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Compound Detail

CHEMBL271417

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CCOC(=O)/C=C/[C@H](CC(C)C)NC(=O)[C@@H]1CC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N1

Basic Information

ChEMBL ID CHEMBL271417
Phase Preclinical
Structure Type MOL
InChI Key HZDZHLMMFJYUEB-OSEDVSKHSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

655.8
MW (Da)
2.31
ALogP
7
HBA
5
HBD
171.8
PSA (Ų)
0.16
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H53N5O7
MW 655.84
Aromatic Rings 1
Heavy Atoms 47
NP-Likeness 0.69

Activity Summary

IC50 2 meas. best 6.69

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.69 6.52 206.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 206.0 nM 6.69 Inhibition of chymotrypsin-like activity of 20S proteasome 18294845
Unchecked IC50 = 447.0 nM 6.35 Inhibition of trypsin-like activity of 20S proteasome 18294845

Literature References

PubMed DOI Target Context # Activities
18294845 10.1016/j.bmcl.2008.02.016 Unchecked 3

Data from ChEMBL 36 via Core Engine