CAMAIONI, Emidio

CAMAIONI, Emidio  

DIPARTIMENTO DI SCIENZE FARMACEUTICHE  

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Risultati 1 - 20 di 155 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
1μs Molecular Dynamics Simulations to study the poisoning effect of the PARP-1 full length enzyme 1-gen-2014 Marchand, Jean Rémy; Carotti, Andrea; Camaioni, Emidio; Pellicciari, Roberto; Macchiarulo, Antonio
2-Alkenyl and 2-alkyl derivatives of adenosine and adenosine-5'-N-ethyluronamide: different affinity and selectivity of E- and Z-diastereomers at A2A adenosine receptors. 1-gen-1996 Vittori, S; Camaioni, Emidio; Di Francesco, E; Volpini, R; Monopoli, A; Dionisotti, S; Ongini, E; Cristalli, G.
2-Alkynyl derivatives of adenosine-5'-N-ethyluronamide: selective A2 adenosine receptor agonists with potent inhibitory activity on platelet aggregation. 1-gen-1994 Cristalli, G; Volpini, R; Vittori, S; Camaioni, Emidio; Monopoli, A; Conti, A; Dionisotti, S; Zocchi, C; Ongini, E.
2-Aralkynyl and 2-heteroalkynyl derivatives of adenosine-5'-N-ethyluronamide as selective A2a adenosine receptor agonists. 1-gen-1995 Cristalli, G; Camaioni, Emidio; Vittori, S; Volpini, R; Borea, Pa; Conti, A; Dionisotti, S; Ongini, E; Monopoli, A.
2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors 1-gen-1999 Klotz, K.; Camaioni, Emidio; Volpini, R.; Kachler, S.; Vittori, S.; Cristalli, G.
3alpha-6alpha-Dihydroxy-7alpha-fluoro-5beta-cholanoate (UPF-680), physicochemical and physiological properties of a new fluorinated bile acid that prevents 17alpha-ethynyl-estradiol-induced cholestasis in rats. 1-gen-2006 Clerici, C; Castellani, D; Asciutti, S; Pellicciari, R; Setchell, Kd; O'Connell, Nc; Sadeghpour, B; Camaioni, Emidio; Fiorucci, Stefano; Renga, B; Nardi, E; Sabatino, G; Clementi, M; Giuliano, V; Baldoni, Monia; Orlandi, S; Mazzocchi, A; Morelli, Antonio; Morelli, Olivia
3alpha-6alpha-Dihydroxy-7alpha-fluoro-5beta-cholanoate (UPF-680), physicochemical and physiological properties of a new fluorinated bile acid that prevents 17alpha-ethynyl-estradiol-induced cholestasis in rats.. 1-gen-2006 Clerici, C; Castellani, D; Asciutti, S; Pellicciari, R; Setchell, Kd; O'Connell, Nc; Sadeghpour, B; Camaioni, Emidio; Fiorucci, Stefano; Renga, Barbara; Nardi, E; Sabatino, G; Clementi, M; Giuliano, V; Baldoni, M; Orlandi, S; Mazzocchi, A; Morelli, A; Morelli, O.
6a-Ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity. 1-gen-2002 Pellicciari, Roberto; Fiorucci, Stefano; Camaioni, Emidio; Clerici, C.; Costantino, G.; Moloney, P.; Morelli, A.; Parks, D.; Willson, T.
6α-Ethyl-Chenodeoxycholic Acid (6-ECDCA), a Potent and Selective FXR Agonist Endowed with Anticholestatic Activity 1-gen-2002 Roberto, Pellicciari; Fiorucci, Stefano; Camaioni, Emidio; Carlo, Clerici; Gabriele, Costantino; Patrick R., Maloney; Antonio, Morelli; Derek J., Parks; Timothy M., Willson
8-Bromo-9-etiladenine come tools per l’ottenimento di antagonisti selettivi per il recettore adenosinico A2B 1-gen-2002 S., Taffi; C., Lambertucci; Camaioni, Emidio; S., Costanzi; R., Volpini; S., Vittori; G., Cristalli
Adenosine deaminase inhibitors: Structure-activity relationships in 1-deazaadenosine and erythro-9-(2-hydroxy-3-nonyl)adenine analogues 1-gen-1993 G., Cristalli; A., Eleuteri; S., Vittori; R., Volpini; Camaioni, Emidio; G., Lupidi
Adenosine deaminase inhibitors: synthesis and structure-activity relationships of 2-hydroxy-3-nonyl derivatives of azoles. 1-gen-1994 Cristalli, G; Eleuteri, A; Volpini, R; Vittori, S; Camaioni, Emidio; Lupidi, G.
Adenosine deaminase inhibitors: synthesis, diastereoisomeric resolution and biological activity of 1-(2-hydroxy-3-nonyl)-1,2,4-triazole-3-carboxamide. 1-gen-1997 Volpini, R; Camaioni, Emidio; Lupidi, G; Vittori, S; Cristalli, G.
Adenosine deaminase – A target for new piperazine derivatives 1-gen-2021 Bakaryan, Anahit; Karapetyan, Luiza; Hakobyan, Naira; Camaioni, Emidio; Mardanyan, Sona; Antonyan, Alvard
Adenosine Deaminase: Functional Implications and Different Classes of Inhibitors 1-gen-2001 Cristalli, G.; Costanzi, S.; Lambertucci, C.; Lupidi, G.; Vittori, S.; Volpini, R.; Camaioni, Emidio
Adenosine receptor agonists: Synthesis and biological evaluation of the diastereoisomers of 2-(3-hydroxy-3-phenyl-1-propyn-1-yl)NECA 1-gen-1997 Camaioni, Emidio; Di Francesco, E; Vittori, S; Volpini, R; Cristalli, G.
Advances in indoleamine 2,3-dioxygenase 1 medicinal chemistry 1-gen-2017 Coletti, Alice; Greco, Francesco Antonio; Dolciami, Daniela; Camaioni, Emidio; Sardella, Roccaldo; Pallotta, Maria Teresa; Volpi, Claudia; Orabona, Ciriana; Grohmann, Ursula; Macchiarulo, Antonio
BF3·Et2O-Promoted Decomposition of Cyclic α-Diazo-β-Hydroxy Ketones: Novel Insights into Mechanistic Aspects 1-gen-2018 Venturoni, Francesco; Cerra, Bruno; Marinozzi, Maura; Camaioni, Emidio; Gioiello, Antimo; Pellicciari, Roberto
Bile Acid Derivatives as Ligands of the Farnesoid X Receptor. Synthesis, Evaluation, and Structure Activity Relationship of a Series of Body and Side Chain Modified Analogs of Chenodeoxycholic Acid 1-gen-2004 Pellicciari, Roberto; Costantino, Gabriele; Camaioni, Emidio; Sadeghpour, B. M.; Entrena Guadix, A.; Willson, T.; Fiorucci, Stefano; Clerici, C.; Gioiello, Antimo
Bile acids: property-activity relationship and molecular modelling studies 1-gen-2007 Natalini, Benedetto; Sardella, Roccaldo; Camaioni, Emidio; Macchiarulo, Antonio; Pellicciari, Roberto