Antiviral and antimicrobial nucleoside derivatives: structural features and mechanisms of action

AA Zenchenko, MS Drenichev, IA Il'Icheva… - Molecular biology, 2021 - Springer
The emergence of new viruses and resistant strains of pathogenic microorganisms has
become a powerful stimulus in the search for new drugs. Nucleosides are a promising class …

Prodrugs of phosphonates and phosphates: crossing the membrane barrier

AJ Wiemer, DF Wiemer - … Chemistry I: Asymmetric Synthesis and Bioactive …, 2015 - Springer
A substantial portion of metabolism involves transformation of phosphate esters, including
pathways leading to nucleotides and oligonucleotides, carbohydrates, isoprenoids and …

Overview of biologically active nucleoside phosphonates

E Groaz, S De Jonghe - Frontiers in Chemistry, 2021 - frontiersin.org
The use of the phosphonate motif featuring a carbon-phosphorous bond as bioisosteric
replacement of the labile P–O bond is widely recognized as an attractive structural concept …

Enzymatic transition states and drug design

VL Schramm - Chemical reviews, 2018 - ACS Publications
Transition state theory teaches that chemically stable mimics of enzymatic transition states
will bind tightly to their cognate enzymes. Kinetic isotope effects combined with …

Kinetic Characterization and Inhibition of Trypanosoma cruzi Hypoxanthine–Guanine Phosphoribosyltransferases

K Glockzin, D Kostomiris, YVT Minnow, K Suthagar… - Biochemistry, 2022 - ACS Publications
Chagas disease, caused by the parasitic protozoan Trypanosoma cruzi, affects over 8
million people worldwide. Current antiparasitic treatments for Chagas disease are ineffective …

Plasmodium purine metabolism and its inhibition by nucleoside and nucleotide analogues

T Cheviet, I Lefebvre-Tournier, S Wein… - Journal of Medicinal …, 2019 - ACS Publications
Malaria still affects around 200 million people and is responsible for more than 400,000
deaths per year, mostly children in subequatorial areas. This disease is caused by parasites …

Acyclic nucleoside phosphonates containing a second phosphonate group are potent inhibitors of 6-oxopurine phosphoribosyltransferases and have antimalarial …

DT Keough, P Spacek, D Hockova, T Tichy… - Journal of medicinal …, 2013 - ACS Publications
Acyclic nucleoside phosphonates (ANPs) that contain a 6-oxopurine base are good
inhibitors of the Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) 6-oxopurine …

Aza-acyclic Nucleoside Phosphonates Containing a Second Phosphonate Group As Inhibitors of the Human, Plasmodium falciparum and vivax 6-Oxopurine …

DT Keough, D Hockova, Z Janeba… - Journal of medicinal …, 2015 - ACS Publications
Hypoxanthine–guanine–[xanthine] phosphoribosyltransferase (HG [X] PRT) is considered
an important target for antimalarial chemotherapy as it is the only pathway for the synthesis …

A comprehensive review on bioactive fused heterocycles as purine-utilizing enzymes inhibitors

M Chauhan, R Kumar - Medicinal Chemistry Research, 2015 - Springer
Purine-utilizing enzymes (PUEs) are involved in the control of biological actions of nitrogen-
containing bases, purines and pyrimidines, by participating in their catabolism, and this has …

New approaches for the identification of drug targets in protozoan parasites

J Müller, A Hemphill - International review of cell and molecular biology, 2013 - Elsevier
Antiparasitic chemotherapy is an important issue for drug development. Traditionally, novel
compounds with antiprotozoan activities have been identified by screening of compound …