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An inhibitor of Chk1 and WEE1 (IC50s = 47 and 97 nM, respectively), selective for Chk1 and WEE1 over PKC (IC50 = 3.4 µM) and Cdk4 (IC50 = 3.75 µM), selective for Chk1 and WEE1 over c-Src and the PDGF and FGF receptors (IC50s = >50 µM for all), and other CDKs (IC50s = >50 µM), sensitizes SKOV3 and OVCAR-3 ovarian cancer cells, as well as cisplatin-resistant A2780cis cells, to cisplatin at 0.5 µM, induces myoblast differentiation into mature osteoblasts and hESC differentiation into cells with mesoderm or cytotrophoblast stem cell lineages when used in combination with BMP4. SMILES: O=C1NC(C2=C3C4=C(C=CC(O)=C4)NC3=CC(C5=CC=CC=C5)=C21)=O.O. InChi Code: InChI=1S/C20H12N2O3.H2O/c23-11-6-7-14-13(8-11)16-15(21-14)9-12(10-4-2-1-3-5-10)17-18(16)20(25)22-19(17)24,/h1-9,21,23H,(H,22,24,25),1H2. InChi Key: BYBJRPZQCMIOPE-UHFFFAOYSA-N
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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