17 articles for DM Shackleford
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
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
Synthesis and biological evaluation of polysulfated oligosaccharide glycosides as inhibitors of angiogenesis and tumor growth.

Progen Pharmaceuticals
Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential.

Glaxosmithkline
Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice.

University of Washington
Phenylaminopyrimidines as inhibitors of Janus kinases (JAKs).

Cytopia Research
Development of [

Monash University
Discovery and Structure-Activity Relationships of Quinazolinone-2-carboxamide Derivatives as Novel Orally Efficacious Antimalarials.

Medicines For Malaria Venture
Potent Antimalarials with Development Potential Identified by Structure-Guided Computational Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series.

Medicines For Malaria Venture
Discovery of Potent and Fast-Acting Antimalarial Bis-1,2,4-triazines.

University of Melbourne
Systematic evaluation of structure-property relationships and pharmacokinetics in 6-(hetero)aryl-substituted matched pair analogs of amiloride and 5-(N,N-hexamethylene)amiloride.

University of Wollongong
Revisiting the SAR of the Antischistosomal Aryl Hydantoin (Ro 13-3978).

University of Nebraska Medical Center
Lead Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series for the Treatment of Malaria.

University of Washington
Discovery of Acylsulfonohydrazide-Derived Inhibitors of the Lysine Acetyltransferase, KAT6A, as Potent Senescence-Inducing Anti-Cancer Agents.

Monash University (Parkville Campus)
Two analogues of fenarimol show curative activity in an experimental model of Chagas disease.

Epichem
Design, structure-activity relationship and in vivo efficacy of piperazine analogues of fenarimol as inhibitors of Trypanosoma cruzi.

Epichem
Synthesis and profiling of benzylmorpholine 1,2,4,5-tetraoxane analogue N205: Towards tetraoxane scaffolds with potential for single dose cure of malaria.

University of Liverpool
Autotaxin inhibitors

Novartis