Reaction Details |
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Target | Nucleoside triphosphate diphosphohydrolase 3 |
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Ligand | BDBM50227032 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_612641 (CHEMBL1065678) |
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Ki | 14300±n/a nM |
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Citation | Baqi, Y; Lee, SY; Iqbal, J; Ripphausen, P; Lehr, A; Scheiff, AB; Zimmermann, H; Bajorath, J; Müller, CE Development of potent and selective inhibitors of ecto-5'-nucleotidase based on an anthraquinone scaffold. J Med Chem53:2076-86 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Nucleoside triphosphate diphosphohydrolase 3 |
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Name: | Nucleoside triphosphate diphosphohydrolase 3 |
Synonyms: | Ectonucleoside triphosphate diphosphohydrolase 3, isoform CRA_a | Protein Entpd3 |
Type: | PROTEIN |
Mol. Mass.: | 59110.31 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_612641 |
Residue: | 529 |
Sequence: | MFTVMTRQPCEQAGFRALSRTPAIVTLVVLLVSIVVLVTLTLIQIHHPQVLSPGLKYGIV
LDAGSSRTTVYVYQWPAEKENNTGVVSQTFRCSVKGSGISSYENNPQDAPKAFEDCMLKV
KEQVPKHLHESTRVYLGATAGMRLLRLQNETAAHEVLESIQSYFKSQPFDFRGAQIISGQ
EEGVYGWITANYIMGNFLEKNLWHMWVHPHGVDTTGALDLGGASTQISFVSEEKMEPNAS
DTVQVSLYGYTYTLYTHSFQCYGRNEAEKKFLAMLLQSPSTDANISNPCYPHGYSTTFTM
GHVFGSLCTEKQRPKSYNPSDTITFTGTGDPQLCREKVASVFDFSACQEQDACSFDGIYQ
PKVQGPFVAFAGFYYTASALNLSGSFSLTSFNDSSWDFCRHTWSELPSLLPRFDETYARS
YCFSAHYIYHLLINGYKFTEATWPQIRFEKEVGNSSIAWSLGYMLSLTNQIPAGSPLIQL
PIQPPVFMGVLAFFTAIALLCLAFLFYLCSAFRTKERSENAFDQAVDSD
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BDBM50227032 |
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n/a |
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Name | BDBM50227032 |
Synonyms: | CHEMBL256057 | acid blue 25 | sodium 1-amino-9,10-dioxo-4-(phenylamino)-9,10-dihydroanthracene-2-sulfonate |
Type | Small organic molecule |
Emp. Form. | C20H13N2O5S |
Mol. Mass. | 393.393 |
SMILES | Nc1c2C(=O)c3ccccc3C(=O)c2c(Nc2ccccc2)cc1S([O-])(=O)=O |
Structure |
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