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Target
Glycoprotein 42
Ligand
BDBM51009
Substrate
n/a
Meas. Tech.
Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus
IC50
420±n/a nM
Citation
 PubChem, PC Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus PubChem Bioassay (2008)[AID] 
Target
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:
MVSFKQVRVPLFTAIALVIVLLLAYFLPPRVRGGGRVSAAAITWVPKPNVEVWPVDPPPPVNFNKTAEQEYGDKEIKLPHWTPTLHTFQVPKNYTKANCTYCNTREYTFSYKERCFYFTKKKHTWNGCFQACAELYPCTYFYGPTPDILPVVTRNLNAIESLWVGVYRVGEGNWTSLDGGTFKVYQIFGSHCTYVSKFSTVPVSHHECSFLKPCLCVSQRSNS
  
Inhibitor
Name:
BDBM51009
Synonyms:
2-[(5-benzylsulfanyl-1,3,4-thiadiazol-2-yl)sulfanyl]-N-[[(Z)-3-(furan-2-yl)prop-2-enylidene]amino]acetamide | 2-[[5-(benzylthio)-1,3,4-thiadiazol-2-yl]thio]-N-[[(Z)-3-(2-furyl)prop-2-enylidene]amino]acetamide | 2-{[5-(benzylthio)-1,3,4-thiadiazol-2-yl]thio}-N'-[(1E,2Z)-3-(2-furyl)prop-2-enylidene]acetohydrazide | MLS000584788 | N-[[(Z)-3-(2-furanyl)prop-2-enylidene]amino]-2-[[5-(phenylmethylthio)-1,3,4-thiadiazol-2-yl]thio]acetamide | N-[[(Z)-3-(furan-2-yl)prop-2-enylidene]amino]-2-[[5-(phenylmethylsulfanyl)-1,3,4-thiadiazol-2-yl]sulfanyl]ethanamide | SMR000203751 | cid_12004791
Type:
Small organic molecule
Emp. Form.:
C18H16N4O2S3
Mol. Mass.:
416.54
SMILES:
O=C(CSc1nnc(SCc2ccccc2)s1)NN=C\C=C/c1ccco1 |w:18.19|
Structure:
Search PDB for entries with ligand similarity: