Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51131 |
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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 | 570±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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BDBM51131 |
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n/a |
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Name | BDBM51131 |
Synonyms: | 8,10a-bis(oxidanyl)-1H-chromeno[2,3-d]pyrimidine-2,4-dione | 8,10a-dihydroxy-1,10a-dihydro-2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione | 8,10a-dihydroxy-1H-[1]benzopyrano[2,3-d]pyrimidine-2,4-dione | 8,10a-dihydroxy-1H-chromeno[2,3-d]pyrimidine-2,4-dione | 8,10a-dihydroxy-1H-chromeno[2,3-d]pyrimidine-2,4-quinone | MLS000690629 | SMR000298896 | cid_2920363 |
Type | Small organic molecule |
Emp. Form. | C11H8N2O5 |
Mol. Mass. | 248.1916 |
SMILES | Oc1ccc2C=C3C(=O)NC(=O)NC3(O)Oc2c1 |t:5| |
Structure |
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