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

CHEMBL235593

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
CS(=O)(=O)N1C[C@H](NC(=O)c2ccc(-n3ccccc3=O)cc2)[C@H](NC(=O)c2ccc(Cl)s2)C1

Basic Information

ChEMBL ID CHEMBL235593
Phase Preclinical
Structure Type MOL
InChI Key RIWVVRAWKVPOCH-DLBZAZTESA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

521.0
MW (Da)
1.72
ALogP
7
HBA
2
HBD
117.6
PSA (Ų)
0.51
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H21ClN4O5S2
MW 521.02
Aromatic Rings 3
Heavy Atoms 34
NP-Likeness -1.57

Activity Summary

Ki 1 meas. best 9.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
Ki 9.36 9.36 0.4 1

Pharmacokinetic Data

Parameter Value Units Species
CL - nmol/mg/min Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X Ki = 0.44 nM 9.36 Inhibition of human factor 10a 17643988

Literature References

PubMed DOI Target Context # Activities
17643988 10.1016/j.bmcl.2007.07.020 Coagulation factor X 1
17643988 10.1016/j.bmcl.2007.07.020 Plasma 1
17643988 10.1016/j.bmcl.2007.07.020 Liver microsomes 1
17643988 10.1016/j.bmcl.2007.07.020 ADMET 1

Data from ChEMBL 36 via Core Engine