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Compound Detail

CHEMBL4740844

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CC[C@H]1[C@@H](O)[C@@H]2[C@H](C[C@@H](O)[C@]3(C)[C@@H]([C@H](C)CCC(=O)O)CC[C@@H]23)[C@@]2(C)CC[C@@H](O)C[C@@H]12

Basic Information

ChEMBL ID CHEMBL4740844
Phase Preclinical
Structure Type MOL
InChI Key QUAACMKIRHXEPE-AESFTPQLSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

436.6
MW (Da)
4.08
ALogP
4
HBA
4
HBD
98.0
PSA (Ų)
0.52
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H44O5
MW 436.63
Aromatic Rings 0
Heavy Atoms 31
NP-Likeness 2.66

Activity Summary

EC50 2 meas. best 5.33

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 5.33 5.33 4700.0 1
G-protein coupled bile acid receptor 1
CHEMBL5409
EC50 4.21 4.21 62000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
27652492 10.1021/acs.jmedchem.6b01126 Bile acid receptor 2
27652492 10.1021/acs.jmedchem.6b01126 G-protein coupled bile acid receptor 1 2

Data from ChEMBL 36 via Core Engine