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Results: 1-22 |
Results: 22
INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE AS TOOLS FOR STUDYING THE MECHANISM AND FUNCTION OF THE ENZYME
Authors: CATTEL L CERUTI M
Citation: L. Cattel et M. Ceruti, INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE AS TOOLS FOR STUDYING THE MECHANISM AND FUNCTION OF THE ENZYME, Critical reviews in biochemistry and molecular biology, 33(5), 1998, pp. 353-373
29-METHYLIDENE-2,3-OXIDOSQUALENE DERIVATIVES AS STEREOSPECIFIC MECHANISM-BASED INHIBITORS OF LIVER AND YEAST OXIDOSQUALENE CYCLASE
Authors: CERUTI M ROCCO F VIOLA F BALLIANO G MILLA P ARPICCO S CATTEL L
Citation: M. Ceruti et al., 29-METHYLIDENE-2,3-OXIDOSQUALENE DERIVATIVES AS STEREOSPECIFIC MECHANISM-BASED INHIBITORS OF LIVER AND YEAST OXIDOSQUALENE CYCLASE, Journal of medicinal chemistry, 41(4), 1998, pp. 540-554
MASS-SPECTROMETRIC BEHAVIOR OF SOME 19-AZA AND 2-AZA SQUALENE DERIVATIVES
Authors: CERUTI M SERAGLIA R
Citation: M. Ceruti et R. Seraglia, MASS-SPECTROMETRIC BEHAVIOR OF SOME 19-AZA AND 2-AZA SQUALENE DERIVATIVES, Rapid communications in mass spectrometry, 11(3), 1997, pp. 321-324
IN-VITRO SUSCEPTIBILITY OF FUNGI TO ACYCLIC INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASES
Authors: AIRAUDI D CERUTI M BIANCO C MARCHISIO VF
Citation: D. Airaudi et al., IN-VITRO SUSCEPTIBILITY OF FUNGI TO ACYCLIC INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASES, Mycoses, 39(1-2), 1996, pp. 51-56
INHIBITION OF HIGHER-PLANT 2,3-OXIDOSQUALENE CYCLASES BY NITROGEN-CONTAINING OXIDOSQUALENE ANALOGS
Authors: TATON M CERUTI M CATTEL L RAHIER A
Citation: M. Taton et al., INHIBITION OF HIGHER-PLANT 2,3-OXIDOSQUALENE CYCLASES BY NITROGEN-CONTAINING OXIDOSQUALENE ANALOGS, Phytochemistry, 43(1), 1996, pp. 75-81
ENHANCEMENT OF RICIN TOXIN-A CHAIN IMMUNOTOXIN ACTIVITY - SYNTHESIS, IONOPHORETIC ABILITY, AND IN-VITRO ACTIVITY OF MONENSIN DERIVATIVES
Authors: DOSIO F FRANCESCHI A CERUTI M BRUSA P CATTEL L COLOMBATTI M
Citation: F. Dosio et al., ENHANCEMENT OF RICIN TOXIN-A CHAIN IMMUNOTOXIN ACTIVITY - SYNTHESIS, IONOPHORETIC ABILITY, AND IN-VITRO ACTIVITY OF MONENSIN DERIVATIVES, Biochemical pharmacology, 52(1), 1996, pp. 157-166
PRELIMINARY SCREENING OF SOME SQUALENOID DERIVATIVES FOR TOXICITY TOWARDS DERMATOPHYTES
Authors: AIRAUDI D CERUTI M GIANNETTA A MARCHISIO VF
Citation: D. Airaudi et al., PRELIMINARY SCREENING OF SOME SQUALENOID DERIVATIVES FOR TOXICITY TOWARDS DERMATOPHYTES, Mycoses, 38(7-8), 1995, pp. 311-315
STEREOCONTROLLED SYNTHESIS OF FLUOROSQUALENES AND FLUOROEPOXYSQUALENES AS INHIBITORS OF SQUALENE EPOXIDASE AND 2,3-OXIDOSQUALENE CYCLASE
Authors: CERUTI M AMISANO S MILLA P VIOLA F ROCCO F JUNG M CATTEL L
Citation: M. Ceruti et al., STEREOCONTROLLED SYNTHESIS OF FLUOROSQUALENES AND FLUOROEPOXYSQUALENES AS INHIBITORS OF SQUALENE EPOXIDASE AND 2,3-OXIDOSQUALENE CYCLASE, Journal of the Chemical Society. Perkin transactions. I, (7), 1995, pp. 889-893
2,3-OXIDOSQUALENE CYCLASE - FROM AZASQUALENES TO NEW SITE-DIRECTED INHIBITORS
Authors: CATTEL L CERUTI M BALLIANO G VIOLA F GROSA G ROCCO F BRUSA P
Citation: L. Cattel et al., 2,3-OXIDOSQUALENE CYCLASE - FROM AZASQUALENES TO NEW SITE-DIRECTED INHIBITORS, Lipids, 30(3), 1995, pp. 235-246
INHIBITION OF 2,3-OXIDOSQUALENE CYCLASE AND STEROL BIOSYNTHESIS BY 10-AZASQUALENE AND 19-AZASQUALENE DERIVATIVES
Authors: VIOLA F BRUSA P BALLIANO G CERUTI M BOUTAUD O SCHUBER F CATTEL L
Citation: F. Viola et al., INHIBITION OF 2,3-OXIDOSQUALENE CYCLASE AND STEROL BIOSYNTHESIS BY 10-AZASQUALENE AND 19-AZASQUALENE DERIVATIVES, Biochemical pharmacology, 50(6), 1995, pp. 787-796
RETENTION OF THE LABEL DURING THE CONVERSION OF [3-H-3]SQUALENE INTO (3S)-2,3-OXIDOSQUALENE CATALYZED BY MAMMALIAN SQUALENE OXIDASE
Authors: BOUTAUD O CERUTI M CATTEL L SCHUBER F
Citation: O. Boutaud et al., RETENTION OF THE LABEL DURING THE CONVERSION OF [3-H-3]SQUALENE INTO (3S)-2,3-OXIDOSQUALENE CATALYZED BY MAMMALIAN SQUALENE OXIDASE, Biochemical and biophysical research communications, 208(1), 1995, pp. 42-47
MASS-SPECTROMETRIC STUDIES ON AZASQUALENES, A CLASS OF 2,3-OXIDOSQUALENE CYCLASE INHIBITORS
Authors: CERUTI M SERAGLIA R TRALDI P
Citation: M. Ceruti et al., MASS-SPECTROMETRIC STUDIES ON AZASQUALENES, A CLASS OF 2,3-OXIDOSQUALENE CYCLASE INHIBITORS, Rapid communications in mass spectrometry, 8(1), 1994, pp. 59-64
A CONVENIENT SYNTHESIS OF [3-H-3]SQUALENE AND [3-H-3]-2,3-OXIDOSQUALENE
Authors: CERUTI M GROSA G ROCCO F DOSIO F CATTEL L
Citation: M. Ceruti et al., A CONVENIENT SYNTHESIS OF [3-H-3]SQUALENE AND [3-H-3]-2,3-OXIDOSQUALENE, Journal of labelled compounds & radiopharmaceuticals, 34(6), 1994, pp. 577-585
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A SQUALENOID MALEIMIDE AND OTHERCLASSES OF SQUALENE DERIVATIVES AS IRREVERSIBLE INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE
Authors: GROSA G VIOLA F CERUTI M BRUSA P DELPRINO L DOSIO F CATTEL L
Citation: G. Grosa et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A SQUALENOID MALEIMIDE AND OTHERCLASSES OF SQUALENE DERIVATIVES AS IRREVERSIBLE INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE, European journal of medicinal chemistry, 29(1), 1994, pp. 17-23
INHIBITION OF STEROL BIOSYNTHESIS IN SACCHAROMYCES-CEREVISIAE AND CANDIDA-ALBICANS BY 22,23-EPOXY-2-AZA-2,3-DIHYDROSQUALENE AND THE CORRESPONDING N-OXIDE
Authors: BALLIANO G MILLA P CERUTI M CARRANO L VIOLA F BRUSA P CATTEL L
Citation: G. Balliano et al., INHIBITION OF STEROL BIOSYNTHESIS IN SACCHAROMYCES-CEREVISIAE AND CANDIDA-ALBICANS BY 22,23-EPOXY-2-AZA-2,3-DIHYDROSQUALENE AND THE CORRESPONDING N-OXIDE, Antimicrobial agents and chemotherapy, 38(9), 1994, pp. 1904-1908
A NEW APPROACH IN THE SYNTHESIS OF IMMUNOTOXINS - RIBOSOME-INACTIVATING PROTEIN NONCOVALENTLY BOUND TO MONOCLONAL-ANTIBODY
Authors: DOSIO F BRUSA P DELPRINO L GROSA G CERUTI M CATTEL L
Citation: F. Dosio et al., A NEW APPROACH IN THE SYNTHESIS OF IMMUNOTOXINS - RIBOSOME-INACTIVATING PROTEIN NONCOVALENTLY BOUND TO MONOCLONAL-ANTIBODY, Journal of pharmaceutical sciences, 83(2), 1994, pp. 206-211
2,3,4,5-TETRAHYDROXY-5-(4-HYDROXYPHENYL)VALERIC ACID - A NEW CLEAVABLE MONOFUNCTIONAL REAGENT FOR MONOCLONAL-ANTIBODY LABELING
Authors: GROSA G DOSIO F BRUSA P CERUTI M DELPRINO L CATTEL L
Citation: G. Grosa et al., 2,3,4,5-TETRAHYDROXY-5-(4-HYDROXYPHENYL)VALERIC ACID - A NEW CLEAVABLE MONOFUNCTIONAL REAGENT FOR MONOCLONAL-ANTIBODY LABELING, Il Farmaco, 49(5), 1994, pp. 349-355
AN NMR AND MOLECULAR MECHANICS STUDY OF SQUALENE AND SQUALENE DERIVATIVES
Authors: POGLIANI L CERUTI M RICCHIARDI G VITERBO D
Citation: L. Pogliani et al., AN NMR AND MOLECULAR MECHANICS STUDY OF SQUALENE AND SQUALENE DERIVATIVES, Chemistry and physics of lipids, 70(1), 1994, pp. 21-34
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF 19-AZASQUALENE 2,3-EPOXIDE AS INHIBITOR OF 2,3-OXIDOSQUALENE CYCLASE
Authors: CERUTI M ROCCO F VIOLA F BALLIANO G GROSA G DOSIO F CATTEL L
Citation: M. Ceruti et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF 19-AZASQUALENE 2,3-EPOXIDE AS INHIBITOR OF 2,3-OXIDOSQUALENE CYCLASE, European journal of medicinal chemistry, 28(9), 1993, pp. 675-682
TOXIN-TARGETED DESIGN FOR ANTICANCER THERAPY .2. PREPARATION AND BIOLOGICAL COMPARISON OF DIFFERENT CHEMICALLY LINKED GELONIN ANTIBODY CONJUGATES
Authors: DELPRINO L GIACOMOTTI M DOSIO F BRUSA P CERUTI M GROSA G CATTEL L
Citation: L. Delprino et al., TOXIN-TARGETED DESIGN FOR ANTICANCER THERAPY .2. PREPARATION AND BIOLOGICAL COMPARISON OF DIFFERENT CHEMICALLY LINKED GELONIN ANTIBODY CONJUGATES, Journal of pharmaceutical sciences, 82(7), 1993, pp. 699-704
TOXIN-TARGETED DESIGN FOR ANTICANCER THERAPY .1. SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW THIOIMIDATE HETEROBIFUNCTIONAL REAGENTS
Authors: DELPRINO L GIACOMOTTI M DOSIO F BRUSA P CERUTI M GROSA G CATTEL L
Citation: L. Delprino et al., TOXIN-TARGETED DESIGN FOR ANTICANCER THERAPY .1. SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW THIOIMIDATE HETEROBIFUNCTIONAL REAGENTS, Journal of pharmaceutical sciences, 82(5), 1993, pp. 506-512
IN-VITRO METABOLISM OF 1,3-DIOXANE, 1,3-OXATHIOLANE, AND 1,3-DITHIANEDERIVATIVES OF THEOPHYLLINE - A STRUCTURE-METABOLISM CORRELATION STUDY
Authors: GROSA G ROCCO F CERUTI M DOSIO F BRUSA P BIGLINO G
Citation: G. Grosa et al., IN-VITRO METABOLISM OF 1,3-DIOXANE, 1,3-OXATHIOLANE, AND 1,3-DITHIANEDERIVATIVES OF THEOPHYLLINE - A STRUCTURE-METABOLISM CORRELATION STUDY, Il Farmaco, 48(5), 1993, pp. 677-690
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