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Cytotoxic sesquiterpene lactones from Eupatorium kiirunense, a coastal plant of Taiwan.
J Nat Prod. 2005 May; 68(5):745-50.JN

Abstract

Phytochemical investigation of Eupatorium kiirunense has resulted in the isolation of eight new sesquiterpene lactones, constituted by five germacranolides, eupakirunsins A-E (1-5), and three heliangolides, eupaheliangolide A (6), 15-acetoxyheliangin (7), and 3-epi-heliangin (8), in addition to the known heliangin (9) and 8,10-epoxy-9-acetoxythymol angelate (10). The structures of the new compounds were established through detailed analysis of their spectroscopic data. Compounds 6, 8, and 9 exhibited cytotoxicity against human oral epidermoid (KB), cervical epitheloid (Hela), and liver (hepa59T/VGH) carcinoma cells.

Authors+Show Affiliations

Institute of Marine Resources, National Sun Yat-sen University, 70 Lien-Hai Road, Kaohsiung, Taiwan 80424, Republic of China.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15921421

Citation

Shen, Ya-Ching, et al. "Cytotoxic Sesquiterpene Lactones From Eupatorium Kiirunense, a Coastal Plant of Taiwan." Journal of Natural Products, vol. 68, no. 5, 2005, pp. 745-50.
Shen YC, Lo KL, Kuo YH, et al. Cytotoxic sesquiterpene lactones from Eupatorium kiirunense, a coastal plant of Taiwan. J Nat Prod. 2005;68(5):745-50.
Shen, Y. C., Lo, K. L., Kuo, Y. H., & Khalil, A. T. (2005). Cytotoxic sesquiterpene lactones from Eupatorium kiirunense, a coastal plant of Taiwan. Journal of Natural Products, 68(5), 745-50.
Shen YC, et al. Cytotoxic Sesquiterpene Lactones From Eupatorium Kiirunense, a Coastal Plant of Taiwan. J Nat Prod. 2005;68(5):745-50. PubMed PMID: 15921421.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cytotoxic sesquiterpene lactones from Eupatorium kiirunense, a coastal plant of Taiwan. AU - Shen,Ya-Ching, AU - Lo,Kuang-Liang, AU - Kuo,Yao Haur, AU - Khalil,Ashraf Taha, PY - 2005/6/1/pubmed PY - 2005/7/8/medline PY - 2005/6/1/entrez SP - 745 EP - 50 JF - Journal of natural products JO - J Nat Prod VL - 68 IS - 5 N2 - Phytochemical investigation of Eupatorium kiirunense has resulted in the isolation of eight new sesquiterpene lactones, constituted by five germacranolides, eupakirunsins A-E (1-5), and three heliangolides, eupaheliangolide A (6), 15-acetoxyheliangin (7), and 3-epi-heliangin (8), in addition to the known heliangin (9) and 8,10-epoxy-9-acetoxythymol angelate (10). The structures of the new compounds were established through detailed analysis of their spectroscopic data. Compounds 6, 8, and 9 exhibited cytotoxicity against human oral epidermoid (KB), cervical epitheloid (Hela), and liver (hepa59T/VGH) carcinoma cells. SN - 0163-3864 UR - https://www.unboundmedicine.com/medline/citation/15921421/Cytotoxic_sesquiterpene_lactones_from_Eupatorium_kiirunense_a_coastal_plant_of_Taiwan_ DB - PRIME DP - Unbound Medicine ER -