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The trypanocidal benzoxaborole AN7973 inhibits trypanosome mRNA processing

PLoS pathogens, 2018-09, Vol.14 (9), p.e1007315

2018

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Veterinary trypanocidal benzoxaboroles are peptidase-activated prodrugs

PLoS pathogens, 2020-11, Vol.16 (11), p.e1008932-e1008932

2020

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Athenaeus describes the most ancient intellectual property

Prometheus (Saint Lucia, Brisbane, Qld.), 2017-04, Vol.35 (2), p.137-143

Witty, Michael

2017

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Fast in vitro methods to determine the speed of action and the stage-specificity of anti-malarials in Plasmodium falciparum

Malaria journal, 2013-11, Vol.12 (1), p.424-424, Article 424

2013

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Transformation of struvite from wastewater to a hydrogen fuel storage compound ammonia borane

Frontiers in chemistry, 2023-11, Vol.11, p.1269845-1269845

2023

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Identification of a 4-fluorobenzyl l-valinate amide benzoxaborole (AN11736) as a potential development candidate for the treatment of Animal African Trypanosomiasis (AAT)

Bioorganic & medicinal chemistry letters, 2018-01, Vol.28 (1), p.6-10

2018

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UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria

Antimicrobial agents and chemotherapy, 2018-09, Vol.62 (9)

2018

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Repositioning of a Diaminothiazole Series Confirmed to Target the Cyclin-Dependent Kinase CRK12 for Use in the Treatment of African Animal Trypanosomiasis

Journal of medicinal chemistry, 2022-04, Vol.65 (7), p.5606-5624

2022

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Medicinal Chemistry Optimization of Antiplasmodial Imidazopyridazine Hits from High Throughput Screening of a SoftFocus Kinase Library: Part 2

Journal of medicinal chemistry, 2014-11, Vol.57 (21), p.8839-8848

2014

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

Journal of medicinal chemistry, 2013-10, Vol.56 (20), p.7750-7754

2013

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Mission possible

Nature (London), 2007-09, Vol.449 (7159), p.166-169

2007

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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

Journal of medicinal chemistry, 2013-11, Vol.56 (21), p.8860-8871

2013

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Antimalarial aminothiazoles and aminopyridines from phenotypic whole-cell screening of a SoftFocus(®) library

Future medicinal chemistry, 2012-12, Vol.4 (18), p.2265-2277

2012

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Cell-Based Medicinal Chemistry Optimization of High Throughput Screening Hits for Orally Active Antimalarials. Part 2: Hits from SoftFocus Kinase and other Libraries: Miniperspectives Series on Phenotypic Screening for Antiinfective Targets

Journal of medicinal chemistry, 2013-10, Vol.56 (20), p.7750-7754

2013

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Erratum for Brunschwig et al., "UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria"

Antimicrobial agents and chemotherapy, 2018-11, Vol.62 (11)

2018

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The Deipnosophists and Dr Johnson

Lexicographica, 2020-11, Vol.36 (1), p.311-324

Witty, Michael

2020

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Synthesis and evaluation of 2-pyridyl pyrimidines with in vitro antiplasmodial and antileishmanial activity

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.401-405

2009

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Chloroquine–astemizole hybrids with potent in vitro and in vivo antiplasmodial activity

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.481-484

2009

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Plant-based Heterologous Expression of Mal d 2, a Thaumatin-like Protein and Allergen of Apple (Malus domestica), and its Characterization as an Antifungal Protein

Journal of molecular biology, 2003-06, Vol.329 (4), p.721-730

2003

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Athenaeus and the Control

Revista de Filosofia Antiga, 2020-05, Vol.14 (1), p.161-170

Witty, Michael

2020

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Wolffia columbiana Can Switch Between Two Anatomically and Physiologically Separate States: Buoyant for Invasion and Starch Rich for Colonization

International journal of botany : IJB, 2009-09, Vol.5 (4), p.307-313

Witty, Michael

2009

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Ancient Roman Urine Chemistry

Acta archaeologica, 2016-12, Vol.87 (1), p.179-191

Witty, Michael

2016

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Hooke’s Gravel was Struvite

Notes and queries, 2016-12, Vol.63 (4), p.gjw218

Witty, Michael

2016

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Ancient Roman Urine Chemistry

Acta archaeologica, 2016-04, Vol.87 (1), p.179-191

Witty, Michael

2016

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Daniel and the Control

Revista de Filosofia Antiga, 2022-04, Vol.16 (1), p.204-207

Witty, Michael

2022

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The trypanocidal benzoxaborole AN7973 inhibits trypanosome mRNA processing

Veterinary trypanocidal benzoxaboroles are peptidase-activated prodrugs

Athenaeus describes the most ancient intellectual property

Fast in vitro methods to determine the speed of action and the stage-specificity of anti-malarials in Plasmodium falciparum

Transformation of struvite from wastewater to a hydrogen fuel storage compound ammonia borane

Identification of a 4-fluorobenzyl l-valinate amide benzoxaborole (AN11736) as a potential development candidate for the treatment of Animal African Trypanosomiasis (AAT)

UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria

Repositioning of a Diaminothiazole Series Confirmed to Target the Cyclin-Dependent Kinase CRK12 for Use in the Treatment of African Animal Trypanosomiasis

Medicinal Chemistry Optimization of Antiplasmodial Imidazopyridazine Hits from High Throughput Screening of a SoftFocus Kinase Library: Part 2

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

Mission possible

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

Antimalarial aminothiazoles and aminopyridines from phenotypic whole-cell screening of a SoftFocus(®) library

Cell-Based Medicinal Chemistry Optimization of High Throughput Screening Hits for Orally Active Antimalarials. Part 2: Hits from SoftFocus Kinase and other Libraries: Miniperspectives Series on Phenotypic Screening for Antiinfective Targets

Erratum for Brunschwig et al., "UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria"

The Deipnosophists and Dr Johnson

Synthesis and evaluation of 2-pyridyl pyrimidines with in vitro antiplasmodial and antileishmanial activity

Chloroquine–astemizole hybrids with potent in vitro and in vivo antiplasmodial activity

Plant-based Heterologous Expression of Mal d 2, a Thaumatin-like Protein and Allergen of Apple (Malus domestica), and its Characterization as an Antifungal Protein

Athenaeus and the Control

Wolffia columbiana Can Switch Between Two Anatomically and Physiologically Separate States: Buoyant for Invasion and Starch Rich for Colonization

Ancient Roman Urine Chemistry

Hooke’s Gravel was Struvite

Ancient Roman Urine Chemistry

Daniel and the Control

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