Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM50771 |
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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 | 1150±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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BDBM50771 |
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n/a |
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Name | BDBM50771 |
Synonyms: | 3-(5-methylfuran-2-yl)carbonyl-4-oxidanyl-2-(3-prop-2-enoxyphenyl)-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 4-hydroxy-3-(5-methylfuran-2-carbonyl)-2-(3-prop-2-enoxyphenyl)-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 4-hydroxy-3-[(5-methyl-2-furanyl)-oxomethyl]-2-(3-prop-2-enoxyphenyl)-1-(2-thiazolyl)-2H-pyrrol-5-one | 5-(3-Allyloxy-phenyl)-3-hydroxy-4-(5-methyl-furan-2-carbonyl)-1-thiazol-2-yl-1,5-dihydro-pyrrol-2-one | 5-(3-allyloxyphenyl)-3-hydroxy-4-(5-methyl-2-furoyl)-1-thiazol-2-yl-3-pyrrolin-2-one | MLS000033775 | SMR000013770 | cid_654648 |
Type | Small organic molecule |
Emp. Form. | C22H18N2O5S |
Mol. Mass. | 422.454 |
SMILES | Cc1ccc(o1)C(=O)C1C(N(C(=O)C1=O)c1nccs1)c1cccc(OCC=C)c1 |
Structure |
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