Výsledky vyhledávání

Non-peptide NK(1) receptor ligands based on the 4-phenylpyridine moiety

Autor: Giuliani G. 1, Cappelli A. 1, Matarrese M. 2, 3, Masiello V. 2, Turolla E.A. 2, Monterisi C. 2, Fazio F. 3, Anzini M. 1, Pericot Mohr G.L. 1, Riitano D. 3, Finetti F. 4, Morbidelli L. 4, Ziche M. 4, Giorgi G. 5, Vomero S. 1

Publikováno v: Bioorganic & medicinal chemistry
19 (2011): 2242–2251.
info:cnr-pdr/source/autori:Giuliani G. 1, Cappelli A. 1, Matarrese M. 2,3, Masiello V. 2,3, Turolla E.A. 2,3, Monterisi C. 2,3, Fazio F. 3, Anzini M. 1, Pericot Mohr G.L. 1, Riitano D. 3, Finetti F. 4, Morbidelli L. 4, Ziche M. 4, Giorgi G. 5, Vomero S. 1/titolo:Non-peptide NK(1) receptor ligands based on the 4-phenylpyridine moiety./doi:/rivista:Bioorganic & medicinal chemistry (Print)/anno:2011/pagina_da:2242/pagina_a:2251/intervallo_pagine:2242–2251/volume:19

The quinoline nucleus of the previously described 4-phenylquinoline-3-carboxamides NK(1) receptor ligands 7 has been transformed into either substituted or azole-(i.e., triazole or tetrazole) fused pyridine moieties of compounds 9 and 10, respectivel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::198f0595b462c82e9a680b2aaecb5b43
https://publications.cnr.it/doc/10528

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Radiosynthesis and preliminary biological evaluation of [18F]VC701, antagonist of PBR receptor, potentially useful for the study of neurodegenerative diseases

Autor: Monterisi C. 1, Masiello V. 1, Moresco R.M. 1, Cappelli A. 3, Valtorta S1., Di Grigoli G. 2, Valenti S. 3, Anzini M. 3, Vomero S. 3, Fazio F. 1, Gianolli L. 1, Messa C. 1, Matarrese M. 1

Publikováno v: 4th European Molecular Imaging Meeting, Barcellona (Spagna), 2009
info:cnr-pdr/source/autori:Monterisi C. 1, Masiello V. 1, Moresco R.M. 1, Cappelli A. 3, Valtorta S1., Di Grigoli G. 2, Valenti S. 3, Anzini M. 3, Vomero S. 3, Fazio F. 1, Gianolli L. 1, Messa C. 1, Matarrese M. 1/congresso_nome:4th European Molecular Imaging Meeting/congresso_luogo:Barcellona (Spagna)/congresso_data:2009/anno:2009/pagina_da:/pagina_a:/intervallo_pagine

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::25eeea7937ffd969c940c7b069a445ae
https://publications.cnr.it/doc/101735

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Akademický článek

Current advances in the structure-activity relationship (SAR) analysis of the old/new 18-kDa translocator protein ligands.

Autor: Singh P; Department of Chemistry, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, 226025, India., Singh VK; Department of Chemistry, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, 226025, India., Gond C; Department of Chemistry, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, 226025, India., Singh D; Department of Chemistry, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, 226025, India., Tiwari AK; Department of Chemistry, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, 226025, India. anjanik2003@gmail.com.

Publikováno v: Molecular diversity [Mol Divers] 2024 Dec 04. Date of Electronic Publication: 2024 Dec 04.

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Anionic polymerization of a benzoful-vene monomer leading to a thermoreversible p-stacked polymer. Studies in macromolecular and aggregate structure

Autor: Cappelli A., Galeazzi S., Giuliani G., Anzini M., Aggravi M., Donati A., Zetta L., Boccia A., Mendichi R., Giorgi G., Paccagnini E., Vomero S.

Publikováno v: Macromolecules
41 (2008): 2324–2334.
info:cnr-pdr/source/autori:Cappelli A., Galeazzi S., Giuliani G., Anzini M., Aggravi M., Donati A., Zetta L., Boccia A., Mendichi R., Giorgi G., Paccagnini E., Vomero S.,/titolo:Anionic polymerization of a benzoful-vene monomer leading to a thermoreversible p-stacked polymer. Studies in macromolecular and aggregate structure/doi:/rivista:Macromolecules (Print)/anno:2008/pagina_da:2324/pagina_a:2334/intervallo_pagine:2324–2334/volume:41

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::e5245bf4d5aa3c232d04378f35f3d632
https://publications.cnr.it/doc/54403

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Structure-affinity relationship studies on arylpiperazine derivatives related to quizapine as serotonin transporter ligands. Molecular basis of the selectivity SERT/5HT3 receptor

Autor: Cappelli A. 1, Giuliani G. 1, Gallelli A. 1, Valenti S. 1, Anzini M. 1, Mennuni L. 2, Makovec F. 2, Cupello A. 3, Vomero S. 1

Publikováno v: Bioorganic & medicinal chemistry
13 (2005): 3455–3460.
info:cnr-pdr/source/autori:Cappelli A. 1, Giuliani G. 1, Gallelli A. 1, Valenti S. 1, Anzini M. 1, Mennuni L. 2, Makovec F. 2, Cupello A. 3, Vomero S. 1/titolo:Structure-affinity relationship studies on arylpiperazine derivatives related to quizapine as serotonin transporter ligands. Molecular basis of the selectivity SERT%2F5HT3 receptor/doi:/rivista:Bioorganic & medicinal chemistry (Print)/anno:2005/pagina_da:3455/pagina_a:3460/intervallo_pagine:3455–3460/volume:13

A series of quipazine derivatives, previously synthesized to probe the 5-HT(3) receptor, was evaluated for its potential interaction with serotonin transporter (SERT). Some of them show nanomolar affinity for the rodent SERT comparable to or slightly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::cd2543961f8d38abd60b6f5f7cc61891
http://www.cnr.it/prodotto/i/10153

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A new p-stacked Benzofulvene polymer showing a thermoreversible polymerization behavior. Studies of the macromolecular and supramolecular architectures and of the polymerization mechanism

Autor: Cappelli A., Anzini M., Vomero S., Donati A., Zetta L., Mendichi R., Casolaro M., Lupetti P., Salvatici P., Giorgi G.

Publikováno v: 43 (2005): 3289–3304.
info:cnr-pdr/source/autori:Cappelli A., Anzini M., Vomero S., Donati A., Zetta L., Mendichi R., Casolaro M., Lupetti P., Salvatici P., Giorgi G./titolo:A new p-stacked Benzofulvene polymer showing a thermoreversible polymerization behavior. Studies of the macromolecular and supramolecular architectures and of the polymerization mechanism/doi:/rivista:/anno:2005/pagina_da:3289/pagina_a:3304/intervallo_pagine:3289–3304/volume:43

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::fb2754b4f1d0bf9916a0ec55ea5e0c5d
http://www.cnr.it/prodotto/i/54164

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Synthesis and characterization of a new Benzofulvene polymer showing self-assembling and thermal-induced disassembling properties

Autor: Cappelli A. Pericot Mohr G. Anzini A. Vomero S. Donati A., Casolaro M. Mendichi R., Giorgi G., Makovec F.

Publikováno v: Journal of organic chemistry 68 (2003): 9473–9476.
info:cnr-pdr/source/autori:Cappelli A. Pericot Mohr G. Anzini A. Vomero S. Donati A., Casolaro M. Mendichi R., Giorgi G., Makovec F./titolo:Synthesis and characterization of a new Benzofulvene polymer showing self-assembling and thermal-induced disassembling properties/doi:/rivista:Journal of organic chemistry/anno:2003/pagina_da:9473/pagina_a:9476/intervallo_pagine:9473–9476/volume:68

A new polymer based on a functionalized benzofulvene moiety has been synthesized by spontaneous polymerization of the monomer in the solid state. This polymer shows a very high molar mass, high solubility in the most common organic solvents and therm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::cde072bbc04cfb547322feb6427afa8e
http://www.cnr.it/prodotto/i/54134

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