34 results on '"Kandale, Ajit"'
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2. Enhancing the Thermal and Kinetic Stability of Ketol-Acid Reductoisomerase, a Central Catalyst of a Cell-Free Enzyme Cascade for the Manufacture of Platform Chemicals
3. C–N bond formation under Cu-catalysis: Synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin-4(3H)-ones against chorismate mutase
4. Synthesis and in vitro cholesteryl ester transfer protein inhibitory activity of novel esters of 2, 10-dichloro-12H-dibenzo [d,g] 1,3-dioxocin-6-carboxylic acid
5. Tackling the opioid crisis - development of kappa-opioid receptor peptide agonists for safer analgesic therapy
6. Crystal structure of Mycobacterium tuberculosis ketol-acid reductoisomerase at 1.0 Å resolution – a potential target for anti-tuberculosis drug discovery
7. Pharmacophore modeling and 3D QSAR analysis of isothiazolidinedione derivatives as PTP1B inhibitors
8. In vitro screening of dry fruit extracts of Piper attenuatum for antioxidant and anticancer activity
9. Analogues of the Herbicide, N-Hydroxy-N-isopropyloxamate, Inhibit Mycobacterium tuberculosis Ketol-Acid Reductoisomerase and Their Prodrugs Are Promising Anti-TB Drug Leads
10. Crystal Structures of Staphylococcus aureus Ketol‐Acid Reductoisomerase in Complex with Two Transition State Analogues that Have Biocidal Activity
11. Ultrasound-based approach to spiro-2,3-dihydroquinazolin-4(1H)-ones: their in vitro evaluation against chorismate mutase
12. Pd-mediated functionalization of polysubstituted pyrroles: Their evaluation as potential inhibitors of PDE4
13. Conformationally restricted novel pyrazole derivatives: Synthesis of 1,8-disubstituted 5,5-dimethyl-4,5-dihydro-1H-benzo[g]indazoles as a new class of PDE4 inhibitors
14. Design and synthesis of 4-alkynyl pyrazoles as inhibitors of PDE4: A practical access via Pd/C–Cu catalysis
15. ChemInform Abstract: AgNO3Mediated C-N Bond Forming Reaction: Synthesis of 3-Substituted Benzothiazines as Potential COX Inhibitors.
16. ChemInform Abstract: AlCl3‐Induced C—N Bond Formation Followed by Pd/C—Cu‐Mediated Coupling—Cyclization Strategy: Synthesis of Pyrrolo[2,3‐b]quinoxalines as Anticancer Agents.
17. Crystal structure of Mycobacterium tuberculosis ketolacid reductoisomerase at 1.0 Å resolution - a potential target for anti-tuberculosis drug discovery.
18. Pharmacophore modeling and 3D QSAR analysis of isothiazolidinedione derivatives as PTP1B inhibitors
19. AlCl3 induced C–N bond formation followed by Pd/C–Cu mediated coupling–cyclization strategy: synthesis of pyrrolo[2,3-b]quinoxalines as anticancer agents
20. AgNO3 mediated C–N bond forming reaction: synthesis of 3-substituted benzothiazines as potential COX inhibitors
21. ChemInform Abstract: Design and Synthesis of 4-Alkynyl Pyrazoles as Inhibitors of PDE4: A Practical Access via Pd/C-Cu Catalysis.
22. In vitro screening of dry fruit extracts of Piper attenuatum for antioxidant and anticancer activity
23. Yb(OTf)3 mediated MCR: a new and regioselective approach towards polysubstituted pyrroles of pharmacological interest
24. Novel thieno[2,3-d]pyrimidines: their design, synthesis, crystal structure analysis and pharmacological evaluation
25. Design, synthesis and in vitro activity of Mycobacterium tuberculosis Ketol-acid reductoisomerase (KARI)inhibitors
26. Synthesis and in vitro cholesteryl ester transfer protein inhibitory activity of novel esters of 2, 10-dichloro-12 H-dibenzo [d,g] 1,3-dioxocin-6-carboxylic acid.
27. Analogues of the Herbicide, N-Hydroxy-N-isopropyloxamate, Inhibit Mycobacterium tuberculosisKetol-Acid Reductoisomerase and Their Prodrugs Are Promising Anti-TB Drug Leads
28. ChemInform Abstract: AgNO3 Mediated C-N Bond Forming Reaction: Synthesis of 3-Substituted Benzothiazines as Potential COX Inhibitors.
29. ChemInform Abstract: AlCl3-Induced C-N Bond Formation Followed by Pd/C-Cu-Mediated Coupling-Cyclization Strategy: Synthesis of Pyrrolo[2,3-b]quinoxalines as Anticancer Agents.
30. Standardisation of Desmodium gangeticum- A Tradition Ayurvedic Plant.
31. AgNO3 mediated C–N bond forming reaction: synthesis of 3-substituted benzothiazines as potential COX inhibitors
32. AlCl3 induced C–N bond formation followed by Pd/C–Cu mediated coupling–cyclization strategy: synthesis of pyrrolo[2,3-b]quinoxalines as anticancer agents
33. Crystal Structures of Staphylococcus aureus Ketol-Acid Reductoisomerase in Complex with Two Transition State Analogues that Have Biocidal Activity.
34. Conformationally restricted novel pyrazole derivatives: synthesis of 1,8-disubstituted 5,5-dimethyl-4,5-dihydro-1H-benzo[g]indazoles as a new class of PDE4 inhibitors.
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