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28609

Sigma-Aldrich

Cholesterol β-D-glucoside

≥97% (TLC)

Sinônimo(s):

Cholesteryl β-D-glucopyranoside

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About This Item

Fórmula empírica (Notação de Hill):
C33H56O6
Número CAS:
7073-61-2
Peso molecular:
548.79
Número MDL:
MFCD00273002
Código UNSPSC:
12352211
eCl@ss:
39023139
ID de substância PubChem:
329753275
NACRES:
NA.25

Nível de qualidade

100

Ensaio

≥97% (TLC)

forma

solid

atividade óptica

[α]/D -49.0±3.0°, c = 0.5 in pyridine

cadeia de caracteres SMILES

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O

InChI

1S/C33H56O6/c1-19(2)7-6-8-20(3)24-11-12-25-23-10-9-21-17-22(13-15-32(21,4)26(23)14-16-33(24,25)5)38-31-30(37)29(36)28(35)27(18-34)39-31/h9,19-20,22-31,34-37H,6-8,10-18H2,1-5H3/t20-,22+,23+,24-,25+,26+,27-,28-,29+,30-,31-,32+,33-/m1/s1

chave InChI

FSMCJUNYLQOAIM-UQBZCTSOSA-N

Ações bioquímicas/fisiológicas

A lipid mediator in heat stress responses in animals, shows anti-ulcer effect.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

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B Steinbrueckner et al.
FEMS microbiology letters, 168(2), 209-212 (1998-12-03)
Helicobacter pullorum and Campylobacter lari are rarely isolated from humans with acute enteritis. Hitherto the two species could only be identified by genotypic techniques. Gas liquid chromatography of whole cell fatty acid extracts is described as the first phenotypic method
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The Journal of membrane biology, 237(2-3), 71-77 (2010-10-13)
The cluster of neurodegenerative disorders in the western Pacific termed amyotrophic lateral sclerosis-parkinsonism dementia complex (ALS-PDC) has been repeatedly linked to the use of seeds of various species of cycad. Identification and chemical synthesis of the most toxic compounds in
Michio Shimamura
Archivum immunologiae et therapiae experimentalis, 60(5), 351-359 (2012-09-01)
Steryl glycosides, sterols glycosylated at the 3β-hydroxy group, have been widely found in plants, algae, and fungi, but are rare in bacteria and animals. Glycosylation of sterols is known to modify properties of the cell membrane and confer resistance against
Hung-Jung Wang et al.
Molecular microbiology, 83(1), 67-84 (2011-11-08)
Helicobacter pylori infection is an aetiological cause of gastric disorders worldwide. H. pylori has been shown to assimilate and convert host cholesterol into cholesteryl glucosides (CGs) by cholesterol-α-glucosyltransferase encoded by capJ. Here, we show that CapJ-deficient (ΔcapJ) H. pylori resulted
W Abraham et al.
Journal of lipid research, 28(4), 446-449 (1987-04-01)
The structures of two classes of glycolipids, acylglucosylsterol and glucosylsterol, from snake epidermis have been determined by chemical, spectroscopic, and gas-liquid chromatographic methods. The acylglucosylsterol consists of a glucose molecule attached to cholesterol and an ester-linked fatty acid on carbon
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