N
Nidhi Gupta
Researcher at Central University of Rajasthan
Publications - 31
Citations - 332
Nidhi Gupta is an academic researcher from Central University of Rajasthan. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 8, co-authored 29 publications receiving 227 citations. Previous affiliations of Nidhi Gupta include Jawaharlal Nehru University & University of Delhi.
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High throughput virtual screening reveals SARS-CoV-2 multi-target binding natural compounds to lead instant therapy for COVID-19 treatment.
TL;DR: Three novel multi-target natural compounds were predicted to subdue the activity of three/more major drug targets simultaneously and are proposed as excellent lead candidates for the development of therapeutic drugs against SARS-CoV-2.
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Biologically Relevant Macrocyclic Complexes of Copper Spectral, Magnetic, Thermal and Antibacterial Approach
TL;DR: In this paper, copper(II) macrocyclic complexes were synthesized with five novel ligands: L1-1,7,10,16,tetraaza-2,6,11,15,15-tetrasena-4,13-dithiacycloocta-decane, L2-1.7,14,20,21,20.
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High throughput and comprehensive approach to develop multiepitope vaccine against minacious COVID-19.
Rupal Ojha,Nidhi Gupta,Biswajit Naik,Satyendra Singh,Vijay Verma,Dhaneswar Prusty,Vijay Kumar Prajapati +6 more
TL;DR: Encouraging data obtained from the various in-silico works indicated this vaccine as an effective therapeutic against COVID-19 as well as good docking scores affirmed the stringency of engineered vaccine.
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Synthesis and EPR Spectral Studies of Mono- and Binuclear Cobalt(II) and Nickel(II) Complexes with New 20‐Membered Dithiatetraazamacrocyclic [N4S2] Ligand
TL;DR: In this paper, a new ligand, 6,10,16,20,tetraketo [N4S2] (L), and its complexes with cobalt(II) and nickel(II), have been synthesized and characterized by elemental analyses, molar conductance, magnetic susceptibility measurements, EPR and electronic spectral studies.
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Regulation of Plasmodium falciparum Origin Recognition Complex subunit 1 (PfORC1) function through phosphorylation mediated by CDK‐like kinase PK5
Abhijit S. Deshmukh,Abhijit S. Deshmukh,Meetu Agarwal,Parul Mehra,Ashish Gupta,Nidhi Gupta,Christian Doerig,Suman Kumar Dhar +7 more
TL;DR: It is shown that phosphorylation of the PfORC1‐N terminal domain by the cyclin‐dependent kinase (CDK) PfPK5 abolishes DNA‐binding activity and leads to changes in subcellular localization and proteasome‐mediated degradation of the protein in schizonts.