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Semi-synthetic studies of α-onocerin derivatives for cytotoxicity

Author:
Pongpamorn, Pornkanok, Wan-erlor, Sakuna, Ruchirawat, Somsak, Thasana, Nopporn
Source:
Phytochemistry letters 2018 v.23 pp. 106-115
ISSN:
1874-3900
Subject:
Lycopodium, acetylcholinesterase, acylation, cell lines, cytotoxicity, humans, lung neoplasms, lymphocytic leukemia, mass spectrometry, moieties, nuclear magnetic resonance spectroscopy, oxidation
Abstract:
Up to 0.064% of α-onocerin (1) was isolated from Lycopodium clavatum. Twenty-one of its derivatives, 18 being new, were semi-synthesized through acylation, reduction, oxidation, and various other reactions. Their molecular structures were confirmed by means of NMR spectroscopy and mass spectrometry. The derivatives were evaluated for their inhibitory activities against acetylcholinesterase (AChE) and four cancer cell lines: HuCCA-1 (human cholangiocarcinoma), A-549 (lung carcinoma), HepG2 (hepatocarcinoma), and MOLT-3 (acute lymphoblastic leukemia). Introduction of a hydroxyl group at C-2/C-20 on α-onocerin (1) enhanced the cytotoxic activity. Most notably, the α-onocerin oxime derivative (22) selectively and significantly exerted cytotoxic activity against only the HepG2 cancer cell line.
Agid:
5915529