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TargetGlycoprotein 42
LigandBDBM50771
Substrate/Competitorn/a
Meas. Tech.Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus
IC50 1150±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:
BDBM50771
n/a
NameBDBM50771
Synonyms:3-(5-methylfuran-2-yl)carbonyl-4-oxidanyl-2-(3-prop-2-enoxyphenyl)-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 4-hydroxy-3-(5-methylfuran-2-carbonyl)-2-(3-prop-2-enoxyphenyl)-1-(1,3-thiazol-2-yl)-2H-pyrrol-5-one | 4-hydroxy-3-[(5-methyl-2-furanyl)-oxomethyl]-2-(3-prop-2-enoxyphenyl)-1-(2-thiazolyl)-2H-pyrrol-5-one | 5-(3-Allyloxy-phenyl)-3-hydroxy-4-(5-methyl-furan-2-carbonyl)-1-thiazol-2-yl-1,5-dihydro-pyrrol-2-one | 5-(3-allyloxyphenyl)-3-hydroxy-4-(5-methyl-2-furoyl)-1-thiazol-2-yl-3-pyrrolin-2-one | MLS000033775 | SMR000013770 | cid_654648
TypeSmall organic molecule
Emp. Form.C22H18N2O5S
Mol. Mass.422.454
SMILESCc1ccc(o1)C(=O)C1C(N(C(=O)C1=O)c1nccs1)c1cccc(OCC=C)c1
Structure
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