Reaction Details |
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Target | Adenosine receptor A2a |
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Ligand | BDBM50061950 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_935777 (CHEMBL2317357) |
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Ki | 35±n/a nM |
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Citation | Rivara, S; Piersanti, G; Bartoccini, F; Diamantini, G; Pala, D; Riccioni, T; Stasi, MA; Cabri, W; Borsini, F; Mor, M; Tarzia, G; Minetti, P Synthesis of (E)-8-(3-chlorostyryl)caffeine analogues leading to 9-deazaxanthine derivatives as dual A(2A) antagonists/MAO-B inhibitors. J Med Chem56:1247-61 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Adenosine receptor A2a |
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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: | MGSSVYITVELAIAVLAILGNVLVCWAVWINSNLQNVTNFFVVSLAAADIAVGVLAIPFA
ITISTGFCAACHGCLFFACFVLVLTQSSIFSLLAIAIDRYIAIRIPLRYNGLVTGVRAKG
IIAICWVLSFAIGLTPMLGWNNCSQKDGNSTKTCGEGRVTCLFEDVVPMNYMVYYNFFAF
VLLPLLLMLAIYLRIFLAARRQLKQMESQPLPGERTRSTLQKEVHAAKSLAIIVGLFALC
WLPLHIINCFTFFCSTCRHAPPWLMYLAIILSHSNSVVNPFIYAYRIREFRQTFRKIIRT
HVLRRQEPFQAGGSSAWALAAHSTEGEQVSLRLNGHPLGVWANGSATHSGRRPNGYTLGL
GGGGSAQGSPRDVELPTQERQEGQEHPGLRGHLVQARVGASSWSSEFAPS
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BDBM50061950 |
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n/a |
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Name | BDBM50061950 |
Synonyms: | 8-((E)-2-Benzo[1,3]dioxol-5-yl-vinyl)-3,7-dimethyl-1-prop-2-ynyl-3,7-dihydro-purine-2,6-dione | CHEMBL342229 |
Type | Small organic molecule |
Emp. Form. | C19H16N4O4 |
Mol. Mass. | 364.3547 |
SMILES | Cn1c(\C=C\c2ccc3OCOc3c2)nc2n(C)c(=O)n(CC#C)c(=O)c12 |
Structure |
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