Literature DB >> 14738403

Highly hydroxylated triterpenes from Salvia kronenburgii.

Gülaçti Topçu1, Zeynep Türkmen, Ayhan Ulubelen, Jennifer K Schilling, David G I Kingston.   

Abstract

The three new triterpenes (1-3) and five known triterpenes and a sterol were isolated from the acetone extract of a Turkish collection of Salvia kronenburgii. The structures of the new triterpenes were established as 1beta,2alpha-dihydroxy-3beta-acetoxy-11-oxours-12-ene (1), 2alpha,20beta-dihydroxy-3beta-acetoxyurs-9(11),12-diene (2), and 1beta,2alpha-dihydroxy-3beta-acetoxyurs-9(11),12-diene (3) on the basis of spectral analyses, including 1D and 2D NMR and mass spectroscopy. It is probable that compounds 2 and 3 are artifacts from dehydration of the corresponding allylic alcohols. 1beta,2alpha,3beta,11alpha-Tetrahydroxyurs-12-ene (5), the most abundant compound in the extract, was found to be highly cytotoxic to renal, non-small cell lung, and breast cancer cell lines.

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Year:  2004        PMID: 14738403     DOI: 10.1021/np030359b

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  A theoretical biogenesis overview of diterpenes isolated from Salvia microphylla.

Authors:  J Alejandro Posada-Salgado; Elihú Bautista; Gabriel Cuevas; Karina Martinez-Mayorga
Journal:  J Mol Model       Date:  2015-11-10       Impact factor: 1.810

  1 in total

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