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Hybrid approach for the design of highly affine and selective dopamine D(3) receptor ligands using privileged scaffolds of biogenic amine GPCR ligands.
Sasse, Britta C; Mach, Ulrich R; Leppaenen, Jukka; Calmels, Thierry; Stark, Holger.
Affiliation
  • Sasse BC; Institute of Pharmaceutical Chemistry, Johann Wolfgang Goethe-University, Max-von-Laue-Strasse 9, 60438 Frankfurt, Germany.
Bioorg Med Chem ; 15(23): 7258-73, 2007 Dec 01.
Article in En | MEDLINE | ID: mdl-17826096
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Collection: 01-internacional Database: MEDLINE Main subject: Drug Design / Receptors, Dopamine D3 / Histamine H1 Antagonists Limits: Animals / Humans Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2007 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido
Search on Google
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Collection: 01-internacional Database: MEDLINE Main subject: Drug Design / Receptors, Dopamine D3 / Histamine H1 Antagonists Limits: Animals / Humans Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2007 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido