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Receptor models Portoghese

Metzger, T. G., Paterlini, M. G., Portoghese, P. S., Ferguson, D. M. (1996). Application of the message-address concept to the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor models. Neurochemical Research, 21, 1287-1294. [Pg.551]

Paterlini G, Portoghese P, Ferguson D. Molecular simulation of dynorphin A-(1—10) binding to extracellular loop 2 of the kappa opioid receptor. A model for receptor activation. J Med Chem 1997 40 3254-3262. [Pg.487]

Linner KM, Stickney BJ, Quist HE, Sharp BM, Portoghese PS (1998) The 5i opioid receptor antagonist, 7-benzylspiroindanylnaltrexone, prolongs renal allograft survival in a rat model. Eur J Pharmacol 354 R3-R5... [Pg.90]

Portoghese, P. S. From models to molecules opioid receptor dimers, bivalent ligands, and selective opioid receptor probes. J. Med. Chem. 2001, 44, 2259-2269. [Pg.571]

Fig. 24.13. A representation of the bimodal binding model of the p opioid receptor as proposed by Portoghese (84). Different opioid series bind to different surface areas of the same receptor protein. Fig. 24.13. A representation of the bimodal binding model of the p opioid receptor as proposed by Portoghese (84). Different opioid series bind to different surface areas of the same receptor protein.

See other pages where Receptor models Portoghese is mentioned: [Pg.367]    [Pg.444]    [Pg.226]    [Pg.456]    [Pg.478]    [Pg.486]    [Pg.487]    [Pg.367]    [Pg.381]    [Pg.996]    [Pg.90]   
See also in sourсe #XX -- [ Pg.475 , Pg.482 ]




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