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Adavosertib Chemical Structure

Adavosertib

Data Sheet For research use only. Not for human use.
Cat. No. :BCP01928CAS No. :955365-80-7Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 955365-80-7 Cat. No. BCP01928
Name Adavosertib
Synonyms MK1775; MK 1775; AZD1775; AZD-1775; AZD 1775;MK-1775;
SMILES
Chemical Name
Formula C27H32N8O2 M. Wt 500.6
Purity 98% Storage Store at 4-8°C
Description MK-1775 inhibits Wee1 kinase in an ATP-competitive manner. Compared to Wee1, MK-1775 displays 2- to 3-fold less potency against Yes with IC50 of 14 nM, 10-fold less potency against seven other kinases with >80% inhibition at 1 μM, and >100-fold selectivity over human Myt 1, another kinase that inhibits cyclin-dependent kinase 1 (CDC2) by phosphorylation at an alternative site (Thr14). By abrogating the DNA damage checkpoint via blockade of Wee1 activity in WiDr cells bearing mutated p53, MK-1775 treatment inhibits the basal phosphorylation of CDC2 at Tyr15 (CDC2Y15) with EC50 of 49 nM, and suppresses gemcitabine-, carboplatin- or cisplatin-induced phosphorylation of CDC2 and cell cycle arrest in a dose-dependent manner, with EC50 of 82 nM and 81 nM, 180 nM and 163 nM, as well as 159 nM and 160 nM, respectively. MK-1775 treatment alone at 30-100 nM has no significant antiproliferative effect in WiDr and H1299 cells, whereas MK-1775 at 300 nM, sufficient to inhibit Wee1 by >80%, displays
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