Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51262 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus |
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IC50 | 910±n/a nM |
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Citation | PubChem, PC Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus PubChem Bioassay(2008)[AID] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Glycoprotein 42 |
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Name: | Glycoprotein 42 |
Synonyms: | BZLF2 | GP42_EBVA8 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 25424.12 |
Organism: | Human herpesvirus 4 type 2 |
Description: | gi_139424501 |
Residue: | 223 |
Sequence: | MVSFKQVRVPLFTAIALVIVLLLAYFLPPRVRGGGRVSAAAITWVPKPNVEVWPVDPPPP
VNFNKTAEQEYGDKEIKLPHWTPTLHTFQVPKNYTKANCTYCNTREYTFSYKERCFYFTK
KKHTWNGCFQACAELYPCTYFYGPTPDILPVVTRNLNAIESLWVGVYRVGEGNWTSLDGG
TFKVYQIFGSHCTYVSKFSTVPVSHHECSFLKPCLCVSQRSNS
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BDBM51262 |
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n/a |
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Name | BDBM51262 |
Synonyms: | 3-(1-benzofuran-2-carbonyl)-4-hydroxy-2-phenyl-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 3-(1-benzofuran-2-ylcarbonyl)-4-oxidanyl-2-phenyl-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 3-[2-benzofuranyl(oxo)methyl]-4-hydroxy-2-phenyl-1-(2-thiazolyl)-2H-pyrrol-5-one | 4-(Benzofuran-2-carbonyl)-3-hydroxy-5-phenyl-1-thiazol-2-yl-1,5-dihydro-pyrrol-2-one | 4-(benzofuran-2-carbonyl)-3-hydroxy-5-phenyl-1-thiazol-2-yl-3-pyrrolin-2-one | MLS000332351 | SMR000434941 | cid_3830309 |
Type | Small organic molecule |
Emp. Form. | C22H14N2O4S |
Mol. Mass. | 402.423 |
SMILES | O=C(C1C(N(C(=O)C1=O)c1nccs1)c1ccccc1)c1cc2ccccc2o1 |
Structure |
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