Literature DB >> 22370472

Przewalskone: a cytotoxic adduct of a danshenol type terpenoid and an icetexane diterpenoid via hetero-Diels-Alder reaction from Salvia przewalskii.

Gang Xu1, Xing-Wei Yang, Chun-Yan Wu, Xiao-Nian Li, Jia Su, Xu Deng, Yan Li, Hong-Bo Qin, Li-Xin Yang, Qin-Shi Zhao.   

Abstract

Przewalskone (1), an unprecedented adduct of two different terpenoid units via a hetero-Diels-Alder cycloaddition, was isolated from the roots of Salvia przewalskii. The structure and absolute configurations were elucidated by extensive analysis of NMR spectra and crystal X-ray diffractions. Compound 1 exhibited significant cytotoxicities against five human cancer lines in vitro (IC(50) 0.69-2.35 μM). This journal is © The Royal Society of Chemistry 2012

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Year:  2012        PMID: 22370472     DOI: 10.1039/c2cc30405h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Tandem C-H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (-)-brussonol and (-)-przewalskine E.

Authors:  Zhi-Wei Jiao; Yong-Qiang Tu; Qing Zhang; Wen-Xing Liu; Shu-Yu Zhang; Shao-Hua Wang; Fu-Min Zhang; Sen Jiang
Journal:  Nat Commun       Date:  2015-06-17       Impact factor: 14.919

2.  Regioisomers Salviprolin A and B, Unprecedented Rosmarinic Acid Conjugated Dinorditerpenoids from Salvia przewalskii Maxim.

Authors:  Xiangdong Su; Yichuang Wu; Meifang Wu; Jielang Lu; Shujie Jia; Xin He; Shuna Liu; Yuyang Zhou; Hui Xing; Yongbo Xue
Journal:  Molecules       Date:  2021-11-18       Impact factor: 4.411

  2 in total

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