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

CHEMBL390528

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=C1NC(=S)S/C1=C\c1ccc(-c2cc(Cl)ccc2Cl)o1

Basic Information

ChEMBL ID CHEMBL390528
Phase Preclinical
Structure Type MOL
InChI Key PQCBMLVRDBJEMS-SDQBBNPISA-N
1
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

356.2
MW (Da)
4.74
ALogP
4
HBA
1
HBD
42.2
PSA (Ų)
0.62
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H7Cl2NO2S2
MW 356.25
Aromatic Rings 2
Heavy Atoms 21
NP-Likeness -1.95

Activity Summary

Ki 2 meas. best 5.7
IC50 1 meas. best 5.22

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Enoyl-acyl-carrier protein reductase
CHEMBL4150
Ki 5.7 5.65 2000.0 2
Enoyl-acyl-carrier protein reductase
CHEMBL4150
IC50 5.22 5.22 6000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
17477517 10.1021/jm061257w Enoyl-acyl-carrier protein reductase 3
17948976 10.1021/jm0700159 Transthyretin 2

Data from ChEMBL 36 via Core Engine