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Compound Detail

CHEMBL3392121

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CS(=O)(=NC(=O)CN1CCCC1)c1ccc(C(=O)Nc2ccc(Cl)cc2C(=O)Nc2ccc(Cl)cn2)cc1

Basic Information

ChEMBL ID CHEMBL3392121
Phase Preclinical
Structure Type MOL
InChI Key LUNONISXCVTTAB-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

574.5
MW (Da)
4.97
ALogP
6
HBA
2
HBD
120.8
PSA (Ų)
0.41
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H25Cl2N5O4S
MW 574.49
Aromatic Rings 3
Heavy Atoms 38
NP-Likeness -1.81

Activity Summary

IC50 1 meas. best 8.49

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
IC50 8.49 8.49 3.2 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X IC50 = 3.2 nM 8.49 Inhibition of human F10a using S-2765 as substrate after 45 mins 23124211

Literature References

PubMed DOI Target Context # Activities
23124211 10.1016/j.ejmech.2012.10.005 Coagulation factor X 2
23124211 10.1016/j.ejmech.2012.10.005 Plasma 2
23124211 10.1016/j.ejmech.2012.10.005 Rattus norvegicus 1

Data from ChEMBL 36 via Core Engine