الصفحة الرئيسية>>Signaling Pathways>> Cell Cycle/Checkpoint>> Cyclin-Dependent Kinases>>SCH900776 S-isomer

SCH900776 S-isomer (Synonyms: SCH 900776 S-isomer;SCH-900776 S-isomer)

رقم الكتالوجGC17792

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SCH900776 S-isomer التركيب الكيميائي

Cas No.: 891494-64-7

الحجم السعر المخزون الكميّة
5mg
84٫00
متوفر
10mg
131٫00
متوفر
20mg
236٫00
متوفر
50mg
458٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products
SCH900776 is a potent, selective and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50 = 3 nM), highly selective against Chk2 (IC50 = 1500 nM) and cyclin-dependent kinase CDK2 (IC50 = 160 nM). SCH900776 exposure phenocopies short interfering RNA-mediated CHK1 ablation and interacts synergistically with DNA antimetabolite agents in vitro and in vivo to selectively induce dsDNA breaks and cell death in tumor cell backgrounds. Chk1 inhibitor SCH 900776 abrogates cytarabine-induced S-phase arrest and enhances cytarabine cytotoxicity in acute leukemia cell lines and leukemic blasts in vitro.

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