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Inhibition of human aromatase by mammalian lignans and isoflavonoid phytoestrogens

✍ Scribed by Adlercreutz, Herman; Bannwart, Christoph; Wähälä, Kristiina; Mäkelä, Taru; Brunow, Gösta; Hase, Tapio; Arosemena, P.J.; Kellis, J.T.; Vickery, Larry E.

Book ID
123378392
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
603 KB
Volume
44
Category
Article
ISSN
0960-0760

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Site. -Depending on the reaction time, indan-1-ones (III) and inden-1-ones (V) are prepared. They are further used to study the active binding site of human aromatase inhibitors. Two compounds (Vb) and (Vc) are good inhibitors of human aromatase whereas they weakly inhibit the equine enzyme.