Shenzhen Wenzhi Bio-Technology Co.,Ltd
Shenzhen Wenzhi Bio-Technology Co.,Ltd
Shenzhen Wenzhi Bio-Technology Co.,Ltd Professional Supplier of Raw steroid powder & injectable & o
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Home>Products>Steroid Hormones Powder>Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements

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  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements
  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements
  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements
  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements
  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements
  • Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements

Healthy Steroid Hormones Powder 98% Assy Androsterone Bodybuilding Supplements

  • HW Steroid Hormones Powder
  • Steroid Hormones Powder

  • China
  • GMP,SGS,UKAS,ISO
  • Negotiable
  • Negotiable
  • foil bag or as your requirement
  • Within 1-2 working days upon receipt payment
  • T/T, Western union, MoneyGram
  • 1000kgs/month
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Shenzhen Wenzhi Bio-Technology Co.,Ltd

Shenzhen Wenzhi Bio-Technology Co.,LtdChina

  • Shenzhen Wenzhi Bio-Technology Co.,Ltd2020-07-10 09:46:19
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Product Details

CAS: 53-41-8 M.F.: C19H30O2 M.W.: 290.44
Assay: 98% Melting Point: 181-184℃ Appearance: White or white crystalline powder
Keywords: China Steroid Hormones Powder, China Steroid Hormones Powder manufacturers, Steroid Hormones Powder catalog, Steroid Hormones Powder

Product Description

Healthy Steroid Hormones Powder 98% Assy Androsterone For Bodybuilding Supplements


Basic Information

Item Specification
CAS 53-41-8
Formula C19H30O2
Molecular Weight 290.44
EINECS N/A
Assay 98%

Description

Androsterone, or 3α-hydroxy-5α-androstan-17-one, is an endogenous steroid hormone, neurosteroid, and putative pheromone. It is a weak androgen with a potency that is approximately 1/7th that of testosterone. In addition, it can be converted to dihydrotestosterone (DHT) from 3α-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase, bypassing conventional intermediates such as androstenedione and testosterone, and as such, can be considered to be a metabolic intermediate in its own right. Androsterone is also known to be an inhibitory androstane neurosteroid, acting as a positive allosteric modulator of the GABAA receptor, and possesses anticonvulsant effects.The unnatural enantiomer of androsterone is more potent as a positive allosteric modulator of GABAA receptors and as an anticonvulsant than the natural form. Androsterones 3β-isomer is epiandrosterone, and its 5β-epimer is etiocholanolone.


History


It was first isolated in 1931, by Adolf Friedrich Johann Butenandt and Kurt Tscherning. They distilled over 17,000 liters (3,700 imp gal; 4,500 U.S. gal) of male urine, from which they got 50 milligrams (0.77 gr) of crystalline androsterone, which was sufficient to find that the chemical formula was very similar to estrone.


Sources


Androsterone has been shown to naturally occur in pine pollen and is well known in many animal species.


Biological role


Androsterone is generally considered to be an inactive metabolite of testosterone, which when conjugated by glucuronidation and sulfation allows testosterone to be removed from the body, but it is a weak neurosteroid that can cross into the brain and could have effects on brain function.


Pheromone


Androsterone is found in the human axilla and skin as well as in the urine. It may also be secreted by human sebaceous glands. It is described as having a musky odor similar to that of androstenol. Androsterone has been found to affect human behavior when smelled.


Biosynthesis


Androsterone and its 5β-isomer, etiocholanolone, are produced in the body as metabolites of testosterone. Testosterone is converted to 5α-dihydrotestosterone and 5β-dihydrotestosterone by 5α-reductase and 5β-reductase, respectively. The enzyme 3α-hydroxysteroid dehydrogenase converts the reduced forms to 5α-androstanediol and 5β-androstanediol, which are subsequently converted by 17β-hydroxysteroid dehydrogenase to androsterone and etiocholanolone, respectively. Androsterone and etiocholanolone can also be formed from androstenedione via the action of 5α-reductase and 5β-reductase forming 5α-androstanedione and 5β-androstanedione which are then converted to androsterone and etiocholanolone by 3α-hydroxysteroid dehydrogenase and 3β-hydroxysteroid dehydrogenase, respectively.


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