Novel pyrrolopyridine compounds of formula (I),
1
and their derivatives open potassium channels and are useful for treating a variety of diseases modulated by potassium channels.
式(I)的新型吡咯吡啶化合物及其衍生物能够打开钾通道,对于治疗受钾通道调节的多种疾病有用。
DAISLEY, R. W.;HANBALI, J. R., J. HETEROCYCL. CHEM., 1983, 20, N 4, 999-1001
作者:DAISLEY, R. W.、HANBALI, J. R.
DOI:——
日期:——
CINNAMOYL DISTAMYCIN ANALOGOUS DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS ANTITUMOR AGENTS
申请人:Pharmacia Italia S.p.A.
公开号:EP1084120B1
公开(公告)日:2004-03-10
[EN] PYRROLOPYRIDINE POTASSIUM CHANNEL OPENERS<br/>[FR] REGULATEURS DU CANAL POTASSIQUE A BASE DE PYRROLOPYRIDINE
申请人:ABBOTT LAB
公开号:WO2004060893A1
公开(公告)日:2004-07-22
Novel pyrrolopyridine compounds of formula (I), and their derivatives open potassium channels and are useful for treating a variety of diseases modulated by potassium channels.
The discovery of a new class of large-conductance Ca2+-activated K+ channel opener targeted for overactive bladder: synthesis and structure–activity relationships of 2-amino-4-azaindoles
作者:Sean C. Turner、William A. Carroll、Tammie K. White、Murali Gopalakrishnan、Michael J. Coghlan、Char-Chang Shieh、Xu-Feng Zhang、Ashutosh S. Parihar、Steven A. Buckner、Ivan Milicic、James P. Sullivan
DOI:10.1016/s0960-894x(03)00324-x
日期:2003.6
2-Amino-4-azaindoles have been identified as a structurally novel class of BKCa channel openers. Their synthesis from 2-chloro-3-nitropyridine is described together with their in vitro properties assessed by Rb-86(+) efflux and whole-cell patch-clamp assays using HEK293 cells stably transfected with the BKCa alpha subunit. In vitro functional characterization of BKCa channel opening activity was also assessed by measurement of relaxation of smooth muscle tissue strips obtained from Landrace pig bladders. The preliminary SAR data indicate the importance of steric bulk around the 2-amino substituent. (C) 2003 Elsevier Science Ltd. All rights reserved.