File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1021/jm101206p
- Scopus: eid_2-s2.0-78649857797
- PMID: 21073191
- WOS: WOS:000284738400007
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect
Title | A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect |
---|---|
Authors | |
Issue Date | 2010 |
Citation | Journal of Medicinal Chemistry, 2010, v. 53, n. 23, p. 8274-8286 How to Cite? |
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. © 2010 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/225086 |
ISSN | 2023 Impact Factor: 6.8 2023 SCImago Journal Rankings: 1.986 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Liu, Xia | - |
dc.contributor.author | Chan, Chi Bun | - |
dc.contributor.author | Jang, Sung Wuk | - |
dc.contributor.author | Pradoldej, Sompol | - |
dc.contributor.author | Huang, Junjian | - |
dc.contributor.author | He, Kunyan | - |
dc.contributor.author | Phun, Lien H. | - |
dc.contributor.author | France, Stefan | - |
dc.contributor.author | Xiao, Ge | - |
dc.contributor.author | Jia, Yonghui | - |
dc.contributor.author | Luo, Hongbo R. | - |
dc.contributor.author | Ye, Keqiang | - |
dc.date.accessioned | 2016-04-18T11:16:44Z | - |
dc.date.available | 2016-04-18T11:16:44Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Journal of Medicinal Chemistry, 2010, v. 53, n. 23, p. 8274-8286 | - |
dc.identifier.issn | 0022-2623 | - |
dc.identifier.uri | http://hdl.handle.net/10722/225086 | - |
dc.description.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. © 2010 American Chemical Society. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Medicinal Chemistry | - |
dc.title | A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/jm101206p | - |
dc.identifier.pmid | 21073191 | - |
dc.identifier.scopus | eid_2-s2.0-78649857797 | - |
dc.identifier.volume | 53 | - |
dc.identifier.issue | 23 | - |
dc.identifier.spage | 8274 | - |
dc.identifier.epage | 8286 | - |
dc.identifier.eissn | 1520-4804 | - |
dc.identifier.isi | WOS:000284738400007 | - |
dc.identifier.issnl | 0022-2623 | - |