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Compound Detail

CHEMBL427854

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CCn1c(CC[C@@H](O)C[C@@H](O)CC(=O)[O-])c(-c2ccc(F)cc2)c(C)c1C(=O)Nc1ccccc1.[Na+]

Basic Information

ChEMBL ID CHEMBL427854
Phase Preclinical
Structure Type MOL
InChI Key NVHGQEYDPZXONX-HLUKFBSCSA-M
Parent Compound CHEMBL1207673
Active Moiety CHEMBL1207673
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

482.6
MW (Da)
4.39
ALogP
5
HBA
4
HBD
111.8
PSA (Ų)
0.32
QED
0
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H30FN2NaO5
MW 504.53
Aromatic Rings 3
Heavy Atoms 35
NP-Likeness -0.33

Activity Summary

IC50 3 meas. best 9.54

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.54 9.54 0.3 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 8.55 8.55 2.8 1
L6
CHEMBL614793
IC50 6.99 6.99 102.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
17560788 10.1016/j.bmc.2007.05.031 L6 2
17560788 10.1016/j.bmc.2007.05.031 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
17560788 10.1016/j.bmc.2007.05.031 Hepatocyte 1
17560788 10.1016/j.bmc.2007.05.031 Mus musculus 1

Data from ChEMBL 36 via Core Engine