R7 (drug)

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R7
R7.svg
Clinical data
Other names4-Oxo-2-phenyl-4H-chromene-7,8-diyl bis(dimethylcarbamate)
Routes of
administration
By mouth[1]
Legal status
Legal status
Pharmacokinetic data
Bioavailability~35% (in mice)[2]
MetabolitesTropoflavin[1]
Elimination half-life~3.25 hours (in mice[2]
Identifiers
  • [8-(Dimethylcarbamoyloxy)-4-oxo-2-phenylchromen-7-yl] N,N-dimethylcarbamate
CAS Number
PubChem CID
UNII
Chemical and physical data
FormulaC21H20N2O6
Molar mass396.399 g·mol−1
3D model (JSmol)
  • CN(C)C(=O)OC1=C(C2=C(C=C1)C(=O)C=C(O2)C3=CC=CC=C3)OC(=O)N(C)C
  • InChI=1S/C21H20N2O6/c1-22(2)20(25)28-16-11-10-14-15(24)12-17(13-8-6-5-7-9-13)27-18(14)19(16)29-21(26)23(3)4/h5-12H,1-4H3
  • Key:KHUMQRAGNPGBIE-UHFFFAOYSA-N

R7 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 treatment of Alzheimer's disease.[1][3][2] It is a structural modification and prodrug of tropoflavin (7,8-DHF) with improved potency and pharmacokinetics, namely oral bioavailability and duration.[2] R7 was synthesized by the same researchers who were involved in the discovery of tropoflavin.[2][4] A patent was filed for R7 in 2013 and was published in 2015.[2] In 2016, it was reported to be in the preclinical stage of development.[1][3] R7 was superseded by R13 because while R7 had a good drug profile in animals, it showed almost no conversion into tropoflavin in human liver microsomes.[5]

In 2010, tropoflavin, a naturally occurring flavonoid, was found to act as an agonist of the TrkB with nanomolar affinity (Kd ≈ 320 nM).[4] Subsequently, tropoflavin demonstrated robust efficacy in animal models of Alzheimer's disease and a variety of other conditions, making it a highly promising potential therapeutic agent.[1] Due to the presence of a vulnerable catechol group on its 2-phenyl-4H-chromene ring, tropoflavin is extensively conjugated via glucuronidation, sulfation, and methylation during first-pass metabolism in the liver and has a poor oral bioavailability of only 5% in mice upon oral administration.[2] As such, tropoflavin itself is a poor candidate for clinical development as an oral medication.[2] R7 is a derivative of tropoflavin with carbamate moieties on its hydroxyl groups, thereby protecting it from metabolism.[2]

As R7 is a slightly larger molecule than tropoflavin, 72.5 mg R7 is molecularly equivalent to 50 mg tropoflavin.[2] Relative to a roughly molecularly equivalent dose of tropoflavin, the area-under-curve levels of R7 were found to be 7.2-fold higher upon oral administration to mice, and R7 hence has a greatly improved oral bioavailability in mice of approximately 35%.[2] Moreover, whereas tropoflavin itself is mostly metabolized in mice within 30 minutes, tropoflavin as a metabolite was still detectable in plasma at 8 hours after administration with R7, indicating that R7 sustainably releases tropoflavin into circulation.[2] In accordance, the terminal half-life of R7 is about 195 minutes (3.25 hours) in mice.[2] The Tmax of R7 is about 60 minutes in mice, and its Cmax for a 78 mg/kg dose was 262 ng/mL, whereas that for a 50 mg/kg dose of tropoflavin was 70 ng/mL.[2]

Like tropoflavin, administration of R7 has been found to activate the TrkB in vivo in the mouse brain.[2] Moreover, R7 was found to potently activate the TrkB and the downstream Akt signaling pathway upon oral administration, an action that was tightly correlated with plasma concentrations of tropoflavin.[2] As such, R7 has shown in vivo efficacy as an agonist of the TrkB, including central activity, similarly to tropoflavin.[2]

See also

References

  1. ^ a b c d e Liu, Chaoyang; Chan, Chi Bun; Ye, Keqiang (2016). "7,8-dihydroxyflavone, a small molecular TrkB agonist, is useful for treating various BDNF-implicated human disorders". Translational Neurodegeneration. 5 (1): 2. doi:10.1186/s40035-015-0048-7. ISSN 2047-9158. PMC 4702337. PMID 26740873.
  2. ^ a b c d e f g h i j k l m n o p q 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 
  3. ^ a b Kazim, Syed Faraz; Iqbal, Khalid (2016). "Neurotrophic factor small-molecule mimetics mediated neuroregeneration and synaptic repair: emerging therapeutic modality for Alzheimer's disease". Molecular Neurodegeneration. 11 (1): 50. doi:10.1186/s13024-016-0119-y. ISSN 1750-1326. PMC 4940708. PMID 27400746.
  4. ^ a b Jang SW, Liu X, Yepes M, Shepherd KR, Miller GW, Liu Y, Wilson WD, Xiao G, Blanchi B, Sun YE, Ye K (2010). "A selective TrkB agonist with potent neurotrophic activities by 7,8-dihydroxyflavone". Proc. Natl. Acad. Sci. U.S.A. 107 (6): 2687–92. Bibcode:2010PNAS..107.2687J. doi:10.1073/pnas.0913572107. PMC 2823863. PMID 20133810.
  5. ^ 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.

External links