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公开(公告)号:NZ526313A
公开(公告)日:2004-11-26
申请号:NZ52631301
申请日:2001-11-30
Applicant: ABBOTT LAB
Inventor: CLAIBORNE AKIYO K , GWALTNEY STEPHEN L , HASVOLD LISA A , LI QUN , LI TOMGMEI , LIN NAN-HORNG , MANTEI ROBERT A , ROCKWAY TODD W , SHAM HING L , SULLIVAN GERARD M , TONG YUNSONG , WANG GARY T , WANG LE , WANG XILU , WANG WEIBO
IPC: A61K31/4164 , A61K31/4178 , A61K31/426 , A61K31/4439 , A61K31/4709 , A61P35/00 , A61P43/00 , C07D233/54 , C07D233/64 , C07D277/20 , C07D277/30 , C07D401/12 , C07D405/12 , C07D409/12
Abstract: A compound of formula (I); a pharmaceutical composition comprising the compound; the use of the compound in the preparation of a medicament for inhibiting farnesyltransferase in a patient in need of such treatment; and the use of the compound in the preparation of a medicament for treating cancer in a patient.
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公开(公告)号:BG107908A
公开(公告)日:2004-01-30
申请号:BG10790803
申请日:2003-06-13
Applicant: ABBOTT LAB
Inventor: CLAIBORNE AKYO K , GWALTNEY II STEPHEN L , HASVOLD LISA A , LI QUN , LI TOMGMEI , LIN NAN-HORNG , MANTEI ROBERT A , ROCKWAY TODD W , SHAM HING L , SULLIVAN GERARD M , TONG YUNSONG , WANG GARY T , WANG LE , WANG XILU , WANG WEIBO
IPC: A61K31/4164 , A61K31/4178 , A61K31/426 , A61K31/4439 , A61K31/4709 , A61P35/00 , A61P43/00 , C07D233/54 , C07D233/64 , C07D277/20 , C07D277/30 , C07D401/12 , C07D405/12 , C07D409/12
Abstract: Substituted imidazoles and thiazoles having formula are used for inhibiting farnesyltransferase. Also disclosed are farnesylransferase-inhibiting compositions and methods of inhibiting farnesyltransferase in a patient. 10 claims
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公开(公告)号:NO20032471L
公开(公告)日:2003-07-25
申请号:NO20032471
申请日:2003-05-30
Applicant: ABBOTT LAB
Inventor: CLAIBORNE AKIYO K , GWALTNEY II STEPHEN L , HASVOLD LISA A , LI QUN , LI TOMGMEI , LIN NAN-HORNG , MANTEI ROBERT A , ROCKWAY TODD W , SHAM HING L , SULLIVAN GERARD M , TONG YUNSONG , WANG GARY T , WANG LE , WANG XILU , WANG WEIBO
IPC: A61K31/4164 , A61K31/4178 , A61K31/426 , A61K31/4439 , A61K31/4709 , A61P35/00 , A61P43/00 , C07D233/54 , C07D233/64 , C07D277/20 , C07D277/30 , C07D401/12 , C07D405/12 , C07D409/12
Abstract: Substituted imidazoles and thiazoles having the formula are useful for inhibiting farnesyltransferase. Also disclosed are farnesyltransferase-inhibiting compositions and methods of inhibiting farnesyltransferase in a patient.
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公开(公告)号:NO20032471D0
公开(公告)日:2003-05-30
申请号:NO20032471
申请日:2003-05-30
Applicant: ABBOTT LAB
Inventor: CLAIBORNE AKIYO K , GWALTNEY II STEPHEN L , HASVOLD LISA A , LI QUN , LI TOMGMEI , LIN NAN-HORNG , MANTEI ROBERT A , ROCKWAY TODD W , SHAM HING L , SULLIVAN GERARD M , TONG YUNSONG , WANG GARY T , WANG LE , WANG XILU , WANG WEIBO
IPC: A61K31/4164 , A61K31/4178 , A61K31/426 , A61K31/4439 , A61K31/4709 , A61P35/00 , A61P43/00 , C07D233/54 , C07D233/64 , C07D277/20 , C07D277/30 , C07D401/12 , C07D405/12 , C07D409/12 , C07D
Abstract: Substituted imidazoles and thiazoles having the formula are useful for inhibiting farnesyltransferase. Also disclosed are farnesyltransferase-inhibiting compositions and methods of inhibiting farnesyltransferase in a patient.
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公开(公告)号:UY27046A1
公开(公告)日:2002-07-31
申请号:UY27046
申请日:2001-11-29
Applicant: ABBOTT LAB
Inventor: WANG GARY T , HASVOLD LISA A , SHAM HING L , SULLIVAN GERARD M , CLAIBORNE AKIYO , LI QUN , MANTEI ROBERT A , WANG LE , GWALTNEY STEPHEN , LI TONGMEI , ROCKWAY TODD W , TONG YUNSONG , WANG XILO , LIN NAN-HORNG , WANG WEIBO
IPC: A61K31/4164 , A61K31/4178 , A61K31/426 , A61K31/4439 , A61K31/4709 , A61P35/00 , A61P43/00 , C07D233/54 , C07D233/64 , C07D277/20 , C07D277/30 , C07D401/12 , C07D405/12 , C07D409/12 , A61K31/00
Abstract: Imidazol y tiazoles sustituidos que tienen la fórmula (I) son útiles para inhibir la farnesiltransferasa. También se revelan composiciones inhibidoras de la farnesiltransferasa y métodos para inhibir la farnesiltransferasa en un paciente.
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公开(公告)号:CA1337909C
公开(公告)日:1996-01-09
申请号:CA615201
申请日:1989-09-29
Applicant: ABBOTT LAB
Inventor: FUNG ANTHONY K L , PLATTNER JACOB J , BAKER WILLIAM R , BOYD STEVEN A , ARMIGER YOEK-LIN , KEMPF DALE J , ROSENBERG SAUL H , SHAM HING LEUNG , DE BISWANATH , KLEINERT HOLLIS D , MANTEI ROBERT A
IPC: A61K31/16 , A61K31/19 , A61K31/265 , A61K31/415 , A61K31/4166 , A61K31/445 , A61K31/4465 , A61K31/66 , A61P9/00 , A61P9/12 , A61P43/00 , C07C237/08 , C07C237/22 , C07C317/28 , C07C323/57 , C07C323/58 , C07D203/18 , C07D211/44 , C07D211/46 , C07D211/62 , C07D211/96 , C07D233/36 , C07D233/54 , C07D233/56 , C07D263/22 , C07D295/185 , C07D401/12 , C07D407/12 , C07D413/12 , C07D521/00
Abstract: A renin inhibiting compound of the formula: wherein A is a substituent; R1 is hydrogen, loweralkyl, substituted loweralkyl or loweralkenyl; X is CH2, CHOH, C(O), O, S, S(O), SO2, NH, N(O) or -P(O)O-; R3 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.
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公开(公告)号:NZ230894A
公开(公告)日:1991-07-26
申请号:NZ23089489
申请日:1989-10-04
Applicant: ABBOTT LAB
Inventor: FUNG ANTHONY K L , PLATTNER JACOB J , BAKER WILLIAM R , BOYD STEPHEN A , ARMIGER YOEK-LIN , KEMPF DALE J , ROSENBERG SAUL H , HING LEUNG SHAM , DE BISWANATH , KLEINERT HOLLIS D , MANTEI ROBERT A
IPC: A61K31/16 , A61K31/19 , A61K31/265 , A61K31/415 , A61K31/4166 , A61K31/445 , A61K31/4465 , A61K31/66 , A61P9/00 , A61P9/12 , A61P43/00 , C07C237/08 , C07C237/22 , C07C317/28 , C07C323/57 , C07C323/58 , C07D203/18 , C07D211/44 , C07D211/46 , C07D211/62 , C07D211/96 , C07D233/36 , C07D233/54 , C07D233/56 , C07D263/22 , C07D295/185 , C07D401/12 , C07D407/12 , C07D413/12 , C07D521/00 , C07D405/12 , C07D265/30 , C07D205/04 , C07D207/10 , C07D211/48 , C07D307/16 , C07D317/04 , C07D317/14 , C07K5/06 , C07C215/08 , C07C215/12 , C07C215/14 , C07C229/10 , C07C237/06 , C07C237/10 , C07C237/12 , C07C237/14 , C07C307/02 , C07C311/05 , C07C317/24 , C07C317/26 , C07F7/02 , C07F9/22 , A61K31/535
Abstract: A renin inhibiting compound of the formula: wherein A is a substituent; R1 is hydrogen, loweralkyl, substituted loweralkyl or loweralkenyl; X is CH2, CHOH, C(O), O, S, S(O), SO2, NH, N(O) or -P(O)O-; R3 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.
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