34123-66-5Relevant articles and documents
Lamellarin-inspired potent topoisomerase I inhibitors with the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one scaffold
Fukuda, Tsutomu,Nanjo, Yusuke,Fujimoto, Masahiro,Yoshida, Kenyu,Natsui, Yuko,Ishibashi, Fumito,Okazaki, Fumiyasu,To, Hideto,Iwao, Masatomo
, p. 265 - 277 (2019/01/04)
A new class of topoisomerase I inhibitors containing the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one (abbreviated as BBPI) ring system have been developed based on structure-activity relationship studies of the cytotoxic marine alkaloid la
A 2-phenyl-substituted-3-benzoyl-substituted indole preparation method
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Paragraph 0035-0037, (2017/05/13)
The invention relates to a preparing method of 2-(phenyl-substituted)-3-(benzoyl-substituted)indole, and particularly discloses a preparing method of 2-(3'-hydroxy-4'-methoxyphenyl)-3-(3'',4'',5''-triethoxybenzoyl)-6-methoxyindole (OXi8006). The structure formula of the OXi8006 is shown in the specification. The OXi8006 can generate good antitumor activity (IC50=1.1 muM) by inhibiting tubulin polymerization and is an important clinical candidate for treating tumor. Synthesis of the OXi8006 by the method has characteristics of simple conditions, easy operation, short reaction steps and high total yield.
Isolation, structure characterization, and synthesis of stabilized 1,2,3,4-tetrahydroisoquinoline marine natural product from potassium cyanide pretreated Thai tunicate, Ecteinascidia thurstoni
Kimura, Shinya,Pangkruang, Waree,Yokoya, Masashi,Honda, Amane,Puthongking, Ploenthip,Suwanborirux, Khanit,Saito, Naoki
, p. 363 - 375 (2014/01/17)
A simple 1,2,3,4-tetrahydroisoquinoline marine natural product (2a) together with two known compounds (3 and 4) was isolated from a low polar fraction of the crude extract of KCN pretreated Thai tunicate Ecteinascidia thurstoni. The structure of 2a was de