Subscribe to RSS
DOI: 10.1055/s-0028-1112202
© Georg Thieme Verlag KG Stuttgart · New York
Wittiorumins A – F, Antioxidant Diels-Alder-Type Adducts from Morus wittiorum
Publication History
Received: June 30, 2008
Revised: October 8, 2008
Accepted: October 19, 2008
Publication Date:
09 January 2009 (online)
Abstract
Six new Diels-Alder-type adducts, wittiorumins A-F (1 – 6) along with the three known compounds chalcomoracin (7), mulberrofuran J (8), and mongolicin F (9), were isolated from the stem bark of Morus wittiorum. Their structures including their absolute configurations were determined on the basis of spectroscopic analysis and chemical methods. Some of the isolated compounds (1 – 4) were assayed for their antioxidant activities, among which compounds 1 – 3 were active as antioxidants, with inhibitory ratios of 73.0 %, 82.0 %, and 82.0 %, respectively, at a concentration of 10 – 5 M.
Key words
Morus wittiorum - Moraceae - Diels-Alder-type adducts - flavonoid - antioxidant activities
References
- 1 Sun S G, Chen R Y, Yu D Q. Structures of two new benzofuran derivatives from the bark of mulberry tree. J Asian Nat Prod Res. 2001; 3 253-9
- 2 Lu H, Liu G T. Effect of dibenzocyclooctene lignans isolated from Fructus schizandrae on lipid peroxidation and antioxidative enzyme activities. Chem Biol Interact. 1991; 78 77-84
- 3 Hano Y, Suzuki S, Kohno H, Nomura T. Absolute configuration of kuwanon L, a natural Diels-Alder type adduct from the Morus root bark. Heterocycles. 1988; 27 75-81
- 4 Hano Y, Suzuki S, Nomura T, Iitaka Y. Absolute configuration of natural Diels-Alder type adducts from the Morus root bark. Heterocycles. 1988; 27 2315-24
- 5 Gaffield W. Circular dichroism, optical rotatory dispersion and absolute configuration of flavanones, 3-hydroxyflavanones and their glycosides. Tetrahedron. 1970; 26 4093-108
- 6 Takasugi M, Nagao S, Masamune T, Shirata A, Takahashi K. Chalcomoracin, a natural Diels-Alder adduct from diseased mulberry. Chem Lett. 1980; 33 1573-6
- 7 Kang J, Chen R Y, Yu D Q. Five new Diels-Alder type adducts from the stem and root bark of Morus mongolica. . Planta Med. 2006; 72 52-9
- 8 Hirakura K, Hano Y, Fukai T, Nomura T, Vzawa J, Fukushima K. Structures of three new natural Diels-Alder type adducts, kuwanons P and X, and mulberrofuran J, from the cultivated mulberry tree (Morus Ihou Koidz). Chem Pharm Bull. 1985; 33 1088-96
- 9 Fukai T, Hano Y, Hirakura K, Nomura T, Uzawa J. Structures of a novel 2-arylbenzofuran derivative and two flavone derivatives from the cultivated mulberry tree (Morus lhou Koidz.). Chem Pharm Bull. 1985; 33 4288-95
Prof. Ruo-Yun Chen
Institute of Materia Medica
Chinese Academy of Medical Sciences & Peking Union Medical College
No.1 Xian Nong Tan Street
Xuan Wu District
Beijing 100050
People’s Republic of China
Phone: +86-010-83161622
Fax: +86-010-63017757
Email: ruoyunchen@hotmail.com