AR002945A1 - Acidos 4-biarilbutirico o 5-biarilpentanoico sustituidos y sus derivados como inhibidores de las metaloproteasas de matriz, composicion que los contiene, y metodos para la preparacion de dichos compuestos - Google Patents
Acidos 4-biarilbutirico o 5-biarilpentanoico sustituidos y sus derivados como inhibidores de las metaloproteasas de matriz, composicion que los contiene, y metodos para la preparacion de dichos compuestosInfo
- Publication number
- AR002945A1 AR002945A1 ARP950100171A AR10017195A AR002945A1 AR 002945 A1 AR002945 A1 AR 002945A1 AR P950100171 A ARP950100171 A AR P950100171A AR 10017195 A AR10017195 A AR 10017195A AR 002945 A1 AR002945 A1 AR 002945A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- derivatives
- substituted
- compounds
- preparation
- Prior art date
Links
Classifications
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- 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
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Acidos 4-biarilbutírico o 5-biarilpentanoico substituidos y sus derivados que tienen actividad inhibitoria de la metaloproteasa de la matriz,caracterizados por la fórmula (T)x A-B-D-E-G, donde A y B son anillos de arilo o heteroarilo;ca da T es un grupo de sustitución; x es 0, 1 ó 2; el grupo Drepresenta (II); el grupo E representa una cadena de dos o tres carbonos que lleva de uno a dos grupos de sustitución que son independientes o estánasociados en una formación de anillo,mos trándose las posibles estructuras en el texto y en las afirmaciones; y el grupo G representa -PO3H2, -M, y III en elque M represente -CO2H,-CON(R11)2 ó -CO2R12; y R13 representa cualquiera de las cadenas laterales de 19 aminoácidos no cíclicosque aparecen de forma natural,e incluye, por lo tanto, sales farmacéuticamente aceptables. También se relaciona con una composición que tiene actividad inhibitoria de la metaloproteasa de la matriz y un método para la preparación de dichoscompue stos.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33984694A | 1994-11-15 | 1994-11-15 | |
US08/539,409 US5789434A (en) | 1994-11-15 | 1995-11-06 | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
AR002945A1 true AR002945A1 (es) | 1998-05-27 |
Family
ID=26991840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP950100171A AR002945A1 (es) | 1994-11-15 | 1995-11-14 | Acidos 4-biarilbutirico o 5-biarilpentanoico sustituidos y sus derivados como inhibidores de las metaloproteasas de matriz, composicion que los contiene, y metodos para la preparacion de dichos compuestos |
Country Status (5)
Country | Link |
---|---|
US (1) | US6166082A (es) |
AR (1) | AR002945A1 (es) |
HR (1) | HRP950558A2 (es) |
IL (1) | IL115995A0 (es) |
TR (1) | TR199501429A2 (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2356053A1 (en) | 1998-12-30 | 2000-07-13 | Bayer Aktiengesellschaft | Use of substituted 4-biarylbutyric and 5-biarylpentanoic acid derivatives as matrix metalloprotease inhibitors for the treatment of respiratory diseases |
US7396810B1 (en) * | 2000-08-14 | 2008-07-08 | Oregon Health Sciences University | Compositions and methods for treating cancer by modulating HER-2 and EGF receptors |
US7625859B1 (en) * | 2000-02-16 | 2009-12-01 | Oregon Health & Science University | HER-2 binding antagonists |
US7393823B1 (en) | 1999-01-20 | 2008-07-01 | Oregon Health And Science University | HER-2 binding antagonists |
NZ520657A (en) * | 2000-03-21 | 2004-11-26 | Procter & Gamble | Heterocyclic side chain containing, N-substituted metalloprotease inhibitors |
JP2003528082A (ja) * | 2000-03-21 | 2003-09-24 | ザ プロクター アンド ギャンブル カンパニー | ニフッ化酪酸メタロプロテアーゼ阻害物質 |
EP1265887A2 (en) * | 2000-03-21 | 2002-12-18 | The Procter & Gamble Company | Carbocyclic side chain containing metalloprotease inhibitors |
AU2001245863A1 (en) * | 2000-03-21 | 2001-10-03 | The Procter & Gamble Company | Heterocyclic side chain containing metalloprotease inhibitors |
AU2003300076C1 (en) | 2002-12-30 | 2010-03-04 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
WO2005016864A1 (en) * | 2003-07-29 | 2005-02-24 | The Arizona Disease Control Research Commission | Conjugated nitro alkene anticancer agents based on isoprenoid metabolism |
WO2006042002A2 (en) * | 2004-10-05 | 2006-04-20 | Oregon Health And Science University | Compositions and methods for treating disease |
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-
1995
- 1995-11-14 IL IL11599595A patent/IL115995A0/xx unknown
- 1995-11-14 AR ARP950100171A patent/AR002945A1/es active IP Right Grant
- 1995-11-14 HR HR08/539,409A patent/HRP950558A2/hr not_active Application Discontinuation
- 1995-11-15 TR TR95/01429A patent/TR199501429A2/xx unknown
-
1998
- 1998-04-09 US US09/057,679 patent/US6166082A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
TR199501429A2 (tr) | 1996-06-21 |
IL115995A0 (en) | 1996-01-31 |
US6166082A (en) | 2000-12-26 |
HRP950558A2 (en) | 1997-12-31 |
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