TY - JOUR
T1 - A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect
AU - Liu, Xia
AU - Chan, Chi Bun
AU - Jang, Sung Wuk
AU - Pradoldej, Sompol
AU - Huang, Junjian
AU - He, Kunyan
AU - Phun, Lien H.
AU - France, Stefan
AU - Xiao, Ge
AU - Jia, Yonghui
AU - Luo, Hongbo R.
AU - Ye, Keqiang
PY - 2010/12/9
Y1 - 2010/12/9
N2 - 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.
AB - 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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U2 - 10.1021/jm101206p
DO - 10.1021/jm101206p
M3 - Article
C2 - 21073191
AN - SCOPUS:78649857797
SN - 0022-2623
VL - 53
SP - 8274
EP - 8286
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 23
ER -