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P V Plazzi

Showing results (31-40 of 40) with videos related to

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Farmaco (Societa Chimica Italiana : 1989)|November 1, 1992
Synthesis and binding assays of H3-receptor ligandsF Bordi, M Mor, P V Plazzi, et al.
Farmaco (Societa Chimica Italiana : 1989)|June 1, 1997
Plasma concentration and brain penetration of the H3-receptor antagonist thioperamide in ratsC Silva, M Mor, F Bordi, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1997
Ligands of the histamine H3-receptor: new potent antagonists of the 2-thioimidazole typeP V Plazzi, M Mor, F Bordi, et al.
Farmaco (Societa Chimica Italiana : 1989)|April 8, 2000
Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groupsM Mor, F Bordi, C Silva, et al.
Journal of Medicinal Chemistry|August 1, 1997
H3-receptor antagonists: synthesis and structure-activity relationships of para- and meta-substituted 4(5)-phenyl-2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazolesM Mor, F Bordi, C Silva, et al.
Journal of Medicinal Chemistry|August 25, 2001
2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonistsG Spadoni, C Balsamini, G Diamantini, et al.
Journal of Medicinal Chemistry|September 28, 1998
Melatonin receptor ligands: synthesis of new melatonin derivatives and comprehensive comparative molecular field analysis (CoMFA) studyM Mor, S Rivara, C Silva, et al.
Bioorganic & Medicinal Chemistry|May 17, 2001
Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligandsM Mor, G Spadoni, B Di Giacomo, et al.
Journal of Medicinal Chemistry|June 20, 1997
Conformationally restrained melatonin analogues: synthesis, binding affinity for the melatonin receptor, evaluation of the biological activity, and molecular modeling studyG Spadoni, C Balsamini, G Diamantini, et al.
Journal of Medicinal Chemistry|September 11, 1998
2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonistsG Spadoni, C Balsamini, A Bedini, et al.
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Showing results (31-40 of 40) with videos related to

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Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Farmaco (Societa Chimica Italiana : 1989)|November 1, 1992
Synthesis and binding assays of H3-receptor ligandsF Bordi, M Mor, P V Plazzi, et al.
Farmaco (Societa Chimica Italiana : 1989)|June 1, 1997
Plasma concentration and brain penetration of the H3-receptor antagonist thioperamide in ratsC Silva, M Mor, F Bordi, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1997
Ligands of the histamine H3-receptor: new potent antagonists of the 2-thioimidazole typeP V Plazzi, M Mor, F Bordi, et al.
Farmaco (Societa Chimica Italiana : 1989)|April 8, 2000
Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groupsM Mor, F Bordi, C Silva, et al.
Journal of Medicinal Chemistry|August 1, 1997
H3-receptor antagonists: synthesis and structure-activity relationships of para- and meta-substituted 4(5)-phenyl-2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazolesM Mor, F Bordi, C Silva, et al.
Journal of Medicinal Chemistry|August 25, 2001
2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonistsG Spadoni, C Balsamini, G Diamantini, et al.
Journal of Medicinal Chemistry|September 28, 1998
Melatonin receptor ligands: synthesis of new melatonin derivatives and comprehensive comparative molecular field analysis (CoMFA) studyM Mor, S Rivara, C Silva, et al.
Bioorganic & Medicinal Chemistry|May 17, 2001
Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligandsM Mor, G Spadoni, B Di Giacomo, et al.
Journal of Medicinal Chemistry|June 20, 1997
Conformationally restrained melatonin analogues: synthesis, binding affinity for the melatonin receptor, evaluation of the biological activity, and molecular modeling studyG Spadoni, C Balsamini, G Diamantini, et al.
Journal of Medicinal Chemistry|September 11, 1998
2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonistsG Spadoni, C Balsamini, A Bedini, et al.
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