| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5823807 | Biochemical Pharmacology | 2012 | 9 Pages |
Abstract
Discovery of new chemical entities (NCEs) as potential A3AR ligands that incorporate a benzo-γ-pyrone substructure.
Keywords
EI-MSPHEDADCysLEUNCEASNBOPZM241385tetramethylsilaneDMFMOPACBBr3(benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphatePyBOPTMS4-(2-[7-Amino-2-(2-furyl)[1,2,4]triazolo[2,3-a][1,3,5]triazin-5-ylamino]ethyl)phenol[3H]NECAR-PIATrpSARTLCASPnuclear magnetic resonanceN,N-diisopropylethylamineArginineAsparagineAspartic acidDiode-array detectorArgglutamic acidUltravioletisoleucineIleChoBoron tribromideTryptophanNMRTyrTyrosinedimethylformamidestructure–affinity relationshipChinese hamster ovary cellsCysteinePhenylalanineLeucineMolecular Operating Environmentinhibition constantnew chemical entityDIPEAPROMOEProlinethin layer chromatographyhigh performance liquid chromatographyHPLCDrug discoveryGluPlantsAdenosine receptor
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Authors
Alexandra Gaspar, Joana Reis, Sonja Kachler, Silvia Paoletta, Eugenio Uriarte, Karl-Norbert Klotz, Stefano Moro, Fernanda Borges,