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L5756

Sigma-Aldrich

Lithocholic acid 3-sulfate disodium salt hydrate

Synonym(s):

3α-Hydroxy-5β-cholan-24-oic acid 3-sulfate, Sulfolithocholic acid

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About This Item

Empirical Formula (Hill Notation):
C24H38Na2O6S · xH2O
CAS Number:
Molecular Weight:
500.60 (anhydrous basis)
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:

Assay

≥95% (TLC)

storage temp.

−20°C

SMILES string

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

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Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Serum-sulfated lithocholate as an indicator of cholestasis during parenteral nutrition in infants and children.
M K Farrell et al.
JPEN. Journal of parenteral and enteral nutrition, 6(1), 30-33 (1982-01-01)
H Takikawa et al.
Biochimica et biophysica acta, 1004(2), 147-150 (1989-08-08)
Biliary excretion and biotransformation of tracer doses of [14C]lithocholic acid and its sulfate and glucuronide intravenously injected into bile-drainaged rats were compared. Biliary excretion efficiency was in the order of unconjugate sulfate glucuronide and all conjugates were completely excreted into
Lithocholate sulphation in the baboon.
M J Dew et al.
Journal of medical primatology, 11(1), 59-64 (1982-01-01)
N P Dorvil et al.
The American journal of clinical nutrition, 37(2), 221-232 (1983-02-01)
The hypothesis that the amino acid used for the conjugation of sulfolithocholate (S-LCA) is a critical determinant of its cholestatic potential was tested in the guinea pig which conjugates 90% of its bile acids with glycine. Twelve groups of animals
A Takahashi et al.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), 2(2), 161-167 (1993-03-01)
Peroral sulpholithocholic acid (SLC) promoted colonic tumorigenesis in conventional rats. We then tested this compound in the mouse, a species with different bile acid metabolism from the rat. Female conventional ICR mice received 0.5 mg of N-methyl-N-nitrosourea (MNU) three times

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