A Synthetic 7,8-Dihydroxyflavone Derivative Promotes Neurogenesis and Exhibits Potent Antidepressant Effect

Xia Liu(Emory University), Chi-Bun Chan(Emory University), Sung‐Wuk Jang(Emory University), Pradoldej Sompol(Emory University), Junjian Huang(Emory University), Kunyan He(Emory University), Lien H. Phun(Georgia Institute of Technology), Stefan France(Georgia Institute of Technology), Ge� Xiao(Centers for Disease Control and Prevention), Yonghui Jia(Harvard University), Hongbo R. Luo(Harvard University), Keqiang Ye(Emory University)
Journal of Medicinal Chemistry
November 12, 2010
Cited by 201Open Access
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Abstract

7,8-Dihydroxyflavone is a recently identified small molecular tropomyosin-receptor-kinase B (TrkB) agonist. Our preliminary structural-activity relationship (SAR) study showed that the 7,8-dihydroxy groups are essential for the agonistic effect. To improve the lead compound's agonistic activity, we have conducted an extensive SAR study and synthesized numerous derivatives. We have successfully identified 4'-dimethylamino-7,8-dihydroxyflavone that displays higher TrkB agonistic activity than that of the lead. This novel compound also exhibits a more robust and longer TrkB activation effect in animals. Consequently, this new compound reveals more potent antiapoptotic activity. Interestingly, chronic oral administration of 4'-dimethylamino-7,8-dihydroxyflavone and its lead strongly promotes neurogenesis in dentate gyrus and demonstrates marked antidepressant effects. Hence, our data support that the synthetic 4'-dimethylamino-7,8-dihydroxyflavone and its lead both are orally bioavailable TrkB agonists and possess potent antidepressant effects.


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