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Compound Detail

CHEMBL511069

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CC(=O)O[C@@H]1O[C@@](C)([C@H]2CC(C)=C(C)C(=O)O2)[C@H]2CC[C@H]3[C@@H]4CC=C5[C@@H](OC(C)=O)C=CC(=O)[C@]5(C)[C@H]4CC[C@]123

Basic Information

ChEMBL ID CHEMBL511069
Phase Preclinical
Structure Type MOL
InChI Key GBCVECRLRGQTDA-RTWHLENNSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

552.7
MW (Da)
4.76
ALogP
8
HBA
0
HBD
105.2
PSA (Ų)
0.28
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C32H40O8
MW 552.66
Aromatic Rings 0
Heavy Atoms 40
NP-Likeness 3.29

Activity Summary

IC50 1 meas. best 5.29

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
ADMET
CHEMBL612558
IC50 5.29 5.29 5100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
ADMET IC50 = 5100.0 nM 5.29 Growth inhibition of mouse Hepa-1c1c7 cells by crystal violet staining 12027740

Literature References

PubMed DOI Target Context # Activities
12027740 10.1021/np0106337 Unchecked 2
12027740 10.1021/np0106337 Quinone oxidoreductase 2
12027740 10.1021/np0106337 ADMET 1

Data from ChEMBL 36 via Core Engine