Year |
Citation |
Score |
2005 |
Redoulés D, Perie J, Viodé C, Mavon A, Fournier D, Daunes S, Casas C, Lougarre A, De Viguerie N. Slow internal release of bioactive compounds under the effect of skin enzymes. The Journal of Investigative Dermatology. 125: 270-7. PMID 16098037 DOI: 10.1111/J.0022-202X.2005.23785.X |
0.344 |
|
2004 |
Azema L, Claustre S, Alric I, Blonski C, Willson M, Perié J, Baltz T, Tetaud E, Bringaud F, Cottem D, Opperdoes FR, Barrett MP. Interaction of substituted hexose analogues with the Trypanosoma brucei hexose transporter. Biochemical Pharmacology. 67: 459-67. PMID 15037198 DOI: 10.1016/J.Bcp.2003.09.005 |
0.358 |
|
2003 |
Ladame S, Castilho MS, Silva CH, Denier C, Hannaert V, Périé J, Oliva G, Willson M. Crystal structure of Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-d-glyceric acid. European Journal of Biochemistry / Febs. 270: 4574-86. PMID 14622286 DOI: 10.1046/J.1432-1033.2003.03857.X |
0.645 |
|
2003 |
Soulère L, Delplace P, Davioud-Charvet E, Py S, Sergheraert C, Périé J, Ricard I, Hoffmann P, Dive D. Screening of Plasmodium falciparum iron superoxide dismutase inhibitors and accuracy of the SOD-assays. Bioorganic & Medicinal Chemistry. 11: 4941-4. PMID 14604655 DOI: 10.1016/J.Bmc.2003.09.011 |
0.316 |
|
2003 |
Castilho MS, Pavão F, Oliva G, Ladame S, Willson M, Périé J. Evidence for the two phosphate binding sites of an analogue of the thioacyl intermediate for the Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase-catalyzed reaction, from its crystal structure. Biochemistry. 42: 7143-51. PMID 12795610 DOI: 10.1021/Bi0206107 |
0.628 |
|
2003 |
Maya JD, Bollo S, Nuñez-Vergara LJ, Squella JA, Repetto Y, Morello A, Périé J, Chauvière G. Trypanosoma cruzi: effect and mode of action of nitroimidazole and nitrofuran derivatives. Biochemical Pharmacology. 65: 999-1006. PMID 12623132 DOI: 10.1016/S0006-2952(02)01663-5 |
0.37 |
|
2003 |
Chauvière G, Bouteille B, Enanga B, de Albuquerque C, Croft SL, Dumas M, Périé J. Synthesis and biological activity of nitro heterocycles analogous to megazol, a trypanocidal lead. Journal of Medicinal Chemistry. 46: 427-40. PMID 12540242 DOI: 10.1021/Jm021030A |
0.348 |
|
2002 |
Claustre S, Denier C, Lakhdar-Ghazal F, Lougare A, Lopez C, Chevalier N, Michels PA, Périé J, Willson M. Exploring the active site of Trypanosoma brucei phosphofructokinase by inhibition studies: specific irreversible inhibition. Biochemistry. 41: 10183-93. PMID 12162732 DOI: 10.1021/Bi020082Z |
0.4 |
|
2002 |
Willson M, Sanejouand YH, Perie J, Hannaert V, Opperdoes F. Sequencing, modeling, and selective inhibition of Trypanosoma brucei hexokinase. Chemistry & Biology. 9: 839-47. PMID 12144928 DOI: 10.1016/S1074-5521(02)00169-2 |
0.365 |
|
2002 |
Soulère L, Viodé C, Périé J, Hoffmann P. Selective inhibition of Fe- versus Cu/Zn-superoxide dismutases by 2,3-dihydroxybenzoic acid derivatives. Chemical & Pharmaceutical Bulletin. 50: 578-82. PMID 12036008 DOI: 10.1248/Cpb.50.578 |
0.304 |
|
2002 |
Lakhdar-Ghazal F, Blonski C, Willson M, Michels P, Perie J. Glycolysis and proteases as targets for the design of new anti-trypanosome drugs. Current Topics in Medicinal Chemistry. 2: 439-56. PMID 11966466 DOI: 10.2174/1568026024607472 |
0.413 |
|
2002 |
Bontá M, Chauviere G, Périé J, Núñez-Vergara LJ, Squella JA. Nitro radical anions from megazol and related nitroimidazoles in aprotic media. A father–son type reaction triggered by an acidic proton Electrochimica Acta. 47: 4045-4053. DOI: 10.1016/S0013-4686(02)00390-0 |
0.315 |
|
2002 |
Amari M, Fodili M, Nedjar-Kolli B, Hoffmann AP, PÉriÉ J. Reactivity studies on 4-aminopyrones: Access to benzimidazole and benzimidazolone derivatives Journal of Heterocyclic Chemistry. 39: 811-816. DOI: 10.1002/Jhet.5570390429 |
0.324 |
|
2002 |
Ladame S, Willson M, Périé J. A Convenient Synthesis of Dibenzyl α,α-Difluoromethyl-β-ketophosphonates European Journal of Organic Chemistry. 2002: 2640. DOI: 10.1002/1099-0690(200208)2002:15<2640::Aid-Ejoc2640>3.0.Co;2-9 |
0.574 |
|
2001 |
Ladame S, Bardet M, Périé J, Willson M. Selective inhibition of Trypanosoma brucei GAPDH by 1,3-bisphospho-D-glyceric acid (1,3-diPG) analogues. Bioorganic & Medicinal Chemistry. 9: 773-83. PMID 11310612 DOI: 10.1016/S0968-0896(00)00295-9 |
0.619 |
|
2001 |
Bollo S, Núñez-Vergara LJ, Bontá M, Chauviere G, Périé J, Squella JA. Cyclic voltammetric studies on nitro radical anion formation from megazol and some related nitroimidazole derivatives Journal of Electroanalytical Chemistry. 511: 46-54. DOI: 10.1016/S0022-0728(01)00557-5 |
0.302 |
|
2000 |
Azéma L, Bringaud F, Blonski C, Périé J. Chemical and enzymatic synthesis of fructose analogues as probes for import studies by the hexose transporter in parasites Bioorganic & Medicinal Chemistry. 8: 717-722. PMID 10819160 DOI: 10.1016/S0968-0896(00)00018-3 |
0.339 |
|
1999 |
Page P, Blonski C, Périé J. Synthesis of phosphono analogues of dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. Bioorganic & Medicinal Chemistry. 7: 1403-1412. PMID 10465414 DOI: 10.1016/S0968-0896(99)00065-6 |
0.423 |
|
1999 |
Claustre S, Bringaud F, Azéma L, Baron R, Périé J, Willson M. An easy stereospecific synthesis of 1-amino-2,5-anhydro-1-deoxy-D-mannitol and arylamino derivatives. Carbohydrate Research. 315: 339-44. PMID 10399304 DOI: 10.1016/S0008-6215(99)00040-3 |
0.345 |
|
1999 |
Viodé C, Bettache N, Cenas N, Krauth-Siegel RL, Chauvière G, Bakalara N, Périé J. Enzymatic reduction studies of nitroheterocycles Biochemical Pharmacology. 57: 549-557. PMID 9952319 DOI: 10.1016/S0006-2952(98)00324-4 |
0.392 |
|
1999 |
Willson M, Perie J. Inhibition of yeast hexokinase: a kinetic and phosphorus nuclear magnetic resonance study Spectrochimica Acta Part a: Molecular and Biomolecular Spectroscopy. 55: 911-917. DOI: 10.1016/S1386-1425(98)00315-1 |
0.361 |
|
1999 |
Redoulès D, Perié J. Stereospecific synthesis of retinoic acid glucoconjugates, as pseudo-substrates of epidermal β-glucocerebrosidase Tetrahedron Letters. 40: 4811-4814. DOI: 10.1016/S0040-4039(99)00920-X |
0.369 |
|
1999 |
Page P, Blonski C, Périé J. Origin of the Slow‐Binding Inhibition of Aldolase by D‐glycero‐Tetrulose 1‐Phosphate (D‐Erythrulose 1‐Phosphate) from the Comparison with the Isosteric Phosphonate Analog European Journal of Organic Chemistry. 1999: 2853-2857. DOI: 10.1002/(Sici)1099-0690(199911)1999:11<2853::Aid-Ejoc2853>3.0.Co;2-0 |
0.423 |
|
1998 |
Page P, Blonski C, Périé J. Interaction of phosphonomethyl analog of dihydroxyacetone phosphate with rabbit muscle aldolase. Biochimica Et Biophysica Acta. 1386: 59-64. PMID 9675245 DOI: 10.1016/S0167-4838(98)00061-2 |
0.347 |
|
1998 |
Chauviere G, Rousseau B, Pillon F, Perie J. Synthesis of 2-amino-5-(1-methyl-5-nitro-[4-3H]-2-imidazolyl)-1,3,4-thiadiazole Journal of Labelled Compounds and Radiopharmaceuticals. 41: 47-51. DOI: 10.1002/(Sici)1099-1344(199801)41:1<47::Aid-Jlcr52>3.0.Co;2-C |
0.31 |
|
1997 |
Blonski C, De Moissac D, Périé J, Sygusch J. Inhibition of rabbit muscle aldolase by phosphorylated aromatic compounds Biochemical Journal. 323: 71-77. PMID 9173904 DOI: 10.1042/Bj3230071 |
0.364 |
|
1996 |
Page P, Blonski C, Périé J. An improved chemical and enzymatic synthesis of new fructose derivatives for import studies by the glucose transporter in parasites Tetrahedron. 52: 1557-1572. DOI: 10.1016/0040-4020(95)01001-7 |
0.397 |
|
1996 |
Rameau J, Devillers J, Declercq J, Chauviere G, Perie J. Molecular structure of 2-Amino-5-(1-methyl-5-nitro-2-imidazolyl)-1,3,4-thiadiazol (Megazol) and related compounds: A concerted study using X-ray crystallography, molecular mechanics, and semiempirical methods Structural Chemistry. 7: 187-204. DOI: 10.1007/Bf02281230 |
0.322 |
|
1995 |
Trinquier M, Perie J, Callens M, Opperdoes F, Willson M. Specific inhibitors for the glycolytic enzymes of Trypanosoma brucei. Bioorganic & Medicinal Chemistry. 3: 1423-7. PMID 8634823 DOI: 10.1016/0968-0896(95)00129-5 |
0.407 |
|
1995 |
Bouteille B, Marie-Daragon A, Chauvière G, de Albuquerque C, Enanga B, Dardé ML, Vallat JM, Périé J, Dumas M. Effect of megazol on Trypanosoma brucei brucei acute and subacute infections in Swiss mice. Acta Tropica. 60: 73-80. PMID 8610542 DOI: 10.1016/0001-706X(95)00109-R |
0.307 |
|
1995 |
Gefflaut T, Blonski C, Perie J, Willson M. Class I aldolases: substrate specificity, mechanism, inhibitors and structural aspects. Progress in Biophysics and Molecular Biology. 63: 301-40. PMID 8599032 DOI: 10.1016/0079-6107(95)00008-9 |
0.321 |
|
1994 |
Willson M, Lauth N, Perie J, Callens M, Opperdoes FR. Inhibition of glyceraldehyde-3-phosphate dehydrogenase by phosphorylated epoxides and alpha-enones. Biochemistry. 33: 214-20. PMID 8286343 DOI: 10.1021/Bi00167A028 |
0.416 |
|
1994 |
Gefflaut T, Périé J. Synthesis of β-Keto-phosphotriesters Using Functionalized Diazoketones Synthetic Communications. 24: 29-33. DOI: 10.1080/00397919408012621 |
0.318 |
|
1994 |
Fabre J, Paul F, Monsan P, Blonski C, Périé J. Enzymatic synthesis of amino acid ester of butyl α-D-glucopyranoside Tetrahedron Letters. 35: 3535-3536. DOI: 10.1016/S0040-4039(00)73229-1 |
0.344 |
|
1993 |
Willson M, Callens M, Kuntz DA, Perié J, Opperdoes FR. Synthesis and activity of inhibitors highly specific for the glycolytic enzymes from Trypanosoma brucei. Molecular and Biochemical Parasitology. 59: 201-10. PMID 8341319 DOI: 10.1016/0166-6851(93)90218-M |
0.404 |
|
1993 |
Perie J, Riviere-Alric I, Blonski C, Gefflaut T, Lauth de Viguerie N, Trinquier M, Willson M, Opperdoes FR, Callens M. Inhibition of the glycolytic enzymes in the trypanosome: an approach in the development of new leads in the therapy of parasitic diseases. Pharmacology & Therapeutics. 60: 347-65. PMID 8022865 DOI: 10.1016/0163-7258(93)90016-7 |
0.373 |
|
1993 |
Fabre J, Betbeder D, Paul F, Monsan P, Perie J. Regiospecific enzymic acylation of butyl α-d-glucopyranoside Carbohydrate Research. 243: 407-411. DOI: 10.1016/0008-6215(93)87045-T |
0.36 |
|
1992 |
Willson M, Périé J, Malecaze F, Opperdoes F, Callens M. Biological properties of amidinium sulfinic and sulfonic acid derivatives: inhibition of glycolytic enzymes of Trypanosoma brucei and protective effect on cell growth European Journal of Medicinal Chemistry. 27: 799-808. DOI: 10.1016/0223-5234(92)90114-G |
0.373 |
|
1991 |
Riviere-Alric I, Willson M, Perie J. SYNTHÈSE D'ANALOGUES DE GLUCOSE-6 PHOSPHATE, INHIBITEURS POTENTIELS D'sHEXOKINASE Phosphorus Sulfur and Silicon and the Related Elements. 56: 71-80. DOI: 10.1080/10426509108038068 |
0.332 |
|
1991 |
Pradines A, Klaebe A, Perie J, Paul F, Monsan P. Large-scale enzymatic synthesis of glycerol 1-phosphate Enzyme and Microbial Technology. 13: 19-23. DOI: 10.1016/0141-0229(91)90183-B |
0.352 |
|
1981 |
Michel E, Perie J, Lattes A. NMR investigation of aryl- and benzyl-mercuric compounds; experimental evidence for σπ conjugation involving the carbon-mercury bond Journal of Organometallic Chemistry. 204: 1-12. DOI: 10.1016/S0022-328X(00)82466-3 |
0.309 |
|
1981 |
Nedjar-Kolli B, Hamdi M, Perie J, Herault V. Structure And New Syntheses In The Series Of 4-Amino-5,6-Dihydro-6-Methyl-2-Pyrones Cheminform. 12. DOI: 10.1002/Chin.198150231 |
0.302 |
|
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