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Compound Detail

CHEMBL400973

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CC(C)n1c(CC[C@@H](O)C[C@@H](O)CC(=O)[O-])c(-c2ccc(F)cc2)c(-c2ccccc2)c1C(=O)Nc1ccc(O)cc1.[Na+]

Basic Information

ChEMBL ID CHEMBL400973
Phase Preclinical
Structure Type MOL
InChI Key FGAITSUOTUYAJZ-CNZCJKERSA-M
Parent Compound CHEMBL1207373
Active Moiety CHEMBL1207373
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

574.6
MW (Da)
6.02
ALogP
6
HBA
5
HBD
132.0
PSA (Ų)
0.13
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H34FN2NaO6
MW 596.63
Aromatic Rings 4
Heavy Atoms 42
NP-Likeness -0.23

Activity Summary

IC50 3 meas. best 9.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
IC50 9.4 9.4 0.4 1
Hepatocyte
CHEMBL613362
IC50 9.3 9.3 0.5 1
Unchecked
CHEMBL612545
IC50 6.2 6.2 626.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
17574412 10.1016/j.bmcl.2007.05.096 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
17574412 10.1016/j.bmcl.2007.05.096 Hepatocyte 1
17574412 10.1016/j.bmcl.2007.05.096 Unchecked 1
17574412 10.1016/j.bmcl.2007.05.096 Mus musculus 1

Data from ChEMBL 36 via Core Engine