| Reaction Details |
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 | Report a problem with these data |
| Target | Glycoprotein 42 |
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| Ligand | BDBM48838 |
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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 | 1580±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 |
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| Synonyms: | BZLF2 | GP42_EBVA8 |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 25424.12 |
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| Organism: | Human herpesvirus 4 type 2 |
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| Description: | gi_139424501 |
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| Residue: | 223 |
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| Sequence: | MVSFKQVRVPLFTAIALVIVLLLAYFLPPRVRGGGRVSAAAITWVPKPNVEVWPVDPPPP
VNFNKTAEQEYGDKEIKLPHWTPTLHTFQVPKNYTKANCTYCNTREYTFSYKERCFYFTK
KKHTWNGCFQACAELYPCTYFYGPTPDILPVVTRNLNAIESLWVGVYRVGEGNWTSLDGG
TFKVYQIFGSHCTYVSKFSTVPVSHHECSFLKPCLCVSQRSNS
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| BDBM48838 |
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| n/a |
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| Name | BDBM48838 |
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| Synonyms: | (5Z)-2-(4-hydroxyanilino)-5-(2-ketoindolin-3-ylidene)-2-thiazolin-4-one | (5Z)-2-(4-hydroxyanilino)-5-(2-oxo-1H-indol-3-ylidene)-1,3-thiazol-4-one | (5Z)-2-(4-hydroxyanilino)-5-(2-oxo-1H-indol-3-ylidene)-4-thiazolone | (5Z)-2-[(4-hydroxyphenyl)amino]-5-(2-oxidanylidene-1H-indol-3-ylidene)-1,3-thiazol-4-one | 3-[2-[(4-hydroxyphenyl)amino]-4-oxo-1,3-thiazol-5(4H)-ylidene]-1,3-dihydro-2H-indol-2-one | MLS000676656 | SMR000298307 | cid_5398245 |
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| Type | Small organic molecule |
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| Emp. Form. | C17H11N3O3S |
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| Mol. Mass. | 337.353 |
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| SMILES | Oc1ccc(NC2=NC(=O)C(S2)=C2C(=O)Nc3ccccc23)cc1 |w:12.22,t:6| |
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| Structure | 
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