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Compound Detail

CHEMBL222012

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N=C(c1ccc(C(=O)Nc2ccc(Cl)cc2C(=O)Nc2ccc(Cl)cn2)cc1)N1CCC(C(=O)O)CC1

Basic Information

ChEMBL ID CHEMBL222012
Phase Preclinical
Structure Type MOL
InChI Key XVKPNRRLYPSIOE-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

540.4
MW (Da)
5.01
ALogP
5
HBA
4
HBD
135.5
PSA (Ų)
0.26
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H23Cl2N5O4
MW 540.41
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -1.27

Activity Summary

IC50 1 meas. best 8.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Coagulation factor X
CHEMBL244
IC50 8.7 8.7 2.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Coagulation factor X IC50 = 2.0 nM 8.7 Inhibition of Factor 10a 19297154

Literature References

PubMed DOI Target Context # Activities
16931010 10.1016/j.bmcl.2006.08.039 Voltage-gated inwardly rectifying potassium channel KCNH2 1
19297154 10.1016/j.bmcl.2009.02.111 Coagulation factor X 1
20503967 10.1021/jm100146h Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine