Target
Glycoprotein 42
Ligand
BDBM51113
Substrate
n/a
Meas. Tech.
Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus
IC50
8670±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:
BDBM51113
Synonyms:
4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazolidin-3-yl]-N-(2-pyridyl)butyramide | 4-[(5Z)-5-[(3,4-dimethoxyphenyl)methylidene]-4-oxidanylidene-2-sulfanylidene-1,3-thiazolidin-3-yl]-N-pyridin-2-yl-butanamide | 4-[(5Z)-5-[(3,4-dimethoxyphenyl)methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]-N-pyridin-2-ylbutanamide | 4-[(5Z)-5-[(3,4-dimethoxyphenyl)methylidene]-4-oxo-2-sulfanylidene-3-thiazolidinyl]-N-(2-pyridinyl)butanamide | 4-[5-(3,4-dimethoxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-2-pyridinylbutanamide | MLS000662830 | SMR000270282 | cid_1334116
Type:
Small organic molecule
Emp. Form.:
C21H21N3O4S2
Mol. Mass.:
443.539
SMILES:
COc1ccc(\C=C2/SC(=S)N(CCCC(=O)Nc3ccccn3)C2=O)cc1OC
Structure:
Search PDB for entries with ligand similarity: