treatment.
- GSLs have on several biochemical processes, there remains a need for compounds having improved GlcCer synthase inhibition activity. It would thus be desirable to provide compounds which inhibit GlcCer synthase activity. It would also be desirable to provide compounds which inhibit GlcCer synthase activity, thereby lowering the level of GSLs and increasing GSL precursor levels, e.g. increasing the levels of ceramide and sphingols. It would further be desirable to provide compounds which inhibit GlcCer synthase activity and lower the level of GSLs without also increasing ceramide levels. It would also be desirable to provide compounds and therapeutic methods to treat conditions and diseases associated with altered GSL levels and/or GSL precursor levels. It would be further desirable to provide such compounds in the form of prodrugs that are then transformed into the active compounds within a cell.
- Novel compounds are provided which inhibit GlcCer formation by inhibiting the enzyme GlcCer synthase, thereby lowering the level of GSLs.
- the compounds of the present invention are in the form of prodrugs. As prodrugs, they are in an inactive form unitl they are introduced into a cell or organism, where they are then converted to an active form. Active compounds are also provided that are more hydrophobic to aid in transport across cell membranes thus increasing the concentration of the compounds in the target cells.
- the active forms of the compounds of the present invention have improved GlcCer synthase inhibition activity and are therefore highly useful in therapeutic methods for treating various conditions and diseases associated with altered GSL levels, as well as GSL precursor levels.
- the compounds of the present invention may be useful in methods involving cancer growth and metastasis, the growth of normal tissues, the ability of pathogenic microorganisms to bind to normal cells, the binding between similar cells, the binding of toxins to human cells, and the ability of cancer cells to block the normal process of immunological cytotoxic attack.
- Figure 1 is a schematic showing the structure of carbon-3 substituted homologues of ethylenedioxy-P4;
- Figure 2 is a graph showing the inhibition of glucosylceramide synthase by D-t- ethylenedioxy-P4 and prodrugs of ethylenedioxy-P4; and Figure 3 is an HPLC trace showing the conversion of the prodrug into the active compound in the presence of liver cytosol.
- Novel compounds in the form of prodrugs are provided which inhibit GlcCer formation by inhibiting the enzyme GlcCer synthase, thereby lowering the level of GSLs.
- the compounds of the present invention are converted to their active form once they have been taken up by a cell.
- the compounds of the present invention have improved GlcCer synthase inhibitory activity and are therefore highly useful in therapeutic methods for treating various conditions and diseases associated with altered GSL levels.
- the prodrugs have improved pharmacokinetic properties, including improved transport into the cells. Once the prodrug enters the target cell or organism, it is converted into the active form by metabolic processes.
- the compounds of the present invention generally have the following formula:
- R T is a phenyl group, preferably a substituted phenyl group such as p-methoxy, hydroxy, dioxane substitutions such as methylenedioxy, ethylenedioxy, and trimethylenedioxy, cyclohexyl or other acyclic group, t-butyl or other branched aliphatic group, or a long alkyl or alkenyl chain, preferably 7 to 15 carbons long with a double bond next to the kernel of the structure.
- the aliphatic chain can have a hydroxyl group near the two asymmetric centers, corresponding to phytosphingosine.
- R 2 is an alkyl residue of a fatty acid, 10 to 18 carbons long.
- the fatty acid can be saturated or unsaturated, or possess a small substitution at the C-2 position (e.g., a hydroxyl group).
- R 3 is a tertiary amine, preferably a cyclic amine such as pyrrolidine, azetidine, morpholine or piperidine, in which the nitrogen atom is attached to the kernel (i.e., a tertiary amine).
- R is any group that is selectively hydrolyzed in a target cell, preferrably an
- the compounds of the present invention are converted in the cell to the active, inhibitory forms of the compounds having the general formula:
- R u R 2 and R 3 are defined above for the prodrug compounds.
- the compounds of the present invention include the prodrugs of the GlcCer Synthase inhibitors disclosed in U.S. Patent No. 6,030,995, hereby incorporated by reference.
- the prodrug compounds comprise a hydrolyzable group covalently bonded to the oxygen of the hydroxyl of the 1-propanol backbone.
- Preferred compounds of the present invention are the prodrugs of D-f-3',4'- ethylenedioxy-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol, also referred to herein as D-f-3',4'-ethylenedioxy-P4 (or D-t-EtDO-P4 in the figures), and D-t-4'- hydroxy-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol, also referred to herein as D-t-4'-hydroxy-P4.
- the prodrugs of the present invention comprise a covalently attached hydrolyzable group (R») to the hydroxyl of the 1-propanol backbone that is selectively hydrolyzed within the cell, preferably enzymatically.
- the chemical moeity can be any group that is selectively hydrolyzed to produce an active compound with a unmodified hydroxyl in the cell.
- Figure 3 shows the selective conversion of acetyl-modified D-t-3',4'- ethylenedioxy-P4 in the presence of cytosol. In the absence of cytosol, the prodrug is not converted to the active compound in an aqueous solution.
- the group is attached to the active compound through an ester bond.
- the chemical group preferrably is an acetyl, -CO(CH 2 ) n CH 3
- n is at least 1 or , wherein R 5 is an alkyl group.
- the modified prodrugs are inactive as inhibiters of GlcCer Synthase (open symbols, Figure 2). However, cleavage of the chemical moeity to form an unmodified hydroxyl produces a potent inhibitor ( Figure 2).
- the compounds of the present invention are prodrugs in which Ri is 4'-hydroxy-phenyl and the hydrolyzable group (Re) is covalently bound to the 4'-hydroxy.
- These compounds have the general formula: wherein
- R 2 is an alkyl residue of a fatty acid, 10 to 18 carbons long.
- the fatty acid can be saturated or unsaturated, or possess a small substitution at the C-2 position (e.g., a hydroxyl group).
- R 3 is a tertiary amine, preferably a cyclic amine such as pyrrolidine, azetidine, morpholine or piperidine, in which the nitrogen atom is attached to the kernel (i.e., a tertiary amine).
- Re is any group that is selectively hydrolyzed in a target cell, preferrably an
- the compounds of the present invention are prodrugs in which Ri is 4'-hydroxy-phenyl and where hydrolyzable groups are covalently bound to both the hydroxyl of the 1-propanol backbone (R4) and the 4'- hydroxy of the phenyl (Re).
- R4 1-propanol backbone
- Re 4'- hydroxy of the phenyl
- R 2 is an alkyl residue of a fatty acid, 10 to 18 carbons long.
- the fatty acid can be saturated or unsaturated, or possess a small substitution at the C-2 position (e.g., a hydroxyl group).
- R 3 is a tertiary amine, preferably a cyclic amine such as pyrrolidine, azetidine, morpholine or piperidine, in which the nitrogen atom is attached to the kernel (i.e., a tertiary amine).
- R 4 and Re are any group that is selectively hydrolyzed in a target cell
- an alkyl group is covalently bound to the compound of the present invention.
- n is an integer from about 1 to about 19;
- R 2 is an alkyl residue of a fatty acid, 10 to 18 carbons long.
- the fatty acid can be saturated or unsaturated, or possess a small substitution at the C-2 position (e.g., a hydroxyl group).
- R 3 is a tertiary amine, preferably a cyclic amine such as pyrrolidine, azetidine, morpholine or piperidine, in which the nitrogen atom is attached to the kernel (i.e., a tertiary amine).
- the alkyl chain attached to the phenyl group makes the active compound more lipophilic, allowing a higher concentration to get into the target cells.
- the alkyl chain in unsaturated.
- the presence of the alkyl chain results in an active compound that resembles the naturally occuring substrate of GlcCer Synthase, which comprises a sphingosine.
- the compounds of the present invention are easily synthesized by methods well known in the art.
- the compounds of the present invention can be synthesized by esterification of the hydroxy (or alcohol) with the appropriate anhydride.
- methods of treating patients suffering from inborn genetic errors in the metabolism of GlcCer and its normal anabolic products (lactosylceramide and the more complex GSLs) with the prodrugs are provided.
- the presently known disorders in this category include Gaucher, Fabry, Tay-Sachs, Sandhoff, and GM1 gangliosidosis.
- the genetic errors lie in the patient's inability to synthesize a hydrolytic enzyme having normal efficiency.
- Their inefficient hydrolase allows the GSL to gradually accumulate to a toxic degree, debilitating or killing the victim.
- the compounds of the present invention slow the formation of GSLs, thus allowing the defective hydrolase to gradually "catch up” and restore the concentrations of GSLs to their normal levels and thus the compounds may be administered to treat such patients.
- the compounds of the present invention are administered but only for a relatively short time.
- disorders include cancer, collagen vascular diseases, atherosclerosis, and the renal hypertrophy of diabetic patients.
- Accumulation or changes in the cellular levels of GSLs have been implicated in these disorders and blocking GSL biosynthesis would allow the normal restorative mechanisms of the body to resolve the imbalance.
- Atherosclerosis With atherosclerosis, it has been shown that arterial epithelial cells grow faster in the presence of a GlcCer product (lactosylceramide). Oxidized serum lipoprotein, a material that normally circulates in the blood, stimulates the formation of plaques and lactosylceramide in the inner lining of blood vessels. Treatment with the compounds of the present invention would inhibit this mitogenic effect.
- GlcCer product lactosylceramide
- patients suffering from infections may be treated with the compounds of the present invention.
- Many types of pathogenic bacteria have to bind to specific GSLs before they can induce their toxic effects.
- Svensson, M. et al. "Epithelial Glucosphingolipid Expression as a Determinant of Bacterial Adherence and Cytokine Production," Infect, and Immun. 62:4404-4410 (1994), expressly incorporated by reference, PDMP treatment reduces the adherence of E. coli to mammalian cells.
- viruses such as influenza type A
- Several bacterial toxins, such as the verotoxins cannot themselves act without first binding to a GSL.
- the degree of infection may be ameliorated.
- the compounds of the present invention may slow the further development of the infection by eliminating the binding sites that remain free.
- tumors produce substances, namely gang ⁇ osides, a family of GSLs, that prevent the host i.e., patient, from generating antibodies against the tumor. By blocking the tumor's ability to secrete these substances, antibodies against the tumor can be produced.
- the GlcCer synthase inhibitors of the present invention to the patient, the tumors will become depleted of their GSLs and the body's normal immunological defenses will come into action and destroy the tumor.
- This technique was described in Inokuchi, J. et al., "Antitumor Activity in Mice of an Inhibitor of Glycosphingolipid Biosynthesis," Cancer Lett. 38:23- 30(1987), expressly incorporated by reference.
- the compounds of the present invention and in particular the aliphatic compounds require much lower doses than those previously described. This is particularly important because the lower dose may reduce certain side effects. Moreover, because the aliphatic compounds of the present invention do not produce ceramide accumulation, they are less toxic. In addition, 1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4), may act via two pathways, GSL depletion and ceramide accumulation.
- a vaccine-like preparation is provided.
- cancer cells are removed from the patient (preferably as completely as possible), and the cells are grown in culture in order to obtain a large number of the cancer cells.
- The. cells are then exposed to the inhibitor for a time sufficient to deplete the cells of their GLSs (generally 1 to 5 days) and are reinjected into the patient.
- These reinjected cells act like antigens and are destroyed by the patient's immunodefense system.
- the remaining cancer cells (which could not be physically removed) will also be attacked by the patient's antibodies.
- the patient's circulating gangliosides in the plasma are removed by plasmapheresis, since the circulating gangliosides would tend to block the immunodefense system.
- tumors are particularly dependent on GSL synthesis for maintenance of their growth (Hakomori, S. "New Directions in Cancer Therapy Based on Aberrant Expression of Glycosphingolipids: Anti-adhesion and Ortho-Signaling Therapy," Cancer Cells 3:461-470 (1991)). Accumulation of ceramide in treated tumors also slows their growth or kills them. Tumors also generate large amounts of GSLs and secrete them into the patient's body, thereby preventing the host's normal response by immunoprotective cells, which should generate antibodies against or otherwise destroy tumor cells (e.g., tumors are weakly antigenic). It has also been shown that GSL depletion blocks the metastasis of tumor cells (Inokuchi, J.
- Tumor angiogenesis [e.g., the production of blood capillaries) is strongly influenced by GSLs (Ziche, M. et al., "Angiogenesis Can Be Stimulated or Repressed in In Vivo by a Change in GM3:GD3 Ganglioside Ratio," Lab. Invest. 67:711-715 (1992)). Depleting the tumor of its GSLs should block the tumors from generating the new blood vessels they need for growth.
- a further important characteristic of the compounds of the present invention is their unique ability to block the growth of multidrug resistant (“MDR”) tumor cells even at much lower dosages.
- MDR multidrug resistant
- PDMP multidrug resistant
- Rosenwald, A.G. et al. "Effects of the Glycosphingolipid Synthesis Inhibitor, PDMP, on Lysosomes in Cultured Cells," J. Lipid Res. 35:1232 (1994), expressly incorporated by reference.
- Tumor cells that survive an initial series of therapeutic treatments often reappear some years later with new properties - they are now resistant to a second treatment schedule, even with different drugs. This change has been attributed to the appearance in the tumor of large amounts of a specific MDR protein (P-glycoprotein).
- PKC protein kinase C
- Blobe, G.C. et al., "Regulation of PKC and Its Role in Cancer Biology,” Cancer Metastasis Rev. 13:411-431 (1994) decreases in PKC have other important effects, particularly slowing of growth.
- PDMP does lower the cellular content of PKC (Shayman, J.A. et al., "Modulation of Renal Epithelial Cell Growth by Glucosylceramide: Association with Protein Kinase C, Sphingosine, and Diacylglyceride,” J. Biol. Chem.
- chlorpromazine behaves like the compounds of the present invention, in its ability to lower tissue levels of GlcCer (Hospattankar, AN. et al., "Changes in Liver Lipids After Administration of 2-Decanoylamino-3-Morpholinopropiophenone and Chlorpromazine," Lipids 17:538-543 (1982)).
- the compounds of the present invention can be employed in a wide variety of pharmaceutical forms; the compound can be employed neat or admixed with a pharmaceutically acceptable earner or other excipients or additives. Generally speaking, the compound will be administered orally or intravenously. It will be appreciated that therapeutically acceptable salts of the compounds of the present invention may also be employed. The selection of dosage, rate/frequency and means of administration is well within the skill of the artisan and may be left to the judgment of the treating physician or attending veterinarian. The method of the present invention may be employed alone or in conjunction with other therapeutic regimens. It will also be appreciated that the compounds of the present invention are also useful as a research tool e.g., to further investigate GSL metabolism.
- compositions within the scope of invention include those comprising a compound of the present invention in an effective amount to achieve an intended purpose. Determination of an effective amount and intended purpose is within the skill of the art. Preferred dosages are dependent for example, on the severity of the disease and the individual patient's response to the treatment.
- pharmaceutically acceptable salts is intended to mean salts of the compounds of the present invention with pharmaceutically acceptable acids, e.g., inorganic acids such as sulfuric, hydrochloric, phosphoric, etc. or organic acids such as acetic.
- pharmaceutically acceptable acids e.g., inorganic acids such as sulfuric, hydrochloric, phosphoric, etc. or organic acids such as acetic.
- compositions of the present invention may also include suitable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which may be used pharmaceutically.
- suitable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which may be used pharmaceutically.
- Such preparations can be administered orally (e.g., tablets, dragees and capsules), rectally (e.g., suppositories), as well as administration by injection.
- the pharmaceutical preparations of the present invention are manufactured in a manner which is itself known, e.g., using the conventional mixing, granulating, dragee-making, dissolving or lyophilizing processes.
- pharmaceutical preparations for oral use can be obtained by combining the active compounds with solid excipients, optionally grinding a resulting mixture and processing the mixture of granules, after adding suitable auxiliaries, if desired or necessary, to obtain tablets.
- Suitable excipients are, in particular, fillers such as sugars, e.g., lactose or sucrose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, e.g., tricalcium diphosphate or calcium hydrogen phosphate, as well as binders such as starch paste, using, e.g., maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose and/or polyvinylpyrrolidone.
- fillers such as sugars, e.g., lactose or sucrose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, e.g., tricalcium diphosphate or calcium hydrogen phosphate, as well as binders such as starch paste, using, e.g., maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth,
- disintegrating agents may be added such as the above-mentioned starches and also carboxymethyl starch, cross-linked polyvinylpyrrolidone, agar, or alginic acid or a salt thereof, such as sodium alginate.
- Auxiliaries are, above all, flow-regulating agents and lubricants, e.g., silica, talc, stearic acid or salts thereof, such as magnesium stearate or calcium stearate, and/or polyethylene glycol.
- Dragee cores are provided with suitable coatings which, if desired, are resistant to gastric juices.
- concentrated sugar solutions may be used, which may optionally contain gum arabic, talc, polyvinylpyrrolidone, polyethylene glycol and/or titanium dioxide, lacquer solutions and suitable organic solvent or solvent mixtures.
- suitable cellulose preparations such as acetylcellulose phthalate or hydroxypropylmethylcellulose phthalate, are used.
- Dyestuffs or pigments may be added to the tablets or dragee coatings, e.g., for identification or in order to characterize different combinations of active compound doses.
- Other pharmaceutical preparations which can be used orally include push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer such as glycerol or sorbitol.
- the push-fit capsules may contain the active compounds in the form of granules which may be mixed with fillers such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
- the active compounds are preferably dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
- stabilizers may be used.
- Possible pharmaceutical preparations which can be used rectally include, e.g., suppositories, which consist of a combination of the active compounds with a suppository base.
- Suitable suppository bases are, e.g., natural or synthetic triglycerides, paraffin hydrocarbons, polyethylene glycols or higher alkanols. It is also possible to use gelatin rectal capsules which consist of a combination of the active compounds with a base.
- Possible base materials include, e.g., liquid triglycerides, polyethylene glycols or paraffin hydrocarbons.
- Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, e.g., water-soluble salts.
- suspension of the active compounds as appropriate oily injection suspensions may be administered.
- suitable lipophilic solvents or vehicles include fatty oils, such as sesame oil, or synthetic fatty acid esters, e.g., ethyl oleate or triglycerides.
- Aqueous injection suspensions may contain substances which increase the viscosity of the suspension such as sodium carboxymethylcellulose, sorbitol and/or dextran.
- the suspension may also contain stabilizers.
- the active compounds of the present invention may be administered in the form of liposomes, pharmaceutical compositions wherein the active compound is contained either dispersed or variously present in corpuscles consisting of aqueous concentrate layers adherent to hydrophobic lipidic layer.
- the active compound may be present both in the aqueous layer and in the lipidic layer or in the non-homogeneous system generally known as a lipophilic suspension.
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Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60234421T DE60234421D1 (en) | 2001-01-10 | 2002-01-10 | AMINOCERAMIDIC COMPOUNDS AND THERAPEUTIC APPLICATIONS |
CA2434028A CA2434028C (en) | 2001-01-10 | 2002-01-10 | Amino ceramide-like compounds and therapeutic methods of use |
EP02718827A EP1358172B1 (en) | 2001-01-10 | 2002-01-10 | Amino ceramide-like compounds and therapeutic methods of use |
AT02718827T ATE449089T1 (en) | 2001-01-10 | 2002-01-10 | AMINOCERAMIDE-TYPE COMPOUNDS AND THERAPEUTIC APPLICATIONS |
MXPA03006188A MXPA03006188A (en) | 2001-01-10 | 2002-01-10 | Amino ceramide-like compounds and therapeutic methods of use. |
BR0206400-6A BR0206400A (en) | 2001-01-10 | 2002-01-10 | Amino ceramide compounds and their uses in therapeutic methods |
AU2002249942A AU2002249942B2 (en) | 2001-01-10 | 2002-01-10 | Amino ceramide-like compounds and therapeutic methods of use |
JP2002562732A JP2004531478A (en) | 2001-01-10 | 2002-01-10 | Aminoceramide-like compounds and methods of use for therapeutic purposes |
Applications Claiming Priority (5)
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US26094801P | 2001-01-10 | 2001-01-10 | |
US60/260,948 | 2001-01-10 | ||
US26219601P | 2001-01-17 | 2001-01-17 | |
US60/262,196 | 2001-01-17 | ||
CA002454456A CA2454456A1 (en) | 2001-01-10 | 2003-12-24 | Amino ceramide-like compounds and therapeutic methods of use |
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WO2002062777A2 true WO2002062777A2 (en) | 2002-08-15 |
WO2002062777A3 WO2002062777A3 (en) | 2002-11-28 |
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EP (1) | EP1358172B1 (en) |
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US10220039B2 (en) | 2007-10-05 | 2019-03-05 | Genzyme Corporation | Method of treating polycystic kidney diseases with ceramide derivatives |
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US20060217560A1 (en) * | 2002-04-29 | 2006-09-28 | Shayman James A | Amino ceramide-like compounds and therapeutic methods of use |
JP2011505374A (en) * | 2007-11-29 | 2011-02-24 | ザ・ホスピタル・フォー・シック・チルドレン | Compositions and methods for treating lysosomal disorders |
WO2009132082A2 (en) * | 2008-04-22 | 2009-10-29 | Medical College Of Georgia Research Institute, Inc. | Immunogenic compositions containing ceramide and methods of use thereof |
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WO1997010817A1 (en) * | 1995-09-20 | 1997-03-27 | The Regents Of The University Of Michigan | Amino ceramide-like compounds and therapeutic methods of use |
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HUT73527A (en) | 1993-08-13 | 1996-08-28 | Seikagaku Kogyo Co Ltd | Remedy for nervous diseases |
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WO2002062777A2 (en) | 2001-01-10 | 2002-08-15 | The Regents Of The University Of Michigan | Amino ceramide-like compounds and therapeutic methods of use |
US20040260099A1 (en) | 2001-01-10 | 2004-12-23 | The Regents Of The University Of Michigan | Amino ceramide-like compounds and therapeutic methods of use |
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US6916802B2 (en) | 2002-04-29 | 2005-07-12 | Genzyme Corporation | Amino ceramide-like compounds and therapeutic methods of use |
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2002
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Also Published As
Publication number | Publication date |
---|---|
US7335681B2 (en) | 2008-02-26 |
WO2002062777A9 (en) | 2003-01-09 |
WO2002062777A3 (en) | 2002-11-28 |
JP2004531478A (en) | 2004-10-14 |
CA2434028A1 (en) | 2002-08-15 |
EP1358172A2 (en) | 2003-11-05 |
US20070072916A1 (en) | 2007-03-29 |
CA2434028C (en) | 2010-11-09 |
CA2454456A1 (en) | 2005-06-24 |
EP1358172B1 (en) | 2009-11-18 |
BR0206400A (en) | 2005-01-18 |
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