Reaction Details |
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Target | Adenosine receptor A2b |
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Ligand | BDBM50189815 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_367228 (CHEMBL865365) |
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IC50 | >1000±n/a nM |
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Citation | Lenzi, O; Colotta, V; Catarzi, D; Varano, F; Filacchioni, G; Martini, C; Trincavelli, L; Ciampi, O; Varani, K; Marighetti, F; Morizzo, E; Moro, S 4-amido-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-ones as new potent and selective human A3 adenosine receptor antagonists. synthesis, pharmacological evaluation, and ligand-receptor modeling studies. J Med Chem49:3916-25 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Adenosine receptor A2b |
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Name: | Adenosine receptor A2b |
Synonyms: | AA2BR_HUMAN | ADENOSINE A2B | ADORA2B | Adenosine receptor A2B (A2B) | Adenosine receptors A2b | Adenosine receptors; A2a & A2b |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 36341.22 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 332 |
Sequence: | MLLETQDALYVALELVIAALSVAGNVLVCAAVGTANTLQTPTNYFLVSLAAADVAVGLFA
IPFAITISLGFCTDFYGCLFLACFVLVLTQSSIFSLLAVAVDRYLAICVPLRYKSLVTGT
RARGVIAVLWVLAFGIGLTPFLGWNSKDSATNNCTEPWDGTTNESCCLVKCLFENVVPMS
YMVYFNFFGCVLPPLLIMLVIYIKIFLVACRQLQRTELMDHSRTTLQREIHAAKSLAMIV
GIFALCWLPVHAVNCVTLFQPAQGKNKPKWAMNMAILLSHANSVVNPIVYAYRNRDFRYT
FHKIISRYLLCQADVKSGNGQAGVQPALGVGL
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BDBM50189815 |
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n/a |
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Name | BDBM50189815 |
Synonyms: | 6-amino-4-benzamido-1,2-dihydro-2-(4-methoxyphenyl)-1,2,4-triazolo[4,3-a]quinoxalin-1-one | CHEMBL209122 |
Type | Small organic molecule |
Emp. Form. | C23H18N6O3 |
Mol. Mass. | 426.4274 |
SMILES | COc1ccc(cc1)-n1nc2c(NC(=O)c3ccccc3)nc3c(N)cccc3n2c1=O |
Structure |
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