Xanthanolides, germacranolides, and other constituents from Carpesium longifolium.J Nat Prod. 2003 Dec; 66(12):1554-7.JN
Abstract
Three new xanthanolides, 1-3, along with nine known compounds, were isolated from the aerial parts of Carpesium longifolium. The structures of the new compounds were elucidated as 1beta,4beta-epoxy-5beta-hydroxy-10alphaH-xantha-11(13)-en-12,8beta-olide (1), 1beta,4beta,4alpha,5beta-diepoxy-10alphaH,11alphaH-xantha-12,8beta-olide (2), and 4-acetoxy-1beta,5beta-epoxy-10alphaH-xantha-11(13)-en-12,8beta-olide (3) by spectroscopic methods including IR, EIMS, HRESIMS, and 1D and 2D NMR experiments. Parthenolide and michelenolide exhibited significant cytotoxic activity against cultured SMMC-7721 (human hepatoma) and HO-8910 (human ovarian carcinoma) cells.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
14695795
Citation
Yang, Chao, et al. "Xanthanolides, Germacranolides, and Other Constituents From Carpesium Longifolium." Journal of Natural Products, vol. 66, no. 12, 2003, pp. 1554-7.
Yang C, Yuan C, Jia Z. Xanthanolides, germacranolides, and other constituents from Carpesium longifolium. J Nat Prod. 2003;66(12):1554-7.
Yang, C., Yuan, C., & Jia, Z. (2003). Xanthanolides, germacranolides, and other constituents from Carpesium longifolium. Journal of Natural Products, 66(12), 1554-7.
Yang C, Yuan C, Jia Z. Xanthanolides, Germacranolides, and Other Constituents From Carpesium Longifolium. J Nat Prod. 2003;66(12):1554-7. PubMed PMID: 14695795.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Xanthanolides, germacranolides, and other constituents from Carpesium longifolium.
AU - Yang,Chao,
AU - Yuan,Chengshan,
AU - Jia,Zhongjian,
PY - 2003/12/30/pubmed
PY - 2004/3/26/medline
PY - 2003/12/30/entrez
SP - 1554
EP - 7
JF - Journal of natural products
JO - J Nat Prod
VL - 66
IS - 12
N2 - Three new xanthanolides, 1-3, along with nine known compounds, were isolated from the aerial parts of Carpesium longifolium. The structures of the new compounds were elucidated as 1beta,4beta-epoxy-5beta-hydroxy-10alphaH-xantha-11(13)-en-12,8beta-olide (1), 1beta,4beta,4alpha,5beta-diepoxy-10alphaH,11alphaH-xantha-12,8beta-olide (2), and 4-acetoxy-1beta,5beta-epoxy-10alphaH-xantha-11(13)-en-12,8beta-olide (3) by spectroscopic methods including IR, EIMS, HRESIMS, and 1D and 2D NMR experiments. Parthenolide and michelenolide exhibited significant cytotoxic activity against cultured SMMC-7721 (human hepatoma) and HO-8910 (human ovarian carcinoma) cells.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/14695795/Xanthanolides_germacranolides_and_other_constituents_from_Carpesium_longifolium_
DB - PRIME
DP - Unbound Medicine
ER -