Taurocholic acid-d5

Catalog No.: A74241
Stable Isotope
Taurocholic acid-d5 is a deuterium-labeled derivative of taurocholic acid, a bile acid known for its biological significance. This compound exhibits notable bioactivity, including the ability to inhibit biliary damage induced by hepatic artery ligation through upregulation of VEGF-A expression. Additionally, taurocholic acid is involved in immunoregulatory processes. Its stable isotope labeling makes Taurocholic acid-d5 an important tool for research applications in metabolic studies and the investigation of bile acid functions in various biological systems.
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5mg
10mg
50mg
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Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
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Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionTaurocholic acid-d5 is a deuterium-labeled derivative of taurocholic acid, a bile acid known for its biological significance. This compound exhibits notable bioactivity, including the ability to inhibit biliary damage induced by hepatic artery ligation through upregulation of VEGF-A expression. Additionally, taurocholic acid is involved in immunoregulatory processes. Its stable isotope labeling makes Taurocholic acid-d5 an important tool for research applications in metabolic studies and the investigation of bile acid functions in various biological systems.
Product Information
Catalog NumA74241
FormulaC26H40D5NO7S
Molecular Weight520.73
CAS Number2044276-13-1
SMILESO=C(CC[C@H]([C@@]1([C@]2([C@H](C[C@]3([C@@]([H])([C@@H](C[C@@]4(C([2H])([C@@]([2H])(C([2H])(C[C@@]43C)[2H])O)[2H])[H])O)[C@@]2(CC1)[H])[H])O)C)[H])C)NCCS(=O)(O)=O
SynonymsN-Choloyltaurine-d5
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