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Compound Detail

CHEMBL291954

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CC[C@H](C)C(=O)O[C@@H]1CCC=C2C=C[C@@H](C)[C@@H](COC(=O)C[C@H](O)CC(=O)O)[C@@H]21

Basic Information

ChEMBL ID CHEMBL291954
Phase Preclinical
Structure Type MOL
InChI Key IBEBWEGAFOWZMK-WTCNCPQGSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

408.5
MW (Da)
2.87
ALogP
6
HBA
2
HBD
110.1
PSA (Ų)
0.56
QED
0
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H32O7
MW 408.49
Aromatic Rings 0
Heavy Atoms 29
NP-Likeness 1.95

Activity Summary

IC50 1 meas. best 4.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3-hydroxy-3-methylglutaryl-coenzyme A reductase
CHEMBL3247
IC50 4.6 4.6 25000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
3-hydroxy-3-methylglutaryl-coenzyme A reductase IC50 = 25000.0 nM 4.6 Inhibition of HMG-CoA reductase in rat liver microsomes 3656359

Literature References

PubMed DOI Target Context # Activities
3656359 10.1021/jm00393a030 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1

Data from ChEMBL 36 via Core Engine