Lee, BS Chu, S Lee, BC Chi, DY Choe, YS Jeong, KJ Jin, C 2024-01-21T13:41:31Z 2024-01-21T13:41:31Z 2021-09-04 2000-07-17 0960-894X https://pubs.kist.re.kr/handle/201004/141225 6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [H-3]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD 5-HYDROXYTRYPTAMINE UPTAKE COMPLEX DIFFERENT INTRINSIC EFFICACY I-125 5-IODO-6-NITROQUIPAZINE ARYLPIPERAZINE DERIVATIVES H-3 6-NITROQUIPAZINE SELECTIVE LIGAND UPTAKE SITES POTENT RAT INHIBITION Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1 Article 10.1016/S0960-894X(00)00290-0 1 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.10, no.14, pp.1559 - 1562 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 10 14 1559 1562 scie scopus 000088148700016 2-s2.0-0034679842 Chemistry, Medicinal Chemistry, Organic Pharmacology & Pharmacy Chemistry Article 5-HYDROXYTRYPTAMINE UPTAKE COMPLEX DIFFERENT INTRINSIC EFFICACY I-125 5-IODO-6-NITROQUIPAZINE ARYLPIPERAZINE DERIVATIVES H-3 6-NITROQUIPAZINE SELECTIVE LIGAND UPTAKE SITES POTENT RAT INHIBITION 6-nitroquipazine