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Compound Detail

CHEMBL470210

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O=[N+]([O-])c1cnc(Sc2nnc(O)n2-c2ccc3c(c2)OCO3)s1

Basic Information

ChEMBL ID CHEMBL470210
Phase Preclinical
Structure Type MOL
InChI Key ZXEYSXDRLYOVCP-UHFFFAOYSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

365.4
MW (Da)
2.22
ALogP
11
HBA
1
HBD
125.4
PSA (Ų)
0.55
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C12H7N5O5S2
MW 365.35
Aromatic Rings 3
Heavy Atoms 24
NP-Likeness -1.66

Activity Summary

IC50 2 meas. best 8.48

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 8.48 7.735 3.3 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 3.3 nM 8.48 Inhibition of JNK by time-resolved FRET assay 19271755
Unchecked IC50 = 102.0 nM 6.99 Displacement of biotin-labeled pep-JIP11 from JNK by DELFIA assay 19271755

Literature References

PubMed DOI Target Context # Activities
19271755 10.1021/jm801503n Unchecked 2

Data from ChEMBL 36 via Core Engine