ES2069833T3 - Derivados peptidilicos. - Google Patents
Derivados peptidilicos.Info
- Publication number
- ES2069833T3 ES2069833T3 ES91311254T ES91311254T ES2069833T3 ES 2069833 T3 ES2069833 T3 ES 2069833T3 ES 91311254 T ES91311254 T ES 91311254T ES 91311254 T ES91311254 T ES 91311254T ES 2069833 T3 ES2069833 T3 ES 2069833T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- elevated
- sub
- hydrogen atom
- replaced
- 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.)
- Expired - Lifetime
Links
- -1 CARBOXYL Chemical class 0.000 abstract 7
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 102000013382 Gelatinases Human genes 0.000 abstract 1
- 108010026132 Gelatinases Proteins 0.000 abstract 1
- 206010027476 Metastases Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical class [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000009401 metastasis Effects 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C55/00—Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
- C07C55/02—Dicarboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
- C07C311/46—Y being a hydrogen or a carbon atom
-
- 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
- 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
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
- C07K5/06052—Val-amino acid
-
- 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
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- 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
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Furan Compounds (AREA)
Abstract
SE DESCRIBEN COMPUESTOS QUE TIENEN LA FORMULA (I): EN DONDE R REPRESENTA UN GRUPO DE -CONHOH, CARBOXILO (-CO SUB 2 H) O CARBOXILO ESTERIFICADO; R ELEVADO 1 REPRESENTA UN GRUPO DE ALQUILO, ALQUENILO, ARILO, ARALQUILO, HETEROARALQUILO O HETEROARILTIOALQUILO OPCIONALMENTE SUSTITUIDO; R (AL CUADRADO) REPRESENTA UN GRUPO DE FENILETILO, FENILPROPILO O FENILBUTILO OPCIONALMENTE SUSTITUIDO; R ELEVADO 3 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO DE ALQUILO; R ELEVADO 4 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO DE ALQUILO; R ELEVADO 5 REPRESENTA UN GRUPO DE ALQUILO O ALQUENILO OPCIONALMENTE SUSTITUIDO OPCIONALMENTE INTERRUMPIDO POR UNO O MAS ATOMOS DE -O ELEVADO 7) [ DONDE R ELEVADO 7 ES UN ATOMO DE HIDROGENO O UN GRUPO DE ALQUILO C SUB 1-6]; X REPRESENTA UN GRUPO DE AMINO (-NH SUB 2), O DE AMINO SUSTITUIDO, DE HIDROXILO O DE HIDROXILO SUSTITUIDO; Y LAS SALES, SOLVATOS E HIDRATOS DE LOS MISMOS. LOS COMPUESTOS SON INHIBIDORES DE LA METALOPROTEINASA Y TIENEN EN PARTICULAR UNA ACCION DE GELATINASA SELECTIVA Y PUEDEN SER UTILES EN EL TRATAMIENTO DEL CANCER PARA CONTROLAR EL DESARROLLO DE METASTASIS TUMORALES.
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909026251A GB9026251D0 (en) | 1990-12-03 | 1990-12-03 | Netalloproteinase inhibitors |
| GB919110339A GB9110339D0 (en) | 1991-05-13 | 1991-05-13 | Metalloproteinase inhibitors |
| GB919110338A GB9110338D0 (en) | 1991-05-13 | 1991-05-13 | Metalloproteinase inhibitors |
| GB919112901A GB9112901D0 (en) | 1991-06-14 | 1991-06-14 | Metalloproteinase inhibitors |
| GB919112888A GB9112888D0 (en) | 1991-06-14 | 1991-06-14 | Metalloproteinase inhibitors |
| GB919115038A GB9115038D0 (en) | 1991-07-11 | 1991-07-11 | Metalloproteinase inhibitors |
| GB919115039A GB9115039D0 (en) | 1991-07-11 | 1991-07-11 | Metalloproteinase inhibitors |
| GB919115916A GB9115916D0 (en) | 1991-07-23 | 1991-07-23 | Metalloproteinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2069833T3 true ES2069833T3 (es) | 1995-05-16 |
Family
ID=27571285
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES91311254T Expired - Lifetime ES2069833T3 (es) | 1990-12-03 | 1991-12-03 | Derivados peptidilicos. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5300501A (es) |
| EP (2) | EP0489577B1 (es) |
| JP (2) | JPH05503720A (es) |
| KR (2) | KR927003521A (es) |
| AT (2) | ATE120182T1 (es) |
| AU (2) | AU652793B2 (es) |
| CA (2) | CA2073513A1 (es) |
| DE (2) | DE69108529T2 (es) |
| DK (1) | DK0489579T3 (es) |
| ES (1) | ES2069833T3 (es) |
| FI (2) | FI923494A0 (es) |
| GB (2) | GB2255340B (es) |
| GR (1) | GR3015567T3 (es) |
| HU (3) | HUT61973A (es) |
| NO (2) | NO922968L (es) |
| WO (2) | WO1992009565A1 (es) |
Families Citing this family (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5892112A (en) * | 1990-11-21 | 1999-04-06 | Glycomed Incorporated | Process for preparing synthetic matrix metalloprotease inhibitors |
| US5189178A (en) * | 1990-11-21 | 1993-02-23 | Galardy Richard E | Matrix metalloprotease inhibitors |
| US5268384A (en) * | 1990-11-21 | 1993-12-07 | Galardy Richard E | Inhibition of angiogenesis by synthetic matrix metalloprotease inhibitors |
| EP0520573A1 (en) * | 1991-06-27 | 1992-12-30 | Glaxo Inc. | Cyclic imide derivatives |
| US5525629A (en) * | 1992-04-07 | 1996-06-11 | British Bio-Technology Limited | Inhibition of cytokine production |
| GB9211706D0 (en) * | 1992-06-03 | 1992-07-15 | Celltech Ltd | Peptidyl derivatives |
| GB9211707D0 (en) * | 1992-06-03 | 1992-07-15 | Celltech Ltd | Peptidyl derivatives |
| AU666727B2 (en) * | 1992-06-25 | 1996-02-22 | F. Hoffmann-La Roche Ag | Hydroxamic acid derivatives |
| US5326760A (en) * | 1992-06-29 | 1994-07-05 | Glaxo, Inc. | Aminobutanoic acid compounds having metalloprotease inhibiting properties |
| GB9215665D0 (en) * | 1992-07-23 | 1992-09-09 | British Bio Technology | Compounds |
| AU5292193A (en) * | 1992-10-02 | 1994-04-26 | Merck & Co., Inc. | N-(mercaptoacyl)peptidyl derivatives as antidegenerative agents |
| US6090785A (en) * | 1992-10-15 | 2000-07-18 | Merck & Co., Inc. | Substituted N-carboxyalkylpeptidyl derivatives as antidegenerative agents |
| GB9223904D0 (en) * | 1992-11-13 | 1993-01-06 | British Bio Technology | Inhibition of cytokine production |
| WO1994012169A1 (en) * | 1992-11-25 | 1994-06-09 | Merck & Co., Inc. | Carboxy-peptidyl derivatives as antidegenerative active agents |
| US5506242A (en) * | 1993-01-06 | 1996-04-09 | Ciba-Geigy Corporation | Arylsufonamido-substituted hydroxamic acids |
| US5552419A (en) * | 1993-01-06 | 1996-09-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5455258A (en) * | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5646167A (en) * | 1993-01-06 | 1997-07-08 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamix acids |
| GB2290543B (en) * | 1993-03-16 | 1996-05-22 | British Biotech Pharm | Hydroxamic acid derivatives as metalloproteinase inhibitors |
| CA2160139A1 (en) * | 1993-04-07 | 1994-10-13 | Richard Edward Galardy | Synthetic matrix metalloprotease inhibitors and uses thereof |
| GB9307956D0 (en) * | 1993-04-17 | 1993-06-02 | Walls Alan J | Hydroxamic acid derivatives |
| GB9308695D0 (en) * | 1993-04-27 | 1993-06-09 | Celltech Ltd | Peptidyl derivatives |
| US5714491A (en) * | 1993-04-27 | 1998-02-03 | Celltech Therapeutics Limited | Peptidyl derivatives as metalloproteinase inhibitors |
| AU7270794A (en) * | 1993-08-02 | 1995-02-28 | Celltech Limited | Succinamide derivatives, processes for their preparation and their use as gelatinase and collagenase inhibitors |
| US5594106A (en) * | 1993-08-23 | 1997-01-14 | Immunex Corporation | Inhibitors of TNF-α secretion |
| GB9320660D0 (en) * | 1993-10-07 | 1993-11-24 | British Bio Technology | Inhibition of cytokine production |
| US6037472A (en) * | 1993-11-04 | 2000-03-14 | Syntex (U.S.A.) Inc. | Matrix metalloprotease inhibitors |
| DE69502378T2 (de) * | 1994-01-20 | 1998-10-01 | British Biotech Pharm | Metalloproteinaseinhibitoren |
| US5514716A (en) * | 1994-02-25 | 1996-05-07 | Sterling Winthrop, Inc. | Hydroxamic acid and carboxylic acid derivatives, process for their preparation and use thereof |
| GB9501737D0 (en) * | 1994-04-25 | 1995-03-22 | Hoffmann La Roche | Hydroxamic acid derivatives |
| EP0763012B1 (en) * | 1994-05-28 | 1999-06-09 | British Biotech Pharmaceuticals Limited | Succinyl hydroxamic acid, n-formyl-n-hydroxy amino carboxylic acid and succinic acid amide derivatives as metalloprotease inhibitors |
| GB9411088D0 (en) * | 1994-06-03 | 1994-07-27 | Hoffmann La Roche | Hydroxylamine derivatives |
| JPH10501806A (ja) * | 1994-06-22 | 1998-02-17 | ブリティッシュ バイオテック ファーマシューティカルズ リミテッド | 金属タンパク質分解酵素阻害剤 |
| US5840698A (en) * | 1994-10-27 | 1998-11-24 | Affymax Technologies N.V. | Inhibitors of collagenase-1 and stormelysin-I metalloproteases, pharmaceutical compositions comprising same and methods of their use |
| US5831004A (en) * | 1994-10-27 | 1998-11-03 | Affymax Technologies N.V. | Inhibitors of metalloproteases, pharmaceutical compositions comprising same and methods of their use |
| GB9423914D0 (en) * | 1994-11-26 | 1995-01-11 | British Biotech Pharm | Polyether derivatives as metalloproteinase inhibitors |
| US5919940A (en) * | 1995-01-20 | 1999-07-06 | British Biotech Pharmaceuticals Limited | Metalloproteinase inhibitors |
| US5857961A (en) * | 1995-06-07 | 1999-01-12 | Clarus Medical Systems, Inc. | Surgical instrument for use with a viewing system |
| US5917090A (en) * | 1995-06-30 | 1999-06-29 | British Biotech Pharmaceuticals Ltd. | Matrix metalloproteinase inhibitors |
| IT1277904B1 (it) * | 1995-08-07 | 1997-11-12 | Polifarma Spa | Metodo per determinare l'attivita' terapeutica di composti inibitori di metalloproteinasi, nuovi composti inibitori, e loro impiego |
| US5665777A (en) * | 1995-11-14 | 1997-09-09 | Abbott Laboratories | Biphenyl hydroxamate inhibitors of matrix metalloproteinases |
| ES2164264T3 (es) | 1995-11-23 | 2002-02-16 | British Biotech Pharm | Inhibidores de metaloproteinasas. |
| US6500948B1 (en) | 1995-12-08 | 2002-12-31 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors-compositions, uses preparation and intermediates thereof |
| CA2238306A1 (en) * | 1995-12-08 | 1997-06-12 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses, and methods and intermediates useful for their preparation |
| GB9613547D0 (en) * | 1996-06-27 | 1996-08-28 | Pharmacia Spa | Matrix metalloproteinase inhibitors |
| BR9712019A (pt) | 1996-09-10 | 1999-08-24 | British Biotech Pharm | Derivados de cidos hirox-mico citoest ticos |
| US6462023B1 (en) | 1996-09-10 | 2002-10-08 | British Biotech Pharmaceuticals, Ltd. | Cytostatic agents |
| US6953788B1 (en) | 1996-09-19 | 2005-10-11 | Aventis Pharmaceuticals Inc. | 3-mercaptoacetylamino-1,5-substituted-2-oxo-azepan derivatives useful as inhibitors of matrix metalloproteinase |
| US6008243A (en) * | 1996-10-24 | 1999-12-28 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them, and their use |
| US6174915B1 (en) | 1997-03-25 | 2001-01-16 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses |
| JPH10130217A (ja) * | 1996-11-01 | 1998-05-19 | Kotobuki Seiyaku Kk | カルボン酸及びその誘導体及びその製造法並びにこれを含有する医薬組成物 |
| ZA9818B (en) * | 1997-01-07 | 1998-07-02 | Abbott Lab | C-terminal ketone inhibitors of matrix metalloproteinases and tnf alpha secretion |
| 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 |
| US5985900A (en) * | 1997-04-01 | 1999-11-16 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses |
| EP0887077A1 (de) * | 1997-06-27 | 1998-12-30 | Boehringer Mannheim Gmbh | Verwendung von Azulenderivaten als Metalloproteaseinhibitoren |
| GB9803005D0 (en) | 1998-02-12 | 1998-04-08 | British Biotech Pharm | Anti-inflammatory agents |
| GB9804504D0 (en) * | 1998-03-03 | 1998-04-29 | Leo Pharm Prod Ltd | Matrix metalloproteinase inhibitors |
| US6288261B1 (en) | 1998-12-18 | 2001-09-11 | Abbott Laboratories | Inhibitors of matrix metalloproteinases |
| RU2001133740A (ru) * | 1999-05-17 | 2003-09-27 | Дайити Файн Кемикал Ко., Лтд. (Jp) | Новые производные гидроксамовой кислоты |
| JP2001031637A (ja) * | 1999-05-17 | 2001-02-06 | Fuji Chemical Industries Ltd | 新規なヒドロキサム酸誘導体 |
| PE20010659A1 (es) | 1999-10-01 | 2001-06-20 | Hoffmann La Roche | Derivados de las pirimidin-2,4,6-trionas como inhibidores de metaloproteasas |
| US6797820B2 (en) | 1999-12-17 | 2004-09-28 | Vicuron Pharmaceuticals Inc. | Succinate compounds, compositions and methods of use and preparation |
| AU2001271068A1 (en) * | 2000-07-18 | 2002-01-30 | Chugai Seiyaku Kabushiki Kaisha | Matrix metalloprotease inhibitors |
| US6716845B2 (en) | 2001-03-30 | 2004-04-06 | Hoffmann-La Roche Inc. | Barbituric acid derivatives |
| AR036053A1 (es) | 2001-06-15 | 2004-08-04 | Versicor Inc | Compuestos de n-formil-hidroxilamina, un proceso para su preparacion y composiciones farmaceuticas |
| ES2283589T3 (es) | 2001-06-15 | 2007-11-01 | Vicuron Pharmaceuticals, Inc. | Compuestos biciclicos de pirrolidina. |
| US7605132B2 (en) * | 2001-08-29 | 2009-10-20 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Protective factors against inflammation, burns and noxious stimuli |
| US7528227B2 (en) * | 2004-03-23 | 2009-05-05 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Histone H2A peptide derivatives and uses thereof |
| WO2005090387A2 (en) * | 2004-03-23 | 2005-09-29 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Histone h2a peptide derivatives and analogs and methods of use thereof |
| WO2004060425A2 (en) * | 2002-12-27 | 2004-07-22 | Angiotech International Ag | Compositions and methods of using collagen and mmpi |
| GB0818907D0 (en) * | 2008-10-15 | 2008-11-19 | Isis Innovation | Histone lysine demethylase inhibitors |
| EP3061460A1 (en) | 2009-04-10 | 2016-08-31 | Tufts Medical Center, Inc. | Par-1 activation by metalloproteinase-1 (mmp-1) |
| DE102014206916A1 (de) | 2014-04-10 | 2015-10-15 | Wacker Chemie Ag | Verfahren zur Ruthenium-katalysierten Umvinylierung von Carbonsäuren |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4743587A (en) * | 1985-09-10 | 1988-05-10 | G. D. Searle & Co. | Hydroxamic acid based collagenase inhibitors |
| FR2609289B1 (fr) * | 1987-01-06 | 1991-03-29 | Bellon Labor Sa Roger | Nouveaux composes a activite d'inhibiteurs de collagenase, procede pour les preparer et compositions pharmaceutiques contenant ces composes |
| GB8827308D0 (en) * | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| GB8827305D0 (en) * | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| CA2058797A1 (en) * | 1991-02-01 | 1992-08-02 | Michael John Broadhurst | Amino acid derivatives |
| US5196412A (en) * | 1991-03-06 | 1993-03-23 | Johnson Matthey, Inc. | Gallium compounds |
-
1991
- 1991-12-03 WO PCT/GB1991/002143 patent/WO1992009565A1/en not_active Ceased
- 1991-12-03 JP JP4500489A patent/JPH05503720A/ja active Pending
- 1991-12-03 EP EP91311252A patent/EP0489577B1/en not_active Expired - Lifetime
- 1991-12-03 HU HU9202498A patent/HUT61973A/hu unknown
- 1991-12-03 AT AT91311252T patent/ATE120182T1/de active
- 1991-12-03 AT AT91311254T patent/ATE120451T1/de not_active IP Right Cessation
- 1991-12-03 EP EP91311254A patent/EP0489579B1/en not_active Expired - Lifetime
- 1991-12-03 WO PCT/GB1991/002142 patent/WO1992009564A1/en not_active Ceased
- 1991-12-03 CA CA002073513A patent/CA2073513A1/en not_active Abandoned
- 1991-12-03 US US07/916,108 patent/US5300501A/en not_active Expired - Lifetime
- 1991-12-03 HU HU922497A patent/HUT62263A/hu unknown
- 1991-12-03 AU AU90173/91A patent/AU652793B2/en not_active Ceased
- 1991-12-03 ES ES91311254T patent/ES2069833T3/es not_active Expired - Lifetime
- 1991-12-03 KR KR1019920701788A patent/KR927003521A/ko not_active Withdrawn
- 1991-12-03 JP JP4500488A patent/JPH05503719A/ja active Pending
- 1991-12-03 KR KR1019920701787A patent/KR927003520A/ko not_active Withdrawn
- 1991-12-03 DE DE69108529T patent/DE69108529T2/de not_active Expired - Fee Related
- 1991-12-03 CA CA002073510A patent/CA2073510A1/en not_active Abandoned
- 1991-12-03 HU HU922497Q patent/HU9202497D0/hu unknown
- 1991-12-03 AU AU90233/91A patent/AU652596B2/en not_active Ceased
- 1991-12-03 FI FI923494A patent/FI923494A0/fi not_active Application Discontinuation
- 1991-12-03 DE DE69108363T patent/DE69108363T2/de not_active Expired - Fee Related
- 1991-12-03 DK DK91311254.6T patent/DK0489579T3/da active
-
1992
- 1992-06-02 GB GB9211715A patent/GB2255340B/en not_active Expired - Fee Related
- 1992-06-02 GB GB9211714A patent/GB2255339B/en not_active Expired - Fee Related
- 1992-07-28 NO NO92922968A patent/NO922968L/no unknown
- 1992-07-28 NO NO92922967A patent/NO922967L/no unknown
- 1992-08-03 FI FI923495A patent/FI923495A7/fi not_active Application Discontinuation
-
1995
- 1995-03-30 GR GR940403917T patent/GR3015567T3/el unknown
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