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2-[2,3-dimethyl-4-(1-oxobutyl)phenoxy]propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

858371-30-9

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858371-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858371-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,3,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 858371-30:
(8*8)+(7*5)+(6*8)+(5*3)+(4*7)+(3*1)+(2*3)+(1*0)=199
199 % 10 = 9
So 858371-30-9 is a valid CAS Registry Number.

858371-30-9Relevant academic research and scientific papers

The synthesis of α,β-unsaturated carbonyl derivatives with the ability to inhibit both glutathione S-transferase P1-1 activity and the proliferation of leukemia cells

Zhao, Guisen,Liu, Chuan,Wang, Rui,Song, Dandan,Wang, Xiaobing,Lou, Hongxiang,Jing, Yongkui

, p. 2701 - 2707 (2008/02/07)

Ethacrynic acid (EA), an α,β-unsaturated carbonyl compound, is a glutathione S-transferase P1-1 (GSTP1-1) inhibitor. Twenty-one novel EA derivatives have been synthesized. The effects of these compounds on GSTP1-1 activity and on the proliferation of human leukemia HL-60 cells have been determined. Compounds with a halogen substitution at the 3′-position of the aromatic ring have greater inhibitory effects on GSTP1-1 activity than those of compounds with a methyl substitution there. Compounds with substitutions at both the 2′- and 3′-positions of the aromatic ring have more antiproliferative ability than those with one substitution at 3′-position. Esterification of the carboxyl group appears to increase the antiproliferative ability.

Synthesis and structure-activity relationship of ethacrynic acid analogues on glutathione-s-transferase P1-1 activity inhibition

Zhao, Guisen,Yu, Tao,Wang, Rui,Wang, Xiaobing,Jing, Yongkui

, p. 4056 - 4062 (2007/10/03)

Ethacrynic acid (EA) is a glutathione-s-transferase π (GSTP1-1) inhibitor. Fifteen of EA analogues were designed and synthesized and their inhibition on GSTP1-1 activity was tested in lysate of human leukemia HL-60 cells. These compounds were synthesized

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