Literature DB >> 9397171

N-hydroxyalkyl derivatives of 3 beta-phenyltropane and 1-methylspiro[1H-indoline-3,4'-piperidine]: vesamicol analogues with affinity for monoamine transporters.

S M Efange1, A P Kamath, A B Khare, M P Kung, R H Mach, S M Parsons.   

Abstract

As part of our ongoing structure-activity studies of the vesicular acetylcholine transporter ligand 2-(4-phenylpiperidino)cyclohexanol (vesamicol, 1), 22 N-hydroxy(phenyl)alkyl derivatives of 3 beta-phenyltropane, 6, and 1-methylspiro[1H-indoline-3,4'-piperidine], 7, were synthesized and tested for binding in vitro. Although a few compounds displayed moderately high affinity for the vesicular acetylcholine transporter, no compound was more potent than the prototypical vesicular acetylcholine transporter ligand vesamicol. However, a few derivatives of 6 displayed higher affinity for the dopamine transporter than cocaine. We conclude that modification of the piperidyl fragment of 1 will not lead to more potent vesicular acetylcholine transporter ligands.

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Year:  1997        PMID: 9397171     DOI: 10.1021/jm970326r

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Chemical structural novelty: on-targets and off-targets.

Authors:  Emmanuel R Yera; Ann E Cleves; Ajay N Jain
Journal:  J Med Chem       Date:  2011-09-14       Impact factor: 7.446

2.  Synthesis and in vitro biological evaluation of carbonyl group-containing inhibitors of vesicular acetylcholine transporter.

Authors:  Simon M N Efange; Anil B Khare; Krystyna von Hohenberg; Robert H Mach; Stanley M Parsons; Zhude Tu
Journal:  J Med Chem       Date:  2010-04-08       Impact factor: 7.446

3.  An efficient synthesis of a spirocyclic oxindole analogue.

Authors:  Dawei Teng; Hongxing Zhang; A Mendonca
Journal:  Molecules       Date:  2006-09-14       Impact factor: 4.411

  3 in total

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