Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51123 |
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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 | 2380±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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BDBM51123 |
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n/a |
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Name | BDBM51123 |
Synonyms: | 1-(4-nitro-2,1,3-benzoxadiazol-7-yl)-3-piperidinecarboxylic acid ethyl ester | 1-(7-nitrobenzofurazan-4-yl)nipecotic acid ethyl ester | MLS000729233 | SMR000307511 | cid_4871598 | ethyl 1-(4-nitro-2,1,3-benzoxadiazol-7-yl)piperidine-3-carboxylate | ethyl 1-(7-nitro-2,1,3-benzoxadiazol-4-yl)piperidine-3-carboxylate |
Type | Small organic molecule |
Emp. Form. | C14H16N4O5 |
Mol. Mass. | 320.3006 |
SMILES | CCOC(=O)C1CCCN(C1)c1ccc([N+]([O-])=O)c2nonc12 |
Structure |
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