AAAAAA

   
Results: 1-7 |
Results: 7
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
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
IN-VITRO CHARACTERIZATION OF POTENCY, AFFINITY AND SELECTIVITY OF H-3ANTAGONISTS - FROM THIOPERAMIDE TO THIOPERAMIDE UNRELATED IMIDAZOLE DERIVATIVES
Authors: BAROCELLI E BALLABENI V CARETTA A BERTONI S BORDI F RIVARA S SILVA C MOR M IMPICCIATORE M
Citation: E. Barocelli et al., IN-VITRO CHARACTERIZATION OF POTENCY, AFFINITY AND SELECTIVITY OF H-3ANTAGONISTS - FROM THIOPERAMIDE TO THIOPERAMIDE UNRELATED IMIDAZOLE DERIVATIVES, Il Farmaco, 52(6-7), 1997, pp. 463-469
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
Risultati: 1-7 |