Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

G6132

Sigma-Aldrich

Glycodeoxycholic acid monohydrate

≥97% (TLC)

Synonym(s):

3α,12α-Dihydroxy-5β-cholanoic acid N-(carboxymethyl)amide, Glycodesoxycholic acid, N-(3α,12α-Dihydroxy-24-oxocholan-24-yl)glycine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C26H43NO5
CAS Number:
360-65-6
Molecular Weight:
467.64
Beilstein/REAXYS Number:
2954947
MDL number:
MFCD00150922
UNSPSC Code:
12161900
PubChem Substance ID:
24895246

description

anionic

assay

≥97% (TLC)

SMILES string

[H]O[H].[H][C@]12CC[C@@]3([H])[C@]4([H])CC[C@H]([C@H](C)CCC(=O)NCC(O)=O)[C@@]4(C)[C@@H](O)C[C@]3([H])[C@@]1(C)CC[C@@H](O)C2

InChI

1S/C26H43NO5.H2O/c1-15(4-9-23(30)27-14-24(31)32)19-7-8-20-18-6-5-16-12-17(28)10-11-25(16,2)21(18)13-22(29)26(19,20)3;/h15-22,28-29H,4-14H2,1-3H3,(H,27,30)(H,31,32);1H2/t15-,16-,17-,18+,19-,20+,21+,22+,25+,26-;/m1./s1

InChI key

DLOTUJUSJVIXDW-YEUHZSMFSA-N

Looking for similar products? Visit Product Comparison Guide

Biochem/physiol Actions

Induces apoptosis in hepatocytes; may induce DNA cleavage.

replaced by

Product No.
Description
Pricing

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
070H5015

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Werner Hartwig et al.
American journal of physiology. Gastrointestinal and liver physiology, 291(5), G844-G850 (2006-10-13)
In acute pancreatitis, local as well as systemic organ complications are mediated by the activation of various inflammatory cascades. The role of complement in this setting is unclear. The aim of the present study was to determine the level of
Frank Axel Wenger et al.
Journal of gastroenterology and hepatology, 22(11), 1872-1876 (2007-10-05)
Octreotide is considered to reduce exocrine pancreatic secretion in acute hemorrhagic necrotizing pancreatitis decreasing pancreatic autodigestion. The aim of this study was to determine whether octreotide also has antioxidative effects in acute pancreatitis. Additionally time and dose of application were
Giulia de Petris et al.
The journal of physical chemistry. B, 113(20), 7162-7169 (2009-05-01)
This paper deals with electrospray ionization mass spectrometry (ESIMS), small-angle X-ray scattering (SAXS), and dynamic light scattering (DLS) measurements in order to provide information on the existence, aggregation, composition, and structure of the two-component aggregates of sodium glycocholate (NaGC) and
Yanfeng Wang et al.
International journal of pharmaceutics, 370(1-2), 68-74 (2008-12-17)
HO-1-u-1 (Ueda-1) is a human tumor cell line established from human sublingual squamous cell carcinoma. In previous study, HO-1-u-1 cell line was grown on cell culture inserts and utilized as in vitro model for screening sublingual drug delivery. The aim
Dockyu Kim et al.
Journal of microbiology and biotechnology, 17(3), 403-407 (2007-12-07)
Several marine bacterial strains, which were isolated from seawater off the island Dokdo, Korea, were screened to find new bioactive compounds such as antibiotics. Among them, Donghaeana dokdonensis strain DSW-6 was found to produce antibacterial agents, and the agents were
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service