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1.Cell adhesion-inhibiting anti-inflammatory and immune-suppressive compounds 审中-公开
Title translation: 细胞粘附抑制抗炎和免疫抑制化合物公开(公告)号:EP1481968A2
公开(公告)日:2004-12-01
申请号:EP04020808.4
申请日:2000-04-03
Applicant: Abbott Laboratories
Inventor: Link, James , Liu, Gang , Pei, Zhonghua , von Geldern, Thomas W. , Winn, Martin , Xin, Zhili , Wang, Sheldon , Boyd, Steven A. , Zhu, Gui-Dong , Freeman, Jennifer C. , Gunawardana, Indrani W. , Staeger, Michael A. , Jae, Hwan-Soo , Lynch, John K.
IPC: C07D207/16 , C07D211/60 , C07D211/62 , C07D295/18 , C07D401/04 , A61K31/165 , A61K31/33 , A61P29/00
CPC classification number: C07D207/27 , C07C323/62 , C07C2601/02 , C07D205/04 , C07D207/09 , C07D207/14 , C07D207/16 , C07D209/08 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D213/40 , C07D213/74 , C07D213/81 , C07D217/02 , C07D217/06 , C07D231/12 , C07D233/56 , C07D241/04 , C07D249/08 , C07D295/185 , C07D295/26 , C07D307/68 , C07D317/66 , C07D401/04 , C07D401/12
Abstract: The present invention relates to cinnamide compounds of formula (I), in which at least one of R 1 to R 5 is a "cis-cinnamide" (a) or a "trans-cinnamide" (b) and the other variables are as defined in the claims, that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:EP0342541A2
公开(公告)日:1989-11-23
申请号:EP89108590.4
申请日:1989-05-12
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Plattner, Jacob J. , Norbeck, Daniel W. , Baker, William R. , Fung, Anthony K. L. , Boyd, Steven A. , Erickson, John W. , Crowley, Steven R.
IPC: C07K5/02 , C07K5/04 , A61K37/64 , C07C103/49 , C07D307/22 , C07C125/065 , C07D295/20 , C07D263/38 , C07D307/68
CPC classification number: C07D239/10 , A61K38/00 , C07C271/22 , C07C317/44 , C07C323/60 , C07C2601/06 , C07C2601/14 , C07D233/32 , C07D263/06 , C07D263/20 , C07D263/22 , C07D263/24 , C07D263/26 , C07D265/06 , C07D273/00 , C07D295/205 , C07D295/215 , C07D307/58 , C07D307/68 , C07D317/36 , C07D333/38 , C07D413/06 , C07K5/06026 , C07K5/06043 , C07K5/06078 , C07K5/101 , C07K5/1016 , C07K7/02
Abstract: A retroviral protease inhibiting compound of the formula:
or a pharmaceutically acceptable salt, prodrug or ester thereof.Abstract translation: 具有下式的逆转录病毒蛋白酶抑制化合物:
或其药学上可接受的盐,前药或酯。 -
3.Benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists 失效
Title translation: 苯并-1,3-二恶唑基 - 和苯并呋喃基取代的吡咯烷衍生物内皮素拮抗剂公开(公告)号:EP1609790A2
公开(公告)日:2005-12-28
申请号:EP05106190.1
申请日:1997-02-12
Applicant: ABBOTT LABORATORIES
Inventor: Winn, Martin , Henry, Kenneth J. Jr. , Liu, Gang , Wittenberger, Steven J. , King, Steven A. , Boyd, Steven A. , Hutchins, Charles W. , Jae, Hwan-Soo , Tasker, Andrew S. , Von Geldern, Thomas W. , Kester, Jeffrey A. , Sorensen, Bryan K. , Szczepankiewicz, Bruce G.
IPC: C07D405/04 , C07D405/12 , A61K31/40 , A61K31/41 , A61K31/435
CPC classification number: C07D401/04 , C07D207/16 , C07D405/04 , C07D405/12 , C07D405/14 , Y02P20/55
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
Abstract translation: 公开了式(I)化合物或其药学上可接受的盐,以及其制备方法和中间体,以及拮抗内皮素的方法。
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公开(公告)号:EP0342541A3
公开(公告)日:1991-11-06
申请号:EP89108590.4
申请日:1989-05-12
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Plattner, Jacob J. , Norbeck, Daniel W. , Baker, William R. , Fung, Anthony K. L. , Boyd, Steven A. , Erickson, John W. , Crowley, Steven R.
IPC: C07K5/02 , C07K5/04 , A61K37/64 , C07C103/49 , C07D307/22 , C07C125/065 , C07D295/20 , C07D263/38 , C07D307/68
CPC classification number: C07D239/10 , A61K38/00 , C07C271/22 , C07C317/44 , C07C323/60 , C07C2601/06 , C07C2601/14 , C07D233/32 , C07D263/06 , C07D263/20 , C07D263/22 , C07D263/24 , C07D263/26 , C07D265/06 , C07D273/00 , C07D295/205 , C07D295/215 , C07D307/58 , C07D307/68 , C07D317/36 , C07D333/38 , C07D413/06 , C07K5/06026 , C07K5/06043 , C07K5/06078 , C07K5/101 , C07K5/1016 , C07K7/02
Abstract: A retroviral protease inhibiting compound of the formula:
or a pharmaceutically acceptable salt, prodrug or ester thereof.-
5.Benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists 失效
Title translation: 苯并-1,3-二氧杂环戊烯和苯并呋喃基取代的吡咯烷衍生物作为内皮素拮抗剂公开(公告)号:EP1609790A3
公开(公告)日:2006-01-04
申请号:EP05106190.1
申请日:1997-02-12
Applicant: ABBOTT LABORATORIES
Inventor: Winn, Martin , Henry, Kenneth J. Jr. , Liu, Gang , Wittenberger, Steven J. , King, Steven A. , Boyd, Steven A. , Hutchins, Charles W. , Jae, Hwan-Soo , Tasker, Andrew S. , Von Geldern, Thomas W. , Kester, Jeffrey A. , Sorensen, Bryan K. , Szczepankiewicz, Bruce G.
IPC: C07D405/04 , C07D405/12 , A61K31/40 , A61K31/41 , A61K31/435
CPC classification number: C07D401/04 , C07D207/16 , C07D405/04 , C07D405/12 , C07D405/14 , Y02P20/55
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
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6.Cell adhesion-inhibiting anti-inflammatory and immune-suppressive compounds 审中-公开
Title translation: Zelladhäsionsuppressierendeentzündungshemmendeund immunsuppressive Verbindungen公开(公告)号:EP1481968A3
公开(公告)日:2005-01-19
申请号:EP04020808.4
申请日:2000-04-03
Applicant: Abbott Laboratories
Inventor: Link, James , Liu, Gang , Pei, Zhonghua , von Geldern, Thomas W. , Winn, Martin , Xin, Zhili , Wang, Sheldon , Boyd, Steven A. , Zhu, Gui-Dong , Freeman, Jennifer C. , Gunawardana, Indrani W. , Staeger, Michael A. , Jae, Hwan-Soo , Lynch, John K.
IPC: C07C323/62 , C07D233/61 , C07D207/26 , C07D295/18 , C07D213/74 , C07D211/22 , C07D207/14 , C07D211/46 , C07D211/62 , C07D211/60 , C07D401/04 , C07D217/02 , C07D307/68 , C07D295/26 , C07D317/66 , C07D209/08 , C07D295/205 , C07D401/12 , A61K31/165 , A61K31/33 , A61P29/00
CPC classification number: C07D207/27 , C07C323/62 , C07C2601/02 , C07D205/04 , C07D207/09 , C07D207/14 , C07D207/16 , C07D209/08 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D213/40 , C07D213/74 , C07D213/81 , C07D217/02 , C07D217/06 , C07D231/12 , C07D233/56 , C07D241/04 , C07D249/08 , C07D295/185 , C07D295/26 , C07D307/68 , C07D317/66 , C07D401/04 , C07D401/12
Abstract: The present invention relates to cinnamide compounds of formula (I), in which at least one of R 1 to R 5 is a "cis-cinnamide" (a) or a "trans-cinnamide" (b) and the other variables are as defined in the claims, that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal.
Abstract translation: 本发明涉及式(I)的肉桂酰胺化合物,其中R 1至R 5中的至少一个为“顺式 - 酰胺”(a)或“反式肉桂酰胺”(b),其它变量如 可用于治疗炎症和免疫疾病的权利要求,含有这些化合物的药物组合物和抑制哺乳动物炎症或抑制免疫应答的方法。
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公开(公告)号:EP0364804A1
公开(公告)日:1990-04-25
申请号:EP89118270.1
申请日:1989-10-03
Applicant: ABBOTT LABORATORIES
Inventor: Fung, Anthony K. L. , Plattner, Jacob J. , Baker, William R. , Armiger, Yoek-Lin , Rosenberg, Saul H. , De, Biswanath , Mantei, Robert A. , Boyd, Steven A. , Kempf, Dale J. , Sham, Hing Leung , Kleinert, Hollis D.
IPC: C07D211/30 , C07D211/44 , C07D295/185 , C07D307/12 , C07D401/12 , C07D405/12 , C07D407/12 , C07D409/12 , C07D411/12 , C07D413/12 , A61K31/445
CPC classification number: C07D233/64 , C07C237/08 , C07C317/28 , C07C323/58 , C07C2601/14 , C07D203/18 , C07D211/44 , C07D211/62 , C07D211/96 , C07D295/185 , C07D401/12 , C07D407/12 , C07D413/12
Abstract: A renin inhibiting compound of the formula:
wherein A is a substituent; R 1 is hydrogen, loweralkyl, substituted loweralkyl or loweralkenyl; X is CH 2 , CHOH, C(O), O, S, S(O), S0 2 , NH, N(O) or -P(O)O-; R 3 is loweralkyl, loweralkenyl or substituted loweralkyl; and T is mimic of the Leu-Val cleavage site of angiotensinogen; or a pharmaceutically acceptable salt, ester or prodrug thereof.Abstract translation: 一种下列化学式的肾素抑制化合物:其中A为取代基的
R1是氢,低级烷基,取代的低级烷基或低级烯基; X是CH 2,CHOH,C(O),O,S,S(O),SO 2,NH,N(O)或-P(O) R3是低级烷基,低级烯基或取代的低级烷基; 并且T是模拟血管紧张素原的Leu-Val切割位点; 或其药学上可接受的盐,酯或前药。
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