Archiv der Pharmazie

Synthesis and Biological Evaluation of 4??Phenoxy??6, 7??disubstituted Quinolines Possessing Semicarbazone Scaffolds as Selective c??Met Inhibitors

B Qi, H Tao, D Wu, J Bai, Y Shi, P Gong

Index: Qi, Baohui; Tao, Haiyan; Wu, Di; Bai, Jinying; Shi, Yandan; Gong, Ping Archiv der Pharmazie, 2013 , vol. 346, # 8 p. 596 - 609

Full Text: HTML

Citation Number: 9

Abstract

ABSTRACT Novel quinoline derivatives bearing acyclic semicarbazones were prepared and their chemical structures as well as the relative stereochemistry were confirmed. All the synthesized compounds were evaluated for their c-Met kinase inhibitory activity and their cytotoxicity against the cell lines HT-29, MKN-45, and MDA-MB-231 in vitro. Several potent compounds were further evaluated against A549 cells. Most compounds displayed ...

Related Articles:

A series of α-heterocyclic carboxaldehyde thiosemicarbazones inhibit topoisomerase IIα catalytic activity

[Huang, He; Chen, Qin; Ku, Xin; Meng, Linghua; Lin, Liping; Wang, Xiang; Zhu, Caihua; Wang, Yi; Chen, Zhi; Li, Ming; Jiang, Hualiang; Chen, Kaixian; Ding, Jian; Liu, Hong Journal of Medicinal Chemistry, 2010 , vol. 53, # 8 p. 3048 - 3064]

More Articles...