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Compound Detail

CHEMBL487278

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CC(C)c1c(C(=O)N[C@H](CO)c2ccccc2)c2c(n1CC[C@@H](O)C[C@@H](O)CC(=O)O)CCCC2

Basic Information

ChEMBL ID CHEMBL487278
Phase Preclinical
Structure Type MOL
InChI Key PRJVCDQLGPGUKJ-KCZVDYSFSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

486.6
MW (Da)
2.93
ALogP
6
HBA
5
HBD
132.0
PSA (Ų)
0.31
QED
0
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H38N2O6
MW 486.61
Aromatic Rings 2
Heavy Atoms 35
NP-Likeness -0.14

Activity Summary

IC50 2 meas. best 8.63
Kd 1 meas. best 7.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatocyte
CHEMBL613362
IC50 8.63 8.63 2.3 1
Liver microsomes
CHEMBL613694
IC50 8.11 8.11 7.8 1
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL402
Kd 7.46 7.46 34.8 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

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

Data from ChEMBL 36 via Core Engine