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

CHEMBL411054

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
O=S(=O)(c1ccc2c(c1)OC(c1ccccc1)(c1ccccc1)O2)N1CCCCC1

Basic Information

ChEMBL ID CHEMBL411054
Phase Preclinical
Structure Type MOL
InChI Key PRJGXZKLMDRCRI-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
3
Publications
0
Known Names

Molecular Properties

421.5
MW (Da)
4.53
ALogP
4
HBA
0
HBD
55.8
PSA (Ų)
0.62
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H23NO4S
MW 421.52
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.86

Activity Summary

Ki 1 meas. best 7.42

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cannabinoid receptor 1
CHEMBL218
Ki 7.42 7.42 38.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 137.0 mL.min-1.g-1 Homo sapiens
CL 549.0 mL.min-1.g-1 Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cannabinoid receptor 1 Ki = 38.0 nM 7.42 Displacement of [3H]CP-55940 from human CB1R expressed in HEK293 cells 18335976

Literature References

PubMed DOI Target Context # Activities
18335976 10.1021/jm701487t Liver microsomes 2
18335976 10.1021/jm701487t Cannabinoid receptor 1 2
18335976 10.1021/jm701487t Mus musculus 1

Data from ChEMBL 36 via Core Engine