ChemSpider 2D Image | EFATUTAZONE DIHYDROCHLORIDE | C27H28Cl2N4O4S

EFATUTAZONE DIHYDROCHLORIDE

  • Molecular FormulaC27H28Cl2N4O4S
  • Average mass575.507 Da
  • Monoisotopic mass574.120850 Da
  • ChemSpider ID17623620

More details:

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

2,4-Thiazolidinedione, 5-[[4-[[6-(4-amino-3,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-yl]methoxy]phenyl]methyl]-, hydrochloride (1:2) [ACD/Index Name]
223132-38-5 [RN]
5-(4-{[6-(4-Amino-3,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-yl]methoxy}benzyl)-1,3-thiazolidin-2,4-diondihydrochlorid [German] [ACD/IUPAC Name]
5-(4-{[6-(4-Amino-3,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-yl]methoxy}benzyl)-1,3-thiazolidine-2,4-dione dihydrochloride [ACD/IUPAC Name]
5-(4-{[6-(4-Amino-3,5-diméthylphénoxy)-1-méthyl-1H-benzimidazol-2-yl]méthoxy}benzyl)-1,3-thiazolidine-2,4-dione, dichlorhydrate [French] [ACD/IUPAC Name]
EFATUTAZONE DIHYDROCHLORIDE
2,4-Thiazolidinedione, 5-[[4-[[6-(4-amino-3,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-yl]methoxy]phenyl]methyl]-, dihydrochloride (9CI)
5-(4-((6-(4-amino-3,5-dimethylphenoxy)-1-methyl-1H-benzo[d]imidazol-2-yl)methoxy)benzyl)thiazolidine-2,4-dione dihydrochloride
5-?[[4-?[[6-?(4-?amino-?3,?5-?dimethylphenoxy)?-?1-?methyl-?1H-?benzimidazol-?2-?yl]?methoxy]?phenyl]?methyl]?-2,?4-?Thiazolidinedione?, hydrochloride (1:2)
5-[[4-[[6-(4-amino-3,5-dimethylphenoxy)-1-methylbenzimidazol-2-yl]methoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione;dihydrochloride
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

76B44WEA8O [DBID]
UNII:76B44WEA8O [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Bio Activity:

      Cell Cycle/DNA Damage MedChem Express HY-14792B
      Cell Cycle/DNA Damage; NF-KB; MedChem Express HY-14792B
      Inolitazone 2Hcl(RS5444; CS-7017) is a novel high-affinity PPAR? agonist, which activates PPAR? with an EC50 about 1/50 that of rosiglitazone and has no effect on RIE cells that do not express PPAR?.; IC50 Value: 0.8 nM [1]; Target: PPAR?; in vitro: In vitro, the IC50 for growth inhibition is approximately 0.8 nM while anaplastic thyroid carcinoma (ATC) tumor growth was inhibited three- to fourfold in nude mice. MedChem Express HY-14792B
      PPAR MedChem Express HY-14792B

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


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