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Superdrol Superdrol

HI-TECH Pharmaceuticals SUPERDROL® is a strong anabolic preparation containing efficient anabolic-androgenic prohormones and verified herbal anabolic substances. This product promotes substantial muscle mass building by enhancing the multifarious course of anabolic processes, reducing the activity of excessive myostatin which inhibits muscle development and reducing the amount of intra-arterial stress. In addition it helps keep up high libido and carries low risk of any side effects associated with such products.

HI-TECH Pharmaceuticals SUPERDROL® contains the following ingredients:
4-androstene-3b-ol,17-one - also referred to as 3β-Hydroxy-4-androstene-17-one or 4-Dehydroepiandrosterone, abbreviated as: 4-DHEA, 4-AD, or AKA, a steroid compound structurally similar to 5-Dehydroepiandrosterone (5-DHEA), differentiating with the position of the double bond moved from between the 5th and 6th carbon to a location between the 4th and 5th carbon of sterane. By transforming to androstenedione and androstenediol in reactions catalysed by the following dehydrogenases: 3β-hydroxysteroid (3b-HSD) and 17β-hydroxysteroid (17b-HSD), it leads to production of precursors converted to testosterone in the presence of 17b-HSD or 3b-HSD. Mainly as an effective pre-precursor of testosterone and - to some extent - independently, it has the ability to activate androgen receptors, allowing the development of numerous muscular and bone structures, breakdown of excessive fat tissue and enhancement of erythropoiesis allowing the synthesis of red blood cells. Not being converted to oetrogens and being a much weaker activator of oestrogen receptors than 5-DHEA, it carries a low risk of side effects associated with excessive excitability of female hormones. As an unmethylated compound, it seems relatively safe for the liver. No changes in the lipid profile have been observed during its supplementation. However, it can change blood pressure, cause oily skin, or skin dermatitis.

1-androstene-3b-ol-17-one - otherwise called 3b-hydroxy-5a-androst-1-en-17-one, 1-Androsterone, as well as 1-Dehydroepiandrosterone, abbreviated as 1-DHEA or 1-Andro, is a steroid whose structure is similar to 5-DHEA, with the difference that the double bond is located between the 1st and 2nd carbon atom of sterane, instead of the 5th and 6th atom. It is susceptible to the activity of 3β-hydroxysteroid dehydrogenases (3b-HSD) and 17β-hydroxysteroid (17b-HSD), enabling synthesis of sequentially androstenedione and androstenediol, compounds allowing the formation of 1-testosterone after conversion of the said metabolites using 17b-HSD and 3b-HSD respectively. It also increases the anabolic potential of the body, enhancing the synthesis of muscle and bone structures, while promoting the catabolism of superfluous fat. This is due to its slightly independent action, which is though much stronger through its metabolite - 1-testosterone. As a substance that is not sensitive to aromatase and shows a significantly weaker action on oestrogen receptors than 5-DHEA, it does not lead to noticeable side effects that are a consequence of the increased excitability of female hormones. Although it is not converted to traditional testosterone (4-testosterone), under certain conditions it may exacerbate hair loss, cause skin dermatitis or prostatic hyperplasia. During its supplementation liver and kidney functions may worsen, blood pressure may rise and lipoprotein profile may change, which is manifested by a decrease in high density lipoprotein (HDL) and increase in the level of low density lipoproteins (LDL). In comparison to 1-testosterone, it does not cause discouragement and drowsiness, but promotes a completely different state of arousal and increased willingness to take action.

Androsterone - also called 5α-androstan-3α-ol-17-one or 3α-hydroxy-5α-androstan-17-one is a chemical compound structurally based on the sterane particle, which is a derivative of testosterone, considered by many to be an inactive metabolite. Due to its ability to transform into dihydrotestosterone (DHT), which activates androgenic receptors, this compound is involved in development of manly features and growth of many structures, including muscle tissue. By maintaining a balanced level of DHT and not getting converted to testosterone, it ensures optimum anabolic action and excludes the risk of side effects accompanying excessive excitability of male hormones, such as: prostate overgrowth, skin dermatitis or androgenic baldness. As it is not susceptible to aromatisation to oestrogens, and even exhibits anti-oestrogen properties, this compound minimises excessive activity of female hormones, therefore preventing gynaecomastia, water or fat retention, decrease in sex drive. By modulating response of selected receptors, it increases the will to undertake some actions and their efficiency. It is also often categorized as a pheromone.

Adrostenolon - also called 3β-hydroxyandrost-5-en-17-one, 5-androstene-3β-ol-17-one, Dehydroepiandrosterone or in abbreviation DHEA, is an endogenous steroid hormone naturally synthesized in the human body, reaching the highest concentration among all androgens. It is the precursor of testosterone and several other anabolic derivatives, and also an independently acting agent. It activates androgen receptors, leading to the development of many structures, including muscle and bone tissue, or increasing the efficiency of red blood cell formation. By blocking the excitability of 11β-hydroxysteroid dehydrogenase type 1 (11bHSD1), it reduces the rate of cortisol synthesis, thereby supporting the proper functioning of the insulin-carbohydrate metabolism, reducing the insulin resistance level, decreasing the amount of accumulated adipose tissue, supporting nutrition of muscle cells, protecting them from disintegration and improving mental state . By affecting the GABAA, NMDA and sigma receptors, it has a significant effect on the nervous system.

6-oxo-Δ4-pregnene-3,20-dione - a steroid compound structurally related to progesterone (4-Pregnen-3,20-dione), considered to be a precursor of pregnenolone, a cholesterol derivative otherwise referred to as: 3β-hydroxypregn-5-en-20-one or 5-Pregnen-3b-ol-20-one. It is the precursor for the synthesis of numerous hormones, including DHEA testosterone. It is assumed that effects of pregnenolone activity depend to a large extent on individual predispositions of the given organism, related for example to quality of enzyme system and its priorities. It supports body mass gain and speeds up glycogen accumulation pace. By enhancing myelination process and having neuroprotective effects, it supports the maintenance of good functionality of the nervous system, boosts cognitive processes and supports memorizing. By allowing deep sleep it increases efficacy of overnight regeneration. It reduces anxiety, improves mood and boosts libido.

Ajuga turkestanica extract - this plant from the Lamiaceae family is a semi-bush found on poor soils, including loam and rocky areas of the central part of the Asian continent. It owes its properties mainly to the high content of turkesterone, a chemical compound belonging to the phyto-steroids having 11α-hydroxyl group, which are analogues of the 20-hydroxyekdyzon insect hormone. It stimulates Act phosphorylation by enhancing flow of calcium into the cells, activating Notch receptors and Wnt pathway and blocking the effect of myostatin, which hinders muscle development over the programmed frames. As a result it increases the production of various types of proteins, especially muscle tissue, which significantly accelerates the construction of new and regeneration of existing protein structures. Due to the lack of influence on androgen receptors, it does not carry the risk of side effects related to their excessive activity, including prostatic hyperplasia, cutaneous eczema, excessive greasiness of the skin or androgenic baldness. In addition it alleviates muscle soreness, improves heart rate and digestive system functions.

(3b,5a,6a,25R)-Spirostane-3,6-diol - otherwise called (25R)-5a-Spirostane-3b,6a-diol or chlorogenin, a compound belonging to the sapogenin group. By combining with androgen receptors, it enhances the synthesis of numerous protein structures, including muscle or bone structures. Due to the low anabolic-androgenic potential of 33:1, it focuses on the induction of intra-aortic anabolism, without unnecessary side effects associated with androgenic effects, including prostatic hyperplasia, male pattern baldness or skin dermatitis. By eliminating the effects of cortisol, it reduces insulin resistance of hepatocytes and myocytes, promotes the transport of glucose to muscle cells, reduces the amount of stored fat and improves mental well-being. Due to certain adaptogenic properties, it increases vitality and durability. It is commonly used as a substance that enhances action of other stronger anabolic-androgenic compounds.

HI-TECH PharmaceuticalsSUPERDROL® is a powerful anabolic product based on the precursors of the most effective anabolic hormones, which are: testosterone, 1-testosterone and DHT. They activate androgen receptors and therefore effectively stimulate the development of muscle and bone structures, erythropoiesis, and initiate the breakdown of superfluous fat tissue. Involvement of additional pathways, including Notch receptors and Wnt pathway, broadens the possibilities to increase anabolic potential. By increasing the anabolic potential of the body, reducing activity of myostatin and decreasing cortisol concentration, the supplement creates favourable conditions for building substantial muscle mass and strong bone structure forming its basis. Moderate androgenic action reduces the risk of adverse side effects associated with excessive excitability of androgens. In addition, oestrogenic activity has been almost entirely eliminated, which minimizes the risk of possible side effects associated with female hormones. What is more, the product helps maintain high libido, strong focus and motivation. Application of innovative Cyclosome TM technology to contain active substances in a capsule ensures high bioavailability of the supplement ingredients and efficiency of their action. To sum up, HI-TECH Pharmaceuticals SUPERDROL® is an extremely efficient supplement ensuring development of strong, dense and lean muscle mass in a relatively short time, with low risk of developing unsolicited side effects. 

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Since 2005
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Superdrol Superdrol 42 tab.
Hi-tech
67.59 $

Superdrol 42 tab.

features

Strength:
Mass:
Endurance:
Regeneration:

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01709231594 (mon.-fri 900-1700)

67.59 $
Notify me of availability

- Delivery even day after tomorrow

- Foreign shippment from 5.59 $ Every 81.43 $ reduces shipping costs by 2.71 $

You have got questions about the product

sales@mz-store.co.uk

01709231594 (mon.-fri 900-1700)

Description
  • Strong anabolic product
  • Combination of efficient prohormones
  • Enriched with herbal substances
  • Increases testosterone and 1-testosterone levels
  • Decreases myostatin activity
  • Decreases cortisol activity
  • Improves insulin activity
  • Boosts anabolism in many ways
  • Reduces androgenic potential
  • Minimises oestrogenic effect
  • Significant anti-catabolic effect
  • Promotes muscle tissue development
  • Strengthens bone tissue
  • Speeds up fat burning
  • Promotes building strong solid musculature

HI-TECH Pharmaceuticals SUPERDROL® is a strong anabolic preparation containing efficient anabolic-androgenic prohormones and verified herbal anabolic substances. This product promotes substantial muscle mass building by enhancing the multifarious course of anabolic processes, reducing the activity of excessive myostatin which inhibits muscle development and reducing the amount of intra-arterial stress. In addition it helps keep up high libido and carries low risk of any side effects associated with such products.

HI-TECH Pharmaceuticals SUPERDROL® contains the following ingredients:
4-androstene-3b-ol,17-one - also referred to as 3β-Hydroxy-4-androstene-17-one or 4-Dehydroepiandrosterone, abbreviated as: 4-DHEA, 4-AD, or AKA, a steroid compound structurally similar to 5-Dehydroepiandrosterone (5-DHEA), differentiating with the position of the double bond moved from between the 5th and 6th carbon to a location between the 4th and 5th carbon of sterane. By transforming to androstenedione and androstenediol in reactions catalysed by the following dehydrogenases: 3β-hydroxysteroid (3b-HSD) and 17β-hydroxysteroid (17b-HSD), it leads to production of precursors converted to testosterone in the presence of 17b-HSD or 3b-HSD. Mainly as an effective pre-precursor of testosterone and - to some extent - independently, it has the ability to activate androgen receptors, allowing the development of numerous muscular and bone structures, breakdown of excessive fat tissue and enhancement of erythropoiesis allowing the synthesis of red blood cells. Not being converted to oetrogens and being a much weaker activator of oestrogen receptors than 5-DHEA, it carries a low risk of side effects associated with excessive excitability of female hormones. As an unmethylated compound, it seems relatively safe for the liver. No changes in the lipid profile have been observed during its supplementation. However, it can change blood pressure, cause oily skin, or skin dermatitis.

1-androstene-3b-ol-17-one - otherwise called 3b-hydroxy-5a-androst-1-en-17-one, 1-Androsterone, as well as 1-Dehydroepiandrosterone, abbreviated as 1-DHEA or 1-Andro, is a steroid whose structure is similar to 5-DHEA, with the difference that the double bond is located between the 1st and 2nd carbon atom of sterane, instead of the 5th and 6th atom. It is susceptible to the activity of 3β-hydroxysteroid dehydrogenases (3b-HSD) and 17β-hydroxysteroid (17b-HSD), enabling synthesis of sequentially androstenedione and androstenediol, compounds allowing the formation of 1-testosterone after conversion of the said metabolites using 17b-HSD and 3b-HSD respectively. It also increases the anabolic potential of the body, enhancing the synthesis of muscle and bone structures, while promoting the catabolism of superfluous fat. This is due to its slightly independent action, which is though much stronger through its metabolite - 1-testosterone. As a substance that is not sensitive to aromatase and shows a significantly weaker action on oestrogen receptors than 5-DHEA, it does not lead to noticeable side effects that are a consequence of the increased excitability of female hormones. Although it is not converted to traditional testosterone (4-testosterone), under certain conditions it may exacerbate hair loss, cause skin dermatitis or prostatic hyperplasia. During its supplementation liver and kidney functions may worsen, blood pressure may rise and lipoprotein profile may change, which is manifested by a decrease in high density lipoprotein (HDL) and increase in the level of low density lipoproteins (LDL). In comparison to 1-testosterone, it does not cause discouragement and drowsiness, but promotes a completely different state of arousal and increased willingness to take action.

Androsterone - also called 5α-androstan-3α-ol-17-one or 3α-hydroxy-5α-androstan-17-one is a chemical compound structurally based on the sterane particle, which is a derivative of testosterone, considered by many to be an inactive metabolite. Due to its ability to transform into dihydrotestosterone (DHT), which activates androgenic receptors, this compound is involved in development of manly features and growth of many structures, including muscle tissue. By maintaining a balanced level of DHT and not getting converted to testosterone, it ensures optimum anabolic action and excludes the risk of side effects accompanying excessive excitability of male hormones, such as: prostate overgrowth, skin dermatitis or androgenic baldness. As it is not susceptible to aromatisation to oestrogens, and even exhibits anti-oestrogen properties, this compound minimises excessive activity of female hormones, therefore preventing gynaecomastia, water or fat retention, decrease in sex drive. By modulating response of selected receptors, it increases the will to undertake some actions and their efficiency. It is also often categorized as a pheromone.

Adrostenolon - also called 3β-hydroxyandrost-5-en-17-one, 5-androstene-3β-ol-17-one, Dehydroepiandrosterone or in abbreviation DHEA, is an endogenous steroid hormone naturally synthesized in the human body, reaching the highest concentration among all androgens. It is the precursor of testosterone and several other anabolic derivatives, and also an independently acting agent. It activates androgen receptors, leading to the development of many structures, including muscle and bone tissue, or increasing the efficiency of red blood cell formation. By blocking the excitability of 11β-hydroxysteroid dehydrogenase type 1 (11bHSD1), it reduces the rate of cortisol synthesis, thereby supporting the proper functioning of the insulin-carbohydrate metabolism, reducing the insulin resistance level, decreasing the amount of accumulated adipose tissue, supporting nutrition of muscle cells, protecting them from disintegration and improving mental state . By affecting the GABAA, NMDA and sigma receptors, it has a significant effect on the nervous system.

6-oxo-Δ4-pregnene-3,20-dione - a steroid compound structurally related to progesterone (4-Pregnen-3,20-dione), considered to be a precursor of pregnenolone, a cholesterol derivative otherwise referred to as: 3β-hydroxypregn-5-en-20-one or 5-Pregnen-3b-ol-20-one. It is the precursor for the synthesis of numerous hormones, including DHEA testosterone. It is assumed that effects of pregnenolone activity depend to a large extent on individual predispositions of the given organism, related for example to quality of enzyme system and its priorities. It supports body mass gain and speeds up glycogen accumulation pace. By enhancing myelination process and having neuroprotective effects, it supports the maintenance of good functionality of the nervous system, boosts cognitive processes and supports memorizing. By allowing deep sleep it increases efficacy of overnight regeneration. It reduces anxiety, improves mood and boosts libido.

Ajuga turkestanica extract - this plant from the Lamiaceae family is a semi-bush found on poor soils, including loam and rocky areas of the central part of the Asian continent. It owes its properties mainly to the high content of turkesterone, a chemical compound belonging to the phyto-steroids having 11α-hydroxyl group, which are analogues of the 20-hydroxyekdyzon insect hormone. It stimulates Act phosphorylation by enhancing flow of calcium into the cells, activating Notch receptors and Wnt pathway and blocking the effect of myostatin, which hinders muscle development over the programmed frames. As a result it increases the production of various types of proteins, especially muscle tissue, which significantly accelerates the construction of new and regeneration of existing protein structures. Due to the lack of influence on androgen receptors, it does not carry the risk of side effects related to their excessive activity, including prostatic hyperplasia, cutaneous eczema, excessive greasiness of the skin or androgenic baldness. In addition it alleviates muscle soreness, improves heart rate and digestive system functions.

(3b,5a,6a,25R)-Spirostane-3,6-diol - otherwise called (25R)-5a-Spirostane-3b,6a-diol or chlorogenin, a compound belonging to the sapogenin group. By combining with androgen receptors, it enhances the synthesis of numerous protein structures, including muscle or bone structures. Due to the low anabolic-androgenic potential of 33:1, it focuses on the induction of intra-aortic anabolism, without unnecessary side effects associated with androgenic effects, including prostatic hyperplasia, male pattern baldness or skin dermatitis. By eliminating the effects of cortisol, it reduces insulin resistance of hepatocytes and myocytes, promotes the transport of glucose to muscle cells, reduces the amount of stored fat and improves mental well-being. Due to certain adaptogenic properties, it increases vitality and durability. It is commonly used as a substance that enhances action of other stronger anabolic-androgenic compounds.

HI-TECH PharmaceuticalsSUPERDROL® is a powerful anabolic product based on the precursors of the most effective anabolic hormones, which are: testosterone, 1-testosterone and DHT. They activate androgen receptors and therefore effectively stimulate the development of muscle and bone structures, erythropoiesis, and initiate the breakdown of superfluous fat tissue. Involvement of additional pathways, including Notch receptors and Wnt pathway, broadens the possibilities to increase anabolic potential. By increasing the anabolic potential of the body, reducing activity of myostatin and decreasing cortisol concentration, the supplement creates favourable conditions for building substantial muscle mass and strong bone structure forming its basis. Moderate androgenic action reduces the risk of adverse side effects associated with excessive excitability of androgens. In addition, oestrogenic activity has been almost entirely eliminated, which minimizes the risk of possible side effects associated with female hormones. What is more, the product helps maintain high libido, strong focus and motivation. Application of innovative Cyclosome TM technology to contain active substances in a capsule ensures high bioavailability of the supplement ingredients and efficiency of their action. To sum up, HI-TECH Pharmaceuticals SUPERDROL® is an extremely efficient supplement ensuring development of strong, dense and lean muscle mass in a relatively short time, with low risk of developing unsolicited side effects. 

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Composition

Composition

Container size: 42 tabletsServing size: 1 tabletServings per container: 42
per 1 tabletamount%DV
Proprietary Prohormone & Anabolic Blend™:4-Androstene3b-ol, 17-one, 1-Androstene-3b-ol, 17-one, Androsterone Undecanoate, Androstenolone Acetate, 6-oxo-^4-pregnene-3,20-dione, Ajuga Turkestanica Extract (Whole Plant), [(3b,5a,6a,25R)-Spirostan-3,6-diol]300 mg-

Other ingrednients

Microcrystalline Cellulose, Phosphatidylcholine 75%, Hydroxypropyl Beta Cyclodextrin, Phytosterols, Magnesium Stearate, Silica, FD&C Blue #2, FD&C Red #40

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