JPH1160551A5 - - Google Patents
Info
- Publication number
- JPH1160551A5 JPH1160551A5 JP1998162706A JP16270698A JPH1160551A5 JP H1160551 A5 JPH1160551 A5 JP H1160551A5 JP 1998162706 A JP1998162706 A JP 1998162706A JP 16270698 A JP16270698 A JP 16270698A JP H1160551 A5 JPH1160551 A5 JP H1160551A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- phenyl
- integer
- substituted
- formula
- 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.)
- Granted
Links
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19719621A DE19719621A1 (de) | 1997-05-09 | 1997-05-09 | Sulfonylaminocarbonsäuren |
| DE19719621:7 | 1997-05-09 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPH1160551A JPH1160551A (ja) | 1999-03-02 |
| JPH1160551A5 true JPH1160551A5 (https=) | 2005-09-29 |
| JP4177483B2 JP4177483B2 (ja) | 2008-11-05 |
Family
ID=7829102
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16270698A Expired - Fee Related JP4177483B2 (ja) | 1997-05-09 | 1998-05-08 | スルホニルアミノカルボン酸 |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US6451824B1 (https=) |
| EP (1) | EP0877018B1 (https=) |
| JP (1) | JP4177483B2 (https=) |
| KR (1) | KR100572494B1 (https=) |
| CN (1) | CN1280267C (https=) |
| AR (1) | AR012674A1 (https=) |
| AT (1) | ATE238984T1 (https=) |
| AU (1) | AU732723B2 (https=) |
| BR (1) | BR9801606B1 (https=) |
| CA (1) | CA2237099C (https=) |
| CZ (1) | CZ295527B6 (https=) |
| DE (2) | DE19719621A1 (https=) |
| DK (1) | DK0877018T3 (https=) |
| ES (1) | ES2195220T3 (https=) |
| HU (1) | HU224959B1 (https=) |
| ID (1) | ID20807A (https=) |
| PL (1) | PL191876B1 (https=) |
| PT (1) | PT877018E (https=) |
| RU (1) | RU2193027C2 (https=) |
| TR (1) | TR199800815A2 (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2208609C2 (ru) * | 1998-02-04 | 2003-07-20 | Новартис Аг | Сульфониламинопроизводные, которые ингибируют разлагающие матрикс металлопротеиназы |
| US6410580B1 (en) | 1998-02-04 | 2002-06-25 | Novartis Ag | Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases |
| ATE227295T1 (de) * | 1998-07-16 | 2002-11-15 | Aventis Pharma Gmbh | Phosphin- und phosphonsäurederivate als arzneimittel |
| DE19851184A1 (de) * | 1998-11-06 | 2000-05-11 | Aventis Pharma Gmbh | N-Arylsulfonyl-aminosäure-omega-amide |
| US6420396B1 (en) * | 1998-12-16 | 2002-07-16 | Beiersdorf Ag | Biphenyl and biphenyl-analogous compounds as integrin antagonists |
| US6677360B2 (en) | 1998-12-16 | 2004-01-13 | Bayer Aktiengesellschaft | Biphenyl and biphenyl-analogous compounds as integrin antagonists |
| US6492394B1 (en) * | 1998-12-22 | 2002-12-10 | Syntex (U.S.A.) Llc | Sulfonamide hydroxamates |
| HK1044935A1 (zh) | 1999-03-03 | 2002-11-08 | The Procter & Gamble Company | 双异取代的金属蛋白酶抑制剂 |
| WO2000058278A1 (fr) * | 1999-03-26 | 2000-10-05 | Shionogi & Co., Ltd. | Derives d'acides amines $g(b) |
| GB9918684D0 (en) | 1999-08-09 | 1999-10-13 | Novartis Ag | Organic compounds |
| IL151250A0 (en) | 2000-03-21 | 2003-04-10 | Procter & Gamble | Difluorobutyric acid metalloprotease inhibitors |
| WO2001070690A1 (en) * | 2000-03-21 | 2001-09-27 | The Procter & Gamble Company | Heterocyclic side chain containing metalloprotease inhibitors |
| EP1265864A1 (en) * | 2000-03-21 | 2002-12-18 | The Procter & Gamble Company | Heterocyclic side chain containing, n-substituted metalloprotease inhibitors |
| EP1208092B1 (en) * | 2000-04-07 | 2006-06-21 | Samsung Electronics Co., Ltd. | Sulfonamide derivative as a matrix metalloproteinase inhibitor |
| GB0103303D0 (en) | 2001-02-09 | 2001-03-28 | Novartis Ag | Organic compounds |
| PA8557501A1 (es) | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | Benzamida, heteroarilamida y amidas inversas |
| WO2003042190A1 (en) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | N-alkyl-adamantyl derivatives as p2x7-receptor antagonists |
| PE20030701A1 (es) | 2001-12-20 | 2003-08-21 | Schering Corp | Compuestos para el tratamiento de trastornos inflamatorios |
| PA8591801A1 (es) | 2002-12-31 | 2004-07-26 | Pfizer Prod Inc | Inhibidores benzamidicos del receptor p2x7. |
| US7071223B1 (en) | 2002-12-31 | 2006-07-04 | Pfizer, Inc. | Benzamide inhibitors of the P2X7 receptor |
| MXPA05012086A (es) * | 2003-05-12 | 2006-02-22 | Pfizer Prod Inc | Inhibidores de benzamida del receptor p2x7. |
| EP1493740A1 (fr) * | 2003-07-03 | 2005-01-05 | Warner-Lambert Company LLC | Dérivés de 5-fluoro-thiophene, leur procédé de preparation, les compositions pharmaceutiques les contenant et leur utilisation comme inhibiteurs de métalloprotéinases |
| US7618981B2 (en) * | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
| GB0412553D0 (en) * | 2004-06-04 | 2004-07-07 | Univ Aberdeen | Therapeutic agents for the treatment of bone conditions |
| WO2006003500A1 (en) * | 2004-06-29 | 2006-01-12 | Pfizer Products Inc. | Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers |
| BRPI0512915A (pt) * | 2004-06-29 | 2008-04-15 | Warner Lambert Co | terapias de combinação utilizando inibidores benzamida do receptor p2x7 |
| JP2008504362A (ja) * | 2004-06-29 | 2008-02-14 | ファイザー・プロダクツ・インク | P2x7阻害活性をもつ5−[4−(2−ヒドロキシ−エチル)−3,5−ジオキソ−4,5−ジヒドロ−3h−[1,2,4]トリアジン−2−イル]−ベンズアミド誘導体を、トリアジンの4−位において置換されていない誘導体とオキシランをルイス酸の存在下で反応させることにより製造する方法 |
| US7576222B2 (en) | 2004-12-28 | 2009-08-18 | Wyeth | Alkynyl-containing tryptophan derivative inhibitors of TACE/matrix metalloproteinase |
| GB0705400D0 (en) | 2007-03-21 | 2007-05-02 | Univ Aberdeen | Therapeutic compounds andm their use |
| SA08290668B1 (ar) * | 2007-10-25 | 2012-02-12 | شيونوجي آند كو.، ليمتد | مشتقات أمين لها نشاط مضاد لمستقبل npy y5 واستخداماتها |
| GB0817208D0 (en) | 2008-09-19 | 2008-10-29 | Pimco 2664 Ltd | Therapeutic apsap compounds and their use |
| GB0817207D0 (en) | 2008-09-19 | 2008-10-29 | Pimco 2664 Ltd | therapeutic apsac compounds and their use |
| KR101682427B1 (ko) * | 2008-12-23 | 2016-12-05 | 아쿠일루스 파마슈티컬즈, 인코포레이티드 | 통증 및 기타 질병을 치료하기 위한 화합물 및 방법 |
| GB201311361D0 (en) | 2013-06-26 | 2013-08-14 | Pimco 2664 Ltd | Compounds and their therapeutic use |
| SI3262028T1 (sl) | 2014-12-17 | 2022-02-28 | Pimco 2664 Limited | N-(4-hidroksi-4-metil-cikloheksil)-4-fenil-benzensulfonamidne in N-(-4hidroksi-4-metil-cikloheksil)-4-(2-piridil)-benzensulfonamidne spojine in njihova terapevtska uporaba |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2764262B2 (ja) * | 1987-08-28 | 1998-06-11 | 持田製薬株式会社 | ヒダントイン誘導体及びそれを有効成分とする医薬組成物 |
| TW201303B (https=) * | 1990-07-05 | 1993-03-01 | Hoffmann La Roche | |
| GB9200210D0 (en) * | 1992-01-07 | 1992-02-26 | British Bio Technology | Compounds |
| US5506242A (en) * | 1993-01-06 | 1996-04-09 | Ciba-Geigy Corporation | Arylsufonamido-substituted hydroxamic acids |
| US5455258A (en) * | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| 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 |
| US5863949A (en) * | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| DK0821671T3 (da) * | 1995-04-20 | 2001-04-23 | Pfizer | Arylsulfonylhydroxamsyrederivater som MMP- og TNF-inhibitorer |
| KR980009238A (ko) * | 1995-07-28 | 1998-04-30 | 우에노 도시오 | 설포닐아미노산 유도체 |
| IL123901A (en) * | 1995-11-17 | 2003-06-24 | Warner Lambert Co | Sulfonamide inhibitors of matrix metalloproteinases and pharmaceutical compositions comprising them |
| CA2242416C (en) * | 1996-01-23 | 2006-03-21 | Shionogi & Co., Ltd. | Sulfonated amino acid derivatives and metalloproteinase inhibitors containing the same |
| CN100413859C (zh) * | 1996-01-23 | 2008-08-27 | 盐野义制药株式会社 | 磺化的氨基酸衍生物及含有它的金属蛋白酶抑制剂 |
| NZ332711A (en) * | 1996-05-17 | 2000-06-23 | Warner Lambert Co | Biphenylsulfonylamino carboxylic acid derivatives as matrix metalloproteinase inhibitors |
| US5756545A (en) * | 1997-04-21 | 1998-05-26 | Warner-Lambert Company | Biphenysulfonamide matrix metal alloproteinase inhibitors |
| DE59802394D1 (de) * | 1997-05-09 | 2002-01-24 | Hoechst Ag | Substituierte Diaminocarbonsäuren |
-
1997
- 1997-05-09 DE DE19719621A patent/DE19719621A1/de not_active Withdrawn
-
1998
- 1998-05-02 DE DE59808121T patent/DE59808121D1/de not_active Expired - Lifetime
- 1998-05-02 PT PT98108038T patent/PT877018E/pt unknown
- 1998-05-02 ES ES98108038T patent/ES2195220T3/es not_active Expired - Lifetime
- 1998-05-02 AT AT98108038T patent/ATE238984T1/de active
- 1998-05-02 EP EP98108038A patent/EP0877018B1/de not_active Expired - Lifetime
- 1998-05-02 DK DK98108038T patent/DK0877018T3/da active
- 1998-05-07 CZ CZ19981438A patent/CZ295527B6/cs not_active IP Right Cessation
- 1998-05-07 TR TR1998/00815A patent/TR199800815A2/xx unknown
- 1998-05-07 AR ARP980102139A patent/AR012674A1/es active IP Right Grant
- 1998-05-07 ID IDP980667A patent/ID20807A/id unknown
- 1998-05-07 CA CA2237099A patent/CA2237099C/en not_active Expired - Fee Related
- 1998-05-08 US US09/074,693 patent/US6451824B1/en not_active Expired - Lifetime
- 1998-05-08 CN CNB981152651A patent/CN1280267C/zh not_active Expired - Fee Related
- 1998-05-08 HU HU9801044A patent/HU224959B1/hu not_active IP Right Cessation
- 1998-05-08 AU AU64823/98A patent/AU732723B2/en not_active Ceased
- 1998-05-08 BR BRPI9801606-7A patent/BR9801606B1/pt not_active IP Right Cessation
- 1998-05-08 KR KR1019980016385A patent/KR100572494B1/ko not_active Expired - Fee Related
- 1998-05-08 PL PL326216A patent/PL191876B1/pl not_active IP Right Cessation
- 1998-05-08 RU RU98108979/04A patent/RU2193027C2/ru not_active IP Right Cessation
- 1998-05-08 JP JP16270698A patent/JP4177483B2/ja not_active Expired - Fee Related
-
2002
- 2002-06-13 US US10/170,870 patent/US7160903B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH1160551A5 (https=) | ||
| JPH11228529A5 (https=) | ||
| RU2010133903A (ru) | Способ и промежуточные соединения для получения производных 5-бифенил-4-ил-2-метилпентановой кислоты | |
| CA2457054A1 (en) | Activator of peroxisome proliferator-activated receptor .delta. | |
| KR910019989A (ko) | 비스-아릴 아미드 및 우레아 화합물들, 이들로 구성된 조성물 이들을 이용한 paf 억제 방법 및 이들의 생산 방법 | |
| JPH10316662A5 (https=) | ||
| JP2004521124A5 (https=) | ||
| RU2008119651A (ru) | Производные дикарбоновых кислот и их применение | |
| EA201070782A1 (ru) | Производные оксадиазола, активные в отношении сфингозин-1-фосфата(sip) | |
| CO5280046A1 (es) | Agonistas alfa 7 y sus composiciones farmaceuticas | |
| JP2004525117A5 (https=) | ||
| JP2009523146A5 (https=) | ||
| TR201901246T4 (tr) | Kimyasal bileşikler. | |
| HUP0203902A2 (hu) | Szubsztituált oxazolidinonok, eljárás az előállításukra, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk | |
| RU2010126105A (ru) | Производные пиридина, замещенные гетероциклическим кольцом и фосфоноксиметильной группой, и содержащие их противогрибковые средства | |
| RU2012109545A (ru) | Использование лигандов ppar дельта для лечения или предотвращения воспалений или заболеваний, связанных с метаболизмом/выработкой энергии | |
| JP2005538944A5 (https=) | ||
| NO20054791D0 (no) | Forbindelser for behandling av stoffskiftesykdommer | |
| JP2002514649A5 (https=) | ||
| SE8205870L (sv) | Nya produkter 3-amino-2-oxo-azetidin-1-sulfonsyraderivat, sett for framstellning derav, anvendning derav som lekemedel, kompositioner innehallande dem och erhallna nya mellanprodukter | |
| JP2006517201A5 (https=) | ||
| HUP0001603A2 (hu) | Cikloalkil-alkánkarbonsavamidok, előállításuk és alkalmazásuk | |
| KR910004569A (ko) | 고리형 치환체를 갖는 (퀴놀린-2-일-메톡시)페닐아세트산 유도체 | |
| RU2010116779A (ru) | Производное амида индазолакриловой кислоты | |
| ATE286503T1 (de) | (hetero)aryl-sulfonamid derivate, deren herstellung und deren verwenddung als faktor xa inhibitoren |