15 articles for VU Jeankumar
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Engineering another class of anti-tubercular lead: Hit to lead optimization of an intriguing class of gyrase ATPase inhibitors.

Birla Institute of Technology
Discovery of potent and selective nonplanar tankyrase inhibiting nicotinamide mimics.

University of Oulu
Design, synthesis, biological evaluation of substituted benzofurans as DNA gyraseB inhibitors of Mycobacterium tuberculosis.

Institute of Technology & Science-Pilani
Development of benzo[d]oxazol-2(3H)-ones derivatives as novel inhibitors of Mycobacterium tuberculosis InhA.

Birla Institute of Technology
An efficient synthesis and biological screening of benzofuran and benzo[d]isothiazole derivatives for Mycobacterium tuberculosis DNA GyrB inhibition.

TBA
Development of 2-(4-oxoquinazolin-3(4H)-yl)acetamide derivatives as novel enoyl-acyl carrier protein reductase (InhA) inhibitors for the treatment of tuberculosis.

Birla Institute of Technology
Thiazole-aminopiperidine hybrid analogues: design and synthesis of novel Mycobacterium tuberculosis GyrB inhibitors.

Birla Institute of Technology
Structure-guided design of novel thiazolidine inhibitors of O-acetyl serine sulfhydrylase from Mycobacterium tuberculosis.

Karolinska Institutet
Novel acridinedione derivatives: design, synthesis, SIRT1 enzyme and tumor cell growth inhibition studies.

Birla Institute of Technology
Synthesis of various 3-nitropropionamides as Mycobacterium tuberculosis isocitrate lyase inhibitor.

Institute of Technology and Science-Pilani
Structure-guided design and development of novel benzimidazole class of compounds targeting DNA gyraseB enzyme of Staphylococcus aureus.

Birla Institute of Technology & Science-Pilani
Mycobacterium tuberculosis lysine-ɛ-aminotransferase a potential target in dormancy: Benzothiazole based inhibitors.

Birla Institute of Technology & Science-Pilani
Cyclic P1 linkers as factor XIa inhibitors

Bristol-Myers Squibb
Inhibitors designed for the active site of dihydroorotase.

Texas A&M University