1062639-48-8Relevant articles and documents
Design, synthesis, and biological evaluation of 3-(1-benzotriazole)-nor-β-lapachones as NQO1-directed antitumor agents
Wu, Li-Qiang,Ma, Xin,Liu, Zhao-Peng
, (2021)
A series of novel 3-(1-benzotriazole)-nor-β-lapachones 5a–5l were synthesized as the NQO1-targeted anticancer agents. Most of these compounds displayed good antiproliferative activity against the breast cancer MCF-7, lung cancer A549 and hepatocellular ca
On the search for potential antimycobacterial drugs: Synthesis of naphthoquinoidal, phenazinic and 1,2,3-triazolic compounds and evaluation against Mycobacterium tuberculosis
Jardim, Guilherme A. M.,Cruz, Eduardo H. G.,Valen?a, Wagner O.,Resende, Jarbas M.,Rodrigues, Bernardo L.,Ramos, Daniela F.,Oliveira, Ronaldo N.,Silva, Pedro E.A.,Da Silva Júnior, Eufranio N.
, p. 1013 - 1027 (2015/05/20)
Fifteen naphthoquinones, sixteen phenazines and fifteen aryl triazoles were synthesized and evaluated against Mycobacterium tuberculosis. Twenty five substances are reported here for the first time and, among all of the compounds evaluated, six presented MIC (minimal inhibitory concentration) values ≤ 6.25 μg mL-1. These substances are promising antimycobacterial prototypes.
A new approach for the synthesis of 3-substituted cytotoxic nor-β-lapachones
Cardoso, Mariana F. C.,Da Silva, Illana M. C. B.,Dos Santos Jr., Helve?cio M.,Rocha, David R.,Arau?jo, Ana Je?rsia,Pessoa, Claudia,De Moraes, Manoel O.,Lotufo, Leti?cia V. C.,De C. Da Silva, Fernando,Santos, Wilson C.,Ferreira, Vitor F.
, p. 12 - 16 (2013/05/08)
Several studies have demonstrated the cytotoxic potential of nor-β-lapachone derivative against cancer cells. Considering nor-β-lapachone as an important prototype, a set of new 3-substituted nor-β-lapachones was synthesized by a new synthetic route that involves the use of synthetic intermediate generated for coupling with several nucleophiles containing the carbohydrate and 2H-pyrazole substituent moieties. All the compounds were screened against four tumor cell lines. Two of the compounds showed moderate cytotoxicity, while the other compounds strongly inhibit all tested cancer cell lines.