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

CHEMBL4790820

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
CC(C)=CCC/C(C)=C/Cc1c(O)c2c(c(/C=C/C(=O)c3ccc(O)cc3)c1O)OC(C)(C)C=C2

Basic Information

ChEMBL ID CHEMBL4790820
Phase Preclinical
Structure Type MOL
InChI Key HAARNMNSHJNCOP-STOILTMGSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

474.6
MW (Da)
7.12
ALogP
5
HBA
3
HBD
87.0
PSA (Ų)
0.22
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H34O5
MW 474.60
Aromatic Rings 2
Heavy Atoms 35
NP-Likeness 2.20

Activity Summary

IC50 1 meas. best 5.12

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
RAW264.7
CHEMBL612557
IC50 5.12 5.12 7600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
RAW264.7 IC50 = 7600.0 nM 5.12 Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells 32208222

Literature References

PubMed DOI Target Context # Activities
32208222 10.1016/j.ejmech.2020.112216 RAW264.7 1

Data from ChEMBL 36 via Core Engine