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Compound Detail

CHEMBL488300

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Cc1cccc(NC(=O)c2c(-c3ccc(F)cc3)c(-c3ccc(F)cc3)c(CC[C@@H](O)C[C@@H](O)CC(=O)O)n2C)c1

Basic Information

ChEMBL ID CHEMBL488300
Phase Preclinical
Structure Type MOL
InChI Key NFCPEMNXYCPHCR-CLJLJLNGSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

562.6
MW (Da)
5.72
ALogP
5
HBA
4
HBD
111.8
PSA (Ų)
0.19
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H32F2N2O5
MW 562.61
Aromatic Rings 4
Heavy Atoms 41
NP-Likeness -0.34

Activity Summary

IC50 2 meas. best 8.89
Kd 1 meas. best 8.49

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Liver microsomes
CHEMBL613694
IC50 8.89 8.89 1.3 1
Hepatocyte
CHEMBL613362
IC50 8.55 8.55 2.8 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 8.49 8.49 3.2 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

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

Data from ChEMBL 36 via Core Engine