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Merck
CN

SML0623

Iniparib

≥98% (HPLC)

别名:

4-Iodo-3-nitrobenzamide, BSI-201

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关于此项目

经验公式(希尔记法):
C7H5IN2O3
化学文摘社编号:
分子量:
292.03
UNSPSC Code:
12352200
NACRES:
NA.77
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InChI

1S/C7H5IN2O3/c8-5-2-1-4(7(9)11)3-6(5)10(12)13/h1-3H,(H2,9,11)

InChI key

MDOJTZQKHMAPBK-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 5 mg/mL, clear

storage temp.

room temp

General description

Iniparib is also called as BSI-201. It is an anticancer agent.

Biochem/physiol Actions

4-iodo-3-nitrobenzamide, the intracellular metabolite of iniparib has the capability to covalently prevent PARP1 (poly(ADP-Ribose) polymerase 1) under cell-free conditions. PARP inhibitor also plays a role in BRCA (breast cancer susceptibility protein) deficient tumors.
Iniparib (BSI-201) is an antineoplastic originally thought to be a poly(ADP-ribose) polymerase-1 (PARP-1) inhibitor. Recent studies indicate Iniparib is not a PARP-1 inhibitor, and its mechanism of action is currently unknown.
Iniparib (BSI-201) is an antineoplastic.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

Lot/Batch Number

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Failure of iniparib to inhibit poly (ADP-Ribose) polymerase in vitro.
Patel AG, et al.
Clinical Cancer Research, 18(6), 1655?1662-1655?1662 (2012)
Evidence for the efficacy of Iniparib, a PARP-1 inhibitor, in BRCA2-associated pancreatic cancer.
Fogelman DR, et al.
Anticancer Research, 31(4), 1417-1420 (2011)
Iniparib plus chemotherapy in metastatic triple-negative breast cancer.
O'Shaughnessy J, et al.
The New England Journal of Medicine, 364(3), 205-214 (2011)
Hyomin Park et al.
Free radical biology & medicine, 204, 195-206 (2023-05-06)
The important pathway toward liver fibrosis is the TGF-β1-induced activation of hepatic stellate cells (HSCs). To discover chemicals to inhibit liver fibrosis, we screened 3000 chemicals using cell array system where human HSCs line LX2 cells are activated with TGF-β1.

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