Trestolone ace, more popularly known as Ment, has developed quite a reputation over the last several years for being an exceedingly potent steroid. Combined with its initial long-term absence from the market, its current limited availability, and a market nearly devoid of high quality clones, its allure among steroid users has been further increased, taking on an almost super-drug status similar to what we saw when the now defunct Parabolan ceased production.
7-methyl-19-nortestosterone (MENT) (Also known as trestolone acetate). This compound is about 10 times more potent than T in terms of anabolic activities and gonadotropin suppression, is not bound by SHBG in circulation, is not a substrate for 5-reductase, and has a relatively low potency for stimulation of prostate growth: approximately four times less than that of T.94, 95MENT is aromatizable to 7-methyl estradiol, which may confer beneficial tissue effects via the estrogen receptor.
In a randomized crossover trial involving hypogonadal men from two disparate societies (Edinburgh and Hong Kong), patients were allocated to treatment with two MENT acetate 115 mg upper-arm implants for 6 weeks and two i.m. injections of TE 200 mg at 3-week intervals. Compared with a 6-week androgen washout period, both MENT and i.m. TE significantly enhanced sexual function, with no between-group differences.
Stanolone
5F-PB22
Trenavar
Methoxydienon
Trestolone Acetate
Epistane
Dymethazine
Halodrol
1-Androsterone
5a-Hydroxy Laxogenin
MK-677 (Ibutamoren mesylate, Nutrobal)
GW501516 (Cardarine)
S4 (Andarine)
LGD-4033
M1,4ADD
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