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Compound Detail

CHEMBL177545

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CC(=O)[O-].CC(C)c1c(OC[C@@H](O)C[C@@H](O)CC(=O)[O-])c(C(C)C)c(C(C)C)c(O)c1-c1ccc(F)cc1.[Na+].[Na+]

Basic Information

ChEMBL ID CHEMBL177545
Phase Preclinical
Structure Type MOL
InChI Key ZEEXPLFIZFMTMI-SXFSLILVSA-L
Parent Compound CHEMBL1206034
Active Moiety CHEMBL1206034
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

476.6
MW (Da)
5.53
ALogP
5
HBA
4
HBD
107.2
PSA (Ų)
0.34
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H39FNa2O8
MW 580.60
Aromatic Rings 2
Heavy Atoms 34
NP-Likeness 0.32

Activity Summary

IC50 3 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 8.4 8.4 4.0 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
IC50 8.39 8.39 4.1 1
Sus scrofa
CHEMBL613488
IC50 5.22 5.22 6000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
1656041 10.1021/jm00114a004 3-hydroxy-3-methylglutaryl-coenzyme A reductase 4
1656041 10.1021/jm00114a004 Rattus norvegicus 2
1656041 10.1021/jm00114a004 Sus scrofa 2
1656041 10.1021/jm00114a004 Oryctolagus cuniculus 1

Data from ChEMBL 36 via Core Engine