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About This Item
Empirical Formula (Hill Notation):
C24H40 O5
CAS Number:
Molecular Weight:
408.57
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 5 mg (700159P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
lipid type
bile acids
shipped in
dry ice
storage temp.
−20°C
SMILES string
O[C@H]1[C@@H]2[C@@H]([C@@]4([C@H]([C@H]1O)C[C@@H](CC4)O)C)CC[C@]3([C@H]2CC[C@@H]3[C@@H](CCC(=O)O)C)C
InChI
1S/C24H40O5/c1-13(4-7-19(26)27)15-5-6-16-20-17(9-11-23(15,16)2)24(3)10-8-14(25)12-18(24)21(28)22(20)29/h13-18,20-22,25,28-29H,4-12H2,1-3H3,(H,26,27)/t13-,14-,15-,16+,17+,18+,20+,21-,22+,23-,24-/m1/s1
InChI key
DKPMWHFRUGMUKF-KWXDGCAGSA-N
General description
Hyocholic acid, also called the 3α,6α,7α-trihydroxy-5β-cholanoic acid, is synthesized by the 6α-hydroxylation of chenodeoxycholic acid. It is a primary trihydroxylated bile acid associated with pigs. It is a minor bile acid in humans. Hyocholic acid is also synthesized from α-muricholic acid (MCA) in liver by the action of cytochrome P450 3A4 (CYP3A4).
Biochem/physiol Actions
Hyocholic acid levels are elevated in plasma and urine samples of patients with cholestatic liver disease and in hepatic cirrhosis.
Packaging
5 mL Amber Glass Screw Cap Vial (700159P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Tammy L Kindel et al.
Surgical endoscopy, 32(2), 805-812 (2017-08-06)
Bile acids (BAs) are post-prandial hormones that play an important role in glucose and lipid homeostasis as well as energy expenditure. Total and glycine-amidated BAs increase after sleeve gastrectomy (SG) and correlate to improved metabolic disease. No specific bile acid
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 700159P-5MG | 04061835384006 |