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You searched for: Author/Creator Jeankumar, Variam Ullas

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1. Corrigendum to "Structure-guided design and development of novel benzimidazole class of compounds targeting DNA gyraseB enzyme of Staphylococcus aureus" [Bioorg. Med. Chem. 22 (2014) 5970–5987]. Issue 7 (1st April 2015)

2. Design and Biological Evaluation of Furan/Pyrrole/Thiophene‐2‐carboxamide Derivatives as Efficient DNA GyraseB Inhibitors of Staphylococcus aureus. (19th February 2015)

3. Design and development of new class of Mycobacterium tuberculosisl-alanine dehydrogenase inhibitors. Issue 18 (15th September 2016)

4. Discovery of novel lysine ɛ-aminotransferase inhibitors: An intriguing potential target for latent tuberculosis. Issue 6 (December 2015)

5. Discovery of potent and selective nonplanar tankyrase inhibiting nicotinamide mimics. Issue 15 (1st August 2015)

6. Enabling the (3 + 2) cycloaddition reaction in assembling newer anti-tubercular lead acting through the inhibition of the gyrase ATPase domain: lead optimization and structure activity profiling. Issue 8 (8th January 2015)

7. Exploring the gyrase ATPase domain for tailoring newer anti-tubercular drugs: Hit to lead optimization of a novel class of thiazole inhibitors. Issue 3 (1st February 2015)

8. Gyrase ATPase Domain as an Antitubercular Drug Discovery Platform: Structure‐Based Design and Lead Optimization of Nitrothiazolyl Carboxamide Analogues. Issue 8 (24th June 2014)

9. Identification and structure–activity relationship study of carvacrol derivatives as Mycobacterium tuberculosis chorismate mutase inhibitors. (August 2014)

10. Mycobacterium tuberculosis lysine-ɛ-aminotransferase a potential target in dormancy: Benzothiazole based inhibitors. Issue 10 (15th May 2017)