
Publications
A Fragment-based approach to assess the ligandability of ArgB, ArgC, ArgD and ArgF in the L-arginine biosynthetic pathway of Mycobacterium tuberculosis
(2021)
(doi: 10.1101/2021.03.12.435067)
A small-molecule inhibitor of the BRCA2-RAD51 interaction modulates RAD51 assembly and potentiates DNA damage-induced cell death
Cell Chem Biol
(2021)
28
835
Inhibiting Mycobacterium tuberculosis CoaBC by targeting an allosteric site
Nat Commun
(2021)
12
143
(doi: 10.1038/s41467-020-20224-x)
Chemical validation of Mycobacterium tuberculosis phosphopantetheine adenylyltransferase using fragment linking and CRISPR interference
(2020)
2020.09.04.280388
(doi: 10.1101/2020.09.04.280388)
Correction to Fragment-Based Design of Mycobacterium tuberculosis InhA Inhibitors.
J Med Chem
(2020)
63
8650
(doi: 10.1021/acs.jmedchem.0c01187)
A small-molecule inhibitor of the BRCA2-RAD51 interaction modulates RAD51 assembly and potentiates DNA damage-induced cell death
(2020)
(doi: 10.1101/2020.07.15.200709)
Using a Fragment-Based Approach to Identify Alternative Chemical Scaffolds Targeting Dihydrofolate Reductase from Mycobacterium tuberculosis
ACS infectious diseases
(2020)
6
2192
(doi: 10.1021/acsinfecdis.0c00263)
Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modification.
Nucleic Acids Res
(2020)
48
8099
(doi: 10.1093/nar/gkaa539)
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