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Compound Detail

CHEMBL270829

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CCN(CC)CCN(C)C(=O)N(C1CCCN(c2ccc(-c3ccccc3S(C)(=O)=O)cc2F)C1=O)S(=O)(=O)c1ccc2cc(Cl)ccc2c1

Basic Information

ChEMBL ID CHEMBL270829
Phase Preclinical
Structure Type MOL
InChI Key JIKNMSSWPPOSOQ-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

743.3
MW (Da)
6.28
ALogP
7
HBA
0
HBD
115.4
PSA (Ų)
0.18
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H40ClFN4O6S2
MW 743.32
Aromatic Rings 4
Heavy Atoms 50
NP-Likeness -1.36

Activity Summary

Ki 1 meas. best 8.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
Ki 8.96 8.96 1.1 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X Ki = 1.1 nM 8.96 Inhibition of human factor 10a 18329876

Literature References

PubMed DOI Target Context # Activities
18329876 10.1016/j.bmcl.2008.02.054 Unchecked 2
18329876 10.1016/j.bmcl.2008.02.054 Coagulation factor X 1
18329876 10.1016/j.bmcl.2008.02.054 Plasma 1

Data from ChEMBL 36 via Core Engine