Reaction Details |
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Target | Adenosine receptor A2a |
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Ligand | BDBM50151188 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_429600 (CHEMBL919032) |
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Ki | 14±n/a nM |
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Citation | Peng, H; Kumaravel, G; Yao, G; Sha, L; Wang, J; Van Vlijmen, H; Bohnert, T; Huang, C; Vu, CB; Ensinger, CL; Chang, H; Engber, TM; Whalley, ET; Petter, RC Novel bicyclic piperazine derivatives of triazolotriazine and triazolopyrimidines as highly potent and selective adenosine A2A receptor antagonists. J Med Chem47:6218-29 (2004) [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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BDBM50151188 |
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n/a |
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Name | BDBM50151188 |
Synonyms: | 5-(4-((5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)methyl)piperazin-1-yl)-2-(furan-2-yl)-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-amine | 5-[4-(5-Chloro-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethyl)-piperazin-1-yl]-2-furan-2-yl-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamine | CHEMBL189192 |
Type | Small organic molecule |
Emp. Form. | C18H18ClF3N10O |
Mol. Mass. | 482.85 |
SMILES | Cn1nc(c(CN2CCN(CC2)c2nc(N)n3nc(nc3n2)-c2ccco2)c1Cl)C(F)(F)F |
Structure |
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