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TargetGlycoprotein 42
LigandBDBM51003
Substrate/Competitorn/a
Meas. Tech.Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus
IC50 1550±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:
BDBM51003
n/a
NameBDBM51003
Synonyms:3-Amino-8-ethyl-thieno[2,3-b]quinoline-2-carboxylic acid [4-(pyrrolidine-1-sulfonyl)-phenyl]-amide | 3-amino-8-ethyl-N-(4-pyrrolidin-1-ylsulfonylphenyl)thieno[2,3-b]quinoline-2-carboxamide | 3-amino-8-ethyl-N-(4-pyrrolidinosulfonylphenyl)thieno[2,3-b]quinoline-2-carboxamide | 3-amino-8-ethyl-N-[4-(1-pyrrolidinylsulfonyl)phenyl]-2-thieno[2,3-b]quinolinecarboxamide | 3-azanyl-8-ethyl-N-(4-pyrrolidin-1-ylsulfonylphenyl)thieno[2,3-b]quinoline-2-carboxamide | MLS000548793 | SMR000171171 | cid_3231270
TypeSmall organic molecule
Emp. Form.C24H24N4O3S2
Mol. Mass.480.602
SMILESCCc1cccc2cc3c(N)c(sc3nc12)C(=O)Nc1ccc(cc1)S(=O)(=O)N1CCCC1
Structure
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