Krishna K. Sharma

Nagar, PB, India

Last Updated: 09/26/2026

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Found 13 publications

Synthetic amino acids-derived peptides target Cryptococcus neoformans by inducing cell membrane disruption.

Synthetic amino acids-derived peptides target Cryptococcus neoformans by inducing cell membrane disruption.

Journal: Bioorganic chemistry

Published: August 30, 2022

Peptide-based drug discovery: Current status and recent advances.

Peptide-based drug discovery: Current status and recent advances.

Journal: Drug discovery today

Published: August 26, 2022

New structural classes of antimalarials.

New structural classes of antimalarials.

Journal: European journal of medicinal chemistry

Published: June 04, 2022

Design, synthesis, and applications of ring-functionalized histidines in peptide-based medicinal chemistry and drug discovery.

Design, synthesis, and applications of ring-functionalized histidines in peptide-based medicinal chemistry and drug discovery.

Journal: Medicinal research reviews

Published: March 09, 2022

Modified histidine containing amphipathic ultrashort antifungal peptide, His[2-p-(n-butyl)phenyl]-Trp-Arg-OMe exhibits potent anticryptococcal activity.

Modified histidine containing amphipathic ultrashort antifungal peptide, His[2-p-(n-butyl)phenyl]-Trp-Arg-OMe exhibits potent anticryptococcal activity.

Journal: European journal of medicinal chemistry

Published: January 22, 2021

Structural and mechanistic insights into the inhibition of amyloid-β aggregation by Aβ39-42 fragment derived synthetic peptides.

Structural and mechanistic insights into the inhibition of amyloid-β aggregation by Aβ39-42 fragment derived synthetic peptides.

Journal: European journal of medicinal chemistry

Published: November 10, 2020

Effect of C-terminus amidation of Aβ39-42 fragment derived peptides as potential inhibitors of Aβ aggregation.

Effect of C-terminus amidation of Aβ39-42 fragment derived peptides as potential inhibitors of Aβ aggregation.

Journal: RSC advances

Published: May 31, 2020

Discovery of a Membrane-Active, Ring-Modified Histidine Containing Ultrashort Amphiphilic Peptide That Exhibits Potent Inhibition of Cryptococcus neoformans.

Discovery of a Membrane-Active, Ring-Modified Histidine Containing Ultrashort Amphiphilic Peptide That Exhibits Potent Inhibition of Cryptococcus neoformans.

Journal: Journal of medicinal chemistry

Published: July 12, 2017

Synthesis, stability and mechanistic studies of potent anticryptococcal hexapeptides.

Synthesis, stability and mechanistic studies of potent anticryptococcal hexapeptides.

Journal: European journal of medicinal chemistry

Published: January 02, 2017

Regioselective copper-catalyzed N(1)-(hetero)arylation of protected histidine.

Regioselective copper-catalyzed N(1)-(hetero)arylation of protected histidine.

Journal: Organic & biomolecular chemistry

Published: October 08, 2016

Metal-free synthesis of N-fused heterocyclic iodides via C-H functionalization mediated by tert-butylhydroperoxide.

Metal-free synthesis of N-fused heterocyclic iodides via C-H functionalization mediated by tert-butylhydroperoxide.

Journal: Chemical communications (Cambridge, England)

Published: September 02, 2015

Room temperature N-arylation of amino acids and peptides using copper(I) and β-diketone.

Room temperature N-arylation of amino acids and peptides using copper(I) and β-diketone.

Journal: Organic & biomolecular chemistry

Published: March 19, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026