Oxandrolone is aromatase inhibitor

Testosterone Enanthate

Chemical Names: 4-androsten-3-one-17beta-ol 17beta-hydroxy-a ndrost-4-en-3-one
Estrogenic Activity: moderate
Progestational Activity: low
Testosterone enanthate is a slow-acting injectable spring of the androgen testosterone.
Coming after deep intramuscular injection, the drug is planned to offer a persistent release of testosterone into the bloodstream for about two to three weeks.
As with all testosterone injectables, testosterone enanthate is extremely preferred by athletes for its efficiency to advertise strong gains in muscle mass and force.

How Supplied:
Testosterone enanthate is wide disposable in human an ( veterinary drug marketplaces. Composing and dose change by country and manufacturer, but generally involve fifty-one mg/ml, one hundred mg/ml, two hundred mg/ml, or 250 mg/ml of steroid ) soluble in oil.
Structural Characteristics:
Testosterone enanthate is a modified sort of testosterone.
The half-life of testosterone enanthate about 8 days after injection.
Side Effects (Estrogenic):
Testosterone is promptly aromatised in the body to estradiol (estrogen). The aromatase (estrogen synthetase) enzyme is liable for this metabolic process of testosterone. Raised estrogen levels could induce side effects specified raised water retention, body fat gain, and gynecomastia.
An anti-estrogen such as Clomid or tamoxifen citrate may represent required to prevent estrogenic side effects.
Side Effects (Androgenic):
Testosterone is the basal male androgen, liable junior upholding secondary male sexual characteristics. Raised rank of testosterone are likely to make androgenic side effects involving oily skin, acne, and body/facial hair growth.
Side Effects (Hepatotoxicity):
Testosterone doesnt have hepatotoxic effects; liver toxicity is unlikely.

Methandienone (also known as methandrostenolone, Dbol, dianabol) is an orally-effective anabolic steroid originally developed in Germany and released in the US in the early 1960s by Ciba Specialty Chemicals. This is a derivative from testosterone, one of the most popular steroid compounds in the world and the second steroid (after testosterone) ever produced. Methandienone promotes dramatic increases in protein synthesis, glycogenolysis, and muscle strength over a short space of time.  

Research suggests the common table mushroom has anti- aromatase [17] properties and therefore possible anti-estrogen activity. In 2009, a case-control study of the eating habits of 2,018 women in southeast China revealed that women who consumed greater than 10 grams of fresh mushrooms or greater than 4 grams of dried mushrooms per day had an approximately 50% lower incidence of breast cancer. Chinese women who consumed mushrooms and green tea had a 90% lower incidence of breast cancer. [18] However the study was relatively small (2,018 patients participating) and limited to Chinese women of southeast China.

Because Dihydrotestosterone is incapable of interaction with the aromatase enzyme and therefore it is unable to undergo aromatization (conversion) into Estrogen, Oxandrolone 10mg Magnus Pharmaceuticals shares this important trait. Its inability to aromatize into Estrogen translates into a total elimination of the potential for any and all estrogenic and Estrogen-related side effects.  Oxandrolone 10mg Magnus Pharmaceuticals  is alkylated at the 17th carbon atom of its steroid structure (properly known as methylation or C17-alpha alkylation) in order to bypass liver metabolism and allow it to reach the bloodstream to perform its job. Unfortunately, C17-alpha alkylation of oral anabolic steroids is known to express varying degrees of liver toxicity, but Oxandrolone 10mg Magnus Pharmaceuticals has demonstrated far less in the way of liver toxicity than most other C17-alpha alkylated oral anabolic steroids. It is important, however, to still understand that Oxandrolone 10mg Magnus Pharmaceuticals is not void of potential liver toxicity and that caution must still be taken in regards to its use in that respect.

Oxandrolone is aromatase inhibitor

oxandrolone is aromatase inhibitor

Because Dihydrotestosterone is incapable of interaction with the aromatase enzyme and therefore it is unable to undergo aromatization (conversion) into Estrogen, Oxandrolone 10mg Magnus Pharmaceuticals shares this important trait. Its inability to aromatize into Estrogen translates into a total elimination of the potential for any and all estrogenic and Estrogen-related side effects.  Oxandrolone 10mg Magnus Pharmaceuticals  is alkylated at the 17th carbon atom of its steroid structure (properly known as methylation or C17-alpha alkylation) in order to bypass liver metabolism and allow it to reach the bloodstream to perform its job. Unfortunately, C17-alpha alkylation of oral anabolic steroids is known to express varying degrees of liver toxicity, but Oxandrolone 10mg Magnus Pharmaceuticals has demonstrated far less in the way of liver toxicity than most other C17-alpha alkylated oral anabolic steroids. It is important, however, to still understand that Oxandrolone 10mg Magnus Pharmaceuticals is not void of potential liver toxicity and that caution must still be taken in regards to its use in that respect.

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