Chemical compound
Pharmaceutical compound
R13 is a small-molecule flavonoid and orally active , potent , and selective agonist of the tropomyosin receptor kinase B (TrkB) – the main signaling receptor for the neurotrophin brain-derived neurotrophic factor (BDNF) – which is under development for the potential treatment of Alzheimer's disease .[ 1] [ 2] It is a structural modification and prodrug of tropoflavin (7,8-DHF) with improved potency and pharmacokinetics , namely oral bioavailability and duration .[ 1] The compound is a replacement for the earlier tropoflavin prodrug R7 and has similar properties to it.[ 1] [ 3] It was developed because while R7 displayed a good drug profile in animal studies, it showed almost no conversion into tropoflavin in human liver microsomes .[ 1] In contrast to R7, R13 is readily hydrolyzed into tropoflavin in human liver microsomes.[ 1]
See also
References
^ a b c d e f g Chen C, Wang Z, Zhang Z, Liu X, Kang SS, Zhang Y, Ye K (January 2018). "The prodrug of 7,8-dihydroxyflavone development and therapeutic efficacy for treating Alzheimer's disease" . Proc. Natl. Acad. Sci. U.S.A . 115 (3): 578–583. Bibcode :2018PNAS..115..578C . doi :10.1073/pnas.1718683115 . PMC 5777001 . PMID 29295929 .
^ US application 20150274692 , Keqiang Ye, "7,8-Dihydoxyflavone and 7,8-substituted flavone derivatives, compositions, and methods related thereto", published 2015-10-01, assigned to Emory University
^ Liu C, Chan CB, Ye K (2016). "7,8-dihydroxyflavone, a small molecular TrkB agonist, is useful for treating various BDNF-implicated human disorders" . Transl Neurodegener . 5 : 2. doi :10.1186/s40035-015-0048-7 . PMC 4702337 . PMID 26740873 .
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Angiopoietin CNTF EGF (ErbB)
FGF
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Agonists: Ersofermin
FGF (1 , 2 (bFGF) , 3 , 4 , 5 , 6 , 7 (KGF ), 8 , 9 , 10 (KGF2) , 17 , 18 , 22 )
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Negative allosteric modulators: VM-902A
TrkB
Agonists: 3,7-DHF
3,7,8,2'-THF
4'-DMA-7,8-DHF
7,3'-DHF
7,8-DHF
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