• SR9009

    SR9009 is a Rev-ErbA agonist. This essentially means that it binds to our Rev-ErbA proteins and enhances their activity in the body.

  • Pregnyl

    Human chorionic gonadotrophin (hCG) is a glycoprotein hormone produced during pregnancy in humans. I was first discovered in 1920 and later sold under prescription to the market in 1932 as Pregnyl. At that time the hormone was extracted from animal pituitary glands. In the 1940’s new manufacturing techniques were developed that allowed for the hormone to be extracted from purified urine obtained from pregnant women. In the case of Pregnyl this is still done to this day. Recently new techniques of recombinant DNA modification allowed for a new synthetic product called Ovidrel. Other than the differences in manufacturing processes there are some notable differences in effects between Pregnyl and Ovidrel.

  • Proviron Bayer

    Proviron was developed by Schering in 1934, making it one of the first drugs used in hormone replacement therapy. Mesterolone is very similar to dihydrotestosterone in that it is a strong androgen but a very weak anabolic agent.

  • Tamoxifen

    Nolvadex a drug that contains the molecule Tamoxifen has been approved by the FDA for prevention and treatment of breast cancer also known as a Selective Estrogen Receptor Modulator (SERM) which acts as a weak estrogen that competes for the estrogen receptor site. Tamoxifen is also known as an Anti-Estrogen / Estrogen-Blocker since it inhibits the activity of regular estrogens.

  • Cabaser pfizer

    Cabaser Pfizer is a drug that contains Cabergoline, an active ingredient that was initially designed for medical purposes but later on became popular in the bodybuilding world.

  • Letrozole

    As much as everyone raves about Letrozole due to its effects on paper, I personally feel there are better drugs for users on steroid cycles that come with far less potential side effects. It is not the best cancer fighting drug for women in pre-menopausal, actually it’s completely ineffective as the main source of estrogen is from the ovaries. However it has been proven highly effective in post-menopausal women due to estrogens from the peripheral tissues. It is not normally used in a first line defence for cancer fighting as many doctors have found favour with Tamoxifen.

  • Aromasin

    Exemestane (Aromasin) is an oral steroidal aromatase inhibitor, but unlike letrozole and anastrozole it permanently binds to the active site of the aromatase enzymes thus blocking their function of converting androgens into estrogens. This is known as Type I or suicide inhibition because the inhibitor becomes inactive due to the mechanism of its actions. A permanent bond with the aromatase enzyme complex is formed and prolonged effects may be experienced even after the drug has cleared from circulation. The aromatase enzyme’s activity can only be restored by new enzyme synthesis.

  • Proviron

    Proviron is an oral steroid containing 25 mg of the hormone Mesterolone per tablet Proviron is not an anabolic but a very powerful anti-estrogen. It prevents gynecomastia while reducing fat and water retention

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