Enobosarm, better known as Ostarine or MK 2866, is a Selective Androgen Receptor Modulator (SARM) developed by GTx (GTx-024) to combat muscle wasting and osteoporosis. Many speculate Ostarine may find uses in hormone replacement treatment plans, as well as in the treatment of sarcopenia, cachexia and muscle atrophy. This is a highly valuable benefit to those suffering from muscle wasting …

MK 677 (IbutaMoren ) is rather similar to peptides like Ipamorelin and GHRP-6, but is administered orally and unlikely to set off the side effects that the latter can possibly cause during use. Apart from ease of use since you don’t have to do painful and inconvenient injections with MK 677 (IbutaMoren ), you can also expect to have significant …

Androstenedione is the common precursor of male and female sex hormones. Some androstenedione is also secreted into the plasma, and may be converted in peripheral tissues to testosterone and estrogens. Androstenedione can be synthesized in one of two ways. The primary pathway involves conversion of 17-hydroxypregnenolone to dehydroepiandrosterone by way of 17,20-lyase, with subsequent conversion ofdehydroepiandrosterone to androstenedione via the …

Estra-4,9-diene-3,17-dione is a powerful pro-steroid chemically similar to the anabolic agent Trenbolone. When in the body, estra-4,9-diene-3,17-dione completes the conversion to Trenbolone. Trenbolone is a potent anabolic steroid, which binds to specific receptors present in reproductive tissue, muscle and fat. Estra Diene Dione (estra-4,9-diene-3,17-dione) is an anabolic steroid and a precursor to Estra Diene Dione. It became a controlled substance …

Methoxydienone particular to a process of synthesis of levonorgestrel, Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception. Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG …

Raloxifen hydrochloride, a second-generation Selective Estrogen Receptor Modulator (SERM) in the Raloxifene hydrochloride benzothiophene family. On September 13, 2007, the U. S. Food and Drug Administration approved Evista for reduction in the risk of invasive breast cancer in postmenopausal women with and Raloxifene hydrochloride without osteoporosis. It has also been approved as a potent stand-alone osteoporosis treatment. Raloxifene is used …

Fulvestrant also called Faslodex or AstraZeneca,is is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It works by blocking the actions of estrogen in the body. Fulvestrant is a complete estrogen receptor antagonist with no agonist effects, which in addition, accelerates the proteasomal degradation of the estrogen receptor. The drug …

Anastrozole is the generic name for the trade name drug Arimidex. In some cases, health care professionals may use the trade name Arimidex when referring to the generic drug name Anastrozole. It is an aromatase inhibitor, an anti-cancer medication use for the adjuvant or initial treatment of breast cancer in post-menopausal women. Estrogen causes or increases growth of certain breast …

Exemestane is a steroidal Aromatase Inhibitor (AI) that is most commonly known as Aromasin. Exemestane carries the ability to inhibit the aromatase enzyme, which is responsible for the production or conversion of testosterone to estrogen. Aromasin has the ability to block aromatization, which in turn inhibits the production of estrogen, and thereby lowers the body’s serum estrogen levels. Treating advanced …

Fareston will display both estrogen antagonist / agonist properties in the body. This puts Fareston in the same category as Nolvadex and Clomid, the two most popular drugs in Farestons category. FARESTON is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors. Toremifene administration for a period of 3 …

Tamoxifen Citrate is the trade name for the drug tamoxifen citrate, it is a non-steroidal agent that demonstrates potent anti-estrogenic properties. The drug is technically an estrogen agonist/antagonist, which competitively binds to estrogen receptors in various target tissues. With the tamoxifen molecule bound to this receptor, estrogen is blocked from exerting any action, and an anti-estrogenic effect is achieved. Tamoxifen …

Nolvadex is the name of the drug whose scientific name is tamoxifen citrate. Nolvadex is not a steroid – it is a potent anti-estrogen used as an ancillary drug during cycle when symptoms of gyno occur. It can also be used post cycle to restore natural testosterone production. Symptoms of gyno can occur when using a cycle which contains drugs …