700157P

Avanti

Stigmasterol-d5

Name: Stigmasterol-d5
Brand: AVANTI
Price: 13839 MXP

Avanti Research^™ - A Croda Brand

Sinónimos:

Stigmasterol-d5

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1 MG

MXP 13,839.00

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Fórmula empírica (notación de Hill):

C₂₉H₄₃D₅O

Número CAS:

2260669-29-0

Peso molecular:

417.72

MDL number:

MFCD00037705

NACRES:

NA.25

UNSPSC Code:

41141804

Assay:

>99% (HPLC)

Form:

powder

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assay

>99% (HPLC)

form

powder

packaging

pkg of 1 × 1 mg (700157P-1mg)

manufacturer/tradename

Avanti Research^™ - A Croda Brand

shipped in

dry ice

storage temp.

−20°C

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Este artículo	700094P	700062P	700121P
Avanti 700157P Stigmasterol-d5	Avanti 700094P cholestanol-d5	Avanti 700062P stigmasterol	Avanti 700121P sitostanol
assay >99% (HPLC)	assay >99% (TLC)	assay >99% (TLC)	assay >99% (TLC)
form powder	form powder	form powder	form powder
packaging pkg of 1 × 1 mg (700157P-1mg)	packaging pkg of 1 × 1 mg (700094P-1mg)	packaging pkg of 1 × 5 mg (700062P-5mg)	packaging pkg of 1 × 5 mg (700121P-5mg)
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C
manufacturer/tradename Avanti Research^™ - A Croda Brand 700157P	manufacturer/tradename Avanti Research^™ - A Croda Brand	manufacturer/tradename Avanti Research^™ - A Croda Brand	manufacturer/tradename Avanti Research^™ - A Croda Brand 700121P
shipped in dry ice	shipped in dry ice	shipped in dry ice	shipped in dry ice

General description

Stigmasterol-d5 is the deuterated form of the plant sterol, stigmasterol. Stigmasterol is called the “good” sterol. The presence of C24 ethyl group and C22 double bond makes it differ from cholesterol.[1]

Biochem/physiol Actions

Stigmasterol is essential for embryonic development in plants and is also involved in the lipid rafts formation. The presence of an additional ethyl group in stigmasterol promotes membrane cohesion.[2]

Packaging

5 mL Amber Glass Screw Cap Vial (700157P-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Clase de almacenamiento

11 - Combustible Solids

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Complex Lipids and Sterols in the Leaves of Eucalyptus macrorhyncha (Myrtaceae) in the Context of Feeding by an Unnamed Gall-Inducing Species of Glycaspis (Synglycaspis)(Hemiptera: Psylloidea: Aphalaridae)

Sharma A, et al.

Annals of the Entomological Society of America, 109(6), 890-898 (2016)

Sterol/steroid metabolism and absorption in a generalist and specialist caterpillar: effects of dietary sterol/steroid structure, mixture and ratio.

Xiangfeng Jing et al.

Insect biochemistry and molecular biology, 43(7), 580-587 (2013-04-10)

Insects cannot synthesize sterols de novo, so they typically require a dietary source. Cholesterol is the dominant sterol in most insects, but because plants contain only small amounts of cholesterol, plant-feeding insects generate most of their cholesterol by metabolizing plant

The role of phytosterols in plant adaptation to temperature.

Erick J Dufourc

Plant signaling & behavior, 3(2), 133-134 (2008-02-01)

Membranes of composition approaching those found in "rafts" of plants, fungi and mammals were investigated by means of solidstate (2)H-NMR, using deuterated dipalmitoyl-phosphatidylcholine ((2)H-DPPC) as a reporter. The dynamics of such membranes was determined through measuring of membrane ordering or

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Stigmasterol-d5