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Compound Detail

CHEMBL235472

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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(=O)NCc1ccccc1.[Na+]

Basic Information

ChEMBL ID CHEMBL235472
Phase Preclinical
Structure Type MOL
InChI Key YKRIOEYBURABBR-JUJAXGASSA-M
Parent Compound CHEMBL1206163
Active Moiety CHEMBL1206163
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

573.7
MW (Da)
5.39
ALogP
6
HBA
4
HBD
124.7
PSA (Ų)
0.17
QED
2
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H35FN3NaO5
MW 595.65
Aromatic Rings 4
Heavy Atoms 42
NP-Likeness -0.51

Activity Summary

IC50 3 meas. best 9.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.82 9.82 0.1 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 8.43 8.43 3.7 1
L6
CHEMBL614793
IC50 7.55 7.55 28.0 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