Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM75323 |
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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 | 4840±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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BDBM75323 |
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n/a |
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Name | BDBM75323 |
Synonyms: | 2-[4-[[[4-[2-(4-chloroanilino)-1,3-thiazol-4-yl]benzoyl]hydrazinylidene]methyl]phenoxy]acetic acid | 2-[4-[[[4-[2-(4-chloroanilino)thiazol-4-yl]benzoyl]hydrazono]methyl]phenoxy]acetic acid | 2-[4-[[[4-[2-[(4-chlorophenyl)amino]-1,3-thiazol-4-yl]phenyl]carbonylhydrazinylidene]methyl]phenoxy]ethanoic acid | 2-[4-[[[[4-[2-(4-chloroanilino)-4-thiazolyl]phenyl]-oxomethyl]hydrazinylidene]methyl]phenoxy]acetic acid | MLS000703184 | SMR000273648 | cid_3143384 |
Type | Small organic molecule |
Emp. Form. | C25H19ClN4O4S |
Mol. Mass. | 506.961 |
SMILES | OC(=O)COc1ccc(C=NNC(=O)c2ccc(cc2)-c2csc(Nc3ccc(Cl)cc3)n2)cc1 |
Structure |
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