期刊
FITOTERAPIA
卷 127, 期 -, 页码 146-150出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.fitote.2018.02.013
关键词
Plectranthus scutellarioides; Abietane-type diterpenoids; Cytotoxicity
资金
- Ministry of Education, Culture, Sports, Science and Technology, Japan (JSPS KAKENHI) [JP17K08333, JP15H05138, JP17H02203, JP17H05435]
- JSPS
- Kobayashi International Scholarship Foundation
- Grants-in-Aid for Scientific Research [15H05138] Funding Source: KAKEN
Three new diterpenoids, spiroscutelones A-C (1-3), along with known diterpene 4, were isolated from the leaves of Plectranthus scutellarioides. Their structures were established based on extensive spectroscopic analyses, including MS and NMR spectroscopy. Spiroscutelone A (1) represents the first example of an abietane-type terpenoid skeleton with a cyclobutane moiety linking the B and C rings. Of compounds 1-4, spiroscutelone B (2) exhibited the most potent cytotoxicities against the three tested human cancer lines [breast (MCF-7), pancreatic (PSN-1), and cervical (HeLa)) with IC50 values ranging from 17.9 mu M to 29.8 mu M and low cytotoxicity against a lung fibroblast (WI-38) normal cell line.
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