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Neetu Dayal
Purdue University West Lafayette, National Institute of Pharmaceutical Education and Research
Research areas: Chemistry · Organic Chemistry · Catalytic C–H Functionalization Methods · Catalytic Cross-Coupling Reactions · Synthesis and biological activity
0000-0002-2705-7061
About
Neetu Dayal
Employment
- 2016 - Present
Education
-
Purdue University Post-Doctoral Research Associate2016 - Present
- 2012 - 2016
- 2010 - 2012
Projects & Funding
Projects & funding information is unavailable.
Publications (31)
- Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Supplementary Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Boronic Acid-Containing 3H- pyrazolo[4,3-f]quinoline Compounds as Dual CLK/ROCK Inhibitors with Anticancer Properties Save
- Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Supplementary Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Supplementary Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Supplementary Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Supplementary Data from Targeting RET Solvent-Front Mutants with Alkynyl Nicotinamide-Based Inhibitors Save
- Re-sensitization of Multidrug-Resistant and Colistin-Resistant Gram-Negative Bacteria to Colistin by Povarov/Doebner-Derived Compounds Save
- 3H-Pyrazolo[4,3-f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo Save
- SF5 and SCF3-substituted tetrahydroquinoline compounds as potent bactericidal agents against multidrug resistant persister Gram-positive bacteria Save
- HSD1787, a Tetrahydro-3H-Pyrazolo[4,3-f]Quinoline Compound Synthesized via Povarov Reaction, Potently Inhibits Proliferation of Cancer Cell Lines at Nanomolar Concentrations Save
- Inhibitors of Intracellular Gram-Positive Bacterial Growth Synthesized via Povarov–Doebner Reactions Save
- Potently inhibiting cancer cell migration with novel 3H-pyrazolo[4,3-f]quinoline boronic acid ROCK inhibitors Save
- Berenil Binds Tightly to Parallel and Mixed Parallel/Antiparallel G-Quadruplex Motifs with Varied Thermodynamic Signatures Save
- 3H-pyrazolo[4,3-f]quinoline haspin kinase inhibitors and anticancer properties Save
- N-(1,3,4-oxadiazol-2-yl)benzamide analogs, bacteriostatic agents against methicillin- and vancomycin-resistant bacteria Save
- Dual FLT3/TOPK inhibitor with activity against FLT3-ITD secondary mutations potently inhibits acute myeloid leukemia cell lines Save