| Literature DB >> 26707391 |
Yong-Mei Cui1, Xin-Lan Liu2, Wen-Ming Zhang2, Hai-Xia Lin2, Tomohiko Ohwada3, Katsutoshi Ido4, Kohei Sawada4.
Abstract
A series of N-acylaminoalkyloxime derivatives of dehydroabietic acid were synthesized and evaluated for BK channel-opening activities in an assay system of CHO-K1 cells expressing hBKα channels. The structure-activity relationship study revealed that a non-covalent interaction between the S atom of the 2-thiophene and the carbonyl O atom may contribute to conformation restriction for interaction with the ion channel. This research could guide the design and synthesis of novel abietane-based BK channel opener.Entities:
Keywords: BK channels; Dehydroabietic acid; Openers; Oxime
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Year: 2015 PMID: 26707391 DOI: 10.1016/j.bmcl.2015.12.038
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823