DP
Dr. Santhosh Penta
National Institute of Technology Warangal, NATIONAL INSTITUTE OF TECHNOLOGY WARANGAL, UNIVERSITY OF HYDERABAD
About
Current Research Interests are:
Synthesis of novel heterocyclic compounds,
Multicomponent reactions,
One-pot synthesis,
Drug Design of Pharmaceutical Importance,
Novel methodologies,
Catalysis,
Ionic liquids,
C-H activation...
Employment
-
National Institute of Technology Warangal ASSOCIATE PROFESSOR2013 - Present
Education
-
NATIONAL INSTITUTE OF TECHNOLOGY WARANGAL PhD
-
UNIVERSITY OF HYDERABAD RESEARCH ASSOCIATE
Projects & Funding
Projects & funding information is unavailable.
Publications (39)
- Design, synthesis and molecular docking studies of isoquinoline based 1,2,3-triazolyl chalcones as potential anti-cancer agents Save
- Novel thiadiazole-thiazolidinone-quinoxaline molecular hybrids: Synthesis, characterization, antimicrobial, antitubercular potential and in silico evaluation Save
- Design, Synthesis, ADME/Tox, and Molecular Modeling of Novel Bis‐1,2,3‐triazoles‐Linked Quinoxalines as Significant Anticancer Agents Save
- Design, Synthesis, and In‐Silico Molecular Docking Studies of 1,2,3‐Triazole‐Bearing Oxepinopyridine Derivatives as Potent Anticancer Agents Save
- New Quinazolinone‐Tethered 1,2,3‐Triazoles aSs Potent Antimicrobial Agents: Design, Synthesis, Biological Evaluation and in silico Docking Study Save
- Design, Synthesis, in Vitro, and in Silico Evaluations of 1,3,4‐Oxadiazole Derivatives Linked to the Pyrrolo[2,3‐d]pyrimidine Moieties as Potent Antimicrobial Targets Save
- Synthesis of Benzimidazole Based 1,2,4‐Triazole Derivatives as Potential Anticancer Agents: In Silico Techniques Save
- Efficient synthesis of novel 2-deoxy-C-nucleosides containing oxa and thiadiazole derivatives and their biological activity Save
- One-pot, three-component synthesis of novel coumarinyl-pyrazolo[3,4-b]pyridine-3-carboxylate derivatives using [AcMIm]FeCl4 as recyclable catalyst Save
- An efficient synthesis tetrazole and oxadiazole analogues of novel 2′-deoxy-C-nucleosides and their antitumor activity Save