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Compound Detail

CHEMBL2159239

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CO[C@@H]1[C@@H](O)[C@@H](O)[C@H](Oc2ccc(CCNC(C)=O)c(-c3ccc4c(c3)OCO4)c2)OC1(C)C

Basic Information

ChEMBL ID CHEMBL2159239
Phase Preclinical
Structure Type MOL
InChI Key FEKRHVNJCYAFDY-OLKYXYMISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

473.5
MW (Da)
2.01
ALogP
8
HBA
3
HBD
115.7
PSA (Ų)
0.56
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H31NO8
MW 473.52
Aromatic Rings 2
Heavy Atoms 34
NP-Likeness 1.00

Activity Summary

EC50 1 meas. best 7.74

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
EC50 7.74 7.74 18.4 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked EC50 = 18.4 nM 7.74 Cytoprotective activity against glucotoxicity in Sprague-Dawley rat DRG neurons ... 22702513

Literature References

PubMed DOI Target Context # Activities
22702513 10.1021/jm300544c Unchecked 3
22702513 10.1021/jm300544c Nucleic Acid 1

Data from ChEMBL 36 via Core Engine