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Compound Detail

CHEMBL481660

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CCc1c(C(=O)N[C@H](CO)c2ccc(-c3ccccc3)cc2)c2c(n1CC[C@@H](O)C[C@@H](O)CC(=O)O)CCCC2

Basic Information

ChEMBL ID CHEMBL481660
Phase Preclinical
Structure Type MOL
InChI Key JYFVDIKKTIPUJT-RGSZASNESA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

548.7
MW (Da)
4.04
ALogP
6
HBA
5
HBD
132.0
PSA (Ų)
0.22
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H40N2O6
MW 548.68
Aromatic Rings 3
Heavy Atoms 40
NP-Likeness -0.20

Activity Summary

IC50 3 meas. best 9.17
Kd 1 meas. best 7.39

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.17 9.17 0.7 1
Liver microsomes
CHEMBL613694
IC50 7.94 7.94 11.5 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 7.39 7.39 40.7 1
L6
CHEMBL614793
IC50 6.0 6.0 1010.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18540668 10.1021/jm7015057 Hepatocyte 2
18540668 10.1021/jm7015057 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
18540668 10.1021/jm7015057 Liver microsomes 1
18540668 10.1021/jm7015057 L6 1
18540668 10.1021/jm7015057 Mus musculus 1

Data from ChEMBL 36 via Core Engine