875-41-2Relevant articles and documents
Synthesis and evaluation of antitumour activities of novel fused tri-And tetracyclic uracil derivatives
Elkalyoubi, Samar,Fayed, Eman
, p. 771 - 777 (2017/01/03)
Simple one-pot syntheses of indenopyrrolopyrimidines and indolopyrrolopyrimidines were achieved via the cyclocondensation of 6-Aminouracils and, respectively, ninhydrin and isatin in the presence of catalytic amounts of glacial acetic acid. Similarly, 5,6-diaminouracil derivatives were used as starting materials for the synthesis of indenopteridines and indolopteridines via their reaction with ninhydrin and isatin, respectively. The synthesised compounds were evaluated for antitumour activity against a human hepatocellular carcinoma cell line (HepG2), some showing antitumour activity comparable with 5-fluorouracil and imatinib.
Isolation, synthesis, and biological activity of aphrocallistin, an adenine-substituted bromotyramine metabolite from the hexactinellida sponge Aphrocallistes beatrix
Wright, Amy E.,Roth, Gregory P.,Hoffman, Jennifer K.,Divlianska, Daniela B.,Pechter, Diana,Sennett, Susan H.,Guzman, Esther A.,Linley, Patricia,McCarthy, Peter J.,Pitts, Tara P.,Pomponi, Shirley A.,Reed, John K.
experimental part, p. 1178 - 1183 (2011/02/28)
A new adenine-substituted bromotyrosine-derived metabolite designated as aphrocallistin (1) has been isolated from the deep-water Hexactinellida sponge Aphrocallistes beatrix. Its structure was elucidated on the basis of spectral data and confirmed throug