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Results: 1-14 |
Results: 14
Immobilized penicillin G acylase as reactor and chiral selector in liquid chromatography
Authors: Massolini, G Calleri, E De Lorenzi, E Pregnolato, M Terreni, M Felix, G Gandini, C
Citation: G. Massolini et al., Immobilized penicillin G acylase as reactor and chiral selector in liquid chromatography, J CHROMAT A, 921(2), 2001, pp. 147-160
Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivatives
Authors: Salvetti, R Pregnolato, M Verri, A Focher, F Spadari, S Marchand, A Mathe, C Gosselin, G
Citation: R. Salvetti et al., Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivatives, NUCLEOS NUC, 20(4-7), 2001, pp. 1123-1125
Enantioselective enzymatic hydrolysis of racemic glycidyl esters by using immobilized porcine pancreas lipase with improved catalytic properties
Authors: Pregnolato, M Terreni, M de Fuentes, IE Leon, ARA Sabuquillo, P Fernandez-Lafuente, R Guisan, JM
Citation: M. Pregnolato et al., Enantioselective enzymatic hydrolysis of racemic glycidyl esters by using immobilized porcine pancreas lipase with improved catalytic properties, J MOL CAT B, 11(4-6), 2001, pp. 757-763
5-(trifluoromethyl)-beta-L-2 '-deoxyuridine, the L-enantiomer of trifluorothymidine: Stereospecific synthesis and antiherpetic evaluations
Authors: Salvetti, R Marchand, A Pregnolato, M Verri, A Spadari, S Focher, F Briant, M Sommadossi, JP Mathe, C Gosselin, G
Citation: R. Salvetti et al., 5-(trifluoromethyl)-beta-L-2 '-deoxyuridine, the L-enantiomer of trifluorothymidine: Stereospecific synthesis and antiherpetic evaluations, BIO MED CH, 9(7), 2001, pp. 1731-1738
Potentiation of inhibition of wild-type and mutant human immunodeficiency virus type 1 reverse transcriptases by combinations of nonnucleoside inhibitors and D- and L-(beta)-dideoxynucleoside triphosphate analogs
Authors: Maga, C Hubscher, U Pregnolato, M Ubiali, D Gosselin, G Spadari, S
Citation: C. Maga et al., Potentiation of inhibition of wild-type and mutant human immunodeficiency virus type 1 reverse transcriptases by combinations of nonnucleoside inhibitors and D- and L-(beta)-dideoxynucleoside triphosphate analogs, ANTIM AG CH, 45(4), 2001, pp. 1192-1200
Selective interaction of the human immunodeficiency virus type 1 reverse transcriptase nonnucleoside inhibitor efavirenz and its thio-substituted analog with different enzyme-substrate complexes
Authors: Maga, G Ubiali, D Salvetti, R Pregnolato, M Spadari, S
Citation: G. Maga et al., Selective interaction of the human immunodeficiency virus type 1 reverse transcriptase nonnucleoside inhibitor efavirenz and its thio-substituted analog with different enzyme-substrate complexes, ANTIM AG CH, 44(5), 2000, pp. 1186-1194
Synthesis and in vitro anti-Mycobacterium activity of N-alkyl-1,2-dihydro-2-thioxo-3-pyridinecarbothioamides. Preliminary toxicity and pharmacokinetic evaluation
Authors: Pagani, G Pregnolato, M Ubiali, D Terreni, M Piersimoni, C Scaglione, F Fraschini, F Gascon, AR Munoz, JLP
Citation: G. Pagani et al., Synthesis and in vitro anti-Mycobacterium activity of N-alkyl-1,2-dihydro-2-thioxo-3-pyridinecarbothioamides. Preliminary toxicity and pharmacokinetic evaluation, J MED CHEM, 43(2), 2000, pp. 199-204
Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis
Authors: Focher, F Ubiali, D Pregnolato, M Zhi, CX Gambino, J Wright, GE Spadari, S
Citation: F. Focher et al., Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis, J MED CHEM, 43(13), 2000, pp. 2601-2607
3H-[1,2]Dithiolo[3,4-b]pyridine-3-thione and its derivatives - Synthesis and antimicrobial activity
Authors: Pregnolato, M Terreni, M Ubiali, D Pagani, G Borgna, P Pastoni, F Zampollo, F
Citation: M. Pregnolato et al., 3H-[1,2]Dithiolo[3,4-b]pyridine-3-thione and its derivatives - Synthesis and antimicrobial activity, FARMACO, 55(11-12), 2000, pp. 669-679
Highly enantiospecific oxyfunctionalization of nonactivated hydrocarbon sites by perfluoro-cis-2-n-butyl-3-n-propyloxaziridine
Authors: Arnone, A Folettto, S Metrangolo, P Pregnolato, M Resnati, G
Citation: A. Arnone et al., Highly enantiospecific oxyfunctionalization of nonactivated hydrocarbon sites by perfluoro-cis-2-n-butyl-3-n-propyloxaziridine, ORG LETT, 1(2), 1999, pp. 281-284
Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors
Authors: Pregnolato, M Ubiali, D Verri, A Focher, F Spadari, S Sun, H Zhi, C Wright, GE
Citation: M. Pregnolato et al., Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors, NUCLEOS NUC, 18(4-5), 1999, pp. 709-711
High-performance liquid chromatography method for analyzing the antiretroviral agent efavirenz in human plasma
Authors: Villani, P Pregnolato, M Banfo, S Rettani, M Burroni, D Seminari, E Maserati, R Regazzi, MB
Citation: P. Villani et al., High-performance liquid chromatography method for analyzing the antiretroviral agent efavirenz in human plasma, THER DRUG M, 21(3), 1999, pp. 346-350
Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylase
Authors: Sun, HM Zhi, CX Wright, GE Ubiali, D Pregnolato, M Verri, A Focher, F Spadari, S
Citation: Hm. Sun et al., Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylase, J MED CHEM, 42(13), 1999, pp. 2344-2350
Antimicrobial and genotoxic activities of N-(2-hydroxyethyl)-1,2-benzisothiazol-3(2H)-thione carbamic esters
Authors: Zani, F Pregnolato, M Zampollo, F
Citation: F. Zani et al., Antimicrobial and genotoxic activities of N-(2-hydroxyethyl)-1,2-benzisothiazol-3(2H)-thione carbamic esters, FARMACO, 54(10), 1999, pp. 643-647
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