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G2878

Sigma-Aldrich

Glycocholic acid hydrate

synthetic, ≥97% (HPLC)

Sinônimo(s):

3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide, Cholylglycine, N-(3α,7α,12α-Trihydroxy-24-oxocholan-24-yl)-glycine

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About This Item

Fórmula empírica (Notação de Hill):
C26H43NO6 · xH2O
Número CAS:
Peso molecular:
465.62 (anhydrous basis)
Beilstein:
2955826
Número MDL:
Código UNSPSC:
12161900
ID de substância PubChem:
NACRES:
NA.25

fonte biológica

synthetic

Nível de qualidade

descrição

anionic

Ensaio

≥97% (HPLC)

forma

powder

peso molecular

average mol wt 1000

número de agregação

2.1

técnica(s)

enzyme immunoassay: suitable

CMC

7.1

grupo funcional

amide

Condições de expedição

ambient

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

O.C[C@H](CCC(=O)NCC(O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C

InChI

1S/C26H43NO6.H2O/c1-14(4-7-22(31)27-13-23(32)33)17-5-6-18-24-19(12-21(30)26(17,18)3)25(2)9-8-16(28)10-15(25)11-20(24)29;/h14-21,24,28-30H,4-13H2,1-3H3,(H,27,31)(H,32,33);1H2/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-;/m1./s1

chave InChI

WDKPRHOCWKLQPK-ZUHYDKSRSA-N

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Aplicação

Glycocholic acid hydrate has been used in a study to assess the invasiveness of Cryptosporidium spp. Into cultured cells. It has also been used in a study to investigate the interaction of chitosan and oil-in-water emulsions under conditions simulating the digestive system.

Ações bioquímicas/fisiológicas

Bile Acid

produto relacionado

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Gloves


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Protocolos

Investigate bile acid roles in gut hormone profiles and glycemic control, vital for clinical labs exploring potential mechanisms.

Conteúdo relacionado

Bile Acids (BA) are synthesized in the liver and play important roles in cholesterol homeostasis, absorption of vitamins and lipids, and various key metabolic processes.

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