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Compound Detail

CHEMBL261775

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O=C(CCS(=O)(=O)c1ccc2cc(Cl)ccc2c1)N1CCN(c2cccc3ncc([N+](=O)[O-])n23)CC1

Basic Information

ChEMBL ID CHEMBL261775
Phase Preclinical
Structure Type MOL
InChI Key IQPDNNPAWCSXOC-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

528.0
MW (Da)
3.56
ALogP
8
HBA
0
HBD
118.1
PSA (Ų)
0.28
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 C24H22ClN5O5S
MW 527.99
Aromatic Rings 4
Heavy Atoms 36
NP-Likeness -1.88

Activity Summary

IC50 1 meas. best 7.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
IC50 7.62 7.62 24.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X IC50 = 24.0 nM 7.62 Inhibition of human factor 10a 18164204

Literature References

PubMed DOI Target Context # Activities
18164204 10.1016/j.bmc.2007.12.024 Plasma 2
18164204 10.1016/j.bmc.2007.12.024 Coagulation factor X 1
18164204 10.1016/j.bmc.2007.12.024 Cytochrome P450 3A4 1
18164204 10.1016/j.bmc.2007.12.024 Mus musculus 1

Data from ChEMBL 36 via Core Engine