Ki Summary

Reaction Details

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Target

Glycoprotein 42

Ligand

BDBM51082

Substrate/Competitor

n/a

Meas. Tech.

Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus

IC50

1030±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

BDBM51082

n/a

Name

BDBM51082

Synonyms:

2-[(2Z,5Z)-4-keto-2-(2-keto-3,3-dimethyl-butylidene)-5-[[5-(3-nitrophenyl)-2-furyl]methylene]thiazolidin-3-yl]-N-propyl-acetamide | 2-[2-(3,3-dimethyl-2-oxidanylidene-butylidene)-5-[[5-(3-nitrophenyl)furan-2-yl]methylidene]-4-oxidanylidene-1,3-thiazolidin-3-yl]-N-propyl-ethanamide | 2-[2-(3,3-dimethyl-2-oxobutylidene)-5-[[5-(3-nitrophenyl)-2-furanyl]methylidene]-4-oxo-3-thiazolidinyl]-N-propylacetamide | 2-[2-(3,3-dimethyl-2-oxobutylidene)-5-[[5-(3-nitrophenyl)furan-2-yl]methylidene]-4-oxo-1,3-thiazolidin-3-yl]-N-propylacetamide | 2-[4-keto-2-(2-keto-3,3-dimethyl-butylidene)-5-[[5-(3-nitrophenyl)-2-furyl]methylene]thiazolidin-3-yl]-N-propyl-acetamide | MLS000335394 | SMR000250152 | cid_4216653

Type

Small organic molecule

Emp. Form.

C25H27N3O6S

Mol. Mass.

497.563

SMILES

CCCNC(=O)Cn1\c(=C\C(=O)C(C)(C)C)s\c(=C/c2ccc(o2)-c2cccc(c2)[N+]([O-])=O)c1=O

Structure