Chemical Structure : LC-K2CAin-1
Catalog No.: PC-25380Not For Human Use, Lab Use Only.
LC-K2CAin-1 is a potent, highly selective CDK2-Cyclin A2 protein-protein interaction (PPI) inhibitor with IC50 of 59.57 nM in HTRF assays.
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LC-K2CAin-1 is a potent, highly selective CDK2-Cyclin A2 protein-protein interaction (PPI) inhibitor with IC50 of 59.57 nM in HTRF assays.
LC-K2CAin-1 shows no significantly affecting the interactions of CDK2 with Cyclin E1, CDK1 with Cyclin B1, CDK9 with Cyclin T1, or those of CDK4 and CDK6 with Cyclin D3.
LC-K2CAin-1 binds to and stabilizes the A-loop, inducing conformational changes of A-loop and α-C-Helix, which are likely responsible for the disruption of the CDK2–Cyclin A2 interaction.
LC-K2CAin-1 suppresses the proliferation of melanoma cells (A875cell, IC50=3.96 uM), and trigger apoptosis and induce G2/M phase arrest, but markedly less effective in CDK2-low VMM5A cells (IC50 > 14 µM).
M.Wt | 525.57 | |
Formula | C23H29F2N5O5S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Sun G, et al. Angew Chem Int Ed Engl. 2025 Aug 19:e202513542.
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