Sodium taurodeoxycholate hydrate
CAS No. 207737-97-1
Sodium taurodeoxycholate hydrate( Taurodeoxycholic acid sodium salt monohydrate )
Catalog No. M23933 CAS No. 207737-97-1
Sodium taurodeoxycholate hydrate has been used in a study to assess the effect of submicellar concentrations of bile salts on the lipid bilayer membrane.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameSodium taurodeoxycholate hydrate
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NoteResearch use only, not for human use.
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Brief DescriptionSodium taurodeoxycholate hydrate has been used in a study to assess the effect of submicellar concentrations of bile salts on the lipid bilayer membrane.
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DescriptionSodium taurodeoxycholate hydrate has been used in a study to assess the effect of submicellar concentrations of bile salts on the lipid bilayer membrane.
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In VitroThe median plasma concentration of Taurodeoxycholate is 33.9 nM in healthy individuals.Taurodeoxycholate inhibits the binding of N-3H-methylscopolamine to the M3 muscarinic receptor of acetylcholine with an IC50 of 170 μM.Taurodeoxycholate (0.05-1.00 mM; 1-6 days) stimulates intestinal epithelial cell proliferation.Taurodeoxycholate (0.05-1.00 mM; 24 h) induces a significant increase in S-phase concentration and a significant decrease in G1-phase concentration of the cell cycle, increases c-myc protein and mRNA expression in IEC-6 cells. Cell Proliferation Assay Cell Line:IEC-6 and caco-2 cells Concentration:0, 0.05, 0.50, and 1.00 mM Incubation Time:1, 2, 4 and 6 days Result:Significantly stimulated intestinal epithelial cell proliferation in a dose-dependent manner.Cell Cycle Analysis Cell Line:IEC-6 cells Concentration:0, 0.05, 0.50, and 1.00 mM Incubation Time:24 h Result:Significantly increased cells in S phase and decreased cells in G1-phase.Western Blot Analysis Cell Line:IEC-6 cells Concentration:0.5 mM Incubation Time:1 and 6 days Result:Significantly increased c-myc protein expression.
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In VivoTaurodeoxycholate (0.5 mg/kg; i.v.; once) confers protection to C57BL/6N mice with sepsis, but does not protect TGR5 KO mice under sepsis. Animal Model:C57BL/6N mice, Lipopolysaccharides (HY-D1056) injection model of sepsisDosage:0.5 mg/kg Administration:Intravenous injection, 30 min or 24 h after LPS injection Result:Improved the survival rate of mice with sepsis. Decreased liver and kidney damage in septic mice. Ameliorated systemic inflammation and normalized blood pressure in septic mice.
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SynonymsTaurodeoxycholic acid sodium salt monohydrate
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number207737-97-1
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Formula Weight539.7
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Molecular FormulaC26H44NO6S.Na.H2O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 100 mg/mL (191.68 mM)
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SMILESC[C@H](CCC(NCCS(=O)([O-])=O)=O)[C@H]1CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C.[H]O[H].[Na+]
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Barbara, Orioni, Mauro, et al. Polymorphic Behavior in Protein?Surfactant Mixtures:? The Water?Bovine Serum Albumin?Sodium Taurodeoxycholate System[J]. Journal of Physical Chemistry B, 2006.
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