EP0692931A4 - Synthetic matrix metalloprotease inhibitors and uses thereof - Google Patents
Synthetic matrix metalloprotease inhibitors and uses thereofInfo
- Publication number
- EP0692931A4 EP0692931A4 EP94913345A EP94913345A EP0692931A4 EP 0692931 A4 EP0692931 A4 EP 0692931A4 EP 94913345 A EP94913345 A EP 94913345A EP 94913345 A EP94913345 A EP 94913345A EP 0692931 A4 EP0692931 A4 EP 0692931A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- matrix metalloprotease
- metalloprotease inhibitors
- synthetic matrix
- synthetic
- inhibitors
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06156—Dipeptides with the first amino acid being heterocyclic and Trp-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biochemistry (AREA)
- Vascular Medicine (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4432493A | 1993-04-07 | 1993-04-07 | |
US44324 | 1993-04-07 | ||
PCT/US1994/003600 WO1994022309A1 (en) | 1993-04-07 | 1994-04-01 | Synthetic matrix metalloprotease inhibitors and uses thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0692931A1 EP0692931A1 (en) | 1996-01-24 |
EP0692931A4 true EP0692931A4 (en) | 1996-03-20 |
Family
ID=21931747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94913345A Ceased EP0692931A4 (en) | 1993-04-07 | 1994-04-01 | Synthetic matrix metalloprotease inhibitors and uses thereof |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0692931A4 (en) |
JP (1) | JPH08511509A (en) |
AU (1) | AU6554294A (en) |
CA (1) | CA2160139A1 (en) |
WO (1) | WO1994022309A1 (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6037472A (en) * | 1993-11-04 | 2000-03-14 | Syntex (U.S.A.) Inc. | Matrix metalloprotease inhibitors |
GB9501737D0 (en) * | 1994-04-25 | 1995-03-22 | Hoffmann La Roche | Hydroxamic acid derivatives |
EP0934259B1 (en) * | 1996-10-16 | 2002-09-18 | American Cyanamid Company | Beta-sulfonamido hydroxamic acids as matrix metalloproteinase and tace inhibitors |
EP0938548B1 (en) | 1996-11-06 | 2008-08-06 | The Regents of the University of California | Isolated tumor necrosis factor receptor releasing enzyme, compositions comprising the enzyme and methods of the use thereof |
US5952320A (en) * | 1997-01-07 | 1999-09-14 | Abbott Laboratories | Macrocyclic inhibitors of matrix metalloproteinases and TNFα secretion |
US5985911A (en) * | 1997-01-07 | 1999-11-16 | Abbott Laboratories | C-terminal ketone inhibitors of matrix metalloproteinases and TNFα secretion |
GB9818605D0 (en) | 1998-08-26 | 1998-10-21 | Glaxo Group Ltd | Formamide compounds as therepeutic agents |
US6172064B1 (en) | 1998-08-26 | 2001-01-09 | Glaxo Wellcome Inc. | Formamides as therapeutic agents |
US6329400B1 (en) | 1998-08-26 | 2001-12-11 | Glaxo Wellcome Inc. | Formamide compounds as therapeutic agents |
US6288261B1 (en) | 1998-12-18 | 2001-09-11 | Abbott Laboratories | Inhibitors of matrix metalloproteinases |
GB9903598D0 (en) * | 1999-02-18 | 1999-04-07 | Univ Manchester | Connective tissue healing |
US20040235950A1 (en) * | 1999-05-20 | 2004-11-25 | Voorhees John J. | Compositions and methods for use against acne-induced inflammation and dermal matrix-degrading enzymes |
EP1372692A4 (en) * | 2001-03-19 | 2005-10-26 | Sloan Kettering Inst Cancer | Asymmetric synthesis of (s, s, r)-(-)-actinonin and its analogs and uses therefor |
AU2004263900A1 (en) | 2003-08-08 | 2005-02-17 | Arriva Pharmaceuticals, Inc. | Methods of protein production in yeast |
WO2005086915A2 (en) | 2004-03-09 | 2005-09-22 | Arriva Pharmaceuticals, Inc. | Treatment of chronic obstructive pulmonary disease by low dose inhalation of protease inhibitor |
JP5421238B2 (en) * | 2008-03-13 | 2014-02-19 | 株式会社ヤクルト本社 | MMP inhibitor |
KR20170086678A (en) * | 2012-05-21 | 2017-07-26 | 디씨비-유에스에이 엘엘씨 | Methods for drug screen using zebrafish model and the compounds screened therefrom |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0489579A1 (en) * | 1990-12-03 | 1992-06-10 | Celltech Therapeutics Limited | Peptidyl derivatives |
WO1992009563A1 (en) * | 1990-11-21 | 1992-06-11 | Glycomed, Inc. | Improved matrix metalloprotease inhibitors |
WO1992009556A1 (en) * | 1990-11-21 | 1992-06-11 | Galardy Richard E | Improved matrix metalloprotease inhibitors |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4599361A (en) * | 1985-09-10 | 1986-07-08 | G. D. Searle & Co. | Hydroxamic acid based collagenase inhibitors |
FR2609289B1 (en) * | 1987-01-06 | 1991-03-29 | Bellon Labor Sa Roger | NOVEL COMPOUNDS HAVING ACTIVITY OF COLLAGENASE INHIBITORS, PROCESS FOR PREPARING SAME AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
GB8726714D0 (en) * | 1987-11-14 | 1987-12-16 | Beecham Group Plc | Compounds |
WO1991017982A1 (en) * | 1990-05-21 | 1991-11-28 | Sankyo Company, Limited | Novel compound matristatin |
US5268384A (en) * | 1990-11-21 | 1993-12-07 | Galardy Richard E | Inhibition of angiogenesis by synthetic matrix metalloprotease inhibitors |
US5114953A (en) * | 1990-11-21 | 1992-05-19 | University Of Florida | Treatment for tissue ulceration |
US5270326A (en) * | 1990-11-21 | 1993-12-14 | University Of Florida | Treatment for tissue ulceration |
-
1994
- 1994-04-01 JP JP6522412A patent/JPH08511509A/en not_active Ceased
- 1994-04-01 WO PCT/US1994/003600 patent/WO1994022309A1/en not_active Application Discontinuation
- 1994-04-01 EP EP94913345A patent/EP0692931A4/en not_active Ceased
- 1994-04-01 CA CA002160139A patent/CA2160139A1/en not_active Abandoned
- 1994-04-01 AU AU65542/94A patent/AU6554294A/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992009563A1 (en) * | 1990-11-21 | 1992-06-11 | Glycomed, Inc. | Improved matrix metalloprotease inhibitors |
WO1992009556A1 (en) * | 1990-11-21 | 1992-06-11 | Galardy Richard E | Improved matrix metalloprotease inhibitors |
EP0489579A1 (en) * | 1990-12-03 | 1992-06-10 | Celltech Therapeutics Limited | Peptidyl derivatives |
Non-Patent Citations (1)
Title |
---|
See also references of WO9422309A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1994022309A1 (en) | 1994-10-13 |
EP0692931A1 (en) | 1996-01-24 |
JPH08511509A (en) | 1996-12-03 |
CA2160139A1 (en) | 1994-10-13 |
AU6554294A (en) | 1994-10-24 |
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Legal Events
Date | Code | Title | Description |
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PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
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17P | Request for examination filed |
Effective date: 19951006 |
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AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL PT SE |
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RHK1 | Main classification (correction) |
Ipc: C07D209/20 |
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A4 | Supplementary search report drawn up and despatched |
Effective date: 19960131 |
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AK | Designated contracting states |
Kind code of ref document: A4 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL PT SE |
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17Q | First examination report despatched |
Effective date: 19981102 |
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APAB | Appeal dossier modified |
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APAD | Appeal reference recorded |
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APAB | Appeal dossier modified |
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APBJ | Interlocutory revision of appeal recorded |
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STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED |
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18R | Application refused |
Effective date: 20010114 |
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APAF | Appeal reference modified |
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