37 articles for thisTarget
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A Novel Pyrazolopyridine with in Vivo Activity in Plasmodium berghei- and Plasmodium falciparum-Infected Mouse Models from Structure-Activity Relationship Studies around the Core of Recently Identified Antimalarial Imidazopyridazines.

University of Cape Town
Structure-Activity Relationship Studies of Orally Active Antimalarial 2,4-Diamino-thienopyrimidines.

University of Cape Town
Medicinal chemistry optimization of antiplasmodial imidazopyridazine hits from high throughput screening of a softfocus kinase library: part 2.

University of Cape Town
Synthesis and in vitro and in vivo pharmacological evaluation of new 4-aminoquinoline-based compounds.

University of Cape Town
Tetrazole-based deoxyamodiaquines: synthesis, ADME/PK profiling and pharmacological evaluation as potential antimalarial agents.

University of Cape Town
Synthesis, antimalarial and antitubercular activity of acetylenic chalcones.

University of Cape Town
Structure-activity relationship studies of orally active antimalarial 3,5-substituted 2-aminopyridines.

University of Cape Town
3,5-Diaryl-2-aminopyridines as a novel class of orally active antimalarials demonstrating single dose cure in mice and clinical candidate potential.

University of Cape Town
Novel orally active antimalarial thiazoles.

University of Cape Town
Quinoline antimalarials containing a dibemethin group are active against chloroquinone-resistant Plasmodium falciparum and inhibit chloroquine transport via the P. falciparum chloroquine-resistance transporter (PfCRT).

University of Cape Town
Conjugates of plumbagin and phenyl-2-amino-1-thioglucoside inhibit MshB, a deacetylase involved in the biosynthesis of mycothiol.

University of Cape Town
hERG,

University of Cape Town
Novel 3-Trifluoromethyl-1,2,4-oxadiazole Analogues of Astemizole with Multi-stage Antiplasmodium Activity and

University of Cape Town
Synthesis of novel keto-ACE analogues as domain-selective angiotensin I-converting enzyme inhibitors.

University of Cape Town
Synthesis and molecular modeling of a lisinopril-tryptophan analogue inhibitor of angiotensin I-converting enzyme.

University of Cape Town
Spiropyrimidinetrione DNA Gyrase Inhibitors with Potent and Selective Antituberculosis Activity.

University of Cape Town
Probing the Requirements for Dual Angiotensin-Converting Enzyme C-Domain Selective/Neprilysin Inhibition.

University of Cape Town
Benzoheterocyclic Oxime Carbamates Active against

University of Cape Town
Structure-Activity Relationship Studies Reveal New Astemizole Analogues Active against

University of Cape Town
Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain.

University of Cape Town
Chemotherapy for human schistosomiasis: how far have we come? What's new? Where do we go from here?

University of Cape Town
Identification and Profiling of a Novel Diazaspiro[3.4]octane Chemical Series Active against Multiple Stages of the Human Malaria Parasite

University of Cape Town
Identification of a Potential Antimalarial Drug Candidate from a Series of 2-Aminopyrazines by Optimization of Aqueous Solubility and Potency across the Parasite Life Cycle.

University of Cape Town
Antitubercular 2-Pyrazolylpyrimidinones: Structure-Activity Relationship and Mode-of-Action Studies.

University of Cape Town
Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and

University of Cape Town
Antiprotozoal and cytotoxicity evaluation of sulfonamide and urea analogues of quinacrine.

University of Cape Town
Structure-Activity Relationship Studies and Plasmodium Life Cycle Profiling Identifies Pan-Active N-Aryl-3-trifluoromethyl Pyrido[1,2- a]benzimidazoles Which Are Efficacious in an in Vivo Mouse Model of Malaria.

University of Cape Town
Antimalarial Lead-Optimization Studies on a 2,6-Imidazopyridine Series within a Constrained Chemical Space To Circumvent Atypical Dose-Response Curves against Multidrug Resistant Parasite Strains.

University of Cape Town
Structure-activity-relationship studies around the 2-amino group and pyridine core of antimalarial 3,5-diarylaminopyridines lead to a novel series of pyrazine analogues with oral in vivo activity.

University of Cape Town
2,4-Diaminothienopyrimidines as orally active antimalarial agents.

University of Cape Town
Cell-based medicinal chemistry optimization of high throughput screening hits for orally active antimalarials. Part 2: hits from SoftFocus kinase and other libraries.

University of Cape Town
[d4U]-spacer-[HI-236] double-drug inhibitors of HIV-1 reverse-transcriptase.

University of Cape Town
C-2-aryl O-substituted HI-236 derivatives as non-nucleoside HIV-1 reverse-transcriptase inhibitors.

University of Cape Town
Identification, Characterization, and Optimization of 2,8-Disubstituted-1,5-naphthyridines as Novel Plasmodium falciparum Phosphatidylinositol-4-kinase Inhibitors with in Vivo Efficacy in a Humanized Mouse Model of Malaria.

University of Cape Town
Novel Antitubercular 6-Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure-Activity Relationship and Target Identification Studies.

University of Cape Town
4-Aminoquinoline Antimalarials Containing a Benzylmethylpyridylmethylamine Group Are Active against Drug Resistant Plasmodium falciparum and Exhibit Oral Activity in Mice.

University of Cape Town
Novel HIV-1 protease inhibitors active against multiple PI-resistant viral strains: coadministration with indinavir.

Merck Research Laboratories