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Author Details
Full Name
Frederick S Buckner
Affiliation
University of Washington
ORCID
Career Start Year
1986
Papers
136
H Index
41
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
33970891
Case Report: Miltefosine Failure and Spontaneous Resolution of Cutaneous Leishmaniasis braziliensis.
Am J Trop Med Hyg
2021
33493793
The Tryp and the Pendulum.
EBioMedicine
2021
33871981
Early Stages of Drug Discovery in an Academic Institution and Involvement of Pharma for Advancing Promising Leads.
ACS Infect Dis
2021
33753338
Spontaneous Selection of <i>Cryptosporidium</i> Drug Resistance in a Calf Model of Infection.
Antimicrob Agents Chemother
2021
32268005
Hydroxychloroquine for Treatment of SARS-CoV-2 Infection? Improving Our Confidence in a Model-Based Approach to Dose Selection.
Clin Transl Sci
2020
32033395
Phenotypic Drug Discovery for Human African Trypanosomiasis: A Powerful Approach.
Trop Med Infect Dis
2020
31808676
Setting Our Sights on Infectious Diseases.
ACS Infect Dis
2020
31888785
A 71-year-old man with recurrent pulmonary mycobacterial avium complex infections and lymphopenia.
Allergy Asthma Proc
2020
32011682
Methionyl-tRNA synthetase inhibitor has potent in vivo activity in a novel Giardia lamblia luciferase murine infection model.
J Antimicrob Chemother
2020
31706668
A new chemotype with promise against Trypanosoma cruzi.
Bioorg Med Chem Lett
2020
33479683
Structure-guided discovery of selective methionyl-tRNA synthetase inhibitors with potent activity against <i>Trypanosoma brucei</i>.
RSC Med Chem
2020
30745384
Optimization of Methionyl tRNA-Synthetase Inhibitors for Treatment of Cryptosporidium Infection.
Antimicrob Agents Chemother
2019
31192168
Bioactivity of Farnesyltransferase Inhibitors Against <i>Entamoeba histolytica</i> and <i>Schistosoma mansoni</i>.
Front Cell Infect Microbiol
2019
29633973
The crystal structure of the drug target Mycobacterium tuberculosis methionyl-tRNA synthetase in complex with a catalytic intermediate.
Acta Crystallogr F Struct Biol Commun
2018
30655955
Triazolopyrimidines and Imidazopyridines: Structure-Activity Relationships and in Vivo Efficacy for Trypanosomiasis.
ACS Med Chem Lett
2018
27992217
Urea Derivatives of 2-Aryl-benzothiazol-5-amines: A New Class of Potential Drugs for Human African Trypanosomiasis.
J Med Chem
2017
28465105
Optimization of a binding fragment targeting the "enlarged methionine pocket" leads to potent Trypanosoma brucei methionyl-tRNA synthetase inhibitors.
Bioorg Med Chem Lett
2017
28110521
From Cells to Mice to Target: Characterization of NEU-1053 (SB-443342) and Its Analogues for Treatment of Human African Trypanosomiasis.
ACS Infect Dis
2017
28427904
Leishmania donovani tyrosyl-tRNA synthetase structure in complex with a tyrosyl adenylate analog and comparisons with human and protozoan counterparts.
Biochimie
2017
28187957
Discovery of N-(2-aminoethyl)-N-benzyloxyphenyl benzamides: New potent Trypanosoma brucei inhibitors.
Bioorg Med Chem
2017
28835807
1-Benzyl-3-aryl-2-thiohydantoin Derivatives as New Anti-<i>Trypanosoma brucei</i> Agents: SAR and in Vivo Efficacy.
ACS Med Chem Lett
2017
28848016
Development of Methionyl-tRNA Synthetase Inhibitors as Antibiotics for Gram-Positive Bacterial Infections.
Antimicrob Agents Chemother
2017
28740614
New Class of Antitrypanosomal Agents Based on Imidazopyridines.
ACS Med Chem Lett
2017
27500735
Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis.
PLoS One
2016
27788467
Structure-guided design of novel Trypanosoma brucei Methionyl-tRNA synthetase inhibitors.
Eur J Med Chem
2016
27658298
Correction: Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis.
PLoS One
2016
27627628
5-Fluoroimidazo[4,5-b]pyridine Is a Privileged Fragment That Conveys Bioavailability to Potent Trypanosomal Methionyl-tRNA Synthetase Inhibitors.
ACS Infect Dis
2016
27501246
Proteasome inhibition for treatment of leishmaniasis, Chagas disease and sleeping sickness.
Nature
2016
25163684
Identification of potent inhibitors of the Trypanosoma brucei methionyl-tRNA synthetase via high-throughput orthogonal screening.
J Biomol Screen
2015
26249349
A binding hotspot in Trypanosoma cruzi histidyl-tRNA synthetase revealed by fragment-based crystallographic cocktail screens.
Acta Crystallogr D Biol Crystallogr
2015
26324270
Inhibitors of methionyl-tRNA synthetase have potent activity against Giardia intestinalis trophozoites.
Antimicrob Agents Chemother
2015
24354316
Substituted 2-phenylimidazopyridines: a new class of drug leads for human African trypanosomiasis.
J Med Chem
2014
25365529
Recent developments in drug discovery for leishmaniasis and human African trypanosomiasis.
Chem Rev
2014
25033456
Synergy testing of FDA-approved drugs identifies potent drug combinations against Trypanosoma cruzi.
PLoS Negl Trop Dis
2014
24743796
Structures of Trypanosoma brucei methionyl-tRNA synthetase with urea-based inhibitors provide guidance for drug design against sleeping sickness.
PLoS Negl Trop Dis
2014
23587950
Induced resistance to methionyl-tRNA synthetase inhibitors in Trypanosoma brucei is due to overexpression of the target.
Antimicrob Agents Chemother
2013
24120539
Dialkylimidazole inhibitors of Trypanosoma cruzi sterol 14α-demethylase as anti-Chagas disease agents.
Bioorg Med Chem Lett
2013
23665145
Crystal structures of Plasmodium falciparum cytosolic tryptophanyl-tRNA synthetase and its potential as a target for structure-guided drug design.
Mol Biochem Parasitol
2013
22877245
Bioisosteric transformations and permutations in the triazolopyrimidine scaffold to identify the minimum pharmacophore required for inhibitory activity against Plasmodium falciparum dihydroorotate dehydrogenase.
J Med Chem
2012
24533285
Recent highlights in anti-protozoan drug development and resistance research.
Int J Parasitol Drugs Drug Resist
2012
23277882
Recent Developments in Sterol 14-demethylase Inhibitors for Chagas Disease.
Int J Parasitol Drugs Drug Resist
2012
22948920
Structure of the prolyl-tRNA synthetase from the eukaryotic pathogen Giardia lamblia.
Acta Crystallogr D Biol Crystallogr
2012
22720744
Urea-based inhibitors of Trypanosoma brucei methionyl-tRNA synthetase: selectivity and in vivo characterization.
J Med Chem
2012
22777048
Pharmacological characterization, structural studies, and in vivo activities of anti-Chagas disease lead compounds derived from tipifarnib.
Antimicrob Agents Chemother
2012
22902861
Distinct states of methionyl-tRNA synthetase indicate inhibitor binding by conformational selection.
Structure
2012
21282428
Selective inhibitors of methionyl-tRNA synthetase have potent activity against Trypanosoma brucei Infection in Mice.
Antimicrob Agents Chemother
2011
22073170
An essential farnesylated kinesin in Trypanosoma brucei.
PLoS One
2011
21820553
Experimental chemotherapy and approaches to drug discovery for Trypanosoma cruzi infection.
Adv Parasitol
2011
21517059
Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice.
J Med Chem
2011
21750879
Screening a fragment cocktail library using ultrafiltration.
Anal Bioanal Chem
2011
1 - 50 of 136
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