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Glycyrrhetinic acid derivatives: a novel class of inhibitors of gap-junctional intercellular communication. Structure-activity relationships.

作者信息

Davidson J S, Baumgarten I M

机构信息

Department of Chemical Pathology, University of Cape Town Medical School, South Africa.

出版信息

J Pharmacol Exp Ther. 1988 Sep;246(3):1104-7.

PMID:3418512
Abstract

Glycyrrhetinic acid was shown previously to inhibit intercellular gap-junctional communication between human fibroblasts. In the present study 31 derivatives of glycyrrhetinic acid were tested for their ability to inhibit communication. Eight of the compounds inhibited communication with high potency (IC50 less than 3 microM) and showed low toxicity, properties which suggest they may be useful pharmacological probes for studies of gap-junction function.

摘要

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