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SMB00807

Sigma-Aldrich

Glycolithocholate sulfate

≥95% (HPLC)

Synonym(s):

Glycolithocholic acid 3-sulfate, Sulfoglycolithocholic acid, Sulfolithocholylglycine

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About This Item

Empirical Formula (Hill Notation):
C26H43NO7S
CAS Number:
15324-64-8
Molecular Weight:
513.69
UNSPSC Code:
41141802
NACRES:
NA.28
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Assay

≥95% (HPLC)

shipped in

wet ice

storage temp.

−20°C

SMILES string

[S](=O)(=O)([O-])O[C@H]1C[C@@H]2[C@@]([C@@H]3[C@H]([C@H]4[C@@]([C@H](CC4)[C@@H](CCC(=O)NCC(=O)O)C)(CC3)C)CC2)(CC1)C

InChI

1S/C26H43NO7S/c1-16(4-9-23(28)27-15-24(29)30)20-7-8-21-19-6-5-17-14-18(34-35(31,32)33)10-12-25(17,2)22(19)11-13-26(20,21)3/h16-22H,4-15H2,1-3H3,(H,27,28)(H,29,30)(H,31,32,33)/p-1/t16-,17-,18-,19+,20-,21+,22+,25+,26-/m1/s1

InChI key

FHXBAFXQVZOILS-OETIFKLTSA-M

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Show Differences

1 of 4

This Item
B59209B59179B3809
4-Bromobenzoic hydrazide 98%

259624

4-Bromobenzoic hydrazide

4-Bromobenzoyl chloride 98%

B59209

4-Bromobenzoyl chloride

2-Bromobenzoyl chloride 98%

B59179

2-Bromobenzoyl chloride

Benzenesulfonyl hydrazide 98%

B3809

Benzenesulfonyl hydrazide

assay

98%

assay

98%

assay

98%

assay

98%

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

mp

165-167 °C (lit.)

mp

36-39 °C (lit.)

mp

8-10 °C (lit.)

mp

101-103 °C (lit.)

functional group

amine

functional group

-

functional group

-

functional group

-

General description

Sulfoglycolithocholic acid, also known as sulfolithocholylglycine, belongs to the class of compounds referred as glycinated bile acids and derivatives. This compound serves as a valuable asset in both biochemical and metabolomics research due to its significant role in the field of bile acid conjugates and secondary bile acid production. Sulfolithocholylglycine is the 3-O-sulfo derivative of glycolithocholic acid and is synthesized through microbial flora enzymes in the colonic environment. In hepatocytes, bile acids, both primary and secondary, undergo amino acid conjugation at the C-24 carboxylic acid on the side chain, resulting in the predominance of glycine-conjugated forms of bile acids in the bile duct[1]. This compound′s unique properties make it an intriguing subject for research, with potential applications in metabolomics and biochemistry.

Application

Sulfoglycolithocholic acid can be used in biochemical research and metabolomics research. It can be used to study the metabolism of bile acids, the gut microbiome, and the effects of bile acids on various tissues and organs.

Features and Benefits

  • Can be used in Metabolomics and Biochemical research
  • High-quality compound suitable for multiple research applications

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
SLCB0720

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J W McDonald et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 8(8), 859-865 (1995-10-01)
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