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Andrew P. Turnbull

Birkbeck, University of London

16

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268

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A High-Throughput Screening Triage Workflow to Authenticate a Novel Series of PFKFB3 Inhibitors

2018
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Tailoring Hit Identification and Qualification Methods for Targeting Protein–Protein Interactions

2017
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Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3).

2014 Bioorganic & Medicinal Chemistry
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Synthesis and structure–activity relationships for 1-(4-(piperidin-1-ylsulfonyl)phenyl)pyrrolidin-2-ones as novel non-carboxylate inhibitors of the aldo-keto reductase enzyme AKR1C3

2013 European Journal of Medicinal Chemistry
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Targeting cancer using fragment based drug discovery.

2012 Anti-cancer Agents in Medicinal Chemistry
- Andrew P. Turnbull
- Susan M. Boyd
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3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic acids; a New Class of Highly Potent and Selective Inhibitors of the Type 5 17-beta-hydroxysteroid Dehydrogenase AKR1C3

2012 Journal of Medicinal Chemistry
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3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic Acids: highly potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase AKR1C3.

2012 Journal of Medicinal Chemistry
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Current methods in structural proteomics and its applications in biological sciences

2012
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Structural Investigations into Shwachman Bodian Diamond Syndrome SBDS using a Bioinformatics Approach

2010 arXiv: Biomolecules
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The impact of Structural Proteomics on Biotechnology

2009 Biotechnology & Genetic Engineering Reviews
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