Chemical Structure : VPC-13789
Catalog No.: PC-72753Not For Human Use, Lab Use Only.
VPC-13789 (VPC13789) is a potent, selective, orally available inhibitor of androgen receptor binding function-3 (BF3) site with IC50 of 0.19 uM.
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VPC-13789 (VPC13789) is a potent, selective, orally available inhibitor of androgen receptor binding function-3 (BF3) site with IC50 of 0.19 uM.
VPC-13789 suppresses AR-mediated transcription, chromatin binding, and recruitment of coregulatory proteins.
VPC-13789 selectively reduces the growth of both androgen-dependent and enzalutamide-resistant PCa cell lines.
VPC-13789 demonstrated in vitro efficacy that reduced PSA production and tumor volume in animal models of CRPC with no observed toxicity.
M.Wt | 383.37 | |
Formula | C21H16F3N3O | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Eric Leblanc, et al. J. Med. Chem. 2021, 64, 20, 14968–14982.
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