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Nag S. Kumar

Observed names: Nag Kumar, Nag S Kumar
OpenAlex ID: A5033237174
Inhibition of recombinant human maltase glucoamylase by salacinol and derivatives
2006 · Elena J. Rossi, Lyann Sim, et al. · FEBS Journal · 88
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Identification of Pyruvate Kinase in Methicillin-Resistant Staphylococcus aureus as a Novel Antimicrobial Drug Target
2011 · Roya Zoraghi, Raymond H. See, et al. · Antimicrobial Agents and Chemotherapy · 56
Discovery and optimization of a new class of pyruvate kinase inhibitors as potential therapeutics for the treatment of methicillin-resistant Staphylococcus aureus infections
2014 · Nag S. Kumar, Edie M. Dullaghan, et al. · Bioorganic & Medicinal Chemistry · 46
Development of fluorescent peptide substrates and assays for the key autophagy-initiating cysteine protease enzyme, ATG4B
2015 · Lubomir Vezenkov, Nicolette S. Honson, et al. · Bioorganic & Medicinal Chemistry · 44
Development of Fluorescent Substrates and Assays for the Key Autophagy-Related Cysteine Protease Enzyme, ATG4B
2014 · Thanh G. Nguyen, Nicolette S. Honson, et al. · Assay and Drug Development Technologies · 39
Design and synthesis of an all-in-one 3-(1,1-difluoroprop-2-ynyl)-3H-diazirin-3-yl functional group for photo-affinity labeling
2009 · Nag S. Kumar, Robert N. Young · Bioorganic & Medicinal Chemistry · 37
Optimization and structure–activity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents
2012 · Nag S. Kumar, Emily A. Amandoron, et al. · Bioorganic & Medicinal Chemistry · 34
Cheminformatics-Driven Discovery of Selective, Nanomolar Inhibitors for Staphylococcal Pyruvate Kinase
2011 · Peter Axerio-Cilies, Raymond H See, et al. · ACS Chemical Biology · 31
Novel EP4 Receptor Agonist-Bisphosphonate Conjugate Drug (C1) Promotes Bone Formation and Improves Vertebral Mechanical Properties in the Ovariectomized Rat Model of Postmenopausal Bone Loss
2014 · Careesa C Liu, Sally Hu, et al. · Journal of Bone and Mineral Research · 30
Synthesis of a Sulfonium Ion Analogue of the Glycosidase Inhibitor Swainsonine
2005 · Nag S. Kumar, B. Mario Pinto · The Journal of Organic Chemistry · 19
Synthesis of d-lyxitol and d-ribitol analogues of the naturally occurring glycosidase inhibitor salacinol
2005 · Nag S. Kumar, B. Mario Pinto · Carbohydrate Research · 19
Binding of sulfonium‐ion analogues of di‐epi‐swainsonine and 8‐epi‐lentiginosine to Drosophila Golgi α‐mannosidase II: The role of water in inhibitor binding
2007 · Nag S. Kumar, Douglas A. Kuntz, et al. · Proteins Structure Function and Bioinformatics · 18
Novel spirothiazamenthane inhibitors of the influenza A M2 proton channel
2016 · Steve Arns, Aruna D. Balgi, et al. · European Journal of Medicinal Chemistry · 15
Synthesis of thioswainsonine as a potential glycosidase inhibitor
2006 · Nag S. Kumar, B. Mario Pinto · Carbohydrate Research · 15
Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol
2007 · Ramakrishna G. Bhat, Nag S. Kumar, et al. · Carbohydrate Research · 10
Synthesis and Conformational Analysis of Bicyclic Sulfonium Salts. Structures Related to the Glycosidase Inhibitor Australine
2005 · Nag S. Kumar, B. Mario Pinto · The Journal of Organic Chemistry · 9
Synthesis of a tritium‐labeled photo‐affinity probe based on an atypical leukotriene biosynthesis inhibitor
2010 · Nag S. Kumar, Matthew P. Braun, et al. · Journal of Labelled Compounds and Radiopharmaceuticals · 6
Synthesis of Trans-4-cyclohexyl-l-proline by Hydrogenation of Trans-4-phenyl-l-proline Using Ruthenium
2013 · V. Pandu Ranga Rao, Nag S. Kumar, et al.
Works count: 18
Citation count: 516
H-index: 14
I10-index: 15
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