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BI 2536 Chemical Structure

BI 2536

Data Sheet For research use only. Not for human use.
Cat. No. :BCP01743CAS No. :755038-02-9Purity:98%
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  • Publications Citing of Biochempartner's BI 2536
  • Chemical Properties&Biological Activity
CAS No. 755038-02-9 Cat. No. BCP01743
Name BI 2536
Synonyms BI-2536;BI2536;
SMILES
Chemical Name
Formula C28H39N7O3 M. Wt 521.66
Purity 98% Storage Store at 4-8°C
Description BI 2536 blocks the activities of Plk2 and Plk3 to a slightly lesser extent with IC50 of 3.5 nM and 9.0 nM, respectively. In HeLa cells, BI 2536 treatment ranging from 10-100 nM leads to the blocking of the recruitment of γ-tubulin and phosphorylation of Apc6 at mitotic centrosomes, inhibition of cohesin release from chromosome arms, induction of monopolar spindles, as well as a range of other mitotic processes that are known to depend on Plk1. BI 2536 treatment leads to the HeLa cells arrested in G2/M, subsequently a sub-G1 DNA peak indicative of DNA breakdown and apoptosis, and accumulated cleaved PARP p85 fragments in a concentration-dependent manner. BI 2536 inhibits the growth of a panel of 32 human cancer cell lines with EC50 of 2-25 nM, while blocking the proliferation of exponentially growing hTERT-RPE1, human umbilical vein endothelial cells (HUVECs), and normal rat kidney (NRK) cells with EC50 of 12-31 nM. Plk1 inhibition by BI 2536 reduces the growth and viability of anaplast
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