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F5379

Sigma-Aldrich

Fucosterol

≥93%, powder, antioxidant

Synonym(e):

3β-Hydroxy-5,24(28)-stigmastadiene, 5,24(28)-Stigmastadien-3β-ol

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About This Item

Empirische Formel (Hill-System):
C29H48O
CAS-Nummer:
17605-67-3
Molekulargewicht:
412.69
MDL-Nummer:
MFCD00037543
UNSPSC-Code:
41116107
PubChem Substanz-ID:
24894886
NACRES:
NA.77

product name

Fucosterol, ≥93%

Qualitätsniveau

100

Assay

≥93%

Lagertemp.

2-8°C

SMILES String

C\C=C(/CC[C@H](C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C

InChI

1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,10,19-20,23-27,30H,8-9,11-18H2,1-6H3/b21-7+

InChIKey

OSELKOCHBMDKEJ-QPSGOUHRSA-N

Allgemeine Beschreibung

Fucosterol is a phytosterol abundantly present in algae, Ecklonia arborea and Silvetia compressa.

Anwendung

Fucosterol has been used:
  • as an environmental contaminant to study its effect on morphological development in growing zebrafish embryos and larvae
  • to study its anxiolytic effects in mice
  • as an external standard to analyze sterols in seaweed samples

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

D6513

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Uvaol ≥95%

Sigma-Aldrich

U6628

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Fucoxanthin analytical standard

Supelco

16337

Fucoxanthin

Ergosterol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1512

Ergosterol

β-Sitosterin-β-D-glucosid analytical standard

Supelco

89851

β-Sitosterin-β-D-glucosid

stigmasterol Avanti Polar Lipids

Avanti

700062P

stigmasterol

β-Sitosterol ≥70%

Sigma-Aldrich

85451

β-Sitosterol

A Kamal-Eldin et al.
Lipids, 33(11), 1073-1077 (1998-12-31)
This work shows that fucosterol, delta5-avenasterol, and similar ethylidene-side chain sterols can undergo acid-catalyzed isomerization to give a mixture of five isomers. Four isomers formed from fucosterol were analyzed, using gas chromatography-mass spectrometry, and were characterized as delta5-avenasterol, two delta5,23-stigmastadienols
Alice A Ramos et al.
Journal of toxicology and environmental health. Part A, 82(9), 537-549 (2019-07-02)
Colorectal cancer (CRC) is one of the most frequently occurring carcinomas which require effective therapies. Fucosterol is a sterol present in marine brown seaweeds with several biological activities. However, the influence of fucosterol in CRC remains to be determined. Thus
I P Shanura Fernando et al.
Environmental research, 172, 150-158 (2019-02-21)
Particulate matter (PM) air pollution has gradually become a widespread problem in East Asia. PM may cause unfamiliar inflammatory responses, oxidative stress, and pulmonary tissue damage, and a comprehensive understanding of the underlying mechanisms is required in order to develop
H Hagiwara et al.
Biochemical and biophysical research communications, 139(1), 348-352 (1986-08-29)
The modulation of angiotensin converting enzyme (ACE) levels was studied using fucosterol, one of phytosterols, in cultured bovine carotid endothelial cells. Addition of fucosterol to the culture medium resulted in the decrease of ACE activity of endothelial cells; however, fucosterol
Cassandra D Kinch et al.
Aquatic toxicology (Amsterdam, Netherlands), 175, 286-298 (2016-04-24)
Exposure to environmental contaminants has been linked to developmental and reproductive abnormalities leading to infertility, spontaneous abortion, reduced number of offspring, and metabolic disorders. In addition, there is evidence linking environmental contaminants and endocrine disruption to abnormal developmental rate, defects
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