The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
24321832 |
38 |
Synthesis and evaluation of the antiparasitic activity of bis-(arylmethylidene) cycloalkanones. |
Universidade Federal De Minas Gerais |
21795044 |
14 |
Design, synthesis and biological evaluation of novel nitroaromatic compounds as potent glutathione reductase inhibitors. |
Batman University |
19447620 |
24 |
In vitro inhibition of human erythrocyte glutathione reductase by some new organic nitrates. |
Atat£Rk University |
17197182 |
26 |
High-throughput screening affords novel and selective trypanothione reductase inhibitors with anti-trypanosomal activity. |
Harvard Medical School |
16033259 |
7 |
Inhibitors of Trypanosoma cruzi trypanothione reductase revealed by virtual screening and parallel synthesis. |
Universit£T Heidelberg |
10956223 |
41 |
Use of an additional hydrophobic binding site, the Z site, in the rational drug design of a new class of stronger trypanothione reductase inhibitor, quaternary alkylammonium phenothiazines. |
University of Manchester |
8893834 |
30 |
Synthesis, activity, and molecular modeling of a new series of tricyclic pyridazinones as selective aldose reductase inhibitors. |
TBA |
11055357 |
10 |
Optimising inhibitors of trypanothione reductase using solid-phase chemistry. |
University of Southamton |
21851087 |
88 |
Dihydroquinazolines as a novel class of Trypanosoma brucei trypanothione reductase inhibitors: discovery, synthesis, and characterization of their binding mode by protein crystallography. |
University of Dundee |
19015351 |
9 |
Compounds structurally related to ellagic acid show improved antiplasmodial activity. |
Justus-Liebig-University |
19761212 |
76 |
Structure mechanism insights and the role of nitric oxide donation guide the development of oxadiazole-2-oxides as therapeutic agents against schistosomiasis. |
National Human Genome Research Institute |
17967916 |
4 |
Interactions of methylene blue with human disulfide reductases and their orthologues from Plasmodium falciparum. |
Biochemie-Zentrum Der Universit£T Heidelberg |
17194585 |
3 |
Discovery of 2-iminobenzimidazoles as a new class of trypanothione reductase inhibitor by high-throughput screening. |
Institute of Medical Research |
16616495 |
28 |
Novel alkylpolyaminoguanidines and alkylpolyaminobiguanides with potent antitrypanosomal activity. |
Wayne State University |
16279799 |
5 |
Irreversible inactivation of trypanothione reductase by unsaturated Mannich bases: a divinyl ketone as key intermediate. |
Biochemie-Zentrum Der UniversitäT Heidelberg |
16250662 |
2 |
Synthesis of 5-nitro-2-furancarbohydrazides and their cis-diamminedichloroplatinum complexes as bitopic and irreversible human thioredoxin reductase inhibitors. |
Umr 8525 Cnrs-Université |
15537352 |
15 |
5-substituted tetrazoles as bioisosteres of carboxylic acids. Bioisosterism and mechanistic studies on glutathione reductase inhibitors as antimalarials. |
Université |
11708927 |
8 |
A prodrug form of a Plasmodium falciparum glutathione reductase inhibitor conjugated with a 4-anilinoquinoline. |
Umr 8525 Cnrs-Université |
11551771 |
16 |
Antiprotozoal and cytotoxicity evaluation of sulfonamide and urea analogues of quinacrine. |
University of Cape Town |
8691487 |
21 |
Inhibition of human glutathione reductase by 10-arylisoalloxazines: crystalline, kinetic, and electrochemical studies. |
Institut FüR Biochemie Ii Der UniversitäT |