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Merck
CN

739723

Glycocholic-2,2,4,4-d4 acid

98 atom % D, 98% (CP)

别名:

3α,7α,12α-Trihydroxy-5β-cholan-24-oic-2,2,4,4-d4 acid N-(carboxymethyl)amide, N-(3α,7α,12α-Trihydroxy-24-oxocholan-24-yl)-glycine-2,2,4,4-d4, Cholylglycine-2,2,4,4-d4

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关于此项目

经验公式（希尔记法）:
C26D4H39NO6
化学文摘社编号:
1201918-15-1
分子量:
469.65
UNSPSC Code:
12352111
PubChem Substance ID:
329765376
MDL number:
MFCD01861560

主要文件

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产品名称

Glycocholic-2,2,4,4-d4 acid, 98 atom % D, 98% (CP)

InChI

1S/C26H43NO6/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)/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-/m1/s1/i8D2,10D2

SMILES string

[H][C@@]12[C@]([C@](CC([2H])([2H])[C@@H](O)C3([2H])[2H])(C)[C@]3([H])C[C@H]2O)([H])C[C@H](O)[C@@]4(C)[C@@]1([H])CC[C@]4([H])[C@]([H])(C)CCC(NCC(O)=O)=O

InChI key

RFDAIACWWDREDC-WZQUIQSLSA-N

isotopic purity

98 atom % D

assay

98% (CP)

form

powder

technique(s)

mass spectrometry (MS): suitable

mp

165-168 °C (lit.)

mass shift

M+4

相关类别

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MBBF1500
MBBD1474
MBBC6210
TA2250V
TA0262V

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Runbin Sun et al.
Drug metabolism and disposition: the biological fate of chemicals, 49(3), 276-286 (2020-12-31)
Our previous study suggests that berberine (BBR) lowers lipids by modulating bile acids and activating intestinal farnesoid X receptor (FXR). However, to what extent this pathway contributes to the hypoglycemic effect of BBR has not been determined. In this study
Diana M Shih et al.
Journal of lipid research, 56(1), 22-37 (2014-11-08)
We performed silencing and overexpression studies of flavin containing monooxygenase (FMO) 3 in hyperlipidemic mouse models to examine its effects on trimethylamine N-oxide (TMAO) levels and atherosclerosis. Knockdown of hepatic FMO3 in LDL receptor knockout mice using an antisense oligonucleotide

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