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Compound Detail

CHEMBL1957045

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C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(-c4ccc(O)cc4)oc4cc(O)cc(O)c4c3=O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O

Basic Information

ChEMBL ID CHEMBL1957045
Phase Preclinical
Structure Type MOL
InChI Key MFIXKYXSBNIMPX-CHLFRWFTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

756.7
MW (Da)
-3.57
ALogP
20
HBA
12
HBD
328.4
PSA (Ų)
0.10
QED
3
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C33H40O20
MW 756.66
Aromatic Rings 3
Heavy Atoms 53
NP-Likeness 1.86

Activity Summary

IC50 1 meas. best 4.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.75 4.75 17600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 17600.0 nM 4.75 Inhibition of Saccharomyces cerevisiae alcohol dehydrogenase measured every 5 mi... 22377672

Literature References

PubMed DOI Target Context # Activities
22377672 10.1016/j.bmc.2012.02.002 Unchecked 3
22377672 10.1016/j.bmc.2012.02.002 Radical scavenging activity 1

Data from ChEMBL 36 via Core Engine