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Merck

G2878

Sigma-Aldrich

Glycocholic acid hydrate

synthetic, ≥97% (HPLC)

Sinónimos:

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 (notación de Hill):
C26H43NO6 · xH2O
Número de CAS:
Peso molecular:
465.62 (anhydrous basis)
Beilstein:
2955826
Número MDL:
Código UNSPSC:
12161900
ID de la sustancia en PubChem:
NACRES:
NA.25

origen biológico

synthetic

descripción

anionic

Análisis

≥97% (HPLC)

formulario

powder

mol peso

average mol wt 1000

número de agregación

2.1

técnicas

enzyme immunoassay: suitable

CMC

7.1

grupo funcional

amide

Condiciones de envío

ambient

temp. de almacenamiento

room temp

cadena 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

Clave InChI

WDKPRHOCWKLQPK-ZUHYDKSRSA-N

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Aplicación

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.

Acciones bioquímicas o fisiológicas

Bile Acid

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Referencia del producto
Descripción
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Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

Eyeshields, Gloves


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Contenido 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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