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11α-Hydroxy canrenone Powder (192569-17-8)

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SKU: 192569-17-8. Category:

AASraw is with synthesis and production ability from gram to mass order of 11α-Hydroxy canrenone Powder (192569-17-8), under CGMP regulation and trackable quality control system.

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Product Description

 

11α-Hydroxy canrenone Powder (192569-17-8) video

 

 


 

11α-Hydroxy canrenone Powder (192569-17-8) Specification:

Chemical Structure: Product Name:11α-Hydroxy canrenone
Raw 11α-Hydroxy canrenone Powder (192569-17-8) hplc≥98% | AASraw Cas No.: 192569-17-8
Molecular Formula: C22H28O4
Molecular Weight:356.46
Synonyms: 11-alpha-Hydroxycarvenone
Storage: Dry, dark· and at 0 – 4 C for short term (days to weeks) or -20 C for long term (months to years).
Documents(COA & HPLC etc.): Available

11α-Hydroxy canrenone Powder (192569-17-8) Description:

11α-Hydroxy canrenone  works same as Canrenone is an aldosterone antagonist with potassium-sparing diuretic activity. Canrenone specifically antagonizes aldosterone at the mineralocorticoid receptor in the kidneys, thereby increasing sodium excretion and inhibiting potassium excretion.Canrenone is reportedly more potent as an antimineralocorticoid relative to spironolactone, but is considerably less potent and effective as an antiandrogen.11α-Hydroxyprogesterone is an endogenous steroid and metabolite of progesterone.It is a weak antiandrogen, and is devoid of androgenic, estrogenic, and progestogenic activity

 

Reference:

  • Jürg Müller (6 December 2012). Regulation of Aldosterone Biosynthesis: Physiological and Clinical Aspects. Springer Science & Business Media. pp. 164–. ISBN 978-3-642-83120-1.
  • Ford, Donald H. (1954). “EFFECT OF 11α-HYDROXYPROGESTERONE ON REPRODUCTIVE SYSTEM OF NORMAL AND PREGNANT ADULT WISTAR RATS*”. The Journal of Clinical Endocrinology & Metabolism. 14 (10): 1268–1270. doi:10.1210/jcem-14-10-1268. ISSN 0021-972X.
  • Souness GW, Latif SA, Laurenzo JL, Morris DJ (1995). “11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2), confer marked mineralocorticoid activity on corticosterone in the ADX rat”. Endocrinology. 136 (4): 1809–12.

 

 

PRECAUTION AND DISCLAIMER:

This Material is Sold For Research Use Only. Terms of Sale Apply. Not for Human Consumption, nor Medical, Veterinary, or Household Uses.

 


COA

HNMR

10161-35-8 Trenbolone enanthate HNMR

Recipes

Trenbolone enanthate Raw Powder Recipes:

To inquiry our Customer Representitive(CSR) for details, for your reference.

 

References & product citations

All The Things About Trenbolone Enanthate Powder

How to Use Trenbololone Recipe to Mix Trenbolone Enanthate Powder 2019

The Ultimate Guide: How to Use Trenbololone Recipe to Mix Trenbolone Enanthate Powder into oil[2019]

 

References:

William Llewellyn, Molecular Nutrition, Anabolics, Pages 491 – 499, 618, 724, 2011.

Kickman, A.T., Pharmacology of Anabolic Steroids, British Journal of Pharmacology, PMC 2439524, Online, 2018.

Wilson, V.S., Lambright, C., Ostby, J., Gray Jr, L.E., In Vitro and In Vivo Effects of 17beta-Trenbolone: a Feedlot Effluent Contaminant, Toxicological Sciences, 2002.

Yarrow, J.F., McCoy, S.C., Borst, S.E., Tissue Selectivity and Potential Clinical Applications of Trenbolone: A Potent Anabolic Steroid with Reduced Androgenic and Estrogenic Activity, PubMed Publications, Online, 2010.

Ojasoo, Raynaud., Unique Steroid Congeners for Receptor Studies, Cancer Research, 1978.