[CAS NO. 1038915-60-4]  Niraparib (MK-4827)

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PRODUCTS SPECIFICATIONS [1038915-60-4]

Store
Catalog
SLK-S2741
Brand
Selleck
CAS
1038915-60-4

DESCRIPTION [1038915-60-4]

Overview

MDLMFCD17779309
Molecular Weight320.39
Molecular FormulaC19H20N4O
SMILESC(N)(=O)C=1C=2C(=CN(N2)C3=CC=C(C=C3)[C@@]4(CCCNC4)[H])C=CC1

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM3.1212 mL15.6060 mL31.2120 mL
5 mM0.6242 mL3.1212 mL6.2424 mL
10 mM0.3121 mL1.5606 mL3.1212 mL
50 mM0.0624 mL0.3121 mL0.6242 mL

Description

Niraparib (MK-4827) is a selective inhibitor of with of 3.8 nM/2.1 nM, with great activity in cancer cells with mutant BRCA-1 and BRCA-2. It is >330-fold selective against PARP3, V-PARP and Tank1. Niraparib can form PARP–DNA complexes resulting in DNA damage, , and cell death. Phase 3.

Targets

PARP2 [1]
(Cell-free assay)
PARP1 [1]
(Cell-free assay)
2.1 nM3.8 nM

In vitro

In a whole cell assay, MK-4827 inhibited PARP activity with EC50 = 4 nM and inhibited proliferation of cancer cells with mutant BRCA-1 and BRCA-2 with CC50 in the 10-100 nM range. It was demonstrated to be a potent and selective PARP-1 and PARP-2 inhibitor with IC50=3.8 and 2.1 nM, respectively. Furthermore, it displayed at least a 100-fold selectivity over PARP-3, V-PARP, and tankyrase-1, with IC50 = 1300, 330, and 570 nM, respectively. As well as inhibiting the growth of HeLa cell lacking BRCA-1 because of silencing by RNA interference, MK-4827 is able to inhibit the proliferation of cancer cell lines carrying natural BRCA-1 or BRCA-2 mutations. In MDA-MB-436 human mammary gland adenocarcinoma cells carrying BRCA-1 mutations, MK-4827 displayed CC50 = 18 nM, while in CAPAN-1 human pancreatic adenocarcinoma cells, which are BRCA-2 mutant, MK-4827 displayed CC50 = 90 nM. In contrast, normal human prostate and mammary epithelial cells are resistant to MK-4827, displaying antiproliferative effects in the micromolar range, thereby demonstrating the very high selective cytotoxicity from these PARP inhibitors in BRCA-1 and -2 mutant cancer cells compared to surrounding tissue.

In vivo

MK-4827, a novel, orally bioavailable, PARP-1 and PARP-2 inhibitor, strongly enhanced the effect of radiation on a variety of human tumor xenografts, both p53 wild type and p53 mutant. It was well tolerated in vivo and demonstrated efficacy as a single agent in a xenograft model of BRCA-1 deficient cancer.


Synonyms

2H-Indazole-7-carboxamide, 2-[4-(3S)-3-piperidinylphenyl]-
2-[4-(3S)-3-Piperidinylphenyl]-2H-indazole-7-carboxamide
Niraparib
2H-Indazole-7-carboxamide 2-[4-(3S)-3-piperidinylphenyl]-
2-[4-[(3S)-Piperidin-3-yl]phenyl]indazole-7-carboxamide