150059-96-4Relevant articles and documents
Structure-based design, synthesis and biological testing of etoposide analog epipodophyllotoxin-N-mustard hybrid compounds designed to covalently bind to topoisomerase II and DNA
Yadav, Arun A.,Wu, Xing,Patel, Daywin,Yalowich, Jack C.,Hasinoff, Brian B.
, p. 5935 - 5949 (2014)
Drugs that target DNA topoisomerase II isoforms and alkylate DNA represent two mechanistically distinct and clinically important classes of anticancer drugs. Guided by molecular modeling and docking a series of etoposide analog epipodophyllotoxin-N-mustar
Structure-based design, synthesis and biological testing of piperazine-linked bis-epipodophyllotoxin etoposide analogs
Yadav, Arun A.,Chee, Gaik-Lean,Wu, Xing,Patel, Daywin,Yalowich, Jack C.,Hasinoff, Brian B.
, p. 3542 - 3551 (2015)
Drugs that target DNA topoisomerase II, such as the epipodophyllotoxin etoposide, are a clinically important class of anticancer agents. A recently published X-ray structure of a ternary complex of etoposide, cleaved DNA and topoisomerase IIβ showed that
Design, synthesis and potent cytotoxic activity of novel podophyllotoxin derivatives
Li, Wen-Qun,Wang, Xu-Li,Qian, Keduo,Liu, Ying-Qian,Wang, Chih-Ya,Yang, Liu,Tian, Jin,Morris-Natschke, Susan L.,Zhou, Xing-Wen,Lee, Kuo-Hsiung
, p. 2363 - 2369 (2013/05/21)
Twenty new acyl thiourea derivatives of podophyllotoxin and 4′-demethylepipodophyllotoxin were prepared and screened for their cytotoxicity against four human tumor cell lines, A-549, DU-145, KB, and KBvin. With IC50 values of 0.098-1.13 μM, co