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CAS Name: 4-chloro-17a-methyl-17b-hydroxyandrosta-1,4-dien-3-one
Chlorodehydromethyltestosterone is an oral 17-alpha-alkylated steroid with a low androgenic acivity index 0.10-0.15 similar to methenolone and a myotrophic activity index of 0.50. Because of the 4-chloro alteration, chlorodehydromethyltestosterone does not convert into estrogens nor into DHT.
Chlorodehydromethyltestosterone is used in cases of muscle wasting syndrome in HIV patients. Because of it’s low androgenic activity chlorodehydromethyltestosterone can be used by woman and does not cause virilization. Chlorodehydromethyltestosterone on low doses does not suppressive on hypothalamic-pituitary axis (HTPA) function.
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CAS Name: (5a,17b)-17-Methyl-2′H-androst-2-eno[3,2-c]pyrazol-17-ol
Stanozolol is a17-alpha-alkylated anabolic steroid with good oral bioavailability. While stanazolol’s androgenic activity index of stanozolol is nearly the same as testosterone, its myotrophic activity is much higher at 2.0–3.7. Stanozolol does not aromatize and does not cause water retention.
Stanozolol has been used for weight loss management in HIV patients with chronic obstructive pulmonary disease and has showed significant improvement in weight, body mass index, LBM, and muscle size. Stanozolol has been shown in vitro to significantly enhance …
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CAS Name: 17beta-Hydroxy-1-methyl-5alpha-androst-1-en-3-one acetate
Methenolone acetate is an oral steroid derivative of dihydrotestosterone (DHT) with a mild myotrophic activity index 0.85 and a low androgenic index 0.12. Methenolone acetate is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces stress on the liver, but also this steroid’s bioavailability.
It is considered one of the safer steroids, meaning it has few side effects. Because of it’s low androgenic activity, methenolone acetate does not suppress endogenous testosterone secretion. Methenolone is also not overly suppressive …
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CAS Name: (5a,17b)-17-Hydroxy-2-(hydroxymethylene)-17-methylandrostan-3-one
Oxymetholone is a 17-alpha-alkylated oral anabolic-androgenic steroid. Oxymetholone is very effective in promoting muscle gains and has an excellent myotrophic activity index of 3.2 and is similar to testosterone with an androgenic activity index of 0.45. Main clinical uses include: osteoporosis, anemia, as well as stimulating muscle growth in undernourished or underdeveloped patients. Also, oxymetholone has been studied for the treatment of HIV-associated wasting, antithrombin III deficiency, pediatric growth impairment, and damaged myocardium, with varying degrees of success.
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CAS Name: (5a,17b)-17-Hydroxy-17-methyl-2-oxaandrostan-3-one
Oxandrolone is a 17-alpha-alkylated oral anabolic steroid. Oxandrolone has an excellent myotrophic activity index of 3.2 and a low androgenic activity index of 0.2. At low doses, oxandrolone will not cause suppression of endogenous testosterone production and does not aromatize to estrogens.
Oxandrolone was approved for treating alcoholic hepatitis, Turner’s syndrome, and weight loss caused by HIV. In addition, the drug has shown positive results in treating anemia and hereditary angioedema and for preserving muscle mass in burns patients. Oxandronolne …
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CAS Name: (17b)-17-Hydroxy-17-methylandrosta-1,4-dien-3-one
Methandrostenolone is a 17-alpha-alkylated oral anabolic-androgenic steroid with anabolic properties that are more pronounced than its androgenic effects. It has little progestational activity and easily converts to estrogens. Methandrostenolone has an anabolic activity index 0.60 and an androgenic activity index 0.20. Methandrostenolone has an extra double bond in the A-ring and, therefore, is not converted by 5-alpha reduction into DHT. Since methandrostenolone was created in the 1960s, it has been used for many different applications.
At present, the only legitimate …



