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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >DNA damage >PPAR inhibitors >T0070907

T0070907

T0070907 Structure
  • ₹19116.95 - ₹70925.4
  • Product name: T0070907
  • CAS: 313516-66-4
  • MF: C12H8ClN3O3
  • MW: 277.66
  • EINECS:
  • MDL Number:MFCD00121849
  • Synonyms:2-CHLORO-5-NITRO-N-4-PYRIDINYLBENZAMIDE;2-CHLORO-5-NITRO-N-(4-PYRIDYL)BENZAMIDE;T 0070907;N1-(4-PYRIDYL)-2-CHLORO-5-NITROBENZAMIDE;BenzaMide, 2-chloro-5-nitro-N-4-pyridinyl-;T0070907 - CAS 313516-66-4 - Calbiochem;CS-2314;T0070907 (T-0070907
2 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • 25MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberT8703
  • Product descriptionT0070907 ≥98% (HPLC)
  • Packaging5MG
  • Price₹19116.95
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberT8703
  • Product descriptionT0070907 ≥98% (HPLC)
  • Packaging25MG
  • Price₹70925.4
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) T8703 T0070907 ≥98% (HPLC) 5MG ₹19116.95 2022-06-14 Buy
Sigma-Aldrich(India) T8703 T0070907 ≥98% (HPLC) 25MG ₹70925.4 2022-06-14 Buy

Properties

Melting point :>184°C (dec.)
Density :1.498
storage temp. :2-8°C
solubility :DMSO: >10mg/mL
form :White solid
color :white
Water Solubility :Soluble in DMSO at 10mg/ml. Insoluble in water.
Sensitive :Light Sensitive

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
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340 IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405 Store locked up.

Description

The peroxisome proliferator-activated receptor-γ (PPARγ) is the nuclear receptor responsible for transducing the therapeutic activity of the thiazolidinediones (TZDs). TZDs are a group of structurally related synthetic PPARγ receptor agonists with antidiabetic actions in vivo. There are many PPARγ agonists, including 15-deoxy-Δ12,14-prostaglandin J2 and azelaoyl PAF, which are naturally derived. However, only a few antagonists have been reported. T0070907 is a potent and selective antagonist of the human PPARγ with an apparent IC50 of 1 nM for the binding inhibition of rosiglitazone, a reference TZD. T0070907 covalently binds to Cys313 of PPARγ, inducing conformational changes that block the recruitment of transcriptional cofactors to the PPARγ/RXR heterodimer.

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