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57499-41-9

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57499-41-9 Usage

General Description

2,3-dehydrosilychristin A is a naturally occurring flavonoid compound found in the roots of the plant Silybum marianum, commonly known as milk thistle. It has been identified as a potent antioxidant and has displayed potential anti-inflammatory and anti-cancer properties. Studies have shown that 2,3-dehydrosilychristin A exhibits protective effects on liver cells and may be beneficial in treating liver disorders such as hepatitis and cirrhosis. Its antioxidant properties make it valuable in neutralizing harmful free radicals in the body and protecting cells from oxidative damage. Research on 2,3-dehydrosilychristin A continues to explore its potential therapeutic applications in various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 57499-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57499-41:
(7*5)+(6*7)+(5*4)+(4*9)+(3*9)+(2*4)+(1*1)=169
169 % 10 = 9
So 57499-41-9 is a valid CAS Registry Number.

57499-41-9Downstream Products

57499-41-9Relevant articles and documents

Preparation and effects of 2,3-dehydrosilymarin, a promising and potent antioxidant and free radical scavenger

Tong, Shanshan,Chu, Chang,Wei, Yuan,Wang, Li,Gao, Xizhe,Xu, Ximing,Yu, Jiangnan

, p. 238 - 244 (2011)

Objectives Silymarin or silybin has been effectively used for treating liver diseases and acute liver injury partly due to its antioxidant activity. In this study, 2,3-dehydrosilymarin, a compound exhibiting remarkable antiradical/antioxidant activity, wa

STEREOCHEMISTRY OF SILYCHRISTIN MILD DEHYDROGENATION OF FLAVANONOLS

Zanarotti, Antonio

, p. 1585 - 1586 (2007/10/02)

3-Hydroxyflavanones can be quntitatively dehydrogenated by air in pyridine to 2,3-dehydro derivatives.The reaction has been performed on silychristin (1) in order to remove the chirality at the flavanonol ring and to allow the assignment of the stereochemistry of the stereochemistry of the dihydrobenzofuran ring as 2'R,3'S.

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