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Transition state analogue discrimination by related purine nucleoside phosphorylasesCrystal structures of Giardia lamblia guanine phosphoribosyltransferase at 1.75 A(,)Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysisStructures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its piecesAtomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylaseOver-the-barrier transition state analogues and crystal structure with Mycobacterium tuberculosis purine nucleoside phosphorylaseTargeting a novel Plasmodium falciparum purine recycling pathway with specific immucillinsPicomolar inhibitors as transition-state probes of 5'-methylthioadenosine nucleosidasesOne-third-the-sites transition-state inhibitors for purine nucleoside phosphorylaseThe synthesis and antibacterial activity of totarol derivatives. Part 1: modifications of ring-C and pro-drugsAssignment of downfield proton resonances in purine nucleoside phosphorylase immucillin-H complex by saturation-transferred NOEs.A novel mechanism for desulfation of mucin: identification and cloning of a mucin-desulfating glycosidase (sulfoglycosidase) from Prevotella strain RS2A synchrotron radiation study of the one-dimensional complex of sodium with (1S)-N-carboxylato-1-(9-deazaadenin-9-yl)-1,4-dideoxy-1,4-imino-D-ribitol, a member of the 'immucillin' familyStructure and inhibition of a quorum sensing target from Streptococcus pneumoniaeInhibition of ricin A-chain with pyrrolidine mimics of the oxacarbenium ion transition state.Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase.Energetic mapping of transition state analogue interactions with human and Plasmodium falciparum purine nucleoside phosphorylases.Femtomolar transition state analogue inhibitors of 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase from Escherichia coli.1-Deoxy-D-galactonojirimycins with dansyl capped N-substituents as β-galactosidase inhibitors and potential probes for GM1 gangliosidosis affected cell lines.1-Deoxynojirimycins with dansyl capped N-substituents as probes for Morbus Gaucher affected cell lines.Transition state analogues in quorum sensing and SAM recycling.Achieving the ultimate physiological goal in transition state analogue inhibitors for purine nucleoside phosphorylase.Transition state analogue inhibitors of purine nucleoside phosphorylase from Plasmodium falciparum.The synthesis and antibacterial activity of totarol derivatives. Part 2: Modifications at C-12 and O-13.Ricin A-chain inhibitors resembling the oxacarbenium ion transition state.Purine nucleoside phosphorylase from Mycobacterium tuberculosis. Analysis of inhibition by a transition-state analogue and dissection by parts.Addition of lithiated 9-deazapurine derivatives to a carbohydrate cyclic imine: convergent synthesis of the aza-C-nucleoside immucillins.Purine-less death in Plasmodium falciparum induced by immucillin-H, a transition state analogue of purine nucleoside phosphorylase.Synthesis and utility of sulfated chromogenic carbohydrate model substrates for measuring activities of mucin-desulfating enzymes.Glucofuranosylation with penta-O-propanoyl-beta-D-glucofuranose.8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases.Ionic states of substrates and transition state analogues at the catalytic sites of N-ribosyltransferases.Analysis of pyruvylated beta-carrageenan by 2D NMR spectroscopy and reductive partial hydrolysis.Exploring structure-activity relationships of transition state analogues of human purine nucleoside phosphorylase.Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase.Plasmodium falciparum purine nucleoside phosphorylase: crystal structures, immucillin inhibitors, and dual catalytic function.Imino-C-nucleoside synthesis: heteroaryl lithium carbanion additions to a carbohydrate cyclic imine and nitrone.Inhibitors of ADP-ribosylating bacterial toxins based on oxacarbenium ion character at their transition states.Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase.The chemistry of castanospermine. Direct oxidation of the tetraacetate to the corresponding gamma-lactam.
P50
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P50
description
Chemiker
@de
chemist
@en
kimyager
@tr
kémikus
@hu
scheikundige
@nl
name
Richard Furneaux
@hu
Richard H Furneaux
@en
Richard H Furneaux
@es
Richard H Furneaux
@nl
Richard H Furneaux
@sl
type
label
Richard Furneaux
@hu
Richard H Furneaux
@en
Richard H Furneaux
@es
Richard H Furneaux
@nl
Richard H Furneaux
@sl
altLabel
Furneaux
@hu
Richard H. Furneaux
@hu
prefLabel
Richard Furneaux
@hu
Richard H Furneaux
@en
Richard H Furneaux
@es
Richard H Furneaux
@nl
Richard H Furneaux
@sl
P1053
B-4157-2015
P106
P21
P31
P3829
P496
0000-0003-0973-2606