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TargetGlycoprotein 42
LigandBDBM51081
Substrate/Competitorn/a
Meas. Tech.Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus
IC50 1510±n/a nM
Citation PubChem, PC Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus PubChem Bioassay(2008)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Glycoprotein 42
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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  Blast E-value cutoff:
BDBM51081
n/a
NameBDBM51081
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
TypeSmall organic molecule
Emp. Form.C27H22FN3O3
Mol. Mass.455.4803
SMILESFc1ccc(cc1)N1C(=O)NC(=O)C(=Cc2ccc3N(Cc4ccccc4)CCCc3c2)C1=O |w:14.15|
Structure
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