Reaction Details |
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Target | Glycoprotein 42 |
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Ligand | BDBM51003 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus |
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IC50 | 1550±n/a nM |
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Citation | PubChem, PC Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus PubChem Bioassay(2008)[AID] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Glycoprotein 42 |
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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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BDBM51003 |
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n/a |
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Name | BDBM51003 |
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 |
Type | Small organic molecule |
Emp. Form. | C24H24N4O3S2 |
Mol. Mass. | 480.602 |
SMILES | CCc1cccc2cc3c(N)c(sc3nc12)C(=O)Nc1ccc(cc1)S(=O)(=O)N1CCCC1 |
Structure |
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