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Compound Detail

CHEMBL444210

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CC(C)c1c(C(=O)NCc2cccc(-c3ccccc3F)c2)nc(-c2ccc(F)cc2)n1CC[C@@H](O)C[C@@H](O)CC(=O)O

Basic Information

ChEMBL ID CHEMBL444210
Phase Preclinical
Structure Type MOL
InChI Key JGYFNJJVXLVBOL-CLJLJLNGSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

591.7
MW (Da)
5.53
ALogP
6
HBA
4
HBD
124.7
PSA (Ų)
0.16
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 C33H35F2N3O5
MW 591.66
Aromatic Rings 4
Heavy Atoms 43
NP-Likeness -0.76

Activity Summary

IC50 3 meas. best 9.22
Kd 1 meas. best 7.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Liver microsomes
CHEMBL613694
IC50 9.22 9.22 0.6 1
Hepatocyte
CHEMBL613362
IC50 7.86 7.86 13.9 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 7.66 7.66 22.0 1
L6
CHEMBL614793
IC50 6.21 6.21 617.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18540668 10.1021/jm7015057 Hepatocyte 2
18540668 10.1021/jm7015057 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1
18540668 10.1021/jm7015057 Liver microsomes 1
18540668 10.1021/jm7015057 L6 1

Data from ChEMBL 36 via Core Engine