(Q48127563)

8 February 2018

title

Studies of selected phenyltropanes at monoamine transporters (English)

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8 February 2018

author

Richard G. Hunter

3

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8 February 2018

author name string

Kuhar MJ

1

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8 February 2018

McGirr KM

2

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8 February 2018

Lambert PD

4

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8 February 2018

Garrett BE

5

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8 February 2018

Carroll FI

6

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8 February 2018

publication date

1 August 1999

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8 February 2018

Drug and Alcohol Dependence

published in

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8 February 2018

volume

56

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8 February 2018

issue

1

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8 February 2018

page(s)

9-15

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8 February 2018

3 Beta-(4-ethyl-3-iodophenyl)nortropane-2 beta-carboxylic acid methyl ester as a high-affinity selective ligand for the serotonin transporter.

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Cocaine receptor: biochemical characterization and structure-activity relationships of cocaine analogues at the dopamine transporter

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Isopropyl and phenyl esters of 3 beta-(4-substituted phenyl)tropan-2 beta-carboxylic acids. Potent and selective compounds for the dopamine transporter.

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Cocaine and 3 beta-(4'-substituted phenyl)tropane-2 beta-carboxylic acid ester and amide analogues. New high-affinity and selective compounds for the dopamine transporter

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7 January 2021

Compounds Affecting the Central Nervous System. 4. 3.beta.-Phenyltropane-2-carboxylic Esters and Analogs

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Novel 2-substituted cocaine analogs: binding properties at dopamine transport sites in rat striatum

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7 January 2021

Synthesis and pharmacology of potential cocaine antagonists. 2. Structure-activity relationship studies of aromatic ring-substituted methylphenidate analogs

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7 January 2021

Molecular characterization of the dopamine transporter.

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7 January 2021

Synthesis and characterization of radioiodinated N-(3-iodopropen-1-yl)-2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropanes: potential dopamine reuptake site imaging agents

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Synthesis of 3-arylecgonine analogues as inhibitors of cocaine binding and dopamine uptake

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Cellular and molecular mechanisms of drug dependence

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Structure-activity relationship studies of cocaine: replacement of the C-2 ester group by vinyl argues against H-bonding and provides an esterase-resistant, high-affinity cocaine analogue

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The dopamine hypothesis of the reinforcing properties of cocaine

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Heteroaromatic analogs of 1-[2-(diphenylmethoxy)ethyl]- and 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR 12935 and GBR 12909) as high-affinity dopamine reuptake inhibitors.

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Substituted 3-phenyltropane analogs of cocaine: synthesis, inhibition of binding at cocaine recognition sites, and positron emission tomography imaging

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The discovery of an unusually selective and novel cocaine analog: difluoropine. Synthesis and inhibition of binding at cocaine recognition sites

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Cocaine receptors on dopamine transporters are related to self-administration of cocaine

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High affinity dopamine reuptake inhibitors as potential cocaine antagonists: a strategy for drug development.

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7 January 2021

Methoxylation of cocaine reduces binding affinity and produces compounds of differential binding and dopamine uptake inhibitory activity: discovery of a weak cocaine "antagonist".

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7 January 2021

Use of identical assay conditions for cocaine analog binding and dopamine uptake to identify potential cocaine antagonists

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7 January 2021

Rate of binding of various inhibitors at the dopamine transporter in vivo

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7 January 2021

Relationship between subjective effects of cocaine and dopamine transporter occupancy

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7 January 2021

Enantioselectivity of cocaine recognition sites: binding of (1S)- and (1R)-2 beta-carbomethoxy-3 beta-(4-iodophenyl)tropane (beta-CIT) to monoamine transporters.

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7 January 2021

10.1016/S0376-8716(99)00005-8

Identifiers

DOI

1 reference

8 February 2018

release_67t5znzl45gdxcjvvl25n5f32m

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/67t5znzl45gdxcjvvl25n5f32m

24 November 2022

mapped directly with Wikidata item

1 reference

8 February 2018