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T0512

Sigma-Aldrich

Taurolithocholic acid 3-sulfate disodium salt

Synonym(e):

3α-Hydroxy-5β-cholan-24-oic acid N-(2-sulfoethyl)amide 3-sulfate

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About This Item

Lineare Formel:
C26H43NO8S2Na2
CAS-Nummer:
64936-83-0
Molekulargewicht:
607.73
MDL-Nummer:
MFCD00055891
UNSPSC-Code:
12161900
PubChem Substanz-ID:
24899892
NACRES:
NA.25

Beschreibung

anionic

Qualitätsniveau

200

Assay

≥90.0% (TLC)

Mol-Gew.

607.73 g/mol

Verunreinigungen

≤3% (TLC)

SMILES String

[Na].[H][C@]12CC[C@@]3([H])[C@]4([H])CC[C@]([H])([C@H](C)CCC(=O)NCCS(O)(=O)=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](C2)OS(O)(=O)=O

InChI

1S/C26H45NO8S2.Na.H/c1-17(4-9-24(28)27-14-15-36(29,30)31)21-7-8-22-20-6-5-18-16-19(35-37(32,33)34)10-12-25(18,2)23(20)11-13-26(21,22)3;;/h17-23H,4-16H2,1-3H3,(H,27,28)(H,29,30,31)(H,32,33,34);;/t17-,18-,19-,20+,21-,22+,23+,25+,26-;;/m1../s1

InChIKey

POWDNUISUWSLLN-RLHFEMFKSA-N

Verwandte Kategorien

Allgemeine Beschreibung

Taurolithocholic acid 3-sulfate disodium salt is a natural detergent bile salt with potential use as a topical microbicidal agent.

Anwendung

Taurolithocholic acid 3-sulfate disodium salt has been used in a study to assess the electrophysiological effects of bile acids on pancreatic acinar cells. It has also been used in a study to investigate the mechanisms underlying the inhibition of bile acid-induced apoptosis by cyclic AMP in rat hepatocytes.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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(Tyr[SO3H]27)Cholecystokinin-Fragment 26-33 Amid ≥97% (HPLC), powder

Sigma-Aldrich

C2175

(Tyr[SO3H]27)Cholecystokinin-Fragment 26-33 Amid

Hyodesoxycholsäure ≥98%

Sigma-Aldrich

H3878

Hyodesoxycholsäure

Glykoursodeoxycholsäure ≥96.0% (TLC)

Sigma-Aldrich

06863

Glykoursodeoxycholsäure

Glycochenodeoxycholsäure Natriumsalz

Sigma-Aldrich

G0759

Glycochenodeoxycholsäure Natriumsalz

Taurodesoxycholsäure, Natriumsalz, CAS-Nr. 1180-95-6, Calbiochem Detergent useful for the solubilization of lipids and membrane-bound proteins. Aggregation number: 6.

Millipore

580221

Taurodesoxycholsäure, Natriumsalz, CAS-Nr. 1180-95-6, Calbiochem

Ursodesoxycholsäure European Pharmacopoeia (EP) Reference Standard

U0800000

Ursodesoxycholsäure

Natriumtaurocholat BRP, European Pharmacopoeia (EP) Reference Standard

S0900000

Natriumtaurocholat

Inhibition of taurolithocholate 3-sulfate-induced apoptosis by cyclic AMP in rat hepatocytes involves protein kinase A-dependent and -independent mechanisms
Graf, D., et al.
Archives of Biochemistry and Biophysics, 415, 9-9 (2003)
Svetlana G Voronina et al.
The Journal of biological chemistry, 280(3), 1764-1770 (2004-11-13)
Biliary disease is a major cause of acute pancreatitis. In this study we investigated the electrophysiological effects of bile acids on pancreatic acinar cells. In perforated patch clamp experiments we found that taurolithocholic acid 3-sulfate depolarized pancreatic acinar cells. At
B C Herold et al.
Antimicrobial agents and chemotherapy, 43(4), 745-751 (1999-04-02)
The development of new, safe, topical microbicides for intravaginal use for the prevention of sexually transmitted diseases is imperative. Previous studies have suggested that bile salts may inhibit human immunodeficiency virus infection; however, their activities against other sexually transmitted pathogens
Yongjian Wen et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 79, 153328-153328 (2020-10-03)
Chaiqin chengqi decoction (CQCQD) is a Chinese herbal formula derived from dachengqi decoction. CQCQD has been used for the management of acute pancreatitis (AP) in the West China Hospital for more than 30 years. Although CQCQD has a well-established clinical
Hanno Ehlken et al.
PloS one, 6(10), e25942-e25942 (2011-10-25)
Mice lacking the Abc4 protein encoded by the multidrug resistance-2 gene (Mdr2(-/-)) develop chronic periductular inflammation and cholestatic liver disease resulting in the development of hepatocellular carcinoma (HCC). Inhibition of NF-κB by expression of an IκBα super-repressor (IκBαSR) transgene in
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