Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51138 |
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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 | 3070±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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BDBM51138 |
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n/a |
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Name | BDBM51138 |
Synonyms: | (5Z)-5-[(1-methyl-3-indolyl)methylidene]-4-sulfanylidene-2-thiazolidinone | (5Z)-5-[(1-methylindol-3-yl)methylene]-4-thioxo-thiazolidin-2-one | (5Z)-5-[(1-methylindol-3-yl)methylidene]-4-sulfanylidene-1,3-thiazolidin-2-one | 5-[(1-methyl-1H-indol-3-yl)methylene]-4-thioxo-1,3-thiazolidin-2-one | MLS000698017 | SMR000225303 | cid_1236521 |
Type | Small organic molecule |
Emp. Form. | C13H10N2OS2 |
Mol. Mass. | 274.361 |
SMILES | Cn1cc(C=C2SC(O)=NC2=S)c2ccccc12 |w:4.3,c:8| |
Structure |
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