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Cytotoxic 8,9-seco-ent-kaurane diterpenoids from Croton kongensis.
- Source :
-
Journal of Asian natural products research [J Asian Nat Prod Res] 2018 Oct; Vol. 20 (10), pp. 920-927. Date of Electronic Publication: 2017 Sep 12. - Publication Year :
- 2018
-
Abstract
- Chemical study on the ethanolic extract generated from the aerial parts of Croton kongensis led to the isolation of three new 8,9-seco-ent-kaurane diterpenoids, kongeniods A‒C (1‒3), together with seven known analogs (4-10). The structures of these compounds were assigned by spectroscopic data analysis. The vitro cytotoxic tests showed that compounds 1-3 exhibited strong activities against HL-60 cell lines with IC <subscript>50</subscript> values of 0.47, 0.58, and 1.27 μM, respectively.
- Subjects :
- Antineoplastic Agents, Phytogenic chemistry
Antineoplastic Agents, Phytogenic pharmacology
Diterpenes, Kaurane chemistry
Diterpenes, Kaurane pharmacology
HL-60 Cells
Humans
Magnetic Resonance Spectroscopy
Plant Extracts analysis
Antineoplastic Agents, Phytogenic isolation & purification
Croton chemistry
Diterpenes, Kaurane isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1477-2213
- Volume :
- 20
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Journal of Asian natural products research
- Publication Type :
- Academic Journal
- Accession number :
- 28895443
- Full Text :
- https://doi.org/10.1080/10286020.2017.1373100