Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51183 |
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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 | 2000±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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BDBM51183 |
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n/a |
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Name | BDBM51183 |
Synonyms: | (6Z)-5-azanylidene-3-(2-methylpropylsulfanyl)-6-[(4-oxidanylidenechromen-3-yl)methylidene]-[1,2,4]thiadiazolo[4,5-a]pyrimidin-7-one | (6Z)-5-imino-3-(2-methylpropylsulfanyl)-6-[(4-oxochromen-3-yl)methylidene]-[1,2,4]thiadiazolo[4,5-a]pyrimidin-7-one | (6Z)-5-imino-3-(2-methylpropylthio)-6-[(4-oxo-1-benzopyran-3-yl)methylidene]-[1,2,4]thiadiazolo[4,5-a]pyrimidin-7-one | (6Z)-5-imino-3-(isobutylthio)-6-[(4-ketochromen-3-yl)methylene]-[1,2,4]thiadiazolo[4,5-a]pyrimidin-7-one | (6Z)-5-imino-3-(isobutylthio)-6-[(4-oxo-4H-chromen-3-yl)methylene]-5,6-dihydro-7H-[1,2,4]thiadiazolo[4,5-a]pyrimidin-7-one | MLS000731452 | SMR000309727 | cid_16193843 |
Type | Small organic molecule |
Emp. Form. | C19H16N4O3S2 |
Mol. Mass. | 412.485 |
SMILES | CC(C)CSC1=NSC2=NC(=O)\C(=C/c3coc4ccccc4c3=O)C(=N)N12 |t:5,8| |
Structure |
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