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

CHEMBL4127465

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
COc1cc(CCOC(C)=O)cc(-c2cc(CCOC(C)=O)cc(OC)c2O)c1O

Basic Information

ChEMBL ID CHEMBL4127465
Phase Preclinical
Structure Type MOL
InChI Key IPGSGNNHPCJUKB-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

418.4
MW (Da)
2.99
ALogP
8
HBA
2
HBD
111.5
PSA (Ų)
0.60
QED
0
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H26O8
MW 418.44
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness 0.58

Activity Summary

IC50 1 meas. best 5.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.96 5.96 1100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1100.0 nM 5.96 Inhibition of yeast alpha-glucosidase using p-nitrophenyl-alpha-glucopyranoside ... 28497968

Literature References

PubMed DOI Target Context # Activities
28497968 10.1021/acs.jnatprod.7b00250 Unchecked 2

Data from ChEMBL 36 via Core Engine