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Compound Detail

CHEMBL391241

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CCNC(=O)c1c(-c2ccccn2)c(-c2ccc(F)cc2)c(CC[C@@H](O)C[C@@H](O)CC(=O)[O-])n1C(C)C.[Na+]

Basic Information

ChEMBL ID CHEMBL391241
Phase Preclinical
Structure Type MOL
InChI Key HUUOZIVMZLNIKG-MUCZFFFMSA-M
Parent Compound CHEMBL1207317
Active Moiety CHEMBL1207317
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

511.6
MW (Da)
4.21
ALogP
6
HBA
4
HBD
124.7
PSA (Ų)
0.29
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H33FN3NaO5
MW 533.58
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -0.47

Activity Summary

IC50 3 meas. best 8.29

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 8.29 8.29 5.1 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 7.68 7.68 21.0 1
L6
CHEMBL614793
IC50 4.97 4.97 10821.0 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