Sustanon (Sustanon 250, Sustamed)
Sustanon(Sustanon 250, Sustamed)
Sustanon is a mixture of four esters of Testosterone (the main male sex hormone), each ester has a different half-life in the body. If to compare Sustanon with individual forms of Testosterone, it has some advantages, for example ease of use, instead of several separate forms of Testosterone. Also, each of the 4 testosterone esters enhances each other's action. It is a mistake to consider Sustanon, as a combined cycle in one ampoule, since all of it’s active substances are Testosterones, which are different in the speed of exposure in the human body.In 250 mg. Sustanon contains:Testosterone Propionate - 30 mg.Testosterone Phenylpropionate - 60 mg.Testosterone Isocaproate - 60 mg.Testosterone Decanoate - 100 mg.
Dianabol (Dbol, Methandrostenolone, Methandienone, Anabol, Methan)
Dianabol (Dbol, Methandrostenolone, Methandienone, Anabol, Methan)
Dianabol (Dbol) is the most popular steroid in the world. That’s why the steroid has so many trade and alternative names which can confused by amateur sportsmen. So if someone is referring to Dianabol, Danabol, DBOL, Methandienone, Anabol, Methan, Methanabol as androgenic anabolic steroids most likely they mean a substance with Methandrostenolone as its chemical name. There are also thousands websites which are selling Dianabol alternatives, they claim that their products produce the same impact on the organism moreover that it does not have any side effects and it’s legal.
turinabol, Tbol
Turinabol (TBOL, Oral Turinabol, 4-Chlorodehydromethyltestosterone)
Turinabol (Tbol, 4 Chlorodehydromethyltestosterone) also known as tbol, oral tbol, oral turinabol and chlorodehydromethyltestosterone is an oral steroid. The chemical name of turinabol is 4-Chlorodehydromethyltestosterone, from this chemical name you can understand that turinabol is combination of the chemical structures of Dianabol (Methandienone) and Clostebol (4-chlorotestosterone). Basically turinabol is a modified form of Dianabol (Methandienone), in composition attended atom of chloro and double bond between carbon 1 and 2. This small change inhibits the hormone from aromatizing into estrogen, and also reduces its androgenic nature.