
Senior Research Associate
Publications
Development of potent inhibitors by fragment-linking strategies.
– Chemical Biology & Drug Design
(2022)
(DOI: 10.1111/cbdd.14120)
Structural Characterization of Mycobacterium abscessus Phosphopantetheine Adenylyl Transferase Ligand Interactions: Implications for Fragment-Based Drug Design
– Frontiers in Molecular Biosciences
(2022)
9,
880432
(DOI: 10.3389/fmolb.2022.880432)
Potential therapeutic targets from Mycobacterium abscessus (Mab): recently reported efforts towards the discovery of novel antibacterial agents to treat Mab infections
– RSC Medicinal Chemistry
(2022)
13,
392
(DOI: 10.1039/d1md00359c)
Discovery of Novel Inhibitors of Uridine Diphosphate- N-Acetylenolpyruvylglucosamine Reductase (MurB) from Pseudomonas aeruginosa, an Opportunistic Infectious Agent Causing Death in Cystic Fibrosis Patients
– Journal of medicinal chemistry
(2022)
65,
2149
(DOI: 10.1021/acs.jmedchem.1c01684)
Development of Inhibitors of SAICAR Synthetase (PurC) from Mycobacterium abscessus Using a Fragment-Based Approach.
– ACS Infect Dis
(2022)
8,
296
(DOI: 10.1021/acsinfecdis.1c00432)
A new strategy for hit generation: Novel in cellulo active inhibitors of CYP121A1 from Mycobacterium tuberculosis via a combined X-ray crystallographic and phenotypic screening approach (XP screen).
– European journal of medicinal chemistry
(2022)
230,
114105
(DOI: 10.1016/j.ejmech.2022.114105)
Targeting Mycobacterium tuberculosis CoaBC through Chemical Inhibition of 4'-Phosphopantothenoyl-l-cysteine Synthetase (CoaB) Activity.
– ACS Infectious Diseases
(2021)
7,
1666
(DOI: 10.1021/acsinfecdis.0c00904)
A small-molecule inhibitor of the BRCA2-RAD51 interaction modulates RAD51 assembly and potentiates DNA damage-induced cell death
– Cell Chemical Biology
(2021)
28,
1
Inhibiting Mycobacterium tuberculosis CoaBC by targeting an allosteric site.
– Nature Communications
(2021)
12,
143
(DOI: 10.1038/s41467-020-20224-x)
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