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

CHEMBL5187352

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([C@@H]2c3c(O)cc(O)cc3[C@@H]3[C@H]2CO[C@H]3c2ccc(O)c(O)c2)cc(OC)c1O

Basic Information

ChEMBL ID CHEMBL5187352
Phase Preclinical
Structure Type MOL
InChI Key WVOKVBOSAJHZDQ-VHQADYEJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

452.5
MW (Da)
3.85
ALogP
8
HBA
5
HBD
128.8
PSA (Ų)
0.38
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C25H24O8
MW 452.46
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness 1.70

Activity Summary

IC50 1 meas. best 4.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.96 4.96 11000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 11000.0 nM 4.96 Inhibition of Bacillus stearothermophilus alpha-glucosidase type IV using p-nitr... 35367706

Literature References

PubMed DOI Target Context # Activities
35367706 10.1016/j.ejmech.2022.114282 Unchecked 1
35367706 10.1016/j.ejmech.2022.114282 Rattus norvegicus 1

Data from ChEMBL 36 via Core Engine