| Literature DB >> 11378365 |
N Zhang1, B Wu, N Eudy, Y Wang, F Ye, D Powell, A Wissner, L R Feldberg, S C Kim, R Mallon, E D Kovacs, L Toral-Barza, C A Kohler.
Abstract
A series of 4-anilino-3-cyano-6,7-dialkoxyquinolines with different substituents attached to the 4-anilino group has been prepared that are potent MEK (MAP kinase kinase) inhibitors. The best activity is obtained when a phenyl or a thienyl group is attached to the para-position of the aniline through a hydrophobic linker, such as an oxygen, a sulfur, or a methylene group. The most active compounds show low nanomolar IC(50)'s against MEK (MAP kinase kinase), and have potent growth inhibitory activity in LoVo cells (human colon tumor line).Entities:
Mesh:
Substances:
Year: 2001 PMID: 11378365 DOI: 10.1016/s0960-894x(01)00238-4
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823