First pharmacophoric hypothesis for T-type calcium channel blockers

Authors
Doddareddy, MRJung, HKLee, JYLee, YSCho, YSKoh, HYPae, AN
Issue Date
2004-04-01
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.12, no.7, pp.1605 - 1611
Abstract
A three-dimensional pharmacophore model was developed for T-type calcium channel blockers in order to map common structural features of highly active compounds by using CATALYST program. In the absence of three dimensional structure based information like binding mode and unavailability of more number of specific T-type calcium channel blockers, this hypothesis which consists of three hydrophobic regions, one hydrogen bond acceptor and one positive ionizable regions will act as a valuable tool in designing new ligands. Further more after the withdrawal of mibefradil, the first marketed T-type calcium channel blocker, due to the drug-drug interactions, there is an urgent need for more work in this interest. (C) 2004 Elsevier Ltd. All rights reserved.
Keywords
STABLE ANGINA; CA2+ CHANNELS; ANTAGONIST; MIBEFRADIL; RO-40-5967; STABLE ANGINA; CA2+ CHANNELS; ANTAGONIST; MIBEFRADIL; RO-40-5967; pharmacophore; hypothesis; T-type calcium channel
ISSN
0968-0896
URI
https://pubs.kist.re.kr/handle/201004/137678
DOI
10.1016/j.bmc.2004.01.034
Appears in Collections:
KIST Article > 2004
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