Reaction Details |
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Target | Adenosine receptor A2a |
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Ligand | BDBM303313 |
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Substrate/Competitor | n/a |
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Meas. Tech. | A2a Ki assay |
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Ki | 0.500±n/a nM |
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Citation | Ali, A; Kuang, R; Lim, Y; Lo, MM; Ting, PC; Biju, P; de Lera Ruiz, M; Degrado, SJ; Tung, AL; Henderson, TJ; Hong, L; Kim, J; Kim, DW; Lee, J; Wu, J; Wu, H; Xiao, Y; Yu, T; Zhou, G; Zhu, X; McCormick, KD; Tagat, JR; Xiao, D; Khan, T; Cao, J; Berlin, M; Zhang, Y Aminoquinazoline compounds as A2A antagonist US Patent US10138212 Publication Date 11/27/2018 |
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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: | A2A adenosine receptor (hA2A) | AA2AR_HUMAN | ADENOSINE A2 | ADENOSINE A2a | ADORA2 | ADORA2A | Adenosine A2A receptor (A2AAR) |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 44716.46 |
Organism: | Homo sapiens (Human) |
Description: | P29274 |
Residue: | 412 |
Sequence: | MPIMGSSVYITVELAIAVLAILGNVLVCWAVWLNSNLQNVTNYFVVSLAAADIAVGVLAI
PFAITISTGFCAACHGCLFIACFVLVLTQSSIFSLLAIAIDRYIAIRIPLRYNGLVTGTR
AKGIIAICWVLSFAIGLTPMLGWNNCGQPKEGKNHSQGCGEGQVACLFEDVVPMNYMVYF
NFFACVLVPLLLMLGVYLRIFLAARRQLKQMESQPLPGERARSTLQKEVHAAKSLAIIVG
LFALCWLPLHIINCFTFFCPDCSHAPLWLMYLAIVLSHTNSVVNPFIYAYRIREFRQTFR
KIIRSHVLRQQEPFKAAGTSARVLAAHGSDGEQVSLRLNGHPPGVWANGSAPHPERRPNG
YALGLVSGGSAQESQGNTGLPDVELLSHELKGVCPEPPGLDDPLAQDGAGVS
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BDBM303313 |
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n/a |
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Name | BDBM303313 |
Synonyms: | 2-amino-8-fluoro-N-[(3- fluoro-6-methyl-2- pyridyl)methyl] quinazoline-4- carboxamide | US10138212, Example 76 |
Type | Small organic molecule |
Emp. Form. | C16H13F2N5O |
Mol. Mass. | 329.3041 |
SMILES | Cc1ccc(F)c(CNC(=O)c2nc(N)nc3c(F)cccc23)n1 |$;;;;;;;;HN;;;;;;;;;;;;;;;$| |
Structure |
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