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DOI: 10.1055/s-0031-1280163
© Georg Thieme Verlag KG Stuttgart · New York
Clerodane Diterpenoids from Tinospora sagittata (Oliv.) Gagnep
Publication History
received April 22, 2011
revised June 30, 2011
accepted July 15, 2011
Publication Date:
27 September 2011 (online)
Abstract
Three new clerodane diterpene glycosides, tinospinosides A (1), B (2), and C (3) were isolated from the roots of Tinospora sagittata (Oliv.) Gagnep. Their structures were determined to be (2S,4aR,6aR,9R,10aS,10bS)-2-(3-furanyl)-9-(β-D-glucopyranosyloxy)-1,4,4a,5,6,6a,9,10,10a,10b-decahydro-6a,10b-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester (1), (2S,4aS,6aR,9R,10aR,10bS)-2-(3-furanyl)-9-(β-D-glucopyranosyloxy)-1,4,4a,5,6,6a,9,10,10a,10b-decahydro-4a-hydroxyl-6a,10b-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester (2) and (2S,4aR,6aR,9R,10aR,10bS)-2-(3-furanyl)-9-(β-D-glucopyranosyloxy)-1,4,4a,5,6,6a,9,10,10a,10b-decahydro-4a-hydroxyl-6a,10b-dimethyl-4-oxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester (3), by various spectroscopic analyses, chemical reactions, and computer-assisted calculations. The inhibitory activities of NO production by these compounds and their chemical derivatives in lipopolysaccharide and TNFγ-activated macrophage-like cell line J774.1 were tested. Tinospin A, 12-epi-tinospin A, tinospinoside B, and tinospinoside C showed inhibitory activities of NO production with the IC50 values of 162, 182, 290, and 218 µM, respectively.
Key words
Tinospora sagittata - Menispermaceae - clerodane diterpenes - nitric oxide
References
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Dr. Wei Li
Faculty of Pharmaceutical Sciences
Toho University
2-2-1 Myiama, Funabashi
Chiba 274-8510
Japan
Phone: +81 47 4 72 11 61
Fax: +81 47 4 72 14 04
Email: liwei@phar.toho-u.ac.jp