Design, synthesis, and enzymatic evaluation of multisubstrate analogue inhibitors of Escherichia coli thymidine phosphorylase.
A series of acyclic phosphonate derivatives of thymine has been synthesized and tested as multisubstrate analogue inhibitors of Escherichia coli thymidine phosphorylase. The compounds synthesized include 1-(phosphonoalkyl)thymines with six to nine methylenes (1-4, respectively); 1-[(Z)-4-phosphonome...
Main Authors: | Esteban-Gamboa, A, Balzarini, J, Esnouf, R, De Clercq, E, Camarasa, M, Pérez-Pérez, M |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2000
|
Similar Items
-
Kinetic analysis of novel multisubstrate analogue inhibitors of thymidine phosphorylase.
by: Balzarini, J, et al.
Published: (2000) -
7-Deazaxanthine, a novel prototype inhibitor of thymidine phosphorylase.
by: Balzarini, J, et al.
Published: (1998) -
Lack of susceptibility of bicyclic nucleoside analogs, highly potent inhibitors of varicella-zoster virus, to the catabolic action of thymidine phosphorylase and dihydropyrimidine dehydrogenase.
by: Balzarini, J, et al.
Published: (2002) -
The A167Y mutation converts the herpes simplex virus type 1 thymidine kinase into a guanosine analogue kinase.
by: Balzarini, J, et al.
Published: (2002) -
Structural basis for non-competitive product inhibition in human thymidine phosphorylase: implications for drug design.
by: El Omari, K, et al.
Published: (2006)