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Compound Detail

CHEMBL252657

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CC(C)c1c(S(=O)(=O)Nc2ccccc2)c(-c2ccc(F)cc2)c(-c2ccc(F)cc2)n1CC[C@@H](O)C[C@@H](O)CC(=O)[O-].[Na+]

Basic Information

ChEMBL ID CHEMBL252657
Phase Preclinical
Structure Type MOL
InChI Key VOHQKDZHOQWHFF-CNZCJKERSA-M
Parent Compound CHEMBL1206230
Active Moiety CHEMBL1206230
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

612.7
MW (Da)
6.00
ALogP
6
HBA
4
HBD
128.9
PSA (Ų)
0.15
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 C32H33F2N2NaO6S
MW 634.68
Aromatic Rings 4
Heavy Atoms 43
NP-Likeness -0.52

Activity Summary

IC50 3 meas. best 9.02

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.02 9.02 1.0 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 8.7 8.7 2.0 1
L6
CHEMBL614793
IC50 7.35 7.35 45.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18155906 10.1016/j.bmcl.2007.11.124 Hepatocyte 2
18155906 10.1016/j.bmcl.2007.11.124 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
18155906 10.1016/j.bmcl.2007.11.124 L6 1
18155906 10.1016/j.bmcl.2007.11.124 Mus musculus 1

Data from ChEMBL 36 via Core Engine