Stanolone description
Stanolone is an endogenous androgen sex
steroid and hormone. The enzyme 5α-reductase catalyzes the formation of
DHT from testosterone in certain tissues including the prostate gland,
seminal vesicles, epididymides, skin, hair follicles, liver, and brain.
This enzyme mediates reduction of the C4-5 double bond of testosterone.
Relative to testosterone, DHT is considerably more potent as an agonist
of the androgen receptor (AR).
Unlike testosterone and various synthetic AAS, Stanolone DHT Dihydrotestosterone Powder CAS 521-18-6
cannot be aromatized, and for this reason, poses no risk of estrogenic
side effects like gynecomastia at any dosage. In addition, DHT cannot be
metabolized by 5α-reductase (as it is already 5α-reduced), and for this
reason, is not potentiated in so-called androgenic tissues like the
skin, hair follicles, and prostate gland. This provides exogenous DHT
with a greater ratio of anabolic to androgenic effects compared to
testosterone, and DHT may be less prone to producing certain skin and
hair-related side effects like acne, oily skin, seborrhea, hirsutism
(excess facial/body hair growth), and androgenic alopecia (pattern hair
loss), as well as prostate enlargement (which can lead to benign
prostatic hyperplasia) and an increased risk of prostate cancer.
For
a fast buildup of power and muscle mass Androstanolone is of little
value. Androstanolone used to be the athlete's favorite competition
steroid since it helped to obtain a harder muscle through a lower fat
content by increasing the androgen level without aromatizing. Numerous
athletes used Androstanolone during workouts for doping tested
championships since the substance remains in the body for only a short
time and the testosterone/epitestosterone value is not influenced.
Another positive characteristic is that the injectable version is not
liver toxic.
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