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Wilson, Daniel
One or more keywords matched the following items that are connected to Wilson, Daniel
Item TypeName
Concept Molecular Structure
Academic Article Inhibition of siderophore biosynthesis by 2-triazole substituted analogues of 5'-O-[N-(salicyl)sulfamoyl]adenosine: antibacterial nucleosides effective against Mycobacterium tuberculosis.
Academic Article Design, synthesis and biological evaluations of N-Hydroxy thienopyrimidine-2,4-diones as inhibitors of HIV reverse transcriptase-associated RNase H.
Academic Article Methylenebis(sulfonamide) linked nicotinamide adenine dinucleotide analogue as an inosine monophosphate dehydrogenase inhibitor.
Academic Article Antitubercular nucleosides that inhibit siderophore biosynthesis: SAR of the glycosyl domain.
Academic Article Development of a selective activity-based probe for adenylating enzymes: profiling MbtA Involved in siderophore biosynthesis from Mycobacterium tuberculosis.
Academic Article Discovery of potent and selective sirtuin 2 (SIRT2) inhibitors using a fragment-based approach.
Academic Article Aryl acid adenylating enzymes involved in siderophore biosynthesis: fluorescence polarization assay, ligand specificity, and discovery of non-nucleoside inhibitors via high-throughput screening.
Academic Article Design, synthesis, and biological evaluation of beta-ketosulfonamide adenylation inhibitors as potential antitubercular agents.
Academic Article Mechanism-based inactivation by aromatization of the transaminase BioA involved in biotin biosynthesis in Mycobaterium tuberculosis.
Academic Article A mechanism-based aryl carrier protein/thiolation domain affinity probe.
Academic Article Design, Synthesis, and Biological Evaluations of Hydroxypyridonecarboxylic Acids as Inhibitors of HIV Reverse Transcriptase Associated RNase H.
Academic Article Bis(sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: inhibition of inosine monophosphate dehydrogenase.
Academic Article Mycophenolic acid analogs with a modified metabolic profile.
Academic Article Development of small-molecule inhibitors of fatty acyl-AMP and fatty acyl-CoA ligases in Mycobacterium tuberculosis.
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  • Molecular Structure