Chemical Structure : SNX631-6
Catalog No.: PC-24325Not For Human Use, Lab Use Only.
SNX631-6 is an equipotent analog of SNX631 and potent, selective inhibitor of CDK8 and CDK19 with Kd values of 0.25 and 0.3 nM respectively.
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SNX631-6 is an equipotent analog of SNX631 and potent, selective inhibitor of CDK8 and CDK19 with Kd values of 0.25 and 0.3 nM respectively.
SNX631-6 exhibits IC50 of 11.7 nM in cell-based NFκB-dependent reporter assay for CDK8/19 inhibition in wild type (WT) 293 cells, but not CDK8/19-double knockout (KO) 293 cells.
SNX631-6 inhibits cancer growth of MYC-CaP-CR tumors in isogenic FVB mice, with no detrimental effect on body weight.
SNX631-6 enhances the efficacy of platinum-based chemotherapy and paclitaxel in both platinum-sensitive and resistant OCCC cell lines.
SNX631-6 shows strong antitumor and anti-metastatic effects in vivo.
M.Wt | 444.59 | |
Formula | C22H20D6N6O2S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Li J, et al. J Clin Invest. 2024 Mar 28;134(10):e176709.
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