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Compound Detail

CHEMBL1760877

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C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OC(=O)[C@@H]5CCCC[C@H]5C(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C

Basic Information

ChEMBL ID CHEMBL1760877
Phase Preclinical
Structure Type MOL
InChI Key AGWMLHOAKFTMPH-HHAXZDJYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

530.8
MW (Da)
6.95
ALogP
4
HBA
2
HBD
100.9
PSA (Ų)
0.35
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H50O6
MW 530.75
Aromatic Rings 0
Heavy Atoms 38
NP-Likeness 1.59

Activity Summary

IC50 1 meas. best 5.07

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.07 5.07 8500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 8500.0 nM 5.07 Inhibition of chymotrypsin-like activity of 20S proteasome 21388808

Literature References

PubMed DOI Target Context # Activities
21388808 10.1016/j.bmcl.2011.02.041 Unchecked 1

Data from ChEMBL 36 via Core Engine