A. Pacitto

发表

Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH

T. Blundell, V. Mizrahi, J. Pató, 2019, European journal of medicinal chemistry.

Synthesis and Structure-Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH.

T. Blundell, V. Mizrahi, J. Pató, 2019 .

Covalent inactivation of Mycobacterium thermoresistibile inosine-5'-monophosphate dehydrogenase (IMPDH).

T. Blundell, D. Chan, C. Abell, 2019, Bioorganic & medicinal chemistry letters.

The Inosine Monophosphate Dehydrogenase, GuaB2, Is a Vulnerable New Bactericidal Drug Target for Tuberculosis

Tom L. Blundell, Menico Rizzi, Stewart T. Cole, 2016, ACS infectious diseases.

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.

Lst4, the yeast Fnip1/2 orthologue, is a DENN-family protein

T. Blundell, Nianshu Zhang, S. Dokudovskaya, 2015, Open Biology.

Fragment-Based Approach to Targeting Inosine-5′-monophosphate Dehydrogenase (IMPDH) from Mycobacterium tuberculosis

Chris Abell, Vinayak Singh, Tom L Blundell, 2018, Journal of medicinal chemistry.

Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancer

T. Blundell, J. Bazan, D. Chirgadze, 2012, Open Biology.

The Inosine Monophosphate Dehydrogenase, GuaB2, Is a Vulnerable New Bactericidal Drug Target for Tuberculosis

T. Blundell, G. Kéri, S. Cole, 2016, ACS infectious diseases.

Synthesis and StructureeActivity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH

T. Blundell, V. Mizrahi, J. Pató, 2022 .