about
2-Octadecynoic acid as a dual life stage inhibitor of Plasmodium infections and plasmodial FAS-II enzymes.Synthetic chalcones and sulfonamides as new classes of Yersinia enterocolitica YopH tyrosine phosphatase inhibitors.Discovery of new inhibitors of Mycobacterium tuberculosis InhA enzyme using virtual screening and a 3D-pharmacophore-based approach.Advances in prodrug design.The (5Z)-5-Pentacosenoic and 5-Pentacosynoic Acids Inhibit the HIV-1 Reverse Transcriptase.Virtual screening and its integration with modern drug design technologies.Modern drug discovery technologies: opportunities and challenges in lead discovery.Pattern recognition techniques applied to the study of leishmanial glyceraldehyde-3-phosphate dehydrogenase inhibition.A pharmacophore-based virtual screening approach for the discovery of Trypanosoma cruzi GAPDH inhibitors.Discovery of new inhibitors of Schistosoma mansoni PNP by pharmacophore-based virtual screening.Encapsulation of metalloporphyrins improves their capacity to block the viability of the human malaria parasite Plasmodium falciparum.A novel approach to inhibit bone resorption: exosite inhibitors against cathepsin KInhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth.Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor.Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies.Structural basis for selective inhibition of trypanosomatid glyceraldehyde-3-phosphate dehydrogenase: molecular docking and 3D QSAR studies.The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi: the effect of species' specific differences on the immobilization.REPLY to Nanomedicine: NMB, 2015; 11:1035.Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase.Discovery of Marinoquinolines as Potent and Fast-Acting Plasmodium falciparum Inhibitors with in Vivo Activity2D Quantitative structure-activity relationship studies on a series of cholesteryl ester transfer protein inhibitorsStructure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruziQuantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasisIn silico screening strategies for novel inhibitors of parasitic diseasesQSAR studies on benzothiophene derivatives as Plasmodium falciparum N-myristoyltransferase inhibitors: Molecular insights into affinity and selectivityAntiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Rafael V Guido
@nl
Rafael V Guido
@sl
Rafael V. Guido
@en
Rafael V. Guido
@es
type
label
Rafael V Guido
@nl
Rafael V Guido
@sl
Rafael V. Guido
@en
Rafael V. Guido
@es
prefLabel
Rafael V Guido
@nl
Rafael V Guido
@sl
Rafael V. Guido
@en
Rafael V. Guido
@es
P106
P1153
17342054700
P21
P31
P496
0000-0002-7187-0818