Literature DB >> 29689329

Sesquiterpenes and diterpenes with cytotoxic activities from the aerial parts of Carpesium humile.

Dong-Dong Xu1, Yuan Yan2, Chun-Xiao Jiang1, Jing-Jing Liang2, Hong-Fang Li2, Quan-Xiang Wu1, Ying Zhu3.   

Abstract

Carpesium humile Winkl is an endemic Chinese species and no previous phytochemical studies have been reported for this species. Two new germacranolides (1 and 2) and a new phytane diterpene (5), together with five known compounds (two sesquiterpenoids and three diterpenoids), were isolated from the aerial parts of C. humile. Their structures were elucidated on the basis of extensive spectroscopic analysis. The conformations and absolute configurations of 1 and 2 were established by combinative analysis of NMR, CD exciton chirality, and X-ray crystallography data. Four germacranolides (1-4) showed strong cytotoxic activities, with broad spectrum activities against six human cancer (HepG2, HeLa, HL60, SGC7901, Lewis, and MDA231) cell lines in vitro using MTT assay, with IC50 values from 3.09 to 7.71 μg/mL. Diterpenes (5, 6, and 8) also displayed good cytotoxic activities for selected cancer cell lines, with IC50 values in the range 5.46-8.08 μg/mL.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Asteraceae; Atractyligenin (CID: 3034426); Carpehumine A and B; Carpelipine A (PubChem CID: 100988384); Carpesium humile; Cytotoxicity; Dehydroabietic acid (CID: 94391); Divaricin B (101938007); Germacranolide; Phytane diterpene; α-Tocopherylquinone (CID: 15561184)

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Year:  2018        PMID: 29689329     DOI: 10.1016/j.fitote.2018.04.015

Source DB:  PubMed          Journal:  Fitoterapia        ISSN: 0367-326X            Impact factor:   2.882


  2 in total

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Journal:  Biomolecules       Date:  2020-05-06

Review 2.  Microbial Conversion of Toxic Resin Acids.

Authors:  Natalia A Luchnikova; Kseniya M Ivanova; Ekaterina V Tarasova; Victoria V Grishko; Irina B Ivshina
Journal:  Molecules       Date:  2019-11-14       Impact factor: 4.411

  2 in total

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