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

CHEMBL240165

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
Oc1ccccc1-c1nnc(S)o1

Basic Information

ChEMBL ID CHEMBL240165
Phase Preclinical
Structure Type MOL
InChI Key HMIBKGQKYCFESO-UHFFFAOYSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

194.2
MW (Da)
1.73
ALogP
5
HBA
2
HBD
59.1
PSA (Ų)
0.68
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C8H6N2O2S
MW 194.22
Aromatic Rings 2
Heavy Atoms 13
NP-Likeness -0.96

Activity Summary

IC50 1 meas. best 5.51
Kd 1 meas. best 7.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Transthyretin
CHEMBL3194
Kd 7.38 7.38 42.0 1
Transthyretin
CHEMBL3194
IC50 5.51 5.51 3100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Transthyretin Kd = 42.0 nM 7.38 Binding affinity to transthyretin at pH 4.4 17948976
Transthyretin IC50 = 3100.0 nM 5.51 Inhibition of transthyretin fibril formation at pH 4.4 17948976

Literature References

PubMed DOI Target Context # Activities
17948976 10.1021/jm0700159 Transthyretin 9
17948976 10.1021/jm0700159 NON-PROTEIN TARGET 2
20817328 10.1016/j.ejmech.2010.08.003 Staphylococcus aureus 1
20817328 10.1016/j.ejmech.2010.08.003 Staphylococcus epidermidis 1
20817328 10.1016/j.ejmech.2010.08.003 Escherichia coli 1

Data from ChEMBL 36 via Core Engine