Structures of Two Natural Hypotensive Diels-Alder Type Adducts, Mulberrofurans F and G, from the Cultivated Mulberry Tree (Morus Ihou Koidz.)

82Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Two novel 2-arylbenzofuran derivatives named mulberrofurans F and G (= albanol A), as well as albanol B (3), were isolated from the ethyl acetate extract of the root bark of cultivated mulberry tree (Japanese name “Roso,” a cultivated variety of Morus Ihou Koidz.).The structures of mulberrofurans F and G were shown to be 1 and 2, respectively, on the basis of spectral and chemical evidence. Mulberrofurans F (1) and G (2) were derived from chalcomoracin (4) and mulberrofuran C (5), respectively, by photocyclization in acidic solution. The compounds (1, 2, and 3) are optically active and can be regarded biogenetically as variations of Diels-Alder type adducts of chalcone derivatives and a dehydroprenyl-2-arylbenzofuran derivative. Intravenous injection of mulberrofuran F (1), as well as G (2), caused a marked depressor effect in rabbit. © 1985, The Pharmaceutical Society of Japan. All rights reserved.

Cite

CITATION STYLE

APA

Fukai, T., Hano, Y., Hirakura, K., Nomura, T., Uzawa, J., & Fukushima, K. (1985). Structures of Two Natural Hypotensive Diels-Alder Type Adducts, Mulberrofurans F and G, from the Cultivated Mulberry Tree (Morus Ihou Koidz.). Chemical and Pharmaceutical Bulletin, 33(8), 3195–3204. https://doi.org/10.1248/cpb.33.3195

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free