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Dimethylcurcumin

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From Wikipedia, the free encyclopedia
Dimethylcurcumin
Clinical data
Other namesASC-J9; GO-Y025
Routes of
administration		Topical
Drug classNonsteroidal antiandrogen; Selective androgen receptor degrader
Identifiers
  • (1E,4Z,6E)-1,7-Bis(3,4-dimethoxyphenyl)-5-hydroxyhepta-1,4,6-trien-3-one
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC23H24O6
Molar mass396.439 g·mol−1
3D model (JSmol)
  • COC1=C(C=C(C=C1)/C=C/C(=C/C(=O)/C=C/C2=CC(=C(C=C2)OC)OC)/O)OC
  • InChI=1S/C23H24O6/c1-26-20-11-7-16(13-22(20)28-3)5-9-18(24)15-19(25)10-6-17-8-12-21(27-2)23(14-17)29-4/h5-15,24H,1-4H3/b9-5+,10-6+,18-15-
  • Key:ZMGUKFHHNQMKJI-CIOHCNBKSA-N

Dimethylcurcumin (development code ASC-J9) is a nonsteroidal antiandrogen and a synthetic curcuminoid.[1]

In vitro, it is an androgen receptor (AR) inhibitor and shows antiandrogenic activity, although its mechanism of action and effects differ from those of conventional antiandrogens; it is not an antagonist of the AR and instead appears to act as a selective degradation enhancer of certain subpopulations of the AR, for instance those present in the prostate gland.[1]

See also

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References

[edit]
  1. 1 2 Shi Q, Shih CC, Lee KH (2009). "Novel anti-prostate cancer curcumin analogues that enhance androgen receptor degradation activity". Anticancer Agents Med Chem. 9 (8): 904–12. doi:10.2174/187152009789124655. PMID 19663790.
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