110684-46-3Relevant academic research and scientific papers
Diverse C-6 substituted 4-methyl-2-(2-, 3- and 4-pyridinyl)quinolines: synthesis, in vitro anticancer evaluation and in silico studies
Kouznetsov, Vladimir V.,Robles-Castellanos, Mayra L.,Sojo, Felipe,Rojas-Ruiz, Fernando A.,Arvelo, Francisco
, p. 551 - 561 (2017)
A series of twelve 4-methyl-2-(2-, 3- and 4-pyridinyl)quinolines 7–9 was synthesized using modified Kametani reaction protocol and their in vitro cytotoxicity was tested against human cancer cell lines MCF-7, SKBR-3, PC3, HeLa, comparing with human dermis
Synthesis, molecular docking study, and cytotoxic activity of 3,4-diaryl-5-(4-pyridinyl)-1,2,4-oxadiazole
Zareian, Bita,Ghadbeighi, Sajad,Amirhamzeh, Amirali,Ostad, Seyed N.,Shafiee, Abbas,Amini, Mohsen
, p. 394 - 401 (2016/07/06)
Background: Triaryl oxadiazoles have been proven to be useful agents against various types of cancer cell lines. Nevertheless, their mechanism of action is not fully understood. Objective: Synthesis and cytotoxic activity of a new group of triaryl oxadiaz
