Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2159233

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CO[C@@H]1[C@@H](O)[C@@H](O)[C@H](Oc2ccc(CCNC(C)=O)c(-c3ccccc3SC)c2)OC1(C)C

Basic Information

ChEMBL ID CHEMBL2159233
Phase Preclinical
Structure Type MOL
InChI Key USRKXLZYHVZAKQ-OLKYXYMISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

475.6
MW (Da)
3.00
ALogP
7
HBA
3
HBD
97.2
PSA (Ų)
0.51
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H33NO6S
MW 475.61
Aromatic Rings 2
Heavy Atoms 33
NP-Likeness 0.73

Activity Summary

EC50 1 meas. best 6.42

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
EC50 6.42 6.42 384.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked EC50 = 384.0 nM 6.42 Cytoprotective activity against glucotoxicity in Sprague-Dawley rat DRG neurons ... 22702513

Literature References

PubMed DOI Target Context # Activities
22702513 10.1021/jm300544c Unchecked 2

Data from ChEMBL 36 via Core Engine