provinox
- Product Code: proviron
- Availability: 49
-
£24.00
<h1>
Provinox® (Mesterolone)</h1>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>CONTENTS</strong>: 25mg/tab. (50tabs.)</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>CHEMICAL NAMES:</strong><br />
17beta-hydroxy-l alpha-methyl-Salpha-androstan-3-one<br />
l-methyl-Salpha-dihydrotestosterone</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>DESCRIPTION:</strong><br />
Similar to dihydrotestosterone, mesterolone is a strong androgen with only a weak level of anabolic activity.This is due to the fact that like dihydrotestosterone, mesterolone is rapidly reduced to inactive diol metabolites in muscle tissue where concentrations of the 3-hydroxysteroid dehydrogenase enzyme are high. The belief that the weak anabolic nature of this compound indicates a tendency to block the androgen receptor in muscle tissue, thereby reducing the gains of other more potent muscle-building steroids, should likewise not be taken seriously. In fact, due to its extremely high affinity for plasma binding proteins such as SHBG, mesterolone may actually work to potentate the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes, mesterolone is primarily used to increase androgen levels when dieting or preparing for a contest, and as an antiestrogen due to its intrinsic ability to antagonize the aromatase enzyme. Mesterolone is a modified form of dihydrotestosterone. It differs by the addition of a methyl group at carbon 1, which helps protect the hormone from hepatic metabolism during oral administration. The same structural modification is also used with oral Primobolan® (methenolone) tablets. Alkylation at the one position slows hepatic metabolism of the steroid during the first pass, although much less profoundly than c-17 alpha alkylation. Mesterolone is resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability remains much lower than c-17 alpha alkylated oral steroids.</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>SIDE EFFECTS:</strong><br />
<img alt="" class="m20 pull-right" src="https://malaytiger.com/uploads/mt/files/provinox_formula.jpg" />Mesterolone is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth.</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>ADMINISTRATION:</strong><br />
The usual dosage among male athletes is between 50 mg and 150 mg of mesterolone per day, or two to six 25 mg tablets. The drug is typically taken in cycles of 6-12 weeks in length, which is usually a sufficient period of time to notice the benefits of drug therapy. Many bodybuilders favor the use of mesterolone during dieting phases or contest preparation, when low estrogen and high androgen levels are particularly desirable.</p>
Provinox® (Mesterolone)</h1>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>CONTENTS</strong>: 25mg/tab. (50tabs.)</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>CHEMICAL NAMES:</strong><br />
17beta-hydroxy-l alpha-methyl-Salpha-androstan-3-one<br />
l-methyl-Salpha-dihydrotestosterone</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>DESCRIPTION:</strong><br />
Similar to dihydrotestosterone, mesterolone is a strong androgen with only a weak level of anabolic activity.This is due to the fact that like dihydrotestosterone, mesterolone is rapidly reduced to inactive diol metabolites in muscle tissue where concentrations of the 3-hydroxysteroid dehydrogenase enzyme are high. The belief that the weak anabolic nature of this compound indicates a tendency to block the androgen receptor in muscle tissue, thereby reducing the gains of other more potent muscle-building steroids, should likewise not be taken seriously. In fact, due to its extremely high affinity for plasma binding proteins such as SHBG, mesterolone may actually work to potentate the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes, mesterolone is primarily used to increase androgen levels when dieting or preparing for a contest, and as an antiestrogen due to its intrinsic ability to antagonize the aromatase enzyme. Mesterolone is a modified form of dihydrotestosterone. It differs by the addition of a methyl group at carbon 1, which helps protect the hormone from hepatic metabolism during oral administration. The same structural modification is also used with oral Primobolan® (methenolone) tablets. Alkylation at the one position slows hepatic metabolism of the steroid during the first pass, although much less profoundly than c-17 alpha alkylation. Mesterolone is resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability remains much lower than c-17 alpha alkylated oral steroids.</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>SIDE EFFECTS:</strong><br />
<img alt="" class="m20 pull-right" src="https://malaytiger.com/uploads/mt/files/provinox_formula.jpg" />Mesterolone is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth.</p>
<p style="font-size: 13px; line-height: 20.799999237060547px;">
<strong>ADMINISTRATION:</strong><br />
The usual dosage among male athletes is between 50 mg and 150 mg of mesterolone per day, or two to six 25 mg tablets. The drug is typically taken in cycles of 6-12 weeks in length, which is usually a sufficient period of time to notice the benefits of drug therapy. Many bodybuilders favor the use of mesterolone during dieting phases or contest preparation, when low estrogen and high androgen levels are particularly desirable.</p>