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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H46O3
Molecular Weight 406.6416
Optical Activity ( + )
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BAR-501

SMILES

CC[C@@H]1[C@H](O)[C@H]2[C@@H]3CC[C@H]([C@H](C)CCCO)[C@@]3(C)CC[C@@H]2[C@@]4(C)CC[C@@H](O)C[C@@H]14

InChI

InChIKey=DQBAHTQWQZRMFH-CRPAWOMZSA-N
InChI=1S/C26H46O3/c1-5-18-22-15-17(28)10-12-26(22,4)21-11-13-25(3)19(16(2)7-6-14-27)8-9-20(25)23(21)24(18)29/h16-24,27-29H,5-15H2,1-4H3/t16-,17-,18+,19-,20+,21+,22+,23+,24+,25-,26-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.0 µM [EC50]
PubMed

PubMed

TitleDatePubMed
Agonism for the bile acid receptor GPBAR1 reverses liver and vascular damage in a mouse model of steatohepatitis.
2019-02
GPBAR1 Functions as Gatekeeper for Liver NKT Cells and provides Counterregulatory Signals in Mouse Models of Immune-Mediated Hepatitis.
2019
Gpbar1 agonism promotes a Pgc-1α-dependent browning of white adipose tissue and energy expenditure and reverses diet-induced steatohepatitis in mice.
2017-10-20
The Bile Acid Receptor GPBAR1 Regulates the M1/M2 Phenotype of Intestinal Macrophages and Activation of GPBAR1 Rescues Mice from Murine Colitis.
2017-07-15
Reversal of Endothelial Dysfunction by GPBAR1 Agonism in Portal Hypertension Involves a AKT/FOXOA1 Dependent Regulation of H2S Generation and Endothelin-1.
2015
Name Type Language
BAR-501
Code English
(3?,5?,6?,7?)-6-Ethylcholane-3,7,24-triol
Preferred Name English
Cholane-3,7,24-triol, 6-ethyl-, (3?,5?,6?,7?)-
Systematic Name English
Code System Code Type Description
FDA UNII
AVN65GUL86
Created by admin on Wed Apr 02 19:16:44 GMT 2025 , Edited by admin on Wed Apr 02 19:16:44 GMT 2025
PRIMARY
PUBCHEM
101886302
Created by admin on Wed Apr 02 19:16:44 GMT 2025 , Edited by admin on Wed Apr 02 19:16:44 GMT 2025
PRIMARY
CAS
1632118-69-4
Created by admin on Wed Apr 02 19:16:44 GMT 2025 , Edited by admin on Wed Apr 02 19:16:44 GMT 2025
PRIMARY