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Compound Detail

CHEMBL488298

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CC(C)n1c(C(=O)NCc2ccccc2)nc(-c2ccc(F)cc2)c1CC[C@@H](O)C[C@@H](O)CC(=O)O

Basic Information

ChEMBL ID CHEMBL488298
Phase Preclinical
Structure Type MOL
InChI Key XRFGQWQHNSTQDR-FGZHOGPDSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

497.6
MW (Da)
3.72
ALogP
6
HBA
4
HBD
124.7
PSA (Ų)
0.30
QED
0
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H32FN3O5
MW 497.57
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -0.56

Activity Summary

IC50 3 meas. best 9.42
Kd 1 meas. best 7.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.42 9.42 0.4 1
Liver microsomes
CHEMBL613694
IC50 8.44 8.44 3.6 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 7.5 7.5 31.6 1
L6
CHEMBL614793
IC50 7.0 7.0 101.0 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