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

CHEMBL182629

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
C=CCc1cc(OC)c(O)c(-c2cc(CC=C)cc(OC)c2O)c1

Basic Information

ChEMBL ID CHEMBL182629
Phase Preclinical
Structure Type MOL
InChI Key KETPSFSOGFKJJY-UHFFFAOYSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
9
Publications
0
Known Names

Molecular Properties

326.4
MW (Da)
4.24
ALogP
4
HBA
2
HBD
58.9
PSA (Ų)
0.75
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C20H22O4
MW 326.39
Aromatic Rings 2
Heavy Atoms 24
NP-Likeness 0.73

Activity Summary

IC50 2 meas. best 5.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.7 5.7 2000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 2000.0 nM 5.7 Inhibition of yeast alpha-glucosidase using p-nitrophenyl-alpha-glucopyranoside ... 28497968

Literature References

Data from ChEMBL 36 via Core Engine