4.4 Article

Structure-Activity Relationship for (+)-Taxifolin Isolated from Silymarin as an Inhibitor of Amyloid β Aggregation

Journal

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Volume 77, Issue 5, Pages 1100-1103

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1271/bbb.120925

Keywords

Alzheimer's disease; amyloid beta; aggregation; (+)-taxifolin; silymarin

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [21248015, 22603006, 22.4068]
  2. Asahi Group Foundation
  3. Kato Memorial Bioscience Foundation
  4. Grants-in-Aid for Scientific Research [21248015, 22603006] Funding Source: KAKEN

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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 beta-protein. Structure-activity relationship studies revealed the 3',4'-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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