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Manish Kumar Tripathi

Researcher at Indian Institutes of Technology

Publications -  36
Citations -  534

Manish Kumar Tripathi is an academic researcher from Indian Institutes of Technology. The author has contributed to research in topics: Acetylcholinesterase & Docking (molecular). The author has an hindex of 8, co-authored 32 publications receiving 261 citations. Previous affiliations of Manish Kumar Tripathi include Maulana Azad National Institute of Technology & All India Institute of Medical Sciences.

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Identification of bioactive molecule from Withania somnifera (Ashwagandha) as SARS-CoV-2 main protease inhibitor.

TL;DR: The study suggests that Withanoside V in Ashwagandha may be serve as a potential inhibitor against Mpro of SARS-CoV-2 to combat COVID-19 and may have an antiviral effect on nCoV.
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Biphenyl-3-oxo-1,2,4-triazine linked piperazine derivatives as potential cholinesterase inhibitors with anti-oxidant property to improve the learning and memory.

TL;DR: The in vivo behavioral and ex vivo studies of compound 6g indicated significant improvement in cognitive dysfunctions against scopolamine-induced amnesia mouse models and a consensual binding affinity and active site interactions with the PAS and active catalytic site (CAS) residues of AChE.
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Design and Development of Multitarget-Directed N-Benzylpiperidine Analogs as Potential Candidates for the Treatment of Alzheimer's Disease

TL;DR: A series of N-benzylpiperidine analogs were designed and synthesized as multi-functional inhibitors of acetylcholinesterase (AChE) and β-secretase-1 (BACE-1) with moderate to excellent inhibitory activities, establishing the brain AChE inhibitory potential and antioxidant properties of these compounds.
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Design and development of molecular hybrids of 2-pyridylpiperazine and 5-phenyl-1,3,4-oxadiazoles as potential multifunctional agents to treat Alzheimer's disease.

TL;DR: This work has designed and synthesized molecular hybrids of 2-pyridylpiperazine and 5-phenyl-1,3,4-oxadiazoles that show significant and balanced inhibitory potential against target enzymes and ex vivo studies suggested decreased AChE activity and antioxidant potential of compound 49, with good oral absorption characteristics ascertained by pharmacokinetic studies.
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Design and development of novel p-aminobenzoic acid derivatives as potential cholinesterase inhibitors for the treatment of Alzheimer's disease.

TL;DR: In vivo studies of the synthesized compounds exhibited significant reversal of cognitive deficits in the animal models of amnesia as compared to standard drug donepezil, and the ex vivo studies in the specific brain regions like the hippocampus, hypothalamus, and prefrontal cortex regions also exhibited AChE inhibition comparable to standarddonepezil.