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Compound Detail

CHEMBL487632

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CC(C)c1c(C(=O)N(C)[C@@H](C)c2ccccc2)nc(-c2ccc(F)cc2)n1CC[C@@H](O)C[C@@H](O)CC(=O)O

Basic Information

ChEMBL ID CHEMBL487632
Phase Preclinical
Structure Type MOL
InChI Key MWFPRNDXYVUNHJ-WUMKDDEVSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

525.6
MW (Da)
4.62
ALogP
6
HBA
3
HBD
115.9
PSA (Ų)
0.32
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H36FN3O5
MW 525.62
Aromatic Rings 3
Heavy Atoms 38
NP-Likeness -0.73

Activity Summary

IC50 3 meas. best 9.77
Kd 1 meas. best 8.12

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.77 9.77 0.2 1
Liver microsomes
CHEMBL613694
IC50 8.72 8.72 1.9 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 8.12 8.12 7.5 1
L6
CHEMBL614793
IC50 4.63 4.63 23400.0 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