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Compound Detail

CHEMBL559524

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C=COC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)OCc1ccccc1

Basic Information

ChEMBL ID CHEMBL559524
Phase Preclinical
Structure Type BOTH
InChI Key YBKQKCPJYVFHAG-SDHOMARFSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

574.7
MW (Da)
3.19
ALogP
7
HBA
4
HBD
151.9
PSA (Ų)
0.16
QED
1
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H46N4O7
MW 574.72
Aromatic Rings 1
Heavy Atoms 41
NP-Likeness -0.14

Activity Summary

IC50 1 meas. best 6.26

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.26 6.26 545.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 545.0 nM 6.26 Inhibition of post acidic activity of proteasome from human PBMC after 30 mins b... 19577931

Literature References

PubMed DOI Target Context # Activities
19577931 10.1016/j.bmc.2009.06.025 Unchecked 6

Data from ChEMBL 36 via Core Engine