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Chemmedchem|October 30, 2014
Synthetic 1-deoxynojirimycin N-substituted peptides offer prolonged disruption to N-linked glycan processingAimé López Aguilar, Jaime Escribano, Paul Wentworth, et al.
Bioorganic & Medicinal Chemistry Letters|December 29, 2007
Carbonic anhydrase inhibitors. Interaction of 2-N,N-dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studiesClaudia Temperini, Alessandro Cecchi, Nicholas A Boyle, et al.
Chemmedchem|September 17, 2011
4-Substituted thioquinolines and thiazoloquinolines: potent, selective, and Tween-80 in vitro dependent families of antitubercular agents with moderate in vivo activityJaime Escribano, Cristina Rivero-Hernández, Hilda Rivera, et al.
ACS Infectious Diseases|March 21, 2020
Exploring the SAR of the β-Ketoacyl-ACP Synthase Inhibitor GSK3011724A and Optimization around a Genotoxic MetaboliteFraser Cunningham, Jorge Esquivias, Raquel Fernández-Menéndez, et al.
Chemmedchem|January 12, 2013
Fueling open-source drug discovery: 177 small-molecule leads against tuberculosisLluís Ballell, Robert H Bates, Rob J Young, et al.
Antimicrobial Agents and Chemotherapy|May 24, 2022
GSK2556286 Is a Novel Antitubercular Drug Candidate Effective In Vivo with the Potential To Shorten Tuberculosis TreatmentEric L Nuermberger, Maria Santos Martínez-Martínez, Olalla Sanz, et al.
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