Literature DB >> 7772306

Diterpenes from Solidago rugosa.

T Lu1, D Vargas, S G Franzblau, N H Fischer.   

Abstract

Investigation of the roots and aerial parts of Solidago rugosa afforded the known diterpenes kolavenol, hardwickiic acid, (-)-kaur-16-en-19-oic acid, (+)-manool, (+)-3 beta-hydroxymanool, manoyl oxide and ent-abietic acid. In addition, the new labdane diterpene (+)-18-tigloyloxymanool and four new ent-abietanes were obtained. The structures of all known and new compounds were elucidated by spectroscopic methods, especially high-field 1H and 13C NMR, and inverse 1H-13C-correlation techniques, as well as chemical transformations. Six diterpenes were tested against Mycobacterium tuberculosis and M. avium, but showed no significant activities with minimum inhibitory concentrations of > 100 micrograms ml-1.

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Year:  1995        PMID: 7772306     DOI: 10.1016/0031-9422(94)00625-4

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


  1 in total

1.  ORGANIC SYNTHESIS. Response to Comment on "Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence".

Authors:  Zhiqiang Ma; Xiaolei Wang; Xiao Wang; Rodrigo A Rodriguez; Curtis E Moore; Shuanhu Gao; Xianghui Tan; Yuyong Ma; Arnold L Rheingold; Phil S Baran; Chuo Chen
Journal:  Science       Date:  2015-07-09       Impact factor: 47.728

  1 in total

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