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Compound Detail

CHEMBL5408411

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CO[C@H](C[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C)C(=O)O

Basic Information

ChEMBL ID CHEMBL5408411
Phase Preclinical
Structure Type MOL
InChI Key AKDDFJQZKGAQEM-RHBSABBPSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

438.6
MW (Da)
3.07
ALogP
5
HBA
4
HBD
107.2
PSA (Ų)
0.53
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H42O6
MW 438.61
Aromatic Rings 0
Heavy Atoms 31
NP-Likeness 2.59

Activity Summary

EC50 1 meas. best 4.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 4.46 4.46 35000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Bile acid receptor EC50 = 35000.0 nM 4.46 Activation of GST-tagged FXR LBD (unknown origin) using biotinylated Src-1 pepti... 37813065

Literature References

PubMed DOI Target Context # Activities
37813065 10.1016/j.ejmech.2023.115851 Bile acid receptor 2
37813065 10.1016/j.ejmech.2023.115851 G-protein coupled bile acid receptor 1 1

Data from ChEMBL 36 via Core Engine