Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51009 |
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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 | 420±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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BDBM51009 |
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n/a |
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Name | BDBM51009 |
Synonyms: | 2-[(5-benzylsulfanyl-1,3,4-thiadiazol-2-yl)sulfanyl]-N-[[(Z)-3-(furan-2-yl)prop-2-enylidene]amino]acetamide | 2-[[5-(benzylthio)-1,3,4-thiadiazol-2-yl]thio]-N-[[(Z)-3-(2-furyl)prop-2-enylidene]amino]acetamide | 2-{[5-(benzylthio)-1,3,4-thiadiazol-2-yl]thio}-N'-[(1E,2Z)-3-(2-furyl)prop-2-enylidene]acetohydrazide | MLS000584788 | N-[[(Z)-3-(2-furanyl)prop-2-enylidene]amino]-2-[[5-(phenylmethylthio)-1,3,4-thiadiazol-2-yl]thio]acetamide | N-[[(Z)-3-(furan-2-yl)prop-2-enylidene]amino]-2-[[5-(phenylmethylsulfanyl)-1,3,4-thiadiazol-2-yl]sulfanyl]ethanamide | SMR000203751 | cid_12004791 |
Type | Small organic molecule |
Emp. Form. | C18H16N4O2S3 |
Mol. Mass. | 416.54 |
SMILES | O=C(CSc1nnc(SCc2ccccc2)s1)NN=C\C=C/c1ccco1 |w:18.19| |
Structure |
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