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

CHEMBL439585

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
O=C1[C@@H]2O[C@@H]2C2(Oc3cccc4cccc(c34)O2)[C@@]23O[C@@]12CCCC3=O

Basic Information

ChEMBL ID CHEMBL439585
Phase Preclinical
Structure Type MOL
InChI Key RBWNSRYEACJDLO-WNHJNPCNSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

350.3
MW (Da)
1.92
ALogP
6
HBA
0
HBD
77.7
PSA (Ų)
0.68
QED
0
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H14O6
MW 350.33
Aromatic Rings 2
Heavy Atoms 26
NP-Likeness 1.47

Activity Summary

IC50 2 meas. best 5.34

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
MCF7
CHEMBL387
IC50 5.34 5.34 4600.0 1
MDA-MB-231
CHEMBL400
IC50 5.09 5.09 8200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
MCF7 IC50 = 4600.0 nM 5.34 Ability to inhibit the growth of MCF-7 cell line 11551767
MDA-MB-231 IC50 = 8200.0 nM 5.09 Ability to inhibit the growth of MDA-MB-231 cell line 11551767

Literature References

PubMed DOI Target Context # Activities
11551767 10.1016/s0960-894x(01)00525-x Thioredoxin reductase 2
11551767 10.1016/s0960-894x(01)00525-x MDA-MB-231 1
11551767 10.1016/s0960-894x(01)00525-x MCF7 1

Data from ChEMBL 36 via Core Engine