Literature DB >> 8862035

Sesquiterpene O-naphthoquinones from the root bark of Ulmus davidiana.

J P Kim1, W G Kim, H Koshino, J Jung, I D Yoo.   

Abstract

Three new sesquiterpene ortho-naphthoquinones, davidianones A, B and C, together with four known compounds, mansonones E, F, H and I, were isolated from the root bark of Ulmus davidiana. On the basis of spectral data including pulse field gradient two-dimensional NMR spectroscopy, the structures of new compounds were established as 3-hydroxymethyl-6,9-dimethylnaphtho(1,8-b,c)pyran-7,8-dione, 6-methoxycarbonyl-3,9-dimethylnaphtho(1,8-b,c)pyran-7,8-dione, 6-dimethoxymethyl-3,9-dimethylnaphtho(1.8-b,c)pyran-7,8-d ion e, respectively. Their antioxidative activities were evaluated by a thiobarbituric acid method using rat liver microsomes, with mansonone F showing the greatest activity.

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Year:  1996        PMID: 8862035     DOI: 10.1016/0031-9422(96)00279-8

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  7 in total

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6.  Synthesis of Spirooxindole-O-Naphthoquinone-Tetrazolo[1,5-a]Pyrimidine Hybrids as Potential Anticancer Agents.

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Authors:  Yong Joo Park; Dong Min Kim; Mi Ho Jeong; Jae Sik Yu; Hae Min So; In Jae Bang; Ha Ryong Kim; Seung-Hwan Kwon; Ki Hyun Kim; Kyu Hyuck Chung
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  7 in total

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