Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51081 |
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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 | 1510±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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BDBM51081 |
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n/a |
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Name | BDBM51081 |
Synonyms: | (5E)-1-(4-fluorophenyl)-5-[[1-(phenylmethyl)-3,4-dihydro-2H-quinolin-6-yl]methylidene]-1,3-diazinane-2,4,6-trione | (5E)-5-[(1-benzyl-3,4-dihydro-2H-quinolin-6-yl)methylene]-1-(4-fluorophenyl)barbituric acid | (5E)-5-[(1-benzyl-3,4-dihydro-2H-quinolin-6-yl)methylidene]-1-(4-fluorophenyl)-1,3-diazinane-2,4,6-trione | 5-[1-(1-Benzyl-1,2,3,4-tetrahydro-quinolin-6-yl)-meth-(E)-ylidene]-1-(4-fluoro-phenyl)-pyrimidine-2,4,6-trione | MLS000331011 | SMR000221044 | cid_1997460 |
Type | Small organic molecule |
Emp. Form. | C27H22FN3O3 |
Mol. Mass. | 455.4803 |
SMILES | Fc1ccc(cc1)N1C(=O)NC(=O)C(=Cc2ccc3N(Cc4ccccc4)CCCc3c2)C1=O |w:14.15| |
Structure |
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