1593735-91-1Relevant articles and documents
Synthesis, β-haematin inhibition, and in vitro antimalarial testing of isocryptolepine analogues: SAR study of indolo[3,2-c]quinolines with various substituents at C2, C6, and N11
Wang, Ning,Wicht, Kathryn J.,Imai, Kento,Wang, Ming-Qi,Anh Ngoc, Tran,Kiguchi, Ryo,Kaiser, Marcel,Egan, Timothy J.,Inokuchi, Tsutomu
, p. 2629 - 2642 (2014/05/06)
A series of indolo[3,2-c]quinolines were synthesized by modifying the side chains of the ω-aminoalkylamines at the C6 position and introducing substituents at the C2 position, such as F, Cl, Br, Me, MeO and NO2, and a methyl group at the N11 po
