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(2R,3R)-3,5,3'-trihydroxy-7,4'-dimethoxyflavanone is a complex organic compound belonging to the flavanone class, which is a subgroup of flavonoids. Flavonoids are a diverse group of naturally occurring bioactive compounds found in plants, known for their antioxidant, anti-inflammatory, and anticancer properties. This specific flavanone is characterized by its chiral centers at the 2 and 3 positions, with the R configuration, and possesses three hydroxyl groups at the 3, 5, and 3' positions, along with two methoxy groups at the 7 and 4' positions. These structural features contribute to its potential biological activities and interactions with various enzymes and receptors in the body. The compound's stereochemistry and functional groups make it an interesting target for further research in the field of natural products chemistry and pharmacology.

78128-76-4

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78128-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78128-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78128-76:
(7*7)+(6*8)+(5*1)+(4*2)+(3*8)+(2*7)+(1*6)=154
154 % 10 = 4
So 78128-76-4 is a valid CAS Registry Number.

78128-76-4Downstream Products

78128-76-4Relevant academic research and scientific papers

Structure-activity relationship for (+)-taxifolin isolated from silymarin as an inhibitor of amyloid β aggregation

Sato, Mizuho,Murakami, Kazuma,Uno, Mayumi,Ikubo, Haruko,Nakagawa, Yu,Katayama, Sumie,Akagi, Ken-Ichi,Irie, Kazuhiro

, p. 1100 - 1103 (2013)

Silymarin, the seed extract of Silybium marianum, has preventive effects against Alzheimer's disease-like pathogenesis in vivo. We isolated (+)-taxifolin (4) from silymarin as an inhibitor of aggregation of the 42- residue amyloid -protein. Structure-activity relationship studies revealed the 30,40-dihydroxyl groups to be critical to the anti-aggregative ability, whereas the 7-hydroxyl group and the stereochemistry at positions 2 and 3 were not important.

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