Reaction Details |
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Target | Trans-activator protein BZLF1 |
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Ligand | BDBM64853 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Counterscreen for inhibitors of PP1: fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 5 (PP5) |
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IC50 | >67047±n/a nM |
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Citation | PubChem, PC Counterscreen for inhibitors of PP1: fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 5 (PP5) PubChem Bioassay(2010)[AID] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Trans-activator protein BZLF1 |
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Name: | Trans-activator protein BZLF1 |
Synonyms: | BZLF1 | BZLF1_EBVB9 | PPP5C protein |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 26856.37 |
Organism: | Human herpesvirus 4 |
Description: | gi_82503229 |
Residue: | 245 |
Sequence: | MMDPNSTSEDVKFTPDPYQVPFVQAFDQATRVYQDLGGPSQAPLPCVLWPVLPEPLPQGQ
LTAYHVSTAPTGSWFSAPQPAPENAYQAYAAPQLFPVSDITQNQQTNQAGGEAPQPGDNS
TVQTAAAVVFACPGANQGQQLADIGVPQPAPVAAPARRTRKPQQPESLEECDSELEIKRY
KNRVASRKCRAKFKQLLQHYREVAAAKSSENDRLRLLLKQMCPSLDVDSIIPRTPDVLHE
DLLNF
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BDBM64853 |
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n/a |
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Name | BDBM64853 |
Synonyms: | MLS000713953 | N-(2,6-dimethoxy-4-pyrimidinyl)-4-[[4-(2-pyridinyl)-2-thiazolyl]amino]benzenesulfonamide;hydrobromide | N-(2,6-dimethoxypyrimidin-4-yl)-4-[(4-pyridin-2-yl-1,3-thiazol-2-yl)amino]benzenesulfonamide;hydrobromide | N-(2,6-dimethoxypyrimidin-4-yl)-4-[[4-(2-pyridyl)thiazol-2-yl]amino]benzenesulfonamide;hydrobromide | SMR000273434 | cid_16192648 |
Type | Small organic molecule |
Emp. Form. | C20H18N6O4S2 |
Mol. Mass. | 470.525 |
SMILES | COc1cc(NS(=O)(=O)c2ccc(Nc3nc(cs3)-c3ccccn3)cc2)nc(OC)n1 |
Structure |
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