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Niraparib (MK-4827) tosylate - 10mM in DMSO, high purity , CAS No.1038915-73-9(DMSO)

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
N408309
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Availability
Price Qty
N408309-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$227.90

PARP2 Selective Inhibitors

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Compound libraries (12325)

Basic Description

Synonyms Niraparib tosylate, MK 4827 tosylate, ZEJULA | 2H-​Indazole-​7-​carboxamide, 2-​[4-​(3S)​-​3-​piperidinylphenyl]​-​, 4-​methylbenzenesulfona​te (1:1)
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Niraparib tosylate (MK-4827, ZEJULA) is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 nM/2.1 nM. Niraparib increases formation of PARP-DNA complexes resulting in DNA damage, apoptosis, and cell death.
Storage Temp Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Information

Niraparib tosylate (MK-4827, ZEJULA) is a selective inhibitor ofPARP1/PARP2withIC50of 3.8 nM/2.1 nM. Niraparib increases formation of PARP-DNA complexes resulting in DNA damage,apoptosis, and cell death.
In vitro

Micromolar concentrations of niraparib radiosensitizes tumor cell lines derived from lung, breast, and prostate cancers independently of their p53 status but not cell lines derived from normal tissues. Niraparib also sensitizes tumor cells to H2O2 and converts H2O2-induced single strand breaks (SSBs) into DSBs during DNA replication.

In vivo

MK-4827 strongly enhances the effect of radiation on a variety of human tumor xenografts, both p53 wild type and p53 mutant. MK-4827 reduces PAR levels in tumors by 1 h after administration which persisted for up to 24 h. In vivo treatment with MK-4827 and radiation prolonged survival (p<0.01) compared to single modalities. In vivo superiority of MK-4827 plus radiation is further documented by significant elevations of cleaved caspase-3 and γ-H2AX in tumors from the combination group compared to single modality cohorts.
Cell Data

cell lines:

Concentrations:50 nM

Incubation Time:24 h

Powder Purity:≥99%

Product Properties

ALogP 4.267
hba_count 2
HBD Count 2
Rotatable Bond 4

Names and Identifiers

Smiles CC1=CC=C(C=C1)[S](O)(=O)=O.NC(=O)C2=CC=CC3=C[N](N=C23)C4=CC=C(C=C4)C5CCCNC5
Molecular Weight 492.59
Reaxy-Rn 42083915
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42083915&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 81 mg/mL (198.8 mM); Water: Insoluble; Ethanol: Insoluble;
DMSO(mg / mL) Max Solubility 98
DMSO(mM) Max Solubility 198.95
Water(mg / mL) Max Solubility <1

Solution Calculators

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