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Compound Detail

CHEMBL521039

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CC(C)n1c(CC[C@@H](O)C[C@@H](O)CC(=O)O)c(-c2ccc(F)cc2)c2c1C(=O)N(c1ccccc1)CCC2

Basic Information

ChEMBL ID CHEMBL521039
Phase Preclinical
Structure Type MOL
InChI Key OMBVEVHRIQULKW-DNQXCXABSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

522.6
MW (Da)
4.99
ALogP
5
HBA
3
HBD
103.0
PSA (Ų)
0.35
QED
1
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H35FN2O5
MW 522.62
Aromatic Rings 3
Heavy Atoms 38
NP-Likeness -0.30

Activity Summary

IC50 2 meas. best 9.52
Kd 1 meas. best 7.67

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Liver microsomes
CHEMBL613694
IC50 9.52 9.52 0.3 1
Hepatocyte
CHEMBL613362
IC50 8.23 8.23 5.9 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 7.67 7.67 21.6 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