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Clenbuteric

Clenbuteric Pharmaceutical Name: Clenbuteric Chemical Name: Clenbuterol hydrocloride Chem.Abstr.Name: N.A Molecular Structure: C12H18CI2N20 Molecular Weight: 277.193 Presentation: Clenbuteric 20 is not a steroids hormone but a beta 2 symphatomometic. Its effect can compare to steroids. Clenbuteric 20 can cause a solid highly qualitative muscle growth which goes hand in hand with significant strength gain and has a strong anticatabolic effect. This means it decreases the rate at which protein is reduced in the muscle cell, consequently causing an enlargement of muscle cells. For this reason numerous athletes use Clenbuteric 20 after steroids treatment to balance the resulting catabolic phase and thus obtain maximum strength and muscle mass. A further aspect of Clenbuteric 20 is it distinct fat burning effect. Clenbuteric 20 burns fat without dieting because it increase the body temperature slightly, forcing the body to burn fat fr this process. Clenbuteric 20 in the meantime, is not only a favorite competition compound among professional bodybuilders. An epecially intense fat burning occurs when Clenbuteric 20 is combined with the LT3 thyroid hormone compound T3. Due to the higher body temperature Clenbuteric 20 magnifies the effect of anabolic/ androgenic steroids taken simultaneously, since the protein processing is increased. * Over dosages of the Clenbuteric 20 will lead to heart failure. Please consult physician before used. STORAGE Store in a dry, dark place at a temperature of 15-25 ° C. Keep out of reach of children. TERMS OF VALIDITY 3 years. Do not use after expiration date indicated on the packaging.

Dianabol (Methandiennone)

Active Life: 6-8 hours
Drug Class: Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 15-50 mg/day......Women 5-10 mg/day
Acne: Yes, especially in higher dosages
Water Retention: Yes, similar to testosterone
High Blood Pressure: Yes
Liver Toxic: Yes
Aromatization: Yes
DHT Conversion: No
Decrease HPTA function: Yes, dose and cycle length dependant

Description

Dianabol is a derivative of testosterone which help to produce exceptional mass and strength muscle. In order to kick start a dianabol cycle, usually what you do is incorporate a fast acting oral like dianabol (or anadrol) and combine it with long acting injectables (such as Deca or Eq with some Testosterone). The reasoning here is that the oral (Dbol in this case) will give almost immediate results, while the injectable takes time to produce results. The end result is that you start seeing results within the first week of your cycle and continue up until the end with the injectables. This entails taking anywhere from 25-50mgs of dbol (although as little as 20mgs or as much as 100mgs have been reported) for 3-6 weeks at the start of a cycle (average time for a "Kick Start" is 4 weeks, though), and then ceasing their use as the injectables start to produce results.

Winstrol (Stanozolol)

Quick Overview Active Life: around 48 hours Drug Class: Anabolic/Androgenic Steroid (for injection or oral) Average Dose: Men 50-100 mg/day.....Women 25-50 mg/week Acne: Rare Water Retention: Rare High Blood Pressure: Rare Liver Toxic: Yes, it is a 17AA steroid Aromatization: No, it is a DHT derivative DHT Conversion: None Decrease HPTA function: Low Description Winstrol is a popular brand name for the anabolic steroid stanozolol. This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth. The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a ggod, reliable builder of muscle. Its anabolic properties could even be comparable to Dianabol, but Winstrol does not have the same tendency for water retention. Stanozolol also contains the same c17 methylation we see with Dianabol, an alteration used so that oral administration is possible. To spite this design however, there are many injectable versions of this steroid produced.

Proviron (Mesterolon)

Mesterolone

From Wikipedia, the free encyclopedia
Mesterolone
Mesterolone.svg
Systematic (IUPAC) name
1 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one
Clinical data
AHFS/Drugs.com International Drug Names
Legal status Prescription Only (AU)
Pharmacokinetic data
Metabolism Liver
Identifiers
CAS number 1424-00-6
ATC code G03BB01
PubChem CID 15020
ChemSpider 14296 Yes
UNII 0SRQ75X9I9 Yes
KEGG D04947 Yes
ChEMBL CHEMBL258918 Yes
Chemical data
Formula C20H32O2
Mol. mass 304.467 g/mol
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Mesterolone is an orally applicable androgen, and DHT derivative. It is sold under the brand name Proviron (as Provironum in Asia-Pacific region), by Bayer Schering Pharma (earlier by Schering). In the late 70's and early 80's it was used with some success in controlled studies of men suffering from various forms of depression. Mesterolone is a relatively weak androgen and rarely used for replacement therapies.[1]

Trials

In one randomized, double-blind 4-week trial, 38 dysthymic men were administered 75 mg daily. Itil & Colleagues reported an improvement of symptoms which included anxiety, lack of drive and desire. Next, they administered a high dose (450 mg/day) or placebo in a 6-week randomized trial of 52 men with a mean age of 40 years, suffering from dysthymia, unipolar and bipolar depression. Both the mesterolone and placebo groups improved significantly and there were no statistically significant differences between the two groups. In this series of studies mesterolone lead to a significant decrease in LH and testosterone levels. This is probably as a result of the extremely high dose used. In another, 100 mg mesterolone cipionate was administered twice monthly. With regards to plasma T levels, there was no difference between the treated vs untreated group, and baseline LH levels were minimally affected.[2]

Bodybuilding

Mesterolone had seen widespread use in bodybuilding primarily for antiestrogenic activity in anabolic steroid stacks but such use has declined after introduction of aromatase inhibitors and SERMs. Most significant benefits of current Mesterolone use are considered to be maintaining libido off-cycle and also relatively and temporarily improving vascularity.[3]

References

  1. Jump up ^ Nieschlag E, Behre HM, Bouchard P, et al. (2004). "Testosterone replacement therapy: current trends and future directions". Hum. Reprod. Update 10 (5): 409–19. doi:10.1093/humupd/dmh035. PMID 15297434.
  2. Jump up ^ Kövary PM, Lenau H, Niermann H, Zierden E, Wagner H (May 1977). "Testosterone levels and gonadotrophins in Klinefelter's patients treated with injections of mesterolone cipionate". Arch Dermatol Res 258 (3): 289–94. PMID 883846.
  3. Jump up ^ Meso-RX Steroid Profiles - Proviron (Mesterolone)

Anavar (Oxandrolone)

Quick Overview

Active Life: 8-12 hours
Drug Class: Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 20-50 mg/day......Women 5-15 mg/day
Acne: Only in higher doses
Water Retention: Rare
High Blood Pressure: Rare
Liver Toxic: Yes, c17-alfa-alkylated steroid. Due to low doses, toxicity is low to medium
Aromatization: None
DHT Conversion: Low
Decrease HPTA function: Dose depandant

Description

Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (DHT). Although one might think that this would make it a more androgenic steroid, it in fact creates a steroid that is less androgenic because it is already "5-alpha reduced". In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent "dihydro° form. It is a simple matter of where a steroid is capable of being potentiated in the body, and with oxandrolone we do not have the same potential as testosterone, which is several times more active in androgen responsive tissues compared to muscle tissue due to its conversion to DHT. It essence oxandrolone has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances.
This steroid works well for the promotion of strength and duality muscle mass gains, although it's mild nature makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results. It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone. In this case the androgen really helps to harden up the muscles, while at the same time making conditions more favorable for fat reduction. Some athletes do choose to incorporate oxandrolone into bulking stacks, but usually with standard bulking drugs like testosterone or Dianabol. The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol, Primobolan or Durabolin. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup.

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