Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Chiara Ghiron"'
Autor:
Chiara Ghiron
Publikováno v:
Journal of Acupuncture & Meridian Studies, Vol 12, Iss 1, Pp 25-28 (2019)
This literature study article will present the possibility of a correlation between the energy meridians of Traditional Chinese Medicine, which can be traced back to the recently described primo vessels (formerly known as Bong-Han ducts), their compo
Externí odkaz:
https://doaj.org/article/fc00a3427cfb47ccbe8c158ecb826a3c
Autor:
Chiara Ghiron, Russell J. Thomas
The book is comprised of a series of exercises in synthetic organic chemistry based around recent published syntheses. The exercises are designed to provide challenges for people with varying levels of experience from final year students to academic
Autor:
Chiara Ghiron
Publikováno v:
Journal of Acupuncture & Meridian Studies, Vol 12, Iss 1, Pp 25-28 (2019)
This literature study article will present the possibility of a correlation between the energy meridians of Traditional Chinese Medicine, which can be traced back to the recently described primo vessels (formerly known as Bong-Han ducts), their compo
Autor:
John Lunec, Iolanda Micco, Bernard T. Golding, Graeme Robertson, Matteo Magnani, Xiaohong Lu, Junfeng Liu, Ian R. Hardcastle, Alessandro Padova, Chiara Ghiron, Barry Dodd, Roger J. Griffin, Andrey V. Zaytsev, David R. Newell
Publikováno v:
Chemical Biology & Drug Design. 86:180-189
Two libraries of substituted benzimidazoles were designed using a 'scaffold-hopping' approach based on reported MDM2-p53 inhibitors. Substituents were chosen following library enumeration and docking into an MDM2 X-ray structure. Benzimidazole librar
Autor:
Simon N. Haydar, Jean Zhang, John Dunlop, Arianna Nencini, Laura Maccari, Elisa Turlizzi, Riccardo Zanaletti, Thomas A. Comery, Chiara Ghiron, Eva Genesio, Iolanda Micco, Cristiana Castaldo
Publikováno v:
European Journal of Medicinal Chemistry. 78:401-418
α7 nicotinic acetylcholine receptor agonists are promising therapeutic candidates for the treatment of cognitive impairment. As a follow up of our internal medicinal chemistry program we investigated a novel series of α7 nAChR agonists. Starting fr
Autor:
Thomas A. Comery, John Dunlop, Laura Maccari, Eva Genesio, Flora Jow, Carmela Pratelli, Chiara Ghiron, Riccardo Zanaletti, Elisa Turlizzi, Ilaria Ceccarelli, Laura Bettinetti, Iolanda Micco, Carla Scali, Simon N. Haydar, Arianna Nencini, Michela Valacchi, Cristiana Castaldo, Giuseppe Cocconcelli
Publikováno v:
Journal of Medicinal Chemistry. 55:10277-10281
α7 Nicotinic acetylcholine receptors (α7 nAChR) represent promising therapeutic candidates for the treatment of cognitive impairment associated with Alzheimer's disease (AD) and schizophrenia. A medicinal chemistry effort around previously reported
Autor:
Riccardo Zanaletti, John Dunlop, Flora Jow, Laura Maccari, Michela Valacchi, Iolanda Micco, Elisa Turlizzi, Cristiana Castaldo, Giovanni Gaviraghi, Simon N. Haydar, Giuseppe Cocconcelli, Thomas A. Comery, Chiara Ghiron, Laura Bettinetti, Carla Scali, Arianna Nencini
Publikováno v:
Journal of Medicinal Chemistry. 55:4806-4823
Alpha-7 nicotinic acetylcholine receptors (α7 nAChR) are implicated in the modulation of many cognitive functions such as attention, working memory, and episodic memory. For this reason, α7 nAChR agonists represent promising therapeutic candidates
Autor:
Yuhua Yang, Adam Davenport, Michael G. Kelly, Andrew Tasker, Michael Croghan, Guomin Yao, Fred D. Lott, Jeff D. Reagan, Christopher H. Fotsch, James Davis, Minghan Wang, Chiara Ghiron, Steve F. Poon, Qingping Zeng, David Martin, Elena Portero-Larragueta, Thomas Stephen Coulter, David J. St. Jean, Jonathan Hutchinson, Charles Henley, Kelly Regal, Paul E. Harrington, Sean Morony, Jeffrey Clarine, Jenny Ying-Lin Lu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5544-5547
The discovery of a series of novel and orally efficacious type II calcimimetics, developed from the lead compound 1, is described herein. Compound 22 suppressed plasma PTH levels relative to vehicle when dosed orally in a rat pharmacodynamic model.
Publikováno v:
Synthetic Communications. 40:2547-2555
A new and efficient synthesis for the preparation of novel 4-fluoro-2H-pyrazol-3-ylamines is described. It involves the reaction of an acyl chloride with fluoroacetonitrile and sequential ring closure of the α-fluoro-β-ketonitrile with hydrazine. U
Autor:
Federico Corelli, Serena Pasquini, Alessia Ligresti, Claudia Mugnaini, Vincenzo Di Marzo, Antonella Brizzi, Chiara Ghiron
Publikováno v:
Journal of combinatorial chemistry 11 (2009): 795–798. doi:10.1021/cc9000955
info:cnr-pdr/source/autori:Pasquini S; Mugnaini C; Brizzi A; Ligresti A; Di Marzo V; Ghiron C; Corelli F/titolo:Rapid combinatorial access to a library of 1,5-disubstituted-3-indole-N-alkylacetamides as CB2 receptor ligands/doi:10.1021%2Fcc9000955/rivista:Journal of combinatorial chemistry/anno:2009/pagina_da:795/pagina_a:798/intervallo_pagine:795–798/volume:11
info:cnr-pdr/source/autori:Pasquini S; Mugnaini C; Brizzi A; Ligresti A; Di Marzo V; Ghiron C; Corelli F/titolo:Rapid combinatorial access to a library of 1,5-disubstituted-3-indole-N-alkylacetamides as CB2 receptor ligands/doi:10.1021%2Fcc9000955/rivista:Journal of combinatorial chemistry/anno:2009/pagina_da:795/pagina_a:798/intervallo_pagine:795–798/volume:11
In our research program on new cannabinoid receptor modulators,9-11 we decided to investigate the possibility to identify novel CB2 ligands starting from commercially available 5-hydroxyindole-3-acetic acid (Figure 2). This scaffold offers three poin