المؤلفون: Chiara Pecchini, Chiara Cocconcelli, Andrea Mozzarelli, Gabriele Costantino, Barbara Campanini, Claudia Beato, Marco Pieroni, Marialaura Marchetti

المصدر: Journal of enzyme inhibition and medicinal chemistry
31 (2016): 645–652. doi:10.3109/14756366.2015.1057720
info:cnr-pdr/source/autori:Beato C, Pecchini C, Cocconcelli C, Campanini B, Marchetti ML, Pieroni M, Mozzarelli A, Costantino G/titolo:Cyclopropane derivatives as potential human serine racemase inhibitors: unveiling novel insights into a difficult target/doi:10.3109%2F14756366.2015.1057720/rivista:Journal of enzyme inhibition and medicinal chemistry (Print)/anno:2016/pagina_da:645/pagina_a:652/intervallo_pagine:645–652/volume:31

مصطلحات موضوعية: Cyclopropanes, 0301 basic medicine, Stereochemistry, Racemases and Epimerases, Malonic acid, Inhibitory postsynaptic potential, Cyclopropane, Structure-Activity Relationship, 03 medical and health sciences, chemistry.chemical_compound, Drug Discovery, Humans, Enzyme Inhibitors, Inhibition, Binding affinities, Pharmacology, chemistry.chemical_classification, Dose-Response Relationship, Drug, Molecular Structure, General Medicine, Molecular Docking Simulation, Serine recemase, 030104 developmental biology, Dicarboxylic acid, chemistry, Biochemistry, Serine racemase, Molecular docking, Glycine, Conformational ensemble, NMDA receptor

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bf2077a646f095d4b3aa2fb0a0d310f