R13 (drug)
Clinical data | |
---|---|
Other names | 4-Oxo-2-phenyl-4H-chromene-7,8-diyl bis(methylcarbamate) |
Routes of administration | By mouth[1] |
Pharmacokinetic data | |
Metabolites | 7,8-Dihydroxyflavone[1] |
Identifiers | |
| |
PubChem CID | |
Chemical and physical data | |
Formula | C19H16N2O6 |
Molar mass | 368.345 g·mol−1 |
3D model (JSmol) | |
| |
|
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 7,8-dihydroxyflavone (7,8-DHF) with improved potency and pharmacokinetics, namely oral bioavailability and duration.[1] The compound is a replacement for the earlier 7,8-DHF 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 7,8-DHF in human liver microsomes.[1] In contrast to R7, R13 is readily hydrolyzed into 7,8-DHF 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. 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.
{{cite journal}}
: CS1 maint: unflagged free DOI (link)
External links