Boldenone (Equipose) is a veterinary injectable anabolic steroid, derivative of testosterone. It exhibits strong androgenic and anabolic properties. It is moderately aromatised to beta estradiol (E2) compared to nandrolone, therefore leading to less water retention. However estrogenic side effects such
Trenbolone is a 19-nortestosterone derivative with a chemical structure resembling nandrolone. It is of high androgenicity and anabolic activity (about five times higher that testosterone), ideal during precontest preparation and dieting. Trenbolone has a positive effect on fat burning and catabolism
Η βήτα αλανίνη αποτελεί ένα αμινοξύπου συμβάλλει στην αποτροπή της κόπωσης και της γαλακτικής οξέωσης, που εμφανίζονται κατά τη διάρκεια της άσκησης. Αυτό συμβαίνει μέσω της αλκαλοποίησης του pH στο αίμακατά την αναερόβια οξείδωση της γλυκόζης. Έχει την ικανότητα να
Mesterolone is a synthetic form of diydroxytestosterone (DHT). It has a mild anti-estrogenic and androgenic action. Mesterolone improves body composition, through beta oxidation of fatty acids. It improves dramatically libido, since it binds strongly with the sex hormone binding globulin (SHBG).
Drostanolone (Masterone) is medically prescribed as an anti-estrogenic therapy for the treatment of advanced inoperable breast cancer in postmenopausal women. It was originally manufactured under pharmaceutical production by Lilly/Syntex during the 1970s. The drug is an injectable AAS derived from dihydrotestosterone (DHT). It
Επιστημονική ημερίδα της Ελληνικής Ακαδημίας Αντιγήρανσης στις 11-12 Φεβρουαρίου 2017 στο Ζάππειο Μέγαρο Oμιλία Βιοπαθολόγου-Συγγραφέα, Γεωργίου Ν.Τουλιάτου, την Κυριακή 12 Φεβρουαρίου 2017, ώρα 18.20μμ (αίθουσα HYGEIA)
Methenolone is a non aromatized anabolic steroid with a low androgenic index. It is considered as a derivative of dihydrotestosterone (DHT). As a result, it does not lead to any water retention or gynecomastia (E2- beta estradiol elevation). Therefore, methenolone enanthate-acetate are
Oxymetholone (anadrol 50) is medically used for the treatment of severe aplastic anemia. The drug increases erythropoietin (EPO) production from the kidneys, iron absorption improves in small intestine and also stimulates the production of red cells from bone marrow. As
The injectable (parenteral) form of stanozolol is less toxic to the liver, since it avoids the first hepatic entrance and enters directly into circulation. It is a suspension and usually painful, when administrated intramuscularly. Its half life is around 24 hours, which
Methyltrienolone (M3) is perhaps the most hepatotoxic oral, among the 17 alkylated AAS. It was initially medically used against advanced breast cancer, as an alternative treatment to the rise of estrogens. It has a similarity to trenbolone, with an enormous androgenic/anabolic ratio. Its effectiveness is so high,