V. Vecchietti

发表

Alkaloids of Ocotea acutangula

G. Palmisano, B. Danieli, C. Casagrande, 1981 .

Substituted 1-(aminomethyl)-2-(arylacetyl)-1,2,3,4-tetrahydroisoquinolines: a novel class of very potent antinociceptive agents with varying degrees of selectivity for kappa and mu opioid receptors.

G. Dondio, M. Sbacchi, V. Vecchietti, 1992, Journal of medicinal chemistry.

Selective kappa-opioid agonists: synthesis and structure-activity relationships of piperidines incorporating on oxo-containing acyl group.

G. Dondio, M. Sbacchi, V. Vecchietti, 1994, Journal of medicinal chemistry.

(2S)-1-(arylacetyl)-2-(aminomethyl)piperidine derivatives: novel, highly selective kappa opioid analgesics.

A. Giordani, V. Vecchietti, G. Clarke, 1991, Journal of medicinal chemistry.

2-Phenyl-4-quinolinecarboxamides: a novel class of potent and selective non-peptide competitive antagonists for the human neurokinin-3 receptor.

H. Sarau, J. Foley, A. Medhurst, 1996, Journal of medicinal chemistry.

Central and peripheral analgesic agents: chemical strategies for limiting brain penetration in kappa-opioid agonists belonging to different chemical classes.

M. Sbacchi, V. Vecchietti, G. Clarke, 1995, Farmaco.

Discovery of a novel class of selective non-peptide antagonists for the human neurokinin-3 receptor. 1. Identification of the 4-quinolinecarboxamide framework.

H. Sarau, A. Medhurst, C. Farina, 1997, Journal of medicinal chemistry.

Potent and selective non-peptidic delta opioid ligands based on the novel heterocycle-condensed octahydroisoquinoline structure

G. Dondio, P. Petrillo, V. Vecchietti, 1994, Regulatory Peptides.

Alkaloids of Ocotea acutangula

G. Palmisano, B. Danieli, C. Casagrande, 1981 .

Discovery of a novel class of selective non-peptide antagonists for the human neurokinin-3 receptor. 2. Identification of (S)-N-(1-phenylpropyl)-3-hydroxy-2-phenylquinoline-4-carboxamide (SB 223412).

H. Sarau, J. Foley, A. Medhurst, 1999, Journal of medicinal chemistry.

Synthesis and positive inotropic effect of 1-alkyl- and 1-acyl-6,7-dimethoxy-3-dimethylamino-1,2,3,4-tetrahydroquinolines

C. Casagrande, F. Santangelo, V. Vecchietti, 1994 .

Alkaloid and lignan constituents of Cinnamosma madagascariensis

V. Vecchietti, G. Ferrari, F. Pelizzoni, 1979 .

Substituted 1-(Aminomethyl)-2-(arylacetyl)-1,2,3,4- tetrahydroisoquinolines: A Novel Class of Very Potent Antinociceptive Agents with Varying Degrees of Selectivity for and μ Opioid Receptors.

G. Dondio, M. Sbacchi, V. Vecchietti, 1992 .

Enantiospecificity of kappa receptors: comparison of racemic compounds and active enantiomers in two novel series of kappa agonist analgesics.

G. Dondio, M. Sbacchi, V. Vecchietti, 1992, Chirality.

Discovery of a novel class of substituted pyrrolooctahydroisoquinolines as potent and selective delta opioid agonists, based on an extension of the message-address concept.

S Ronzoni, G. Dondio, M. Artico, 1997, Journal of medicinal chemistry.

Dopamine receptor agonists. I. Synthesis and pharmacological evaluation of 4-aryl-substituted analogues of 6,7-dihydroxy-2-amino tetralin (6,7-ADTN) and related indane compounds

M. Mabilia, C. Casagrande, F. Santangelo, 1992 .

(1S)-1-(aminomethyl)-2-(arylacetyl)-1,2,3,4-tetrahydroisoquinoline and heterocycle-condensed tetrahydropyridine derivatives: members of a novel class of very potent kappa opioid analgesics.

M. Sbacchi, V. Vecchietti, G. Clarke, 1991, Journal of medicinal chemistry.

THE ROLE OF THE “SPACER" IN THE OCTAHYDROISOQUINOLINE SERIES: DISCOVERY OF SB 213698, A NON-PEPTIDIC, POTENT AND SELECTIVE DELTA OPIOID AGONIST

G. Dondio, P. Petrillo, V. Vecchietti, 1995 .