AR030197A1 - Compuesto n-sustituido que contiene una cadena lateral heterociclica, composicion farmaceutica que lo comprende y uso de dicho compuesto para la fabricacion de un medicamento - Google Patents
Compuesto n-sustituido que contiene una cadena lateral heterociclica, composicion farmaceutica que lo comprende y uso de dicho compuesto para la fabricacion de un medicamentoInfo
- Publication number
- AR030197A1 AR030197A1 ARP010101310A ARP010101310A AR030197A1 AR 030197 A1 AR030197 A1 AR 030197A1 AR P010101310 A ARP010101310 A AR P010101310A AR P010101310 A ARP010101310 A AR P010101310A AR 030197 A1 AR030197 A1 AR 030197A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- memory
- manufacture
- pharmaceutical composition
- side chain
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/34—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
- C07D211/66—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4 having a hetero atom as the second substituent in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/96—Sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D309/06—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrane Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Un compuesto N-sustituido que contiene una cadena lateral heterocíclica que tiene una estructura segun la formula (1), en donde (A) R1 se selecciona de -OH, -NHOH; (B) R2 se selecciona de hidrogeno, alquilo, alquenilo y otros de acuerdo con la memoria; (C) R3 se selecciona de alquilo, alquenilo, alquinilo y otros de acuerdo con la memoria; (D) A es un heterociclolalquilo monocíclico sustituido o no sustituido que tiene de 3 a 8 átomos en el anillo de los cuales 1 a 3 son heteroátomos; o A está enlazada a R2 donde, juntos, forman un heterocicloalquilo monocíclico sustituido o no sustituido que tiene de 3 a 8 átomos en el anillo de los cuales 1 a 3 son heteroátomos; (E) n es de 0 a 4; (F) E se selecciona de un enlace covalente, alquilo C1-4, -C(=O)-, y otros de acuerdo con la memoria; (G) (1) X se selecciona de hidrogeno, alquilo y otros de acuerdo con la memoria; (H) G se selecciona de -S-, -O-, -N(R5)-, -C(R5)=C(R5')-, y otros de acuerdo con la memoria; (I) G' se selecciona de -S-, -O-, -N(R6)-, =C(R6)- y otros de acuerdo con la memoria; (J) M se selecciona de -CH- y -N-; y (K) Z es -(CH7R7)a-L-R8, donde: (1) a es de 0 a 4; (2) cada 7 y R7' independientemente se seleccionan de hidrogeno, alquilo y otros de acuerdo con la memoria; o un isomero optico, diastereomero o enantiomero para la formula (1), o una sal farmacéuticamente aceptable, o amida biohidrolizable, éster, o imida de estos. Una composicion farmacéutica que comprende: (a) una cantidad segura y eficaz de dicho compuesto; (b) un portador farmacéuticamente aceptable. El uso de un compuesto es que la fabricacion de un medicamento para tratar enfermedad asociada con la actividad no deseada de la metaloproteasa en un sujeto mamífero. Dicho uso en donde el trastorno es artritis, y se selecciona del grupo que consiste de osteoartritis y artritis reumatoide y otros de acuerdo con la memoria.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19130200P | 2000-03-21 | 2000-03-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR030197A1 true AR030197A1 (es) | 2003-08-13 |
Family
ID=22704936
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP010101310A AR030197A1 (es) | 2000-03-21 | 2001-03-20 | Compuesto n-sustituido que contiene una cadena lateral heterociclica, composicion farmaceutica que lo comprende y uso de dicho compuesto para la fabricacion de un medicamento |
Country Status (22)
Country | Link |
---|---|
US (2) | US6949545B2 (es) |
EP (1) | EP1265864A1 (es) |
JP (1) | JP2003528080A (es) |
KR (1) | KR20020081465A (es) |
CN (1) | CN1425004A (es) |
AR (1) | AR030197A1 (es) |
AU (1) | AU2001245891A1 (es) |
BR (1) | BR0109328A (es) |
CA (1) | CA2404131A1 (es) |
CZ (1) | CZ20023145A3 (es) |
HU (1) | HUP0300235A2 (es) |
IL (1) | IL151125A0 (es) |
MA (1) | MA26884A1 (es) |
MX (1) | MXPA02009311A (es) |
NO (1) | NO20024520L (es) |
NZ (1) | NZ520657A (es) |
PE (1) | PE20011137A1 (es) |
PL (1) | PL365444A1 (es) |
RU (1) | RU2245876C2 (es) |
SK (1) | SK12842002A3 (es) |
WO (1) | WO2001070691A1 (es) |
ZA (1) | ZA200206298B (es) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1249239B1 (en) * | 1999-12-28 | 2008-05-21 | Teikoku Seiyaku Co., Ltd. | Antipruritic agents for external use |
NZ520656A (en) * | 2000-03-21 | 2004-05-28 | Procter & Gamble | Heterocyclic side chain containing metalloprotease inhibitors |
JP4294321B2 (ja) * | 2001-03-14 | 2009-07-08 | ノバルティス アクチエンゲゼルシャフト | Mmp阻害剤としての使用のためのアザシクロアルキル置換酢酸誘導体 |
US20070160655A1 (en) * | 2003-04-23 | 2007-07-12 | Sefton Michael V | Hydroxyamate-containing materials for the inhibition of matrix metalloproteinases |
US20040213758A1 (en) * | 2003-04-23 | 2004-10-28 | Rimon Therapeutics Ltd. | Hydroxyamate-containing materials for the inhibition of matrix metalloproteinases |
US7576222B2 (en) | 2004-12-28 | 2009-08-18 | Wyeth | Alkynyl-containing tryptophan derivative inhibitors of TACE/matrix metalloproteinase |
KR100717022B1 (ko) * | 2005-08-27 | 2007-05-10 | 삼성전자주식회사 | 잉크젯 프린트헤드 및 그 제조방법 |
RU2526201C2 (ru) * | 2007-11-16 | 2014-08-20 | Эббви Инк. | Способ лечения артрита |
US20100160322A1 (en) | 2008-12-04 | 2010-06-24 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8557983B2 (en) | 2008-12-04 | 2013-10-15 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
UA108193C2 (uk) * | 2008-12-04 | 2015-04-10 | Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань | |
MY158932A (en) * | 2008-12-05 | 2016-11-30 | Abbvie Inc | Sulfonamide derivatives as bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
US8563735B2 (en) | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
US8586754B2 (en) | 2008-12-05 | 2013-11-19 | Abbvie Inc. | BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
US20100319773A1 (en) * | 2009-06-22 | 2010-12-23 | Solarmation, Inc. | Optics for Concentrated Photovoltaic Cell |
Family Cites Families (68)
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 |
US4771038A (en) | 1986-01-21 | 1988-09-13 | Ici Americas Inc. | Hydroxamic acids |
DK77487A (da) | 1986-03-11 | 1987-09-12 | Hoffmann La Roche | Hydroxylaminderivater |
ZW23187A1 (en) | 1986-12-15 | 1988-06-29 | Hoffmann La Roche | Phosphinic acid derivatives |
US5183900A (en) | 1990-11-21 | 1993-02-02 | Galardy Richard E | Matrix metalloprotease inhibitors |
US5892112A (en) | 1990-11-21 | 1999-04-06 | Glycomed Incorporated | Process for preparing synthetic matrix metalloprotease inhibitors |
GB9102635D0 (en) | 1991-02-07 | 1991-03-27 | British Bio Technology | Compounds |
GB9107368D0 (en) | 1991-04-08 | 1991-05-22 | Smithkline Beecham Plc | Novel compounds |
AU2228292A (en) | 1991-06-14 | 1993-01-12 | Research Corporation Technologies, Inc. | Peptide derivatives of collagenase inhibitor |
JPH05125029A (ja) | 1991-11-06 | 1993-05-21 | Yamanouchi Pharmaceut Co Ltd | 新規なアミド化合物又はその塩 |
JPH07503016A (ja) | 1992-01-15 | 1995-03-30 | メルク エンド カンパニー インコーポレーテッド | 変形防止剤としての置換されたホスフィン酸含有ペプチジル誘導体 |
EP0639982A1 (en) | 1992-05-01 | 1995-03-01 | British Biotech Pharmaceuticals Limited | Use of mmp inhibitors |
US5318964A (en) | 1992-06-11 | 1994-06-07 | Hoffmann-La Roche Inc. | Hydroxamic derivatives and pharmaceutical compositions |
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 |
GB9223904D0 (en) | 1992-11-13 | 1993-01-06 | British Bio Technology | Inhibition of cytokine production |
US5646167A (en) | 1993-01-06 | 1997-07-08 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamix acids |
US5455258A (en) * | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
US5506242A (en) | 1993-01-06 | 1996-04-09 | Ciba-Geigy Corporation | Arylsufonamido-substituted hydroxamic acids |
DE69419473T2 (de) | 1993-04-27 | 2000-03-16 | Celltech Therapeutics Ltd. | Peptidylderivate als inhibitoren von metalloproteinase |
GB9308695D0 (en) | 1993-04-27 | 1993-06-09 | Celltech Ltd | Peptidyl derivatives |
US5827890A (en) | 1993-08-02 | 1998-10-27 | Celltech Therapeutics Ltd. | Succinamide derivatives, processes for their preparation and their use as gelatinase and collagenase inhibitors |
US5545735A (en) | 1993-10-04 | 1996-08-13 | Merck & Co., Inc. | Benzo-Fused Lactams promote release of growth hormone |
US5470834A (en) | 1993-10-06 | 1995-11-28 | Florida State University | Sulfoximine and suldodiimine matrix metalloproteinase inhibitors |
US5403952A (en) | 1993-10-08 | 1995-04-04 | Merck & Co., Inc. | Substituted cyclic derivatives as novel antidegenerative agents |
UA48121C2 (uk) | 1993-11-04 | 2002-08-15 | Сінтекс (С.Ш.А.) Інк. | Інгібітори матричних металопротеаз і фармацетична композиція на їх основі |
GB9323165D0 (en) | 1993-11-10 | 1994-01-05 | Chiros Ltd | Compounds |
WO1995019956A1 (en) | 1994-01-20 | 1995-07-27 | British Biotech Pharmaceuticals Limited | Metalloproteinase inhibitors |
GB9401129D0 (en) | 1994-01-21 | 1994-03-16 | British Bio Technology | Hydroxamic acid derivatives as metalloproteinase inhibitors |
DE69529100T2 (de) | 1994-01-22 | 2003-07-17 | British Biotech Pharmaceuticals Ltd., Cowley | 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 |
US5665753A (en) | 1994-03-03 | 1997-09-09 | Smithkline Beecham Corporation | Cytokine inhibiting imidazole substituted hydroxamic acid derivatives |
GB9405076D0 (en) | 1994-03-16 | 1994-04-27 | Inst Of Ophtalmology | A medical use of matrix metalloproteinase inhibitors |
DE4411311A1 (de) * | 1994-03-31 | 1995-10-05 | Basf Ag | Verfahren zur Herstellung von lagerstabilen wäßrigen Lösungen von Vinylamin-Einheiten enthaltenden Polymerisaten |
GB9501737D0 (en) | 1994-04-25 | 1995-03-22 | Hoffmann La Roche | Hydroxamic acid derivatives |
WO1995029892A1 (en) | 1994-04-28 | 1995-11-09 | The Du Pont Merck Pharmaceutical Company | Hydroxamic acid and amino acid derivatives and their use as anti-arthritic agents |
JPH07304770A (ja) | 1994-05-11 | 1995-11-21 | Kanebo Ltd | 新規ベンゾアゼピノン誘導体 |
ATE181055T1 (de) | 1994-05-28 | 1999-06-15 | British Biotech Pharm | Succinyl hydroxamsäure-, n-formyl-n-hydroxy- aminocarbonsäure- und succinsäureamid-derivate und ihre verwendung als metalloprotease- inhibitoren |
GB9411088D0 (en) | 1994-06-03 | 1994-07-27 | Hoffmann La Roche | Hydroxylamine derivatives |
GB9411598D0 (en) | 1994-06-09 | 1994-08-03 | Hoffmann La Roche | Hydroxamic acid derivatives |
GB9412350D0 (en) | 1994-06-20 | 1994-08-10 | Fujisawa Pharmaceutical Co | New compound and its preparation |
EP0766664B1 (en) | 1994-06-22 | 2000-04-05 | British Biotech Pharmaceuticals Limited | Metalloproteinase inhibitors |
GB9416897D0 (en) | 1994-08-20 | 1994-10-12 | British Biotech Pharm | Metalloproteinase inhibitors |
HRP950558A2 (en) | 1994-11-15 | 1997-12-31 | Scott M. Wilhelm | Substituted 4-biarylbutric or biarylpentanoic acids and derivatives as matrix metalloprotease inhibitors |
US5919940A (en) | 1995-01-20 | 1999-07-06 | British Biotech Pharmaceuticals Limited | Metalloproteinase inhibitors |
US5573438A (en) * | 1995-04-25 | 1996-11-12 | D'andrea; Deborah | Book including candy as a part of the pages |
US5886022A (en) | 1995-06-05 | 1999-03-23 | Bayer Corporation | Substituted cycloalkanecarboxylic acid derivatives as matrix metalloprotease inhibitors |
US6124333A (en) | 1995-06-22 | 2000-09-26 | British Biotech Pharmaceuticals Limited | Metalloproteinase inhibitors |
TW453995B (en) | 1995-12-15 | 2001-09-11 | Novartis Ag | Certain alpha-substituted arylsulfonamido acetohydroxamic acids |
KR100338861B1 (ko) * | 1996-01-23 | 2003-02-20 | 시오노기세이야쿠가부시키가이샤 | 술폰화아미노산유도체및이를함유한메탈로프로테이나제저해제 |
AU4159197A (en) | 1996-09-04 | 1998-03-26 | Warner-Lambert Company | Biphenyl butyric acids and their derivatives as inhibitors of matrix metalloproteinases |
BR9807815A (pt) | 1997-02-03 | 2000-03-08 | Pfizer Prod Inc | Derivados de ácido arilsulfonilamino-hidroxâmico |
ES2234103T3 (es) * | 1997-03-04 | 2005-06-16 | Pharmacia Corporation | Compuestos de acido tioarilsulfonamidohidroxamico. |
DE19719621A1 (de) * | 1997-05-09 | 1998-11-12 | Hoechst Ag | Sulfonylaminocarbonsäuren |
IL134273A0 (en) * | 1997-07-31 | 2001-04-30 | Procter & Gamble | Acyclic metalloprotease inhibitors |
ATE217863T1 (de) * | 1997-08-08 | 2002-06-15 | Pfizer Prod Inc | Arylsulfonylaminohydroxamsäurederivate |
WO1999018079A1 (en) | 1997-10-06 | 1999-04-15 | Warner-Lambert Company | Heteroaryl butyric acids and their derivatives as inhibitors of matrix metalloproteinases |
EP1053226A1 (en) | 1998-02-04 | 2000-11-22 | Novartis AG | Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases |
PA8469501A1 (es) * | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
FR2782080B1 (fr) * | 1998-08-10 | 2001-01-05 | Adir | Nouveaux derives d'acide hydroxamique, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
US6677360B2 (en) * | 1998-12-16 | 2004-01-13 | Bayer Aktiengesellschaft | Biphenyl and biphenyl-analogous compounds as integrin antagonists |
US6225311B1 (en) | 1999-01-27 | 2001-05-01 | American Cyanamid Company | Acetylenic α-amino acid-based sulfonamide hydroxamic acid tace inhibitors |
HUP0201714A3 (en) | 1999-03-03 | 2003-05-28 | Procter & Gamble | Substituted heterocyclic compounds and pharmaceutical compositions containing them |
ES2208315T3 (es) | 1999-05-28 | 2004-06-16 | Pfizer Products Inc. | Hidroxiamidas de acidos 3-(arilsulfonamido)-tetrahidropiran-3-carboxilicos. |
HN2000000052A (es) | 1999-05-28 | 2001-02-02 | Pfizer Prod Inc | Hidroxiamidas de acidos 3- (arilsulfonilamino)- tetrahidrofuran-3-carboxilicos. |
US6696456B1 (en) * | 1999-10-14 | 2004-02-24 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
PA8525601A1 (es) * | 2000-08-21 | 2002-04-25 | Hoffmann La Roche | Profarmacos de (3s,4s)-4-bencil-1-[2-(4-hidroxi-bencenosulfonil)-etil]-piperidin-3-ol |
-
2001
- 2001-03-02 HU HU0300235A patent/HUP0300235A2/hu unknown
- 2001-03-02 PL PL01365444A patent/PL365444A1/xx not_active Application Discontinuation
- 2001-03-02 KR KR1020027012313A patent/KR20020081465A/ko not_active Application Discontinuation
- 2001-03-02 MX MXPA02009311A patent/MXPA02009311A/es unknown
- 2001-03-02 EP EP01918867A patent/EP1265864A1/en not_active Withdrawn
- 2001-03-02 SK SK1284-2002A patent/SK12842002A3/sk unknown
- 2001-03-02 NZ NZ520657A patent/NZ520657A/en unknown
- 2001-03-02 RU RU2002128007/04A patent/RU2245876C2/ru not_active IP Right Cessation
- 2001-03-02 JP JP2001568903A patent/JP2003528080A/ja not_active Withdrawn
- 2001-03-02 CN CN01806655A patent/CN1425004A/zh active Pending
- 2001-03-02 CA CA002404131A patent/CA2404131A1/en not_active Abandoned
- 2001-03-02 BR BR0109328-2A patent/BR0109328A/pt not_active IP Right Cessation
- 2001-03-02 IL IL15112501A patent/IL151125A0/xx unknown
- 2001-03-02 WO PCT/US2001/008931 patent/WO2001070691A1/en not_active Application Discontinuation
- 2001-03-02 AU AU2001245891A patent/AU2001245891A1/en not_active Abandoned
- 2001-03-02 CZ CZ20023145A patent/CZ20023145A3/cs unknown
- 2001-03-20 AR ARP010101310A patent/AR030197A1/es not_active Application Discontinuation
- 2001-03-21 PE PE2001000265A patent/PE20011137A1/es not_active Application Discontinuation
-
2002
- 2002-08-07 ZA ZA200206298A patent/ZA200206298B/en unknown
- 2002-09-13 US US10/243,511 patent/US6949545B2/en not_active Expired - Fee Related
- 2002-09-16 MA MA26819A patent/MA26884A1/fr unknown
- 2002-09-20 NO NO20024520A patent/NO20024520L/no not_active Application Discontinuation
-
2004
- 2004-01-16 US US10/758,791 patent/US20040127498A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
IL151125A0 (en) | 2003-04-10 |
HUP0300235A2 (hu) | 2003-08-28 |
ZA200206298B (en) | 2003-04-11 |
US20040127498A1 (en) | 2004-07-01 |
US20030139414A1 (en) | 2003-07-24 |
CA2404131A1 (en) | 2001-09-27 |
CN1425004A (zh) | 2003-06-18 |
KR20020081465A (ko) | 2002-10-26 |
MA26884A1 (fr) | 2004-12-20 |
PE20011137A1 (es) | 2001-12-04 |
RU2002128007A (ru) | 2004-02-27 |
NO20024520D0 (no) | 2002-09-20 |
CZ20023145A3 (cs) | 2003-01-15 |
AU2001245891A1 (en) | 2001-10-03 |
MXPA02009311A (es) | 2003-03-12 |
US6949545B2 (en) | 2005-09-27 |
SK12842002A3 (sk) | 2003-02-04 |
BR0109328A (pt) | 2003-06-10 |
NZ520657A (en) | 2004-11-26 |
PL365444A1 (en) | 2005-01-10 |
JP2003528080A (ja) | 2003-09-24 |
WO2001070691A1 (en) | 2001-09-27 |
EP1265864A1 (en) | 2002-12-18 |
RU2245876C2 (ru) | 2005-02-10 |
NO20024520L (no) | 2002-09-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR033356A1 (es) | Compuesto que contiene una cadena lateral heterociclica, composicion farmaceutica que lo comprende y uso de dicho compuesto para la fabricacion de un medicamento | |
AR030197A1 (es) | Compuesto n-sustituido que contiene una cadena lateral heterociclica, composicion farmaceutica que lo comprende y uso de dicho compuesto para la fabricacion de un medicamento | |
CO4920242A1 (es) | Compuestos inhibidores de metalopreoteasas 1,4-heterocicli- cos, composiciones farmaceuticas que los contienen y metodos para su utilizacion | |
CO4900035A1 (es) | Compuestos inhibidores de metaloproteasas 1,3-diheterocicli- cos, composiciones farmaceuticas que los contienen y metodos para utilizacion | |
CO4900036A1 (es) | Compuestos inhibidores de metaloproteasas de amina ciclica substituida composiciones farmaceuticas que los contienen y metodos para su utilizacion | |
CO4920240A1 (es) | Compuestos inhibidores de metaloproteasa diheterociclicos, composiciones farmaceuticas que los contienen y metodos para su utilizacion | |
CO4900033A1 (es) | Compuestos inhibidores de metaloproteasas, composiciones farmaceuticas que los contienen . | |
AR040773A1 (es) | Pirazoles utiles como inhibidores de gsk-3 | |
CO4900045A1 (es) | Compuestos inhibidores de metaloproteasas espirociclicos, composiciones farmaceuticas que los contienen y metodos para su utilizacion | |
AR047008A1 (es) | Compuestos de 4-tetrazolil-4-fenilpiperidina como agonistas de los receptores opioides y agentes terapeuticos de utilidad para el tratamiento del dolor y composiciones farmaceuticas que los contienen como principio activo en combinacion con otros agentes terapéuticos. | |
KR940014328A (ko) | 인돌린 화합물 | |
PA8610801A1 (es) | Compuestos de aril o heteroaril amida | |
DK0447285T3 (da) | Nephtalenderivater, fremgangsmåde til fremstilling heraf og farmaceutiske midler indeholdende dem | |
NO843836L (no) | Terapeutisk aktive sulfamatderivater | |
PE58699A1 (es) | Derivados de acido arilsulfonil hidroxamico | |
AR065937A2 (es) | Compuesto derivado indazol, composicion farmaceutica que lo comprende y su uso en la fabricacion de medicamentos para modular la actividad de proteina quinasa | |
RU94044671A (ru) | Применение непептидных антагонистов рецептора тахикинина | |
EA200201201A1 (ru) | Соединения с сульфамидной группой и содержащие эти соединения фармацевтические композиции | |
CY1110904T1 (el) | Φαρμακευτικως ενεργα παραγωγα βενζοσουλφοναμιδιου ως αναστολεις πρωτεϊνικων κινασων jun | |
CO4970730A1 (es) | Tetrahidro prostaglandinas aromaticas c16-c20 sustituidas utilies como agonistas fp | |
AR035071A1 (es) | Compuestos para el tratamiento de la disfuncion endotelial; metodo para producir a dichos compuestos farmaceuticos; uso de dichos compuestos para la manufactura de un medicamento | |
CO5150219A1 (es) | Inhibidores de metaloproteasa que contiene alquenilo y alque nilo que son efectivos en el tratamiento de condiciones ca- racterizadas por actividad excesiva de estas enzimas | |
EA199900135A1 (ru) | Производные пиразолопиридина и их применение в качестве фармацевтического препарата | |
AR019674A1 (es) | Compuestos antitromboticos y composiciones farmaceuticas que los contienen | |
KR920000730A (ko) | 신규 벤즈이미다졸 유도체, 그의 제조방법, 그의 신규 중간체, 그의 약물 용도 및 그를 함유하는 제약 조성물 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |