| Literature DB >> 29913194 |
Ningombam Swapana1, Takehiro Tominaga2, Abdelsamed I Elshamy3, Mahmoud A A Ibrahim4, Mohamed-Elamir F Hegazy5, Ch Brajakishor Singh6, Midori Suenaga2, Hiroshi Imagawa2, Masaaki Noji2, Akemi Umeyama7.
Abstract
A new unusual seco-isopimarane, kaemgalangol A (1) and 12 usual analogs (2-13) were isolated from the rhizomes of Kaempferia galanga (Family: Zingiberaceae). KaemgalangolA (1) represented a rarely isolated 9,10-seco-isopimarane skeleton. The chemical structures of the isolated compounds were mainlyinvestigated by spectroscopic techniques such as 1D, 2D NMR, and HRMS. The absolute configuration of 1-3 was studied by X-ray diffraction analysis as well as experimental and TDDFT-calculated electronic circular dichroism. Among the isolated diterpenoids, 5, 6 and 9 exhibited cytotoxic activity against HeLa (IC50 75.1, 74.2 and 76.5 μM, respectively) and HSC-2 (IC50 69.9, 53.3 and 58.2 μM, respectively) cancer cells.Entities:
Keywords: Absolute configuration; Cytotoxicity; Kaemgalangol A; Kaempferia galanga; Seco-isopimarane; Theoretical calculations; X-ray
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Year: 2018 PMID: 29913194 DOI: 10.1016/j.fitote.2018.06.010
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882