9 research outputs found

    Binding Site of Loperamide: Automated Docking of Loperamide in Human mu- and delta-Opioid Receptors

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    Loperamide is a piperidine analogue, acting as agonist on peripheral opioid receptors, exhibiting affinity and selectivity for the cloned μ human opioid receptor compared with the δ human opioid receptor. Automatic docking studies of loperamide, using AutoDock, on human μ- and δ-opioid receptors is described. Whilst no meaningful difference was detected concerning the docking of the arylpiperidine moiety, μ/δ selectivity could be explained as a different accommodation of the two phenyl groups in two lipophylic pockets of receptor

    New benzo[g]isoquinoline-5,10-diones and dihydrothieno [2,3-b]naphtho-4,9-dione derivatives: synthesis and biological evaluation as potential antitumoral agents.

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    QSAR Studies on Thiazolidines: A Biologically Privileged Scaffold

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