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Results: 1-11 |
Results: 11
MELATONIN RECEPTOR LIGANDS - SYNTHESIS OF NEW MELATONIN DERIVATIVES AND COMPREHENSIVE COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) STUDY
Authors: MOR M RIVARA S SILVA C BORDI F PLAZZI PV SPADONI G DIAMANTINI G BALSAMINI C TARZIA G FRASCHINI F LUCINI V NONNO R STANKOV BM
Citation: M. Mor et al., MELATONIN RECEPTOR LIGANDS - SYNTHESIS OF NEW MELATONIN DERIVATIVES AND COMPREHENSIVE COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) STUDY, Journal of medicinal chemistry, 41(20), 1998, pp. 3831-3844
2-[N-ACYLAMINO(C-1-C-3)ALKYL]INDOLES AS MT1 MELATONIN RECEPTOR PARTIAL AGONISTS, ANTAGONISTS, AND PUTATIVE INVERSE AGONISTS
Authors: SPADONI G BALSAMINI C BEDINI A DIAMANTINI G DIGIACOMO B TONTINI A TARZIA G MOR M PLAZZI PV RIVARA S NONNO R PANNACCI M LUCINI V FRASCHINI F STANKOV BM
Citation: G. Spadoni et al., 2-[N-ACYLAMINO(C-1-C-3)ALKYL]INDOLES AS MT1 MELATONIN RECEPTOR PARTIAL AGONISTS, ANTAGONISTS, AND PUTATIVE INVERSE AGONISTS, Journal of medicinal chemistry, 41(19), 1998, pp. 3624-3634
H-3 RECEPTOR ANTAGONISTS - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PARA-SUBSTITUTED AND META-SUBSTITUTED HENYL-2-[[2-[4(5)-IMIDAZOLYL]ETHYL]THIO]IMIDAZOLES
Authors: MOR M BORDI F SILVA C RIVARA S CRIVORI P PLAZZI PV BALLABENI V CARETTA A BAROCELLI E IMPICCIATORE M CARRUPT PA TESTA B
Citation: M. Mor et al., H-3 RECEPTOR ANTAGONISTS - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PARA-SUBSTITUTED AND META-SUBSTITUTED HENYL-2-[[2-[4(5)-IMIDAZOLYL]ETHYL]THIO]IMIDAZOLES, Journal of medicinal chemistry, 40(16), 1997, pp. 2571-2578
CONFORMATIONALLY RESTRAINED MELATONIN ANALOGS - SYNTHESIS, BINDING-AFFINITY FOR THE MELATONIN RECEPTOR, EVALUATION OF THE BIOLOGICAL-ACTIVITY, AND MOLECULAR MODELING STUDY
Authors: SPADONI G BALSAMINI C DIAMANTINI G DIGIACOMO B TARZIA G MOR M PLAZZI PV RIVARA S LUCINI V NONNO R PANNACCI M FRASCHINI F STANKOV BM
Citation: G. Spadoni et al., CONFORMATIONALLY RESTRAINED MELATONIN ANALOGS - SYNTHESIS, BINDING-AFFINITY FOR THE MELATONIN RECEPTOR, EVALUATION OF THE BIOLOGICAL-ACTIVITY, AND MOLECULAR MODELING STUDY, Journal of medicinal chemistry, 40(13), 1997, pp. 1990-2002
H-3 RECEPTOR ANTAGONISTS - CONFORMATIONAL-ANALYSIS OF THIOPERAMIDE AND X-RAY CRYSTAL-STRUCTURE OF THE ANALOG N-CYCLOHEXYL-4-METHYLPIPERIDINE-1-CARBOTHIOAMIDE
Authors: PLAZZI PV BORDI F MOR M COZZINI P DOMIANO P
Citation: Pv. Plazzi et al., H-3 RECEPTOR ANTAGONISTS - CONFORMATIONAL-ANALYSIS OF THIOPERAMIDE AND X-RAY CRYSTAL-STRUCTURE OF THE ANALOG N-CYCLOHEXYL-4-METHYLPIPERIDINE-1-CARBOTHIOAMIDE, Il Farmaco, 52(6-7), 1997, pp. 399-404
PLASMA-CONCENTRATION AND BRAIN PENETRATION OF THE H-3 RECEPTOR ANTAGONIST THIOPERAMIDE IN RATS
Authors: SILVA C MOR M BORDI F RIVARA S CARETTA A BALLABENI V BAROCELLI E PLAZZI PV
Citation: C. Silva et al., PLASMA-CONCENTRATION AND BRAIN PENETRATION OF THE H-3 RECEPTOR ANTAGONIST THIOPERAMIDE IN RATS, Il Farmaco, 52(6-7), 1997, pp. 457-462
LIGANDS OF THE HISTAMINE H-3 RECEPTOR - NEW POTENT ANTAGONISTS OF THE2-THIOIMIDAZOLE TYPE
Authors: PLAZZI PV MOR M BORDI F SILVA C RIVARA S CARETTA A BALLABENI V IMPICCIATORE M VITALI T
Citation: Pv. Plazzi et al., LIGANDS OF THE HISTAMINE H-3 RECEPTOR - NEW POTENT ANTAGONISTS OF THE2-THIOIMIDAZOLE TYPE, Il Farmaco, 52(5), 1997, pp. 295-302
RAT PROTEIN-BINDING AND CEREBRAL PHOSPHOLIPID AFFINITY OF THE H-3 RECEPTOR ANTAGONIST THIOPERAMIDE
Authors: PLAZZI PV MOR M SILVA C BORDI F MORINI G CRIVORI P CARETTA A
Citation: Pv. Plazzi et al., RAT PROTEIN-BINDING AND CEREBRAL PHOSPHOLIPID AFFINITY OF THE H-3 RECEPTOR ANTAGONIST THIOPERAMIDE, Journal of Pharmacy and Pharmacology, 48(7), 1996, pp. 712-717
BIOLOGICAL STUDIES ON 1,2-BENZISOTHIAZOLE DERIVATIVES .5. ANTIMICROBIAL PROPERTIES OF N-ALKANOIC, N-ARYLALKANOIC AND N-ARYLOXYALKANOIC DERIVATIVES OF 1,2-BENZISOTHIAZOLIN-3-ONE - QSAR STUDY AND GENOTOXICITY EVALUATION
Authors: MOR M ZANI F MAZZA P SILVA C BORDI F MORINI G PLAZZI PV
Citation: M. Mor et al., BIOLOGICAL STUDIES ON 1,2-BENZISOTHIAZOLE DERIVATIVES .5. ANTIMICROBIAL PROPERTIES OF N-ALKANOIC, N-ARYLALKANOIC AND N-ARYLOXYALKANOIC DERIVATIVES OF 1,2-BENZISOTHIAZOLIN-3-ONE - QSAR STUDY AND GENOTOXICITY EVALUATION, Il Farmaco, 51(7), 1996, pp. 493-501
HETEROARYLAMINOETHYL AND HETEROARYLTHIOETHYL IMIDAZOLES - SYNTHESIS AND H-3 RECEPTOR AFFINITY
Authors: PLAZZI PV BORDI F MOR M SILVA C MORINI G CARETTA A BAROCELLI E VITALI T
Citation: Pv. Plazzi et al., HETEROARYLAMINOETHYL AND HETEROARYLTHIOETHYL IMIDAZOLES - SYNTHESIS AND H-3 RECEPTOR AFFINITY, European journal of medicinal chemistry, 30(11), 1995, pp. 881-889
QSAR STUDY ON H3-RECEPTOR AFFINITY OF BENZOTHIAZOLE DERIVATIVES OF THIOPERAMIDE
Authors: BORDI F MOR M MORINI G PLAZZI PV SILVA C VITALI T CARETTA A
Citation: F. Bordi et al., QSAR STUDY ON H3-RECEPTOR AFFINITY OF BENZOTHIAZOLE DERIVATIVES OF THIOPERAMIDE, Il Farmaco, 49(3), 1994, pp. 153-166
Risultati: 1-11 |