Literature DB >> 11133101

Synthesis and structure-activity relationships of 3-cyano-4-(phenoxyanilino)quinolines as MEK (MAPKK) inhibitors.

N Zhang1, B Wu, D Powell, A Wissner, M B Floyd, E D Kovacs, L Toral-Barza, C Kohler.   

Abstract

A series of 3-cyano-4-(phenoxyanilino)cyanoquinolines has been prepared as MEK (MAP kinase kinase) inhibitors. The best activity is seen with alkoxy groups at both the 6- and 7-positions. The lead compounds show low nanomolar IC50's against MAP kinase kinase, and have potent inhibitory activity in tumor cells.

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Year:  2000        PMID: 11133101     DOI: 10.1016/s0960-894x(00)00580-1

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  4 in total

Review 1.  Small-molecule inhibitors of the ERK signaling pathway: Towards novel anticancer therapeutics.

Authors:  Jeremy L Yap; Shilpa Worlikar; Alexander D MacKerell; Paul Shapiro; Steven Fletcher
Journal:  ChemMedChem       Date:  2011-01-03       Impact factor: 3.466

Review 2.  Novel agents for the prevention of breast cancer: targeting transcription factors and signal transduction pathways.

Authors:  Qiang Shen; Powel H Brown
Journal:  J Mammary Gland Biol Neoplasia       Date:  2003-01       Impact factor: 2.673

3.  Synthesis, delivery, and molecular docking of fused quinolines as inhibitor of Hepatitis A virus 3C proteinase.

Authors:  Mehrnaz Rafiei Jorshari; Manouchehr Mamaghani; Parivash Jahanshahi
Journal:  Sci Rep       Date:  2021-09-23       Impact factor: 4.379

Review 4.  Quinoline-Based Molecules Targeting c-Met, EGF, and VEGF Receptors and the Proteins Involved in Related Carcinogenic Pathways.

Authors:  Annamaria Martorana; Gabriele La Monica; Antonino Lauria
Journal:  Molecules       Date:  2020-09-18       Impact factor: 4.411

  4 in total

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