1038915-58-0

1038915-58-0 structure

Name: MK-4827 (R-enantiomer)
Chemical Name: 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide
CAS Number: 1038915-58-0
Molecular Formula: C₁₉H₂₀N₄O
Molecular Weight: 320.38800
Catalog: Research Areas Cancer
Create Date: 2016-03-04 09:31:28
Modify Date: 2024-04-04 18:40:30
Niraparib R-enantiomer (MK-4827 R-enantiomer) is an excellent PARP1 inhibitor with IC50 of 2.4 nM.

Name	2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide
Synonyms	2-{4-[(3R)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide MK-4827 (R-enantiomer)

Description	Niraparib R-enantiomer (MK-4827 R-enantiomer) is an excellent PARP1 inhibitor with IC50 of 2.4 nM.
Related Catalog	Research Areas >> Cancer
Target	PARP-1:2.4 nM (IC50)
In Vitro	Niraparib R-enantiomer (MK-4827 R-enantiomer) resolution of Niraparib R-enantiomer give compounds Niraparib R-enantiomer and Niraparib S-enantiomer, both showing excellent inhibition of PARP-1. Niraparib R-enantiomer has somewhat lower in vitro metabolic clearance than the Niraparib S-enantiomer in rat liver microsomes, but Niraparib S-enantiomer is more potent in cell based assays (PARylation EC50, Niraparib R-enantiomer=30 nM, Niraparib S-enantiomer=4.0 nM; BRCA1-HeLa CC50, Niraparib R-enantiomer=470, Niraparib S-enantiomer=34 nM). Given this improved potency and similar in vitro turnover in human liver microsomes (HLM Clint, Niraparib R-enantiomer=4, Niraparib S-enantiomer=3 μL/min/mgP), Niraparib S-enantiomer (Niraparib) is focused on[1].
References	[1]. Jones P, et al. Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): a novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors. J Med Chem. 2009 Nov 26;52(22):7170-85.