DHEA-S

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Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
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Company Name: Hangzhou J&H Chemical Co., Ltd.  
Tel: 0571-87396432
Email: sales@jhechem.com
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Company Name: Shandong JunRui Pharmaceutical Co., Ltd.  
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Company Name: Chengdu Push Bio-Technology Co., Ltd.  
Tel: 028-85370565-229 18080489829
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DHEA-S Basic information
Product Name:DHEA-S
Synonyms:Formylisoglutamic acid;DEHYDROEPIANDROSTERONESULPHATE;[(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] hydrogen sulfate;sulfuric acid [(3S,8R,9S,10R,13S,14S)-17-keto-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] ester;(3β)-3-(Sulfooxy)androst-5-en-17-one;Prasterone Sulfate Sports Nutrition Supplements Prasterone Sodium Sulfate 651-48-9;Androst-5-en-17-one, 3-(sulfooxy)-, (3β)-;Abiraterone Impurity 73
CAS:651-48-9
MF:C19H28O5S
MW:368.49
EINECS:
Product Categories:
Mol File:651-48-9.mol
DHEA-S Structure
DHEA-S Chemical Properties
Boiling point 468.81°C (rough estimate)
density 1.1763 (rough estimate)
refractive index 1.5300 (estimate)
Melting point 190-192 °C
pKa-3.51±0.18(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
DHEA-S Usage And Synthesis
UsesDehydroepiandrosterone sulfate, a neuroactive neurosteroid, plays a major role in brain development and aging by influencing the migration of neurons, arborization of dendrites, and formation of new synapses[1][2][3].
DefinitionChEBI: A steroid sulfate that is the 3-sulfooxy derivative of dehydroepiandrosterone.
in vivo

DHEAS chronic administration produces a dose-dependent effect on performance[3].

Animal Model:Sixty-four male Sprague-Dawley rats, approximately 90 days of age (300-400 g)[3].
Dosage:5, 10, or 20 mg/kg.
Administration:Subcutaneous injection starting 7 days post-surgery and 1 h prior to all behavioral testing.
Result:Significantly effective in improving latency to reach the platform as compared to injured rats receiving vehicle.
IC 50Human Endogenous Metabolite
References[1] E E Baulieu, et al. Dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) as neuroactive neurosteroids. Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4089-91. DOI:10.1073/pnas.95.8.4089
[2] C R Parker Jr, et al. Dehydroepiandrosterone and dehydroepiandrosterone sulfate production in the human adrenal during development and aging. Steroids. 1999 Sep;64(9):640-7. DOI:10.1016/s0039-128x(99)00046-x
[3] Stuart W Hoffman, et al. The delayed administration of dehydroepiandrosterone sulfate improves recovery of function after traumatic brain injury in rats. J Neurotrauma. 2003 Sep;20(9):859-70. DOI:10.1089/089771503322385791
DHEA-S Preparation Products And Raw materials
Tag:DHEA-S(651-48-9) Related Product Information
Dehydroepiandrosterone Phosphoric acid Dehydroepiandrosterone ABiraterone impurity 15 Abiraterone Acetate Dimer Impurity (3β)-Androsta-5,16-diene-3,17-diol 3-Acetate 17-(Trifluoromethanesulfonate) DIETHYL(3-PYRIDYL)BORANE Abiraterone Sulfate Sodium Salt Abiraterone Impurity 4 Abiraterone Ethyl Ether Dehydroepiandrosterone acetate Abiraterone Abiraterone N-Oxide Abiraterone Related CoMpound 2 (Prasterone Triflate) Abiraterone Sulfate Abiraterone Related Compound 8 Abiraterone DiMer IMpurity (Prasteronyl Abiraterone) 17-Iodoandrosta-5,16-dien-3beta-ol