Literature DB >> 11140724

Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines.

S W Wright1, D L Hageman, L D McClure, A A Carlo, J L Treadway, A M Mathiowetz, J M Withka, P H Bauer.   

Abstract

Anilinoquinazolines currently of interest as inhibitors of tyrosine kinases have been found to be allosteric inhibitors of the enzyme fructose 1,6-bisphosphatase. These represent a new approach to inhibition of F16BPase and serve as leads for further drug design. Enzyme inhibition is achieved by binding at an unidentified allosteric site.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11140724     DOI: 10.1016/s0960-894x(00)00586-2

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


  2 in total

1.  Designing inhibitors against fructose 1,6-bisphosphatase: exploring natural products for novel inhibitor scaffolds.

Authors:  Sabrina Heng; Katharine M Harris; Evan R Kantrowitz
Journal:  Eur J Med Chem       Date:  2010-01-13       Impact factor: 6.514

2.  A library of novel allosteric inhibitors against fructose 1,6-bisphosphatase.

Authors:  Sabrina Heng; Kimberly R Gryncel; Evan R Kantrowitz
Journal:  Bioorg Med Chem       Date:  2009-04-19       Impact factor: 3.641

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.