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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >DNA damage >PARP inhibitors >4-iodo-3-nitrobenzamide

4-iodo-3-nitrobenzamide

4-iodo-3-nitrobenzamide Structure
  • ₹12394.63
  • Product name: 4-iodo-3-nitrobenzamide
  • CAS: 160003-66-7
  • MF: C7H5IN2O3
  • MW: 292.03
  • EINECS:685-396-9
  • MDL Number:MFCD11110639
  • Synonyms:4-iodo-3-nitrobenzamide;IND-71677;NSC-746045;BSI-201 (Iniparib);iniparib/NSC-746045;BSI-201, 4-Iodo-3-nitrobenzamide;109775;INIPARIB; NSC-746045; IND-71677; BSI 201; BSI201
1 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 10MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberSML0623
  • Product descriptionIniparib ≥98% (HPLC)
  • Packaging10MG
  • Price₹12394.63
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) SML0623 Iniparib ≥98% (HPLC) 10MG ₹12394.63 2022-06-14 Buy

Properties

Boiling point :344.8±32.0 °C(Predicted)
Density :2.055±0.06 g/cm3(Predicted)
storage temp. :Sealed in dry,Store in freezer, under -20°C
solubility :DMSO: soluble5mg/mL, clear
pka :14?+-.0.50(Predicted)
form :powder
color :white to beige
Stability :Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
Precautionary statements:
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Poly(ADP-ribose) polymerase (PARP) is a critical DNA repair enzyme involved in DNA single-strand break repair via the base excision repair pathway. PARP1 is activated by DNA damage. Inhibiting its activity has been linked to synthetic lethality and loss of either of the breast cancer susceptibility genes, BRCA1 and BRCA2. BSI-201 is an irreversible, noncompetitive inhibitor of PARP1 that disrupts binding between PARP1 and DNA by interacting with the DNA binding domain. It produces rapid apoptosis in various cancer cell lines with IC50 values ranging from 40-128 μM and is not toxic in Syrian hamsters at doses as high as 200 mg/kg. In phase II clinical studies, BSI-201, in combination with carboplatin and gemcitabine, has produced promising results in "triple-negative" breast cancers, increasing median overall survival from 7.7 months to 12.3 months.

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