PubRank

Manoranjan Panda

Author PubWeight™ 10.73‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Explicit ion, implicit water solvation for molecular dynamics of nucleic acids and highly charged molecules. J Comput Chem 2008 1.13
2 A priori theoretical prediction of selectivity in asymmetric catalysis: design of chiral catalysts by using quantum molecular interaction fields. Angew Chem Int Ed Engl 2006 1.11
3 Computer-aided design of chiral ligands. Part 2. Functionality mapping as a method to identify stereocontrol elements for asymmetric reactions. J Org Chem 2003 1.04
4 Quantum mechanical models correlating structure with selectivity: predicting the enantioselectivity of beta-amino alcohol catalysts in aldehyde alkylation. J Am Chem Soc 2003 0.99
5 Methyl-thiazoles: a novel mode of inhibition with the potential to develop novel inhibitors targeting InhA in Mycobacterium tuberculosis. J Med Chem 2013 0.88
6 Computer-aided design of chiral ligands. Part I. Database search methods to identify chiral ligand types for asymmetric reactions. J Mol Graph Model 2002 0.86
7 4-aminoquinolone piperidine amides: noncovalent inhibitors of DprE1 with long residence time and potent antimycobacterial activity. J Med Chem 2014 0.82
8 Lead optimization of 1,4-azaindoles as antimycobacterial agents. J Med Chem 2014 0.82
9 Synthesis and structure activity relationship of imidazo[1,2-a]pyridine-8-carboxamides as a novel antimycobacterial lead series. Bioorg Med Chem Lett 2013 0.79
10 Structure guided lead generation for M. tuberculosis thymidylate kinase (Mtb TMK): discovery of 3-cyanopyridone and 1,6-naphthyridin-2-one as potent inhibitors. J Med Chem 2014 0.78
11 Pyrazolopyrimidines establish MurC as a vulnerable target in Pseudomonas aeruginosa and Escherichia coli. ACS Chem Biol 2014 0.77
12 Diarylthiazole: an antimycobacterial scaffold potentially targeting PrrB-PrrA two-component system. J Med Chem 2014 0.77
13 Understanding of the mass spectrometric fragmentation pathways of a few potentially genotoxic haloaniline isomers in their protonated form by collision-induced dissociation. J Pharm Biomed Anal 2011 0.75