CITCO

Suppliers

Names

[ CAS No. ]:
338404-52-7

[ Name ]:
CITCO

[Synonym ]:
6-(4-CHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE O-(3,4-DICHLOROBENZYL)OXIME
6-(4-Chlorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime
CITCO

Chemical & Physical Properties

[ Density]:
1.48g/cm3

[ Molecular Formula ]:
C19H12Cl3N3OS

[ Molecular Weight ]:
436.74200

[ Exact Mass ]:
434.97700

[ PSA ]:
67.13000

[ LogP ]:
6.57370

[ Index of Refraction ]:
1.697

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

Articles

Evaluation of the HC-04 cell line as an in vitro model for mechanistic assessment of changes in hepatic cytochrome P450 3A during adenovirus infection.

Drug Metab. Dispos. 42(7) , 1191-201, (2014)

HC-04 cells were evaluated as an in vitro model for mechanistic study of changes in the function of hepatic CYP3A during virus infection. Similar to in vivo observations, infection with a first genera...

Involvement of CAR and PXR in the transcriptional regulation of CYP2B6 gene expression by ingredients from herbal medicines.

Xenobiotica 45 , 773-81, (2015)

1. Induction of hepatic drug-metabolizing enzymes can affect drug efficacy and cause toxicity. However, so far, limited information is available regarding the molecular mechanism how herbal medicines ...

Quantitative high-throughput identification of drugs as modulators of human constitutive androstane receptor.

Sci. Rep. 5 , 10405, (2015)

The constitutive androstane receptor (CAR, NR1I3) plays a key role in governing the transcription of numerous hepatic genes that involve xenobiotic metabolism/clearance, energy homeostasis, and cell p...


More Articles

Related Compounds

  • N-(3-cyano-4,5-dimethylthiophen-2-yl)-1-(methylsulfonyl)pyrrolidine-2-carboxamide
  • [4-(6-Bromo-2-benzothiazolyl)-1-piperazinyl][1-(methylsulfonyl)-2-pyrrolidinyl]methanone
  • [4-(4-Ethyl-2-benzothiazolyl)-1-piperazinyl][1-(methylsulfonyl)-2-pyrrolidinyl]methanone
  • (4-(4-Methoxybenzo[d]thiazol-2-yl)piperazin-1-yl)(1-(methylsulfonyl)pyrrolidin-2-yl)methanone
  • 2-((5-phenyl-1-(4-(trifluoromethoxy)phenyl)-1H-imidazol-2-yl)thio)-1-(pyrrolidin-1-yl)ethanone
  • N-(7-Chloro-4-methoxy-2-benzothiazolyl)-1-(methylsulfonyl)-2-pyrrolidinecarboxamide
  • N-[6-[(Dimethylamino)sulfonyl]-2-benzothiazolyl]-1-(methylsulfonyl)-2-pyrrolidinecarboxamide
  • 1-(methylsulfonyl)-N-(5-(p-tolyl)-1,3,4-oxadiazol-2-yl)pyrrolidine-2-carboxamide
  • N-(4,5-Dimethyl-2-benzothiazolyl)-1-(methylsulfonyl)-N-(2-pyridinylmethyl)-2-pyrrolidinecarboxamide
  • N-(5-Methoxy-2-benzothiazolyl)-1-(methylsulfonyl)-N-(3-pyridinylmethyl)-2-pyrrolidinecarboxamide
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