Ki Summary

Reaction Details

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Target

Glycoprotein 42

Ligand

BDBM51194

Substrate/Competitor

n/a

Meas. Tech.

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

IC50

1480±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

BDBM51194

n/a

Name

BDBM51194

Synonyms:

(1-pyrazin-2-ylethylideneamino) 3-(2,6-dichlorophenyl)-5-methyl-1,2-oxazole-4-carboxylate | (1-pyrazin-2-ylethylideneamino) 3-[2,6-bis(chloranyl)phenyl]-5-methyl-1,2-oxazole-4-carboxylate | 3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolecarboxylic acid [1-(2-pyrazinyl)ethylideneamino] ester | 3-(2,6-dichlorophenyl)-5-methyl-isoxazole-4-carboxylic acid (1-pyrazin-2-ylethylideneamino) ester | MLS000696488 | N-({[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl}oxy)-N-[(Z)-1-(2-pyrazinyl)ethylidene]amine | SMR000336605 | cid_1481882

Type

Small organic molecule

Emp. Form.

C17H12Cl2N4O3

Mol. Mass.

391.208

SMILES

CC(=NOC(=O)c1c(C)onc1-c1c(Cl)cccc1Cl)c1cnccn1 |w:2.2,(11.89,4.02,;12.21,2.52,;11.07,1.49,;9.6,1.96,;8.46,.93,;9.49,-.21,;6.99,1.41,;6.52,2.87,;7.42,4.12,;4.98,2.87,;4.5,1.41,;5.75,.5,;5.75,-1.04,;4.41,-1.81,;3.08,-1.04,;4.41,-3.35,;5.75,-4.12,;7.08,-3.35,;7.08,-1.81,;8.62,-1.81,;13.68,2.04,;14.82,3.07,;16.29,2.6,;16.61,1.09,;15.46,.06,;14,.53,)|

Structure