Parallel solution- and solid-Phase synthesis of spirohydantoin derivatives as neurokinin-1 receptor ligands
摘要:
The combination of the 3,5-bis(trifluoromethyl)phenyl group with a spirohydantoin motive as a central scaffold was the basis for the design of a combinatorial library targeted towards the neurokinin-1 receptor. A solution-and solid-phase procedure is described and binding affinities of representative compounds presented. (C) 2002 Elsevier Science Ltd. All rights reserved.
Parallel solution- and solid-Phase synthesis of spirohydantoin derivatives as neurokinin-1 receptor ligands
摘要:
The combination of the 3,5-bis(trifluoromethyl)phenyl group with a spirohydantoin motive as a central scaffold was the basis for the design of a combinatorial library targeted towards the neurokinin-1 receptor. A solution-and solid-phase procedure is described and binding affinities of representative compounds presented. (C) 2002 Elsevier Science Ltd. All rights reserved.
Piperidine derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man.
哌啶衍生物及其药学上可接受的衍生物,适用于治疗哺乳动物,尤其是人体细菌感染的方法。
PIPERIDINE DERIVATIVES AS ANTIBACTERIAL AGENTS
申请人:SMITHKLINE BEECHAM PLC
公开号:EP1419155A2
公开(公告)日:2004-05-19
[EN] MEDICAMENTS<br/>[FR] MEDICAMENTS
申请人:SMITHKLINE BEECHAM PLC
公开号:WO2003010138A2
公开(公告)日:2003-02-06
Piperidine derivatives (I) and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man. Formula (I):
Parallel solution- and solid-Phase synthesis of spirohydantoin derivatives as neurokinin-1 receptor ligands
作者:Konrad H. Bleicher、Yves Wüthrich、Maxime De Boni、Sabine Kolczewski、Torsten Hoffmann、Andrew J. Sleight
DOI:10.1016/s0960-894x(02)00488-2
日期:2002.9
The combination of the 3,5-bis(trifluoromethyl)phenyl group with a spirohydantoin motive as a central scaffold was the basis for the design of a combinatorial library targeted towards the neurokinin-1 receptor. A solution-and solid-phase procedure is described and binding affinities of representative compounds presented. (C) 2002 Elsevier Science Ltd. All rights reserved.