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Compound Detail

CHEMBL3138060

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C=CC[C@@H]1C2C[C@H](O)CC[C@]2(C)[C@H]2CC[C@]3(C)C([C@H](C)CCC(=O)O)CC[C@H]3[C@@H]2[C@@H]1O

Basic Information

ChEMBL ID CHEMBL3138060
Phase Preclinical
Structure Type MOL
InChI Key BYQIIBTUGRCOBV-VZEOLMJCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

432.6
MW (Da)
5.28
ALogP
3
HBA
3
HBD
77.8
PSA (Ų)
0.50
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H44O4
MW 432.65
Aromatic Rings 0
Heavy Atoms 31
NP-Likeness 2.32

Activity Summary

EC50 1 meas. best 6.32

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 6.32 6.32 480.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Bile acid receptor EC50 = 480.0 nM 6.32 Binding affinity for human Farnesoid X receptor in FRET assay 15317466

Literature References

PubMed DOI Target Context # Activities
15317466 10.1021/jm049904b Bile acid receptor 2

Data from ChEMBL 36 via Core Engine