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700086P

Avanti

DHEA sulfate

Avanti Research™ - A Croda Brand

Szinonimák:

DHEA sulfate; DHEA; DHEA-S; 3β-hydroxy-5-androsten-17-one 3-sulfate (sodium salt); 5-androsten-3β-ol-17-one sulfate (sodium salt Prasterone sulfate (sodium salt)

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About This Item

Tapasztalati képlet (Hill-képlet):
C19H27NaO5S
CAS-szám:
651-48-9
Molekulatömeg:
390.47
UNSPSC kód:
12352211
NACRES:
NA.25

leírás

Dehydroepiandrosterone sulfate (sodium salt)

Teszt

>99% (TLC)

form

powder

kiszerelés

pkg of 1 × 10 mg (700086P-10mg)
pkg of 1 × 25 mg (700086P-25mg)
pkg of 1 × 50 mg (700086P-50mg)

gyártó/kereskedő neve

Avanti Research™ - A Croda Brand

kiszállítva

dry ice

tárolási hőmérséklet

−20°C

InChI

1S/C19H28O5S/c1-18-9-7-13(24-25(21,22)23)11-12(18)3-4-14-15-5-6-17(20)19(15,2)10-8-16(14)18/h3,13-16H,4-11H2,1-2H3,(H,21,22,23)/t13-,14-,15-,16-,18-,19-/m0/s1

Nemzetközi kémiai azonosító kulcs

CZWCKYRVOZZJNM-USOAJAOKSA-N

Általános leírás

DHEA sulfate is a metabolite of dehydroepiandrosterone (DHEA) produced by the addition of a sulfate group, catalyzed by the sulfotransferase enzymes SULT1A1 and SULT1E1, which also produce estrone sulfate from estrone. DHEA sulfate can also be back-converted to DHEA through the action of steroid sulfatase.
Dehydroepiandrosterone (DHEA) sulfate (DHEAS) is an adrenal steroid and is present in abundance in humans. It is the sulfate ester of DHAE and is synthesized by the adrenal glands and the gonads. DHEAS is produced in the zona reticularis.

Alkalmazás

DHEA sulfate has been used:
  • as a sulfated steroid in chemotaxis assay of bone-marrow (BM) neutrophil and also to test its inhibitory effect on the Rac-specific guanine nucleotide exchange factor (Rac GEF)
  • as an internal standard in mass spectrometry
  • as a synthetic lipid standard for spiking low-density lipoprotein (LDL) samples for liquid chromatography-mass spectrometry analysis (LC-MS)

Biokémiai/fiziológiai hatások

Dehydroepiandrosterone (DHEA) sulfate (DHEAS) regulates the synthesis of catecholamines. It modulates neurotransmitter receptors including the γ-aminobutyric acid type A (GABAA) and the N-methyl-D -aspartate (NMDA) receptors. Low levels of DHAES in brain is observed in Alzheimer′s disease (AD) patients.

Kiszerelés

5 mL Amber Glass Screw Cap Vial (700086P-10mg)
5 mL Amber Glass Screw Cap Vial (700086P-25mg)
5 mL Amber Glass Screw Cap Vial (700086P-50mg)

Jogi információk

Avanti Research is a trademark of Avanti Polar Lipids, LLC

gyakran vásárolják ezzel a termékkel együtt

Product No.
Leírás
Árazás

Tárolási osztály kódja

11 - Combustible Solids

Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

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Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Ana Reis et al.
Journal of lipid research, 54(7), 1812-1824 (2013-05-15)
Lipidome profile of fluids and tissues is a growing field as the role of lipids as signaling molecules is increasingly understood, relying on an effective and representative extraction of the lipids present. A number of solvent systems suitable for lipid
Joseph S Dillon
Current drug targets. Inflammation and allergy, 4(3), 377-385 (2005-08-17)
Dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) are metabolic intermediates in the production of potent androgens, estrogens and other less well-characterized steroids. DHEA(S) and closely related steroid hormones have a variety of immunological effects both in vitro and in vivo in
Marco Racchi et al.
CNS drug reviews, 9(1), 21-40 (2003-02-22)
The physiological role of dehydroepiandrosterone (DHEA) and its sulphated ester DHEA(S) has been studied for nearly 2 decades and still eludes final clarification. The major interest in DHEA derives from its unique pattern of activity. Its levels exhibit a dramatic
Julia Junker et al.
Molecules (Basel, Switzerland), 24(13) (2019-06-30)
Sulfoconjugates of sterols play important roles as neurosteroids, neurotransmitters, and ion channel ligands in health and disease. In most cases, sterol conjugate analysis is performed with liquid chromatography-mass spectrometry. This is a valuable tool for routine analytics with the advantage
P Ebeling et al.
Lancet (London, England), 343(8911), 1479-1481 (1994-06-11)
Dehydroepiandrosterone (DHEA), with its sulphate conjugate (DHEAS), is the most abundant steroid hormone in the circulation but its physiological importance is unclear. We propose that DHEA has either oestrogen-like or androgen-like effects depending on the hormonal milieu. In premenopausal women
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