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Compound Detail

CHEMBL488297

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CC(C)c1c(C(=O)NCc2ccccc2)nc(-c2ccc(F)c(F)c2)n1CC[C@@H](O)C[C@@H](O)CC(=O)O

Basic Information

ChEMBL ID CHEMBL488297
Phase Preclinical
Structure Type MOL
InChI Key VBYMTGCWOPVZIK-WOJBJXKFSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

515.6
MW (Da)
3.86
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 C27H31F2N3O5
MW 515.56
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -0.91

Activity Summary

IC50 3 meas. best 9.82
Kd 1 meas. best 8.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 9.82 9.82 0.1 1
Liver microsomes
CHEMBL613694
IC50 9.52 9.52 0.3 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 8.16 8.16 6.9 1
L6
CHEMBL614793
IC50 6.32 6.32 484.0 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