Compounds selective for dopamine receptor subtypes
Novel dopamine (DA) receptor proteins of relatively low natural abundance and uncertain physiology can be expressed selectively in genetically transfected cultured cells to facilitate screening of novel DA receptor ligands. Selective agonists or antagonists for most of the five major DA receptor typ...
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Veröffentlicht in: | Drug discovery today 1997-08, Vol.2 (8), p.333-340 |
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creator | Kebabian, John W. Tarazi, Frank I. Kula, Nora S. Baldessarini, Ross J. |
description | Novel dopamine (DA) receptor proteins of relatively low natural abundance and uncertain physiology can be expressed selectively in genetically transfected cultured cells to facilitate screening of novel DA receptor ligands. Selective agonists or antagonists for most of the five major DA receptor types are emerging, but better D
4 and D
5 agonists, D
3 and D
5 antagonists, and more selective D
2 antagonists are needed. Clinical development of such compounds as diagnostic neuroradiopharmaceuticals or neuropsychiatric drugs remains empirical and somewhat unpredictable. The search for novel receptor-selective agents can be enhanced by better understanding of the physiology and pharmacology of DA neuroreceptors. |
doi_str_mv | 10.1016/S1359-6446(97)01075-1 |
format | Article |
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4 and D
5 agonists, D
3 and D
5 antagonists, and more selective D
2 antagonists are needed. Clinical development of such compounds as diagnostic neuroradiopharmaceuticals or neuropsychiatric drugs remains empirical and somewhat unpredictable. The search for novel receptor-selective agents can be enhanced by better understanding of the physiology and pharmacology of DA neuroreceptors.</description><identifier>ISSN: 1359-6446</identifier><identifier>EISSN: 1878-5832</identifier><identifier>DOI: 10.1016/S1359-6446(97)01075-1</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Catecholaminergic system ; Medical sciences ; Neuropharmacology ; Neurotransmitters. Neurotransmission. Receptors ; Pharmacology. Drug treatments</subject><ispartof>Drug discovery today, 1997-08, Vol.2 (8), p.333-340</ispartof><rights>1997 Elsevier Science Ltd. All rights reserved</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-a4db325714341f8344c5a6834d5991ae27c536e3c7c70c7a4c09376f919530583</citedby><cites>FETCH-LOGICAL-c367t-a4db325714341f8344c5a6834d5991ae27c536e3c7c70c7a4c09376f919530583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S1359-6446(97)01075-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2740478$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kebabian, John W.</creatorcontrib><creatorcontrib>Tarazi, Frank I.</creatorcontrib><creatorcontrib>Kula, Nora S.</creatorcontrib><creatorcontrib>Baldessarini, Ross J.</creatorcontrib><title>Compounds selective for dopamine receptor subtypes</title><title>Drug discovery today</title><description>Novel dopamine (DA) receptor proteins of relatively low natural abundance and uncertain physiology can be expressed selectively in genetically transfected cultured cells to facilitate screening of novel DA receptor ligands. Selective agonists or antagonists for most of the five major DA receptor types are emerging, but better D
4 and D
5 agonists, D
3 and D
5 antagonists, and more selective D
2 antagonists are needed. Clinical development of such compounds as diagnostic neuroradiopharmaceuticals or neuropsychiatric drugs remains empirical and somewhat unpredictable. The search for novel receptor-selective agents can be enhanced by better understanding of the physiology and pharmacology of DA neuroreceptors.</description><subject>Biological and medical sciences</subject><subject>Catecholaminergic system</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Neurotransmitters. Neurotransmission. Receptors</subject><subject>Pharmacology. Drug treatments</subject><issn>1359-6446</issn><issn>1878-5832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFUMtKBDEQDKLguvoJwhxE9DCanrwmJ5HFFyx4UM8hm-mByLxMZhb8e7MPvXqqpqnqripCzoHeAAV5-wZM6FxyLq-0uqZAlcjhgMygVGUuSlYcpvmXckxOYvykFAot5IwUi74d-qmrYhaxQTf6NWZ1H7KqH2zrO8wCOhzGtInTavweMJ6So9o2Ec_2OCcfjw_vi-d8-fr0srhf5o5JNeaWVytWCAWccahLxrkTViashNZgsVBOMInMKaeoU5Y7qpmStQYtGE225-Ryd3cI_deEcTStjw6bxnbYT9FAigNS00QUO6ILfYwBazME39rwbYCaTUNm25DZxDdamW1DBpLuYv_ARmebOtjO-fgnLhSnXG183O1omMKuPQYTncfOYeVTN6Opev_Pox8Cd3jL</recordid><startdate>19970801</startdate><enddate>19970801</enddate><creator>Kebabian, John W.</creator><creator>Tarazi, Frank I.</creator><creator>Kula, Nora S.</creator><creator>Baldessarini, Ross J.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>19970801</creationdate><title>Compounds selective for dopamine receptor subtypes</title><author>Kebabian, John W. ; Tarazi, Frank I. ; Kula, Nora S. ; Baldessarini, Ross J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-a4db325714341f8344c5a6834d5991ae27c536e3c7c70c7a4c09376f919530583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Catecholaminergic system</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Neurotransmitters. Neurotransmission. Receptors</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kebabian, John W.</creatorcontrib><creatorcontrib>Tarazi, Frank I.</creatorcontrib><creatorcontrib>Kula, Nora S.</creatorcontrib><creatorcontrib>Baldessarini, Ross J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Drug discovery today</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kebabian, John W.</au><au>Tarazi, Frank I.</au><au>Kula, Nora S.</au><au>Baldessarini, Ross J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Compounds selective for dopamine receptor subtypes</atitle><jtitle>Drug discovery today</jtitle><date>1997-08-01</date><risdate>1997</risdate><volume>2</volume><issue>8</issue><spage>333</spage><epage>340</epage><pages>333-340</pages><issn>1359-6446</issn><eissn>1878-5832</eissn><abstract>Novel dopamine (DA) receptor proteins of relatively low natural abundance and uncertain physiology can be expressed selectively in genetically transfected cultured cells to facilitate screening of novel DA receptor ligands. Selective agonists or antagonists for most of the five major DA receptor types are emerging, but better D
4 and D
5 agonists, D
3 and D
5 antagonists, and more selective D
2 antagonists are needed. Clinical development of such compounds as diagnostic neuroradiopharmaceuticals or neuropsychiatric drugs remains empirical and somewhat unpredictable. The search for novel receptor-selective agents can be enhanced by better understanding of the physiology and pharmacology of DA neuroreceptors.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S1359-6446(97)01075-1</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Catecholaminergic system Medical sciences Neuropharmacology Neurotransmitters. Neurotransmission. Receptors Pharmacology. Drug treatments |
title | Compounds selective for dopamine receptor subtypes |
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