期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 12, 期 19, 页码 2743-2747出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(02)00514-0
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Electrostatic potential surface mapping of various aromatic ring systems contained in 5-HT3R agonists indicate that some agonists contain an aromatic moiety capable of a favorable cation-pi interaction next to the e-face of pyridine (or its bioisostere). A pharmacophore model has been proposed based on superimposition of two distinct 'aryl' interactions. (C) 2002 Elsevier Science Ltd. All rights reserved.
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