Synthesis of transition state inhibitors for N-riboside hydrolases and transferases
- 1 February 1997
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 53 (8) , 2915-2930
- https://doi.org/10.1016/s0040-4020(96)01172-6
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Purine-specific Nucleoside N-Ribohydrolase from Trypanosoma brucei bruceiJournal of Biological Chemistry, 1996
- Mechanistic Diagnoses of N-Ribohydrolases and Purine Nucleoside PhosphorylaseJournal of the American Chemical Society, 1996
- Inosine−Uridine Nucleoside Hydrolase from Crithidia fasciculata. Genetic Characterization, Crystallization, and Identification of Histidine 241 as a Catalytic Site Residue,Biochemistry, 1996
- Design and Synthesis of D-Ribofuranoamidrazones as Inhibitors of Nucleoside Processing EnzymesSynlett, 1995
- A new class of C-nucleoside analogues. 1-(S)-aryl-1,4-dideoxy-1,4-imino-D-ribitols, transition state analogue inhibitors of nucleoside hydrolaseTetrahedron Letters, 1993
- Electronic nature of the transition state for nucleoside hydrolase. A blueprint for inhibitor designBiochemistry, 1993
- The Challenge of MalariaScience, 1992
- Transition-state analysis of nucleoside hydrolase from Crithidia fasciculataBiochemistry, 1991
- Purine and pyrimidine metabolism in the trypanosomatidaeMolecular and Biochemical Parasitology, 1984
- Partial purification and properties of a nucleoside hydrolase from CrithidiaArchives of Biochemistry and Biophysics, 1973