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J Nat Med ; 78(3): 537-546, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38517624

ABSTRACT

A phytochemical investigation of Kaempferia champasakensis rhizomes led to the isolation of a new 3,4-seco-isopimarane diterpene, kaempferiol A (1), and three new isopimarane diterpenes, kaempferiols B-D (2-4), together with six known isopimarane diterpenes (5-10). The structures of 1-4 were elucidated by extensive spectroscopic analyses, including HR-ESI-MS, UV, IR, and 1D and 2D NMR. The absolute configurations of 1, 3, and 4 were determined by ECD calculations, while that of 2 was established using the modified Mosher method. All isolated compounds were tested for cytotoxicity against three human cancer cell lines, lung cancer (A549), cervical cancer (HeLa), and breast cancer (MCF-7). Among them, 6 and 7 showed moderate cytotoxic activities against the three tested cell lines, with IC50 values ranging from 38.04 to 27.77 µM, respectively.


Subject(s)
Antineoplastic Agents, Phytogenic , Diterpenes , Zingiberaceae , Humans , Diterpenes/chemistry , Diterpenes/pharmacology , Diterpenes/isolation & purification , Zingiberaceae/chemistry , Vietnam , Molecular Structure , Antineoplastic Agents, Phytogenic/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Cell Line, Tumor , Rhizome/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacology
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