Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL521883

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
O=C(Oc1cncc(Cl)c1)c1cc([N+](=O)[O-])[nH]n1

Basic Information

ChEMBL ID CHEMBL521883
Phase Preclinical
Structure Type MOL
InChI Key OZKRGPPMLLQBAY-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
2
Publications
0
Known Names

Molecular Properties

268.6
MW (Da)
1.59
ALogP
6
HBA
1
HBD
111.0
PSA (Ų)
0.51
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C9H5ClN4O4
MW 268.62
Aromatic Rings 2
Heavy Atoms 18
NP-Likeness -1.49

Activity Summary

IC50 1 meas. best 6.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.6 6.6 250.0 1

Pharmacokinetic Data

Parameter Value Units Species
t1/2 - - -

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 250.0 nM 6.6 Inhibition of hepatitis A virus 3C proteinase by microplate assay 18407505

Literature References

PubMed DOI Target Context # Activities
18407505 10.1016/j.bmc.2008.03.059 Unchecked 7
18407505 10.1016/j.bmc.2008.03.059 No relevant target 1

Data from ChEMBL 36 via Core Engine