Identification of potential P. falciparum transketolase inhibitors: pharmacophore design, in silico screening and docking studies

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ISSN Print: 2153-036X
ISSN Online: 2153-0378
www.scirp.org/journal/jbpc
E-mail: jbpc@scirp.org

"Identification of potential P. falciparum transketolase inhibitors: pharmacophore design, in silico screening and docking studies"
written by Shweta Joshi, Alok Ranjan Singh, Uzma Saqib, Prakash Chandra Misra, Mohammad Imran Siddiqi, Jitendra Kumar Saxena,
published by Journal of Biophysical Chemistry, Vol.1 No.2, 2010

has been cited by the following article(s):

[1]	Nouvelles méthodes électrochimiques pour le criblage d'inhibiteurs de transcétolases
	2018

[2]	Recent progress in the identification and development of anti-malarial agents using virtual screening based approaches
	Combinatorial chemistry & high throughput screening, 2015

[3]	Chemical and genetic validation of thiamine utilization as an antimalarial drug target
	Nature communications, 2013

[4]	Molecular Modelling and Docking Studies of Human Blood Coagulation Factor-XIIIA Protein
	SK Gunda, AM Madasu, P Kakarla, M Shaik - ijrpbsonline.com, 2013

[5]	Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparum transketolase and β-hematin inhibitors
	MedChemComm, 2012

[6]	Thiamin (vitamin B1) biosynthesis and regulation: a rich source of antimicrobial drug targets?
	International journal of biological sciences, 2011

[1]	Identification of a Human Anti-Alpha-Toxin Monoclonal Antibody Against Staphylococcus aureus Infection Frontiers in Microbiology, 2021 DOI:10.3389/fmicb.2021.692279

[2]	Innovative Electrochemical Screening Allows Transketolase Inhibitors to Be Identified Analytical Chemistry, 2018 DOI:10.1021/acs.analchem.8b01752

[3]	Innovative Electrochemical Screening Allows Transketolase Inhibitors to Be Identified Analytical Chemistry, 2018 DOI:10.1021/acs.analchem.8b01752

[4]	Chemical and genetic validation of thiamine utilization as an antimalarial drug target Nature Communications, 2013 DOI:10.1038/ncomms3060

[5]	Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparumtransketolase and β-hematin inhibitors Med. Chem. Commun., 2012 DOI:10.1039/C1MD00188D

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