Nian E. Zhou

3-Acylamino-azetidin-2-one as a novel class of cysteine proteases inhibitors.

E. Purisima, R. Ménard, Rajeshwar Singh, 2003, Bioorganic & medicinal chemistry letters.

6-Acylamino-penam derivatives: synthesis and inhibition of cathepsins B, L, K, and S.

E. Purisima, R. Ménard, Rajeshwar Singh, 2002, Bioorganic & medicinal chemistry letters.

Design and synthesis of 6-substituted amino-4-oxa-1-azabicyclo[3,2,0]heptan-7-one derivatives as cysteine proteases inhibitors.

E. Purisima, R. Ménard, Rajeshwar Singh, 2002, Bioorganic & medicinal chemistry letters.

Essential but Not Vulnerable: Indazole Sulfonamides Targeting Inosine Monophosphate Dehydrogenase as Potential Leads against Mycobacterium tuberculosis.

Thomas R. Ioerger, Travis Hartman, Tom L. Blundell, 2017, ACS infectious diseases.

Mycobacterium tuberculosis adenosine kinase bound to 6-methylmercaptopurine riboside

Q. Dang, J. Sacchettini, T. Parish, 2019 .

Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase

Q. Dang, J. Sacchettini, T. Parish, 2019, Journal of medicinal chemistry.