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1H-Imidazole, 2-[(2,2-diethoxyethyl)thio]-4,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137684-79-8

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137684-79-8 Usage

Imidazole derivative

Yes

Contains ethoxy and phenyl groups

Yes

Presence of sulfur

Yes, suggests thiol-like properties

Potential biological activities

Antifungal, antibacterial, and anti-inflammatory properties

Potential pharmacological and medicinal applications

Possible, but requires further research to understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 137684-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,6,8 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137684-79:
(8*1)+(7*3)+(6*7)+(5*6)+(4*8)+(3*4)+(2*7)+(1*9)=168
168 % 10 = 8
So 137684-79-8 is a valid CAS Registry Number.

137684-79-8Downstream Products

137684-79-8Relevant academic research and scientific papers

Acyl-CoA::cholesterol O-Acyl Transferase (ACAT) Inhibitors. 1. 2-(Alkylthio)-4,5-diphenyl-1H-imidazoles as Potent Inhibitors of ACAT

Harris, Neil V.,Smith, Christopher,Asthon, Michael J.,Bridge, Andrew W.,Bush, Raymond C.,et al.

, p. 4384 - 4392 (2007/10/02)

A potent, bioavailable ACAT inhibitor may have beneficial effects in the treatment of atherosclerosis by (i) reducing the absorption of dietary cholesterol, (ii) reducing the secretion of very low density lipoproteins into plasma from the liver, and (iii) preventing the transformation of arterial macrophages into foam cells.We have found that a mevalonate derivative 2, which contains a 4,5-diphenyl-1H-imidazol-2-yl moiety, inhibits rat hepatic microsomal ACAT in vitro and produces a significant hypocholesterolemic effect in the cholesterol-fed rat.Structure-activity relationships for analogues of 2 demonstrate that the 4,5-diphenyl-1H-imidazole moiety is a pharmacophore for inhibition of rat microsomal ACAT.

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