Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2047474

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CN1CCN(C(=O)c2cc3cc(Cl)cc([N+](=O)[O-])c3[nH]2)CC1

Basic Information

ChEMBL ID CHEMBL2047474
Phase Preclinical
Structure Type MOL
InChI Key FKACYPTZQOXPJW-UHFFFAOYSA-N
1
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

322.8
MW (Da)
2.12
ALogP
4
HBA
1
HBD
82.5
PSA (Ų)
0.68
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H15ClN4O3
MW 322.75
Aromatic Rings 2
Heavy Atoms 22
NP-Likeness -1.78

Activity Summary

EC50 2 meas. best 6.4
Ki 1 meas. best 6.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H4 receptor
CHEMBL3759
EC50 6.4 6.2 398.1 2
Histamine H4 receptor
CHEMBL3759
Ki 6.4 6.4 398.1 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29939744 10.1021/acs.jmedchem.8b00435 Histamine H4 receptor 4
22749391 10.1016/j.ejmech.2012.06.016 Histamine H4 receptor 1

Data from ChEMBL 36 via Core Engine