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Merck
CN

G7132

甘胆酸钠 水合物

≥95% (TLC)

别名:

3α,7α,12α-三羟基-5β-胆烷-24-酸 N-（羧甲基）酰胺 钠盐, N-（3α,7α,12α-三羟基-24-氧代胆碱-24-基）甘氨酸 钠盐, 甘氨胆酸 钠盐, 甘氨胆酸 钠盐 水合物

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关于此项目

线性分子式:
C26H42NO6Na · xH2O
化学文摘社编号:
338950-81-5
分子量:
487.60 (anhydrous basis)
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24895292
EC Number:
212-730-9
Beilstein/REAXYS Number:
3854517
MDL number:
MFCD09037360

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产品名称

甘胆酸钠 水合物, ≥95% (TLC)

InChI key

YWROUPFMHKARON-HJRQWJHVSA-M

InChI

1S/C26H43NO6.Na.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/q;+1;/p-1/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-;;/m1../s1

SMILES string

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

description

anionic

assay

≥95% (TLC)

mol wt

micellar avg mol wt 900(lit.)

aggregation number

1.9

CMC

13 mM (20-25°C)(lit.)

mp

210-215 °C (subl.) (lit.)

Quality Level

200

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相关类别

Application

在一项研究中，使用甘胆酸钠水合物通过荧光法和酶法评估血清总胆汁酸。 也用于研究其对睾酮胶束形成和增溶的影响。

Biochem/physiol Actions

胆盐

General description

甘胆酸钠水合物是一种共轭胆盐和离子型生物洗涤剂。

Preparation Note

该产品由天然胆酸（产品号C1129）合成制备而成。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000524017
0000522150
0000522153
0000522150
0000524017

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Micelle formation and testosterone solubilization by sodium glycocholate.
L Martis et al.
Journal of pharmaceutical sciences, 61(11), 1757-1761 (1972-11-01)
Mari Araki et al.
Journal of biochemistry, 160(5), 269-279 (2016-11-02)
DDHD2 has been reported to exhibit phospholipase A
Feilong Sun et al.
Colloids and surfaces. B, Biointerfaces, 170, 521-528 (2018-07-04)
Poorly soluble vitamin K cannot be absorbed by patients suffering from cholestasis due to extremely low level of bile salts in the intestine. A formulation of vitamin K including glycocholic acid (i.e. Konakion® MM), does not increase bioavailability because it
Monalisa Mohapatra et al.
Langmuir : the ACS journal of surfaces and colloids, 27(22), 13461-13467 (2011-10-07)
The interaction of submicellar concentrations of various physiologically important unconjugated [sodium deoxycholate (NaDC), sodium cholate (NaC)] and conjugated [sodium glycodeoxycholate (NaGDC), sodium glycocholate (NaGC), sodium taurodeoxycholate (NaTDC), sodium taurocholate (NaTC)] bile salts with dipalmitoylphosphatidylcholine (DPPC) and dimyristoylphosphatidylcholine (DMPC) small unilamellar
Yuxing Guo et al.
Journal of the science of food and agriculture, 98(3), 976-983 (2017-07-18)
To exert an antihypertensive effect after oral administration, angiotensin I-converting enzyme (ACE)-inhibitory peptides must remain active after intestinal transport. The purpose of this article is to elucidate the transport permeability and route of ACE-inhibitory peptide Arg-Leu-Ser-Phe-Asn-Pro (RLSFNP) across the intestinal
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