Reaction Details | |||
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Target | Adenosine receptor A2a | ||
Ligand | BDBM50393187 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_852589 (CHEMBL2156700) | ||
Ki | 830±n/a nM | ||
Citation | Drabczynska, A; Yuzlenko, O; Köse, M; Paskaleva, M; Schiedel, AC; Karolak-Wojciechowska, J; Handzlik, J; Karcz, T; Kuder, K; Müller, CE; Kiec-Kononowicz, K Synthesis and biological activity of tricyclic cycloalkylimidazo-, pyrimido- and diazepinopurinediones. Eur J Med Chem46:3590-607 (2011) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Adenosine receptor A2a | |||
Name: | Adenosine receptor A2a | ||
Synonyms: | AA2AR_RAT | ADENOSINE A2a | Adenosine A2 receptor | Adenosine A2a receptor (A2a) | Adenosine Receptors A2a (A2a) | Adenosine receptor A2a and A3 | Adenosine receptors A2a | Adora2a | Rat striatal adenosine A2a receptor | ||
Type: | G Protein-Coupled Receptor (GPCR) | ||
Mol. Mass.: | 45015.65 | ||
Organism: | Rattus norvegicus (rat) | ||
Description: | Rat A2A receptors expressed in CHO cells. | ||
Residue: | 410 | ||
Sequence: |
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BDBM50393187 | |||
n/a | |||
Name | BDBM50393187 | ||
Synonyms: | CHEMBL2153607 | ||
Type | Small organic molecule | ||
Emp. Form. | C18H27N5O2 | ||
Mol. Mass. | 345.4393 | ||
SMILES | CC1CCC(CC1)N1CCCCn2c1nc1n(C)c(=O)n(C)c(=O)c21 |(18.08,-19.63,;17.5,-18.21,;15.98,-18,;15.39,-16.59,;16.33,-15.37,;17.86,-15.56,;18.44,-16.99,;15.75,-13.95,;16.79,-12.78,;16.52,-11.25,;15.16,-10.49,;13.73,-11.09,;13.3,-12.59,;14.19,-13.86,;13.29,-15.1,;11.82,-14.62,;10.5,-15.38,;10.5,-16.92,;9.17,-14.62,;7.84,-15.39,;9.17,-13.08,;7.83,-12.32,;10.5,-12.31,;10.5,-10.77,;11.82,-13.08,)| | ||
Structure |