CAS No. 1038915-60-4

Batch: Purity:99.99
Niraparib (MK-4827) Chemical Structure
Chemical Structure
Check the Niraparib (MK-4827) product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 2-[4-[(3S)-piperidin-3-yl]phenyl]indazole-7-carboxamide
CAS Number 1038915-60-4
Molecular Formula

C19H20N4O

Molecular Weight (MW) 320.39
SMILES C1CC(CNC1)C2=CC=C(C=C2)N3C=C4C=CC=C(C4=N3)C(=O)N
InChIKey PCHKPVIQAHNQLW-CQSZACIVSA-N

Ordering Information

Biological Activity

Niraparib (MK-4827) is a selective inhibitor of PARP1 (IC50 3.8 nM) and PARP2 (IC50 2.1 nM). It inhibits PARP activity, inducing the formation of PARP-DNA complexes and preventing DNA repair. This leads to the accumulation of DNA strand breaks, genomic instability, and selective synthetic lethality in homologous recombination-deficient tumor cells, ultimately driving apoptosis and tumor cell death. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 64 mg/mL (199.75 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 64 mg/mL
Water Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.