Ngampong KongkathipSuwaporn LuangkaminBoonsong KongkathipChak SangmaRonald GriggPalangpon KongsaereeSamran PrabpaiNarathip PradidpholSuratsawadee PiyaviriyagulPongpun SiripongKasetsart UniversityUniversity of LeedsMahidol UniversityNational Cancer Institute Thailand2018-07-242018-07-242004-08-26Journal of Medicinal Chemistry. Vol.47, No.18 (2004), 4427-4438002226232-s2.0-4143061295https://repository.li.mahidol.ac.th/handle/20.500.14594/21165Rhinacanthin-M, -N and -Q, natural products isolated from the medicinal plant Rhinacanthus nasutus, and 39 novel naphthoquinone esters have been synthesized in excellent yield by esterification of naphthoquinone-3-(propan- 3′-ols) with benzoic or naphthoic acids. Almost all the naphthoquinone esters that contain a C-3 hydroxy group showed significant cytotoxicities against KB, HeLa, and HepG2 cell lines. In contrast, ester derivatives lacking the C-3 hydroxy group were inactive to the cancer cell lines. Two methyl substituents on the C-2′ of propyl chain conferred more potent cytotoxicity than when there is only one or no methyl group. Naphthoate esters exhibited greater cytotoxicity than benzoate esters. Computer modeling has been done to obtain a first look at the mode of action in connection with these observations.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyPharmacology, Toxicology and PharmaceuticsArticleSCOPUS10.1021/jm030323g