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

CHEMBL152557

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
CCCCC1(C2CCCC2)Cc2cc(OCCCC(=O)O)c(Cl)c(Cl)c2C1=O

Basic Information

ChEMBL ID CHEMBL152557
Phase Preclinical
Structure Type MOL
InChI Key KHKGTPJPBOQECW-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

427.4
MW (Da)
6.34
ALogP
3
HBA
1
HBD
63.6
PSA (Ų)
0.47
QED
1
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H28Cl2O4
MW 427.37
Aromatic Rings 1
Heavy Atoms 28
NP-Likeness 0.70

Activity Summary

IC50 1 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Felis catus
CHEMBL612670
IC50 8.4 8.4 4.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Felis catus IC50 = 4.0 nM 8.4 In vitro inhibition of HCO3- stimulated swelling in cat cerebrocortical tissue s... 7086844

Literature References

PubMed DOI Target Context # Activities
7086844 10.1021/jm00347a017 No relevant target 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
7086844 10.1021/jm00347a017 Rattus norvegicus 1
7086844 10.1021/jm00347a017 Felis catus 1
26588045 10.1021/acs.jmedchem.5b00671 Potassium channel subfamily K member 2 1
34413955 10.1021/acsmedchemlett.1c00240 Leukotriene B4 receptor 2 1

Data from ChEMBL 36 via Core Engine