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Compound Detail

CHEMBL491410

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Oc1ccc(CCc2ccc(O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)cc2O)c(O)c1

Basic Information

ChEMBL ID CHEMBL491410
Phase Preclinical
Structure Type MOL
InChI Key DHNFDTBTJFVKKB-HCXYKTFWSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

378.4
MW (Da)
0.41
ALogP
8
HBA
6
HBD
139.8
PSA (Ų)
0.44
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C19H22O8
MW 378.38
Aromatic Rings 2
Heavy Atoms 27
NP-Likeness 1.37

Activity Summary

IC50 2 meas. best 6.37

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Tyrosinase
CHEMBL1973
IC50 6.37 6.37 430.0 1
Tyrosinase
CHEMBL3318
IC50 6.37 6.37 430.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Tyrosinase IC50 = 430.0 nM 6.37 Inhibition of mushroom tyrosinase 18782667
Tyrosinase IC50 = 430.0 nM 6.37 Inhibition of Tyrosinase 21334791

Literature References

PubMed DOI Target Context # Activities
18782667 10.1016/j.bmcl.2008.08.053 Tyrosinase 1
21334791 10.1016/j.ejmech.2011.01.065 Tyrosinase 1

Data from ChEMBL 36 via Core Engine