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Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter.
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Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter.

Auteur: M Froimowitz Aangesloten bij: Massachusetts College of Pharmacy and Health Sciences, Boston, Massachusetts 02115, USA. mfroimowitz@mcphs.eduY GuLA DakinPM NagafujiCJ KelleyAlle auteurs
Editie/Formaat: Artikel Artikel : Engels
Publicatie:Journal of medicinal chemistry, 2007 Jan 25; 50(2): 219-32
Database:Van MEDLINE®/PubMed®, een database van de Amerikaanse National Library of Medicine.
Overige databases: British Library SerialsArticleFirst
Samenvatting:
Methylphenidate analogues, in which the carbomethoxy has been replaced by an alkyl group and with different phenyl substituents, have been synthesized and tested in monoamine transporter assays. As predicted from a pharmacophore model, most of the RR/SS diastereomers showed high potency as dopamine reuptake inhibitors. Analogues with a 4-chlorophenyl group and an unbranched initial alkyl atom had consistently  Meer lezen...
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Details

Soort document: Artikel
Alle auteurs / medewerkers: M Froimowitz Aangesloten bij: Massachusetts College of Pharmacy and Health Sciences, Boston, Massachusetts 02115, USA. mfroimowitz@mcphs.edu; Y Gu; LA Dakin; PM Nagafuji; CJ Kelley; D Parrish; JR Deschamps; A Janowsky
ISSN:0022-2623
Taalopmerking: English
Uniek kenmerk: 110081487
Onderscheidingen:

Fragment:

Methylphenidate analogues, in which the carbomethoxy has been replaced by an alkyl group and with different phenyl substituents, have been synthesized and tested in monoamine transporter assays. As predicted from a pharmacophore model, most of the RR/SS diastereomers showed high potency as dopamine reuptake inhibitors. Analogues with a 4-chlorophenyl group and an unbranched initial alkyl atom had consistently enhanced selectivity for the dopamine transporter. The most potent compounds were those with a three- or four-carbon chain. The "inactive" RS/SR diastereomers showed substantial activity when the phenyl substituent was 3,4-dichloro. On a locomotor assay, one compound was found to have a slow onset and a long duration of action. The activity of these compounds provides additional evidence for a conformational/superposition model of methylphenidate with cocaine-like structures. A ketone analogue, obtained by hydrogenating a previously described vinylogous amide, had activity similar to that of methylphenidate.

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