Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sabrina Zappitelli"'
Autor:
C.A. Maggi, Laura Quartara, Paola Cucchi, Luigi Rotondaro, Sandro Giuliani, Alessandro Giolitti, Francesca Bellucci, Sabrina Zappitelli, Claudio Catalani, Stefania Meini
Publikováno v:
British Journal of Pharmacology. 162:1202-1212
BACKGROUND AND PURPOSE Icatibant is a well-known kinin B2 receptor antagonist currently used for angiooedema attacks. MEN16132 is a non-peptide B2 receptor antagonist, more potent and long lasting than icatibant in different models. Here we studied t
Autor:
Maria Altamura, Antonio Guidi, Paola Cucchi, Carlo Alberto Maggi, Alessandro Giolitti, Claudio Catalani, Luigi Rotondaro, Franco Pasqui, Stefania Meini, Sabrina Zappitelli, Sandro Giuliani, Francesca Bellucci
Publikováno v:
European Journal of Pharmacology. 516:104-111
The pharmacological outline of a novel and original antagonist at the human tachykinin NK 2 receptor is presented, namely MEN13510 ( N - N ′-bis-[2-(1 H -indol-3-yl)-ethyl]- N , N ′-bis-(3-thiomorpholin-4-yl-propyl)-phthalamide). MEN13510 retaine
Autor:
Alessandro Giolitti, Sandro Giuliani, Francesca Bellucci, Paola Cucchi, Katrin Boels, Stefania Meini, Sabrina Zappitelli, Carlo Alberto Maggi, Laura Quartara, Luigi Rotondaro
Publikováno v:
British Journal of Pharmacology. 143:938-941
The aim of the present report was to investigate the ligand selectivity of the human orphan G-protein-coupled receptor GPR100 (hGPR100), recently identified as a novel bradykinin (BK) receptor, as compared with that of the human B2 receptor (hB2R) st
Autor:
Laura Quartara, Stefania Meini, Carlo Alberto Maggi, Paola Cucchi, Alessandro Giolitti, Luigi Rotondaro, Sandro Giuliani, Francesca Bellucci, Sabrina Zappitelli, Claudio Catalani
Publikováno v:
European Journal of Pharmacology. 491:121-125
The pharmacology of peptide and non-peptide bradykinin B2 receptor ligands was evaluated in the inositol phosphate (IP) production assay in CHO cells expressing the human bradykinin B2 receptor. The effect of single and double alanine mutation of D26
Autor:
Luigi Rotondaro, Carlo Alberto Maggi, Stefania Meini, Alessandro Giolitti, Sabrina Zappitelli, Wolfgang Reichert, Paola Cucchi, Francesca Bellucci, Laura Quartara, Claudio Catalani
Publikováno v:
British Journal of Pharmacology. 140:500-506
Binding affinity at the [3H]-BK binding site and activity as inositol phosphate (IP) production by the peptide bradykinin (BK) and the nonpeptide FR190997 were studied at wild-type or point-mutated human B2 receptors (hB2R) expressed in CHO cells. Th
Autor:
Francesca Bellucci, Stefania Meini, Riccardo Patacchini, Carlo Alberto Maggi, Danilo Giannotti, Sabrina Zappitelli, Luigi Rotondaro, Maria Altamura, Alessandro Giolitti
Publikováno v:
Journal of Medicinal Chemistry. 45:3418-3429
A new series of monocyclic pseudopeptidic tachykinin NK-2 receptor antagonists has been derived from nepadutant with the help of site-directed mutagenesis studies and QSAR models. MEN11558 is the lead compound which is evaluated on a series of 13 new
Autor:
Alessandro Giolitti, Laura Quartara, Stefania Meini, Carlo Alberto Maggi, Paola Cucchi, Sabrina Zappitelli, Luigi Rotondaro
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 80:303-309
FR173657, LF16,0335, and LF16,0687 are nonpeptide antagonists, endowed with high affinity and selectivity for the human kinin B2receptor. The kinin B2receptor belongs to the family of G-protein-coupled receptors with seven transmembrane (TM) helices.
Autor:
Luigi Rotondaro, Paola Cucchi, Sabrina Zappitelli, Carlo Alberto Maggi, Anna Rita Renzetti, Alessandro Giolitti
Publikováno v:
Neuropharmacology. 39:1422-1429
A series of 14 mutants on nine selected residues of the human tachykinin NK 2 receptor was produced and stably transfected into CHO cells to investigate the binding of the peptide MEN 11420 and the nonpeptide SR 48968 antagonists. The main interactio
Autor:
Francesca, Bellucci, Stefania, Meini, Paola, Cucchi, Claudio, Catalani, Wolfgang, Reichert, Sabrina, Zappitelli, Luigi, Rotondaro, Laura, Quartara, Alessandro, Giolitti, Carlo Alberto, Maggi
Publikováno v:
British journal of pharmacology. 140(3)
Binding affinity at the [3H]-BK binding site and activity as inositol phosphate (IP) production by the peptide bradykinin (BK) and the nonpeptide FR190997 were studied at wild-type or point-mutated human B2 receptors (hB2R) expressed in CHO cells. Th
Autor:
Carlo Alberto Maggi, Luigi Rotondaro, Paola Cucchi, Laura Quartara, Alessandro Giolitti, Stefania Meini, Sabrina Zappitelli
Publikováno v:
Peptides. 23(8)
The ligand receptor interactions involving the C-terminal moiety of kinin B 2 receptor antagonists Icatibant (H-DArg-Arg-Pro-Hyp-Gly-Thi-Ser-Dtic-Oic-Arg-OH), MEN 11270 (H-DArg-Arg-Pro-Hyp-Gly-Thi-c(Dab-Dtic-Oic-Arg)c(7γ-10α)) and a series of analo