Methyl Substitution of a Rexinoid Agonist Improves Potency and Reveals Site of Lipid Toxicity

Volume: 57, Issue: 12, Pages: 5370 - 5380
Published: Jun 5, 2014
Abstract
(2E,4E,6Z,8E)-8-(3',4'-Dihydro-1'(2'H)-naphthalen-1'-ylidene)-3,7-dimethyl-2,4,6-octatrienoic acid, 9cUAB30, is a selective rexinoid that displays substantial chemopreventive capacity with little toxicity. 4-Methyl-UAB30, an analogue of 9cUAB30, is a potent RXR agonist but caused increased lipid biosynthesis unlike 9cUAB30. To evaluate how methyl substitution influenced potency and lipid biosynthesis, we synthesized four 9cUAB30 homologues with...
Paper Details
Title
Methyl Substitution of a Rexinoid Agonist Improves Potency and Reveals Site of Lipid Toxicity
Published Date
Jun 5, 2014
Volume
57
Issue
12
Pages
5370 - 5380
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