Pharmacophore-based discovery of substituted pyridines as novel dopamine transporter inhibitors (Q33964160)

30 July 2017

Pharmacophore-based discovery of substituted pyridines as novel dopamine transporter inhibitors (English)

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30 July 2017

Istvan J Enyedy

1

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30 July 2017

Sukumar Sakamuri

2

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30 July 2017

Wahiduz A Zaman

3

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30 July 2017

Kenneth M Johnson

4

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30 July 2017

Shaomeng Wang

5

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30 July 2017

language of work or name

English

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publication date

1 February 2003

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Bioorganic & Medicinal Chemistry Letters

30 July 2017

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30 July 2017

13

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30 July 2017

3

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30 July 2017

513-517

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Structure and function of the dopamine transporter

30 July 2017

1 reference

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Pharmacotherapies for treatment of cocaine abuse: preclinical aspects

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Thiazoloindans and Thiazolobenzopyrans: A Novel Class of Orally Active Central Dopamine (Partial) Agonists

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Imaging studies on the role of dopamine in cocaine reinforcement and addiction in humans

1 reference

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Pharmacophore-based discovery, synthesis, and biological evaluation of 4-phenyl-1-arylalkyl piperidines as dopamine transporter inhibitors

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Pharmacophore-based discovery of 3,4-disubstituted pyrrolidines as a novel class of monoamine transporter inhibitors.

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Discovery of substituted 3,4-diphenyl-thiazoles as a novel class of monoamine transporter inhibitors through 3-D pharmacophore search using a new pharmacophore model derived from mazindol

1 reference

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Molecular modeling, structure--activity relationships and functional antagonism studies of 4-hydroxy-1-methyl-4-(4-methylphenyl)-3-piperidyl 4-methylphenyl ketones as a novel class of dopamine transporter inhibitors.

1 reference

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2D QSAR modeling and preliminary database searching for dopamine transporter inhibitors using genetic algorithm variable selection of Molconn Z descriptors.

1 reference

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Chemistry and biology of the 2 beta-alkyl-3 beta-phenyl analogues of cocaine: subnanomolar affinity ligands that suggest a new pharmacophore model at the C-2 position

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Dopamine transporter site-directed mutations differentially alter substrate transport and cocaine binding

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2-Carbomethoxy-3-aryl-8-oxabicyclo[3.2.1]octanes: potent non-nitrogen inhibitors of monoamine transporters

1 reference

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National Cancer Institute Drug Information System 3D database.

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Further studies on conformationally constrained tricyclic tropane analogues and their uptake inhibition at monoamine transporter sites: synthesis of (Z)-9-(substituted arylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes as a novel class of serotonin t

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7 January 2021

10.1016/S0960-894X(02)00943-5

Identifiers

DOI

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30 July 2017

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