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Sujeet Kumar

Researcher at Amity Institute of Biotechnology

Publications -  60
Citations -  1157

Sujeet Kumar is an academic researcher from Amity Institute of Biotechnology. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 12, co-authored 35 publications receiving 761 citations. Previous affiliations of Sujeet Kumar include University of the Sciences & Pondicherry University.

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An Inhibitor of Nonhomologous End-Joining Abrogates Double-Strand Break Repair and Impedes Cancer Progression

TL;DR: SCR7 impedes tumor progression in mouse models and when coadministered with DSB-inducing therapeutic modalities enhances their sensitivity significantly, suggesting this inhibitor to target NHEJ offers a strategy toward the treatment of cancer and improvement of existing regimens.
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COVID-19 pandemic: Insights into structure, function, and hACE2 receptor recognition by SARS-CoV-2.

TL;DR: The structure of RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2 and its significance in drug discovery is discussed and the receptor recognition mechanisms of coronaviruses are explained.
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COVID-19 Pandemic: Insights into Structure, Function, and hACE2 Receptor Recognition by the SARS-CoV-2

TL;DR: This review summarizes the current knowledge on the origin and evolution of SARS-CoV-2, roles of key viral factors and discuss the receptor recognition mechanisms of coronaviruses, and provides a comparative analysis of the Sars-CoVs S proteins, receptor-binding specificity, and the differences in their antigenicity based on biophysical and structural characteristics.
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Synthesis and biological evaluation of novel 2-aralkyl-5-substituted-6-(4′-fluorophenyl)-imidazo[2,1-b][1,3,4]thiadiazole derivatives as potent anticancer agents

TL;DR: FACS analysis in conjunction with mitochondrial membrane potential and DNA fragmentation studies indicated that 4a induced apoptosis without cell cycle arrest suggesting that it could be used as a potential chemotherapeutic agent.
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Novel Levamisole Derivative Induces Extrinsic Pathway of Apoptosis in Cancer Cells and Inhibits Tumor Progression in Mice

TL;DR: 4a was found to be more potent than its parental analogue Levamisole based on both ex vivo and in vivo studies, suggesting that 4a could be used as a potent chemotherapeutic agent.