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739723

Sigma-Aldrich

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

98 atom % D, 98% (CP)

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Synonym(s):
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
Empirical Formula (Hill Notation):
C26D4H39NO6
CAS Number:
Molecular Weight:
469.65
MDL number:
PubChem Substance ID:

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

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

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

InChI key

RFDAIACWWDREDC-WZQUIQSLSA-N

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

739723

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

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

739707

Glycodeoxycholic-2,2,4,4-d4 acid

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

614149

Cholic acid-2,2,4,4-d4

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

614130

Deoxycholic acid-2,2,4,4-d4

isotopic purity

98 atom % D

isotopic purity

≥98 atom % D

isotopic purity

98 atom % D

isotopic purity

≥98 atom % D

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

assay

98% (CP)

assay

≥98% (CP)

assay

98% (CP)

assay

≥98% (CP)

form

powder

form

powder

form

solid

form

solid

mp

165-168 °C (lit.)

mp

-

mp

200-201 °C (lit.)

mp

171-174 °C

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.

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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
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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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