CAS 17605-67-3|Fucosterol

Introduction:Basic information about CAS 17605-67-3|Fucosterol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameFucosterol
CAS Number17605-67-3Molecular Weight412.69100
Density0.98 g/cm3Boiling Point504.2ºC at 760 mmHg
Molecular FormulaC29H48OMelting Point118-120ºC
MSDSChineseUSAFlash Point220.3ºC

Names

Namefucosterol
SynonymMore Synonyms

Fucosterol BiologicalActivity

DescriptionFucosterol is isolated from E. stolonifera with anti-adipogenic, anti-diabetic and anti-cancer activities. Fucosterol regulates adipogenesis via modulation of PPARαand C/EBPαexpression.
Related CatalogResearch Areas >>CancerSignaling Pathways >>Epigenetics >>PARPSignaling Pathways >>Cell Cycle/DNA Damage >>PARP
Target

PPARα; C/EBPα[1]

In VitroFucosterol (0-50 μM; 7 days) suppresses the expression of PPARα and C/EBPα when compared to fully differentiated control adipocytes[1].Fucosterol shows cytotoxicity against T47D and HT29 cell lines with IC50 values of 27.94 and 70.41 μg/ml, respectively[3]. Fucosterol decreases cell HEK293, MCF-7, and SiHa cells proliferation with IC50 values of 185.4, 43.3, and 34.0 µg/ml, respectively[4]. Cell Viability Assay[1] Cell Line: 3T3-L1 adipocytes Concentration: 0 μM; 25 μM; 50 μM Incubation Time: 7 days Result: Inhibited PPARα and C/EBPα expression.
In VivoFucosterol (orally adminstratin; 30mg/kg) causes a significant decrease in serum glucose concentrations, and exhibits an inhibition of sorbitol accumulations in the lenses[2].
References

[1]. Jung HA, et al. Anti-adipogenic activity of the edible brown alga Ecklonia stolonifera and its constituent fucosterol in 3T3-L1 adipocytes. Arch Pharm Res. 2014 Jun;37(6):713-20.

[2]. Lee YS, et al. Anti-diabetic activities of fucosterol from Pelvetia siliquosa. Arch Pharm Res. 2004 Nov;27(11):1120-2.

[3]. Khanavi M, et al. Cytotoxicity of fucosterol containing fraction of marine algae against breast and colon carcinoma cell line. Pharmacogn Mag. 2012 Jan;8(29):60-4.

[4]. Caamal-Fuentes E, et al. Cytotoxic and antiproliferative constituents from Dictyota ciliolata, Padina sanctae-crucis and Turbinaria tricostata. Pharm Biol. 2014 Oct;52(10):1244-8.

Chemical & Physical Properties

Density0.98 g/cm3
Boiling Point504.2ºC at 760 mmHg
Melting Point118-120ºC
Molecular FormulaC29H48O
Molecular Weight412.69100
Flash Point220.3ºC
Exact Mass412.37100
PSA20.23000
LogP7.94490
Vapour Pressure2.8E-12mmHg at 25°C
Index of Refraction1.53
InChIKeyOSELKOCHBMDKEJ-HRKULPSGSA-N
SMILESCC=C(CCC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C
Storage condition2-8°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADRNONH for all modes of transport
WGK Germany3

Articles27

More Articles
Kinetics and molecular docking studies of an anti-diabetic complication inhibitor fucosterol from edible brown algae Eisenia bicyclis and Ecklonia stolonifera.

Chem. Biol. Interact. 206(1) , 55-62, (2013)

In the present study, we investigated the anti-diabetic potential of fucosterol by evaluating the ability of this compound to inhibit rat lens aldose reductase (RLAR), human recombinant aldose reducta...

The effect of traditional stir-frying process on hydrophilic and lipophilic antioxidant capacities of pine nut kernels.

Int. J. Food Sci. Nutr. 66 , 873-80, (2015)

The effect of traditional stir-frying process at different heating temperatures (50-150 °C) and time periods (5-20 min) on hydrophilic part (total and individual phenolics), lipophilic part (tocophero...

Inhibition of Mycobacterium tuberculosis growth by saringosterol from Lessonia nigrescens.

J. Nat. Prod. 64(11) , 1463-4, (2001)

Assay-guided fractionation of an antitubercular extract obtained from Lessonia nigrescens yielded the phytosterol saringosterol as its active component. No appreciable toxicity against Vero cells was ...

Synonyms

trans-24-Ethylidenecholesterol
D5-avenasterol
MFCD00037543
FUCOSTEROL
Fucosterin
trans-Stigmasta-5,24(28)-dien-3b-ol
24-ETHYLIDENCHOLEST-5-ENE-3B-OL
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