Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers

Authors
Ku, Il WheaCho, SangwonDoddareddy, Munikumar ReddyJang, Min SeokKeum, GyochangLee, Jung-HaChung, Bong YoungKim, YouseungRhim, HyewhonKang, Soon Bang
Issue Date
2006-10-01
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.16, no.19, pp.5244 - 5248
Abstract
Morpholin-2-one-5-carboxamide derivatives were prepared by using the one-pot Ugi multicomponent reaction and evaluated for blocking effects on T- and N-type Ca2+ channels. Among them, compound 5i produced the highest potency (IC50 = 0.45 +/- 0.02 mu M), while compounds 5d, 5f, 5k, 5n, 5o, and 6m produced relatively high potency as well as selectivity on T-type Ca2+ channels. These novel scaffolds showed potent and selective T-type Ca2+ channel blocking activities. (c) 2006 Published by Elsevier Ltd.
Keywords
CALCIUM-CHANNELS; EFFICIENT SYNTHESIS; IN-VITRO; NEURONS; PAIN; DIVERSITY; SUBUNITS; EPILEPSY; RECEPTOR; CALCIUM-CHANNELS; EFFICIENT SYNTHESIS; IN-VITRO; NEURONS; PAIN; DIVERSITY; SUBUNITS; EPILEPSY; RECEPTOR; T-type Ca2+ channel; mibefradil; morpholinone
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/135036
DOI
10.1016/j.bmcl.2006.05.031
Appears in Collections:
KIST Article > 2006
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