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Compound Detail

CHEMBL228528

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CC(C)n1c(CC[C@@H](O)C[C@@H](O)CC(=O)[O-])c(-c2ccc(F)cc2)c2c3ccccc3n(-c3cccc(F)c3)c(=O)c21.[Na+]

Basic Information

ChEMBL ID CHEMBL228528
Phase Preclinical
Structure Type MOL
InChI Key XVSQSSWYHPGJJA-JIMLSGQQSA-M
Parent Compound CHEMBL1206147
Active Moiety CHEMBL1206147
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

574.6
MW (Da)
5.99
ALogP
6
HBA
3
HBD
104.7
PSA (Ų)
0.19
QED
2
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H31F2N2NaO5
MW 596.61
Aromatic Rings 5
Heavy Atoms 42
NP-Likeness -0.36

Activity Summary

IC50 2 meas. best 8.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
IC50 8.72 8.72 1.9 1
Hepatocyte
CHEMBL613362
IC50 6.61 6.61 246.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
17574411 10.1016/j.bmcl.2007.05.097 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
17574411 10.1016/j.bmcl.2007.05.097 Hepatocyte 1

Data from ChEMBL 36 via Core Engine