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• W2056541680 abstract "Analogs of oxytocin containing tetrahydroisoquinoline carboxylic acid (Tic) of L or D configuration in position 2 were synthesized and their biological activities were tested. Both analogs showed negligible agonist activity in uterotonic, galactogogic, and pressor assays, but they are in vitro uterotonic inhibitors. In comparison with oxytocin analogs containing l- or D-phenylalanine in position 2, the analog with the D-configuration of the conformationally fixed aromatic residue has significantly increased inhibitory activity which suggests that the proper conformation for the interaction with the receptor, but not for its activation, was stabilized. 1H NMR and CD studies, supported by theoretical calculations, suggest that the conformational properties of the analog containing D-tetrahydroisoquinoline carboxylic acid are similar to those of [2D-phenylalaninejoxytocin." @default.
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• W2056541680 date "2009-01-12" @default.
• W2056541680 modified "2023-10-10" @default.
• W2056541680 title "Conformationally restricted analogs of oxytocin; stabilization of inhibitory conformation†" @default.
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• W2056541680 doi "https://doi.org/10.1111/j.1399-3011.1990.tb01289.x" @default.
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