Chemical Structure : KY-065
Catalog No.: PC-23612Not For Human Use, Lab Use Only.
KY-065 is a potent, selective and ATP-competitive CDK8/19 inhibitor with IC50 of 4.4/3.6 nM respectively, without affecting the activities of other CDK family members.
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KY-065 is a potent, selective and ATP-competitive CDK8/19 inhibitor with IC50 of 4.4/3.6 nM respectively, without affecting the activities of other CDK family members.
KY-065 also does not markedly inhibit the kinase activities of 30 serine/threonine kinases through a single point inhibition assay.
KY-065 ameliorates the suppressive differentiation in chondrocytes of Fgfr3Ach mice.
KY-065 decreases STAT1Ser727 phosphorylation in chondrocytes of Fgfr3Ach mice, with no significant effect on the phosphorylation level of STAT1Tyr701.
KY-065 elongates the long bone and improves growth plate cytoarchitecture in Fgfr3Ach mice.
M.Wt | 399.44 | |
Formula | C22H25NO6 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Sadamori K, et al. Biochim Biophys Acta Mol Basis Dis. 2024 Dec 12:167626.
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