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Compound Detail

CHEMBL235709

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CC(C)n1c(CC[C@@H](O)C[C@@H](O)CC(=O)[O-])c(-c2ccc(F)cc2)c(-c2ccccn2)c1C(N)=O.[Na+]

Basic Information

ChEMBL ID CHEMBL235709
Phase Preclinical
Structure Type MOL
InChI Key FZLLTCORMNRZCD-STYNFMPRSA-M
Parent Compound CHEMBL1206165
Active Moiety CHEMBL1206165
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

483.5
MW (Da)
3.56
ALogP
6
HBA
4
HBD
138.7
PSA (Ų)
0.33
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 C26H29FN3NaO5
MW 505.52
Aromatic Rings 3
Heavy Atoms 35
NP-Likeness -0.30

Activity Summary

IC50 3 meas. best 8.31

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 8.31 8.31 4.9 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 8.28 8.28 5.3 1
L6
CHEMBL614793
IC50 4.73 4.73 18609.0 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