MDL | - |
---|---|
Molecular Weight | 392.57 |
Molecular Formula | C24H40O4 |
SMILES | C[C@H](CCC(O)=O)[C@H]1CC[C@@]2([H])[C@]3([H])C[C@H](O)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C |
Hyodeoxycholic acid is a secondary bile acid formed in the small intestine by the gut flora, and acts as a TGR5 (GPCR19) agonist, with an EC 50 of 31.6 µM in CHO cells.
Human Endogenous Metabolite |
Hyodeoxycholic acid is a secondary hydrophilic bile acid formed in the small intestine by the gut flora, and acts as an agonist of TGR5, with an EC 50 of 31.6 µM in CHO cells [1] . Hyodeoxycholic acid (50, 100 μM) increases the expression of genes ( Abca1, Abcg1, and Apoe ) involved in cholesterol efflux in RAW 264.7 cells [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Hyodeoxycholic acid (HDCA; 1.25% (wt/wt)) obviously decreases fat mass and increases lean mass but does not raise the serum levels of any organ toxicity markers in LDLRKO mice. Hyodeoxycholic acid inhibits atherosclerotic lesion formation in LDLRKO at multiple sites, improves plasma lipoprotein profiles, decreases plasma glucose level and intestinal cholesterol absorption efficiency and increases daily cholesterol excretion through fecal output. Hyodeoxycholic acid also improves HDL function as measured by a cholesterol efflux assay [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
DMSO : ≥ 100 mg/mL ( 254.73 mM )
H 2 O : < 0.1 mg/mL (insoluble)
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.5473 mL | 12.7366 mL | 25.4732 mL |
5 mM | 0.5095 mL | 2.5473 mL | 5.0946 mL |
10 mM | 0.2547 mL | 1.2737 mL | 2.5473 mL |