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Riviciclib
Products Details
Product Description
– Riviciclib (P276-00 free base) is a potent cyclin-dependent kinase (CDK) inhibitor, which inhibits CDK9-cyclinT1, CDK4-cyclin D1, and CDK1-cyclinB with IC50s of 20 nM, 63 nM, and 79 nM, respectively[1][2].
Riviciclib shows antitumor activity on cisplatin-resistant cells[3].
Web ID
– HY-16559A
Shipping
– Room temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C21H20ClNO5
Citations
– Int J Mol Sci. 2022 Feb 24;23(5):2493.|Elife. 2020 Dec 7;9:e61405.
References
– [1]Roskoski R Jr,Cyclin-dependent protein kinase inhibitors including palbociclib as anticancer drugs.Pharmacol Res. 2016 May;107:249-275.|[2]Joshi KS, et al. In vitro antitumor properties of a novel cyclin-dependent kinase inhibitor, P276-00. Mol Cancer Ther. 2007 Mar;6(3):918-25.|[3]Joshi KS,et al. P276-00, a novel cyclin-dependent inhibitor induces G1-G2 arrest, shows antitumor activity on cisplatin-resistant cells and significant in vivo efficacy in tumor models. Mol Cancer Ther. 2007 Mar;6(3):926-34.
CAS Number
– 920113-02-6
Molecular Weight
– 401.84
SMILES
– O=C1C=C(C2=C(Cl)C=CC=C2)OC3=C([C@H]4[C@H](CO)N(C)CC4)C(O)=CC(O)=C13
Clinical Information
– No Development Reported
Research Area
– Cancer
Solubility
– 10 mM in DMSO
Target
– CDK
Isoform
– CDK1;CDK2;CDK4;CDK6;CDK9
Pathway
– Cell Cycle/DNA Damage
Product type
– Reference compound
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