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Compound Detail

CHEMBL235148

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O=C(N[C@H]1CN(C(=O)C2CC2)C[C@H]1NC(=O)c1ccc(Cl)s1)c1ccc(-n2ccccc2=O)cc1

Basic Information

ChEMBL ID CHEMBL235148
Phase Preclinical
Structure Type MOL
InChI Key CKNBLYXXVHZIRU-RBUKOAKNSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

511.0
MW (Da)
2.70
ALogP
6
HBA
2
HBD
100.5
PSA (Ų)
0.53
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 C25H23ClN4O4S
MW 511.00
Aromatic Rings 3
Heavy Atoms 35
NP-Likeness -1.52

Activity Summary

Ki 1 meas. best 8.68

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
Ki 8.68 8.68 2.1 1

Pharmacokinetic Data

Parameter Value Units Species
CL - - Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X Ki = 2.1 nM 8.68 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