Reaction Details |
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Target | Ectonucleoside triphosphate diphosphohydrolase 1 |
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Ligand | BDBM50336767 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_463990 (CHEMBL929977) |
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Ki | >100000±n/a nM |
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Citation | Weyler, S; Baqi, Y; Hillmann, P; Kaulich, M; Hunder, AM; Müller, IA; Müller, CE Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists. Bioorg Med Chem Lett18:223-7 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Ectonucleoside triphosphate diphosphohydrolase 1 |
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Name: | Ectonucleoside triphosphate diphosphohydrolase 1 |
Synonyms: | ATPDase | CD_antigen=CD39 | Cd39 | ENTP1_RAT | Ecto-ATP diphosphohydrolase | Ecto-apyrase | Entpd1 | Lymphoid cell activation antigen | NTPDase 1 |
Type: | PROTEIN |
Mol. Mass.: | 57412.31 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_463990 |
Residue: | 511 |
Sequence: | MEDIKDSKVKRFCSKNILIILGFSSVLAVIALIAVGLTHNKPLPENVKYGIVLDAGSSHT
NLYIYKWPAEKENDTGVVQLLEECQVKGPGISKYAQKTDEIAAYLAECMKMSTERIPASK
QHQTPVYLGATAGMRLLRMESKQSADEVLAAVSRSLKSYPFDFQGAKIITGQEEGAYGWI
TINYLLGRFTQEQSWLNFISDSQKQATFGALDLGGSSTQVTFVPLNQTLEAPETSLQFRL
YGTDYTVYTHSFLCYGKDQALWQKLAQDIQVSSGGILKDPCFYPGYKKVVNVSELYGTPC
TKRFEKKLPFNQFQVQGTGDYEQCHQSILKFFNNSHCPYSQCAFNGVFLPPLQGSFGAFS
AFYFVMDFFKKMANDSVSSQEKMTEITKNFCSKPWEEVKASYPTVKEKYLSEYCFSGTYI
LSLLLQGYNFTGTSWDQIHFMGKIKDSNAGWTLGYMLNLTNMIPAEQPLSPPLPHSTYIS
LMVLFSLVLVAMVITGLFIFSKPSYFWKEAV
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BDBM50336767 |
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n/a |
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Name | BDBM50336767 |
Synonyms: | CHEMBL257495 | PSB-716 | sodium 1-amino-4-(2-methoxyphenylamino)-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate |
Type | Small organic molecule |
Emp. Form. | C21H15N2O6S |
Mol. Mass. | 423.419 |
SMILES | COc1ccccc1Nc1cc(c(N)c2C(=O)c3ccccc3C(=O)c12)S([O-])(=O)=O |
Structure |
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