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公开(公告)号:DE69619140D1
公开(公告)日:2002-03-21
申请号:DE69619140
申请日:1996-12-06
Applicant: ABBOTT LAB
Inventor: SHAM LEUNG , NORBECK W , CHEN XIAOQI , BETEBENNER A , KEMPF J , HERRIN R , KUMAR N , CONDON L , COOPER J , DICKMAN A , HANNICK M , KOLACZKOWSKI LAWRENCE , OLIVER A , PLATA J , STENGEL J , STONER J , TIEN J , LIU JIH-HUA , PATEL M
IPC: C07D253/00 , A61K31/00 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/415 , A61K31/4164 , A61K31/4166 , A61K31/4184 , A61K31/42 , A61K31/421 , A61K31/425 , A61K31/427 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/4439 , A61K31/47 , A61K31/495 , A61K31/496 , A61K31/4965 , A61K31/505 , A61K31/513 , A61K31/53 , A61K31/55 , A61K38/05 , A61K45/00 , A61P31/18 , A61P43/00 , C07C231/12 , C07C235/20 , C07C273/18 , C07C275/16 , C07D20060101 , C07D207/22 , C07D207/26 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/40 , C07D207/404 , C07D207/408 , C07D207/416 , C07D211/72 , C07D211/84 , C07D223/06 , C07D233/28 , C07D233/30 , C07D233/32 , C07D233/36 , C07D233/40 , C07D233/42 , C07D233/66 , C07D239/06 , C07D239/10 , C07D239/20 , C07D239/22 , C07D241/06 , C07D241/08 , C07D241/18 , C07D243/04 , C07D253/06 , C07D263/16 , C07D263/20 , C07D263/22 , C07D263/34 , C07D265/04 , C07D267/04 , C07D277/12 , C07D277/32 , C07D277/34 , C07D279/06 , C07D281/02 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07D413/12 , C07D417/12
Abstract: A compound comprising a substituent of the formula (II) is disclosed as an HIV protease inhibitor. Intermediates for making such compounds and processes for making such intermediates are also disclosed.
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公开(公告)号:AR039596A1
公开(公告)日:2005-03-02
申请号:ARP030100770
申请日:2003-03-06
Applicant: ABBOTT LAB
Inventor: COWART MARLON , BHATIA P , DAANEN JEROME , PATEL M , KOLASA TEODOZYJ , BRIONI JORGE D , ROHDE J , ENGESTROM K , STEWART A
IPC: C07D403/06 , A61K31/505 , A61K31/506 , A61P15/10 , A61P25/16 , A61P25/18 , A61P25/22 , A61P25/24 , A61P25/30 , A61P29/00 , C07D235/18 , C07D401/12 , C07D401/14 , C07D417/12 , C07D417/14
Abstract: Benzimidazoles para el tratamiento de la disfunción sexual y composiciones que contienen compuestos de fórmula (1) para el tratamiento de la disfunción sexual. Reivindicación 1: Uso de un compuesto de fórmula (1), una sal aceptable para uso farmacéutico, éster, amida o profármaco del mismo, donde; A se selecciona de entre el grupo de fórmulas (2); X se selecciona entre el grupo formado por NH, O y S; L se seleccionan entre el grupo formado por CH2, CH2CH2, CH2CH2CH2 y CH2CH2CH2CH2; R1, R2, R3, R4 y R5 se selecciona cada uno independientemente entre el grupo formado por hidrógeno, alcoxi, alquenilo, alquilo, alquilsulfinilo, alquilsulfonilo, alquiltio, alquinilo, alcoxicarbonilo, alquilcarbonilo, alquilcarboniloxi, carboxi, ciano, formilo, halógeno, haloalcoxi, haloalquilo, hidroxi, hidroxialquilo, mercapto, nitro, -NZ1Z2, (NZ1Z2)carbonilo y (NZ1Z2)sulfonilo donde Z1 y Z2 se seleccionan cada uno independientemente entre el grupo formado por hidrógeno, alquilo, alquilcarbonilo, alquilsulfonilo y formilo; RA, RB, RC y RD se seleccionan cada uno independientemente entre el grupo formado por hidrógeno, alcoxi, alquenilo, alquilo, alquilsulfinilo, alquilsulfonilo, alquiltio, alquinilo, alcoxicarbonilo, alquilcarbonilo, alquilcarboniloxi, carboxi, ciano, formilo, halógeno, haloalcoxi, haloalquilo, hidroxi, hidroxialquilo, mercapto, nitro, -NZ1Z2 y (NZ1Z2)carbonilo; RE se selecciona entre el grupo formado por hidrógeno, alcoxicarbonilo, alquilo, alquilcarbonilo, arilcarbonilo, cicloalquilcarbonilo, heterociclocarbonilo y (NZ1Z2)carbonilo; RF se selecciona entre el grupo formado por hidrógeno y alquilo; Z se selecciona entre el grupo formado por N, C y CH; y --- es un enlace cuando Z es C y --- está ausente cuando Z es N o CH, caracterizado porque es para la fabricación de un medicamento para el tratamiento de la disfunción sexual en un mamífero.
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公开(公告)号:DE69619140T2
公开(公告)日:2002-10-31
申请号:DE69619140
申请日:1996-12-06
Applicant: ABBOTT LAB
Inventor: SHAM LEUNG , NORBECK W , CHEN XIAOQI , BETEBENNER A , KEMPF J , HERRIN R , KUMAR N , CONDON L , COOPER J , DICKMAN A , HANNICK M , KOLACZKOWSKI LAWRENCE , OLIVER A , PLATA J , STENGEL J , STONER J , TIEN J , LIU JIH-HUA , PATEL M
IPC: C07D253/00 , A61K31/00 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/415 , A61K31/4164 , A61K31/4166 , A61K31/4184 , A61K31/42 , A61K31/421 , A61K31/425 , A61K31/427 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/4439 , A61K31/47 , A61K31/495 , A61K31/496 , A61K31/4965 , A61K31/505 , A61K31/513 , A61K31/53 , A61K31/55 , A61K38/05 , A61K45/00 , A61P31/18 , A61P43/00 , C07C231/12 , C07C235/20 , C07C273/18 , C07C275/16 , C07D20060101 , C07D207/22 , C07D207/26 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/40 , C07D207/404 , C07D207/408 , C07D207/416 , C07D211/72 , C07D211/84 , C07D223/06 , C07D233/28 , C07D233/30 , C07D233/32 , C07D233/36 , C07D233/40 , C07D233/42 , C07D233/66 , C07D239/06 , C07D239/10 , C07D239/20 , C07D239/22 , C07D241/06 , C07D241/08 , C07D241/18 , C07D243/04 , C07D253/06 , C07D263/16 , C07D263/20 , C07D263/22 , C07D263/34 , C07D265/04 , C07D267/04 , C07D277/12 , C07D277/32 , C07D277/34 , C07D279/06 , C07D281/02 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07D413/12 , C07D417/12
Abstract: A compound comprising a substituent of the formula (II) is disclosed as an HIV protease inhibitor. Intermediates for making such compounds and processes for making such intermediates are also disclosed.
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