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Results: 1-9 |
Results: 9
Different phyllosilicates as supports for lipase immobilisation
Authors: de Fuentes, IE Viseras, CA Ubiali, D Terreni, M Alcantara, AR
Citation: Ie. De Fuentes et al., Different phyllosilicates as supports for lipase immobilisation, J MOL CAT B, 11(4-6), 2001, pp. 657-663
Modulation of penicillin acylase properties via immobilization techniques:One-pot chemoenzymatic synthesis of cephamandole from cephalosporin C
Authors: Terreni, M Pagani, G Ubiali, D Ferndandez-Lafuente, R Mateo, C Guisan, JM
Citation: M. Terreni et al., Modulation of penicillin acylase properties via immobilization techniques:One-pot chemoenzymatic synthesis of cephamandole from cephalosporin C, BIOORG MED, 11(18), 2001, pp. 2429-2432
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
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
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
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