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DOI: 10.1055/s-0028-1112203
© Georg Thieme Verlag KG Stuttgart · New York
Novel Benzil and Isoflavone Derivatives from Millettia dielsiana
Publikationsverlauf
Received: June 2, 2008
Revised: October 6, 2008
Accepted: October 19, 2008
Publikationsdatum:
12. Januar 2009 (online)
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Abstract
The analysis of vine stem extract from Millettia dielsiana Harms yielded a novel benzil (1) and five new prenylated isoflavones (2 – 6) together with three known isoflavones (7 – 10) and one known flavone (11), and their structures were elucidated on the basis of chemical and spectral analysis. The absolute configuration of the 3′′,4′′-diols in 6 was determined by observing the CD induced after addition of dimolybdenum tetraacetate in DMSO solution (Snatzke’s method). Some isolates were tested for their anti-inflammatory and antithrombase activities and cytotoxicities. Compound 2, barbigerone, and genistein showed significant anti-inflammatory activity, with inhibitory ratios 59.1 %, 59.5 %, and 58.5 %, respectively, at 10 μM, while compound 4 exhibited moderate cytotoxicity.
Abbreviations
CC:column chromatography
PAF:platelet activating-factor
PMN:polymorphonuclear leukocyte
THF:tetrahydrofuran
Key words
Millettia dielsiana Harms - Leguminosae - benzil - prenylated isoflavones - millesianins A–E - Snatzke’s method
- Supporting Information for this article is available online at
- Supporting Information .
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Prof. Ruo-Yun Chen
Institute of Materia Medica
Chinese Academy of Medical Sciences and
Peking Union Medical College
1 Xian Nong Tan Street
Beijing 100050
People’s Republic of China
Telefon: +86-010-8316-1622
Fax: +86-010-6301-7757
eMail: rych@imm.ac.cn
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