Reaction Details |
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Target | P2Y purinoceptor 12 |
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Ligand | BDBM50100269 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1454020 (CHEMBL3367079) |
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IC50 | 4600±n/a nM |
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Citation | Boldron, C; Besse, A; Bordes, MF; Tissandié, S; Yvon, X; Gau, B; Badorc, A; Rousseaux, T; Barré, G; Meneyrol, J; Zech, G; Nazare, M; Fossey, V; Pflieger, AM; Bonnet-Lignon, S; Millet, L; Briot, C; Dol, F; Hérault, JP; Savi, P; Lassalle, G; Delesque, N; Herbert, JM; Bono, F N-[6-(4-butanoyl-5-methyl-1H-pyrazol-1-yl)pyridazin-3-yl]-5-chloro-1-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1H-indole-3-carboxamide (SAR216471), a novel intravenous and oral, reversible, and directly acting P2Y12 antagonist. J Med Chem57:7293-316 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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P2Y purinoceptor 12 |
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Name: | P2Y purinoceptor 12 |
Synonyms: | P2Y purinoceptor 12 | P2Y12_RAT | P2ry12 | P2y12 | Purinergic receptor P2Y12 |
Type: | PROTEIN |
Mol. Mass.: | 39068.50 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_1454020 |
Residue: | 343 |
Sequence: | MEVPGANATSANTTSIPGTSTLCSRDYKITQVLFPLLYTVLFFAGLITNSLAMRIFFQIR
SKSNFIIFLKNTVISDLLMILTFPFKILSDAKLGAGHLRTLVCQVTSVTFYFTMYISISF
LGLITIDRYLKTTRPFKTSSPSNLLGAKILSVAIWAFMFLLSLPNMILTNRRPKDKDITK
CSFLKSEFGLVWHEIVNYICQVIFWINFLIVIVCYSLITKELYRSYVRTRGSAKAPKKRV
NIKVFIIIAVFFICFVPFHFARIPYTLSQTRAVFDCNAENTLFYVKESTLWLTSLNACLD
PFIYFFLCKSFRNSLMSMLRCSTSGANKKKGQEGGDPSEETPM
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BDBM50100269 |
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n/a |
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Name | BDBM50100269 |
Synonyms: | CHEMBL3325627 |
Type | Small organic molecule |
Emp. Form. | C27H28N4O4 |
Mol. Mass. | 472.5356 |
SMILES | CCCC(=O)c1cnn(c1C)-c1ccc(NC(=O)c2cn(CC(O)=O)c3cc(C)c(C)cc23)cc1 |
Structure |
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