E-Control 3.0 is a potent aromatase inhibitor containing Androsta-3 5-diene-7 17-dione which helps with decreasing in circulating levels of estrogen in the body. Simply put it will inhibit or reduce the amount of androgens in the body that can convert into estrogen. The active ingredient is a compound called Androsta-3,5-Diene-7,17-Dione which is a very potent suicide aromatase inhibitor. E-Control 2.0 can be used with all of our pro-hormone products to help reduce any possible water retention, eliminate the chance of the development of male breast tissue, and increase sex drive. E-Control 3.0 should also be taken after using our products as PCT (post cycle therapy) to bring hormone function back to normal once your cycle is completed.
Androsta-3 5-diene-7 17-dione
- Androsta-3 5-diene-7 17-dione – 25mg
- Chlorophytum Borivilianum (50% extract) – 250mg
- Indole-3-carbinol (I3C) – 200mg
The Power Behind E-Control 3.0
Androsta-3 5-diene-7 17-dione is an aromatize inhibiting compound and is a DHEA analog that will reduce estradiol and is mostly used as a post cycle therapy. Androsta-3 5-diene-7 17-dione naturally occurs in the human body. In the 1970s, East German steroid chemists, affiliated with the Research Center for Molecular Biology and Medicine, produced Androsta-3 5-diene-7 17-dione in human urine. Later on, in the early ’90s, researchers from the Ohoku College of Pharmacy in Japan were looking for aromatase inhibitors(AIs). They found out that Androsta-3 5-diene-7 17-dione was one of the best AIs available.
Chlorophytum Borivilianum (extract) the roots are used traditionally in Indian subcontinent as aphrodisiac and sexual stimulant. Ethanolic extract of roots as well as sapogenins isolated from the roots were studied for effect on sexual behavior and spermatogenesis in albino rats. Administration of 100 mg/Kg and 200 mg/Kg b.w. of the sapogenin and ethanolic extract respectively had pronounced anabolic and spermatogenic effect in treated animals as evidenced by weight gains in the body and reproductive organs and histological studies. The treatment also markedly affected sexual behavior of animals as reflected in reduction of mount latency, ejaculation latency, post ejaculatory latency, intromission latency and an increase of mount frequency and attractability towards female.
Indole-3-carbinol (I3C) (a metabolic product of I3C in the gut) have been shown to improve Phase I detoxification of estrogens favoring the less potent 2OH estrone pathway. Although the 2OH estrone can also make DNA-damaging quinones, they are less adhesive to the DNA and therefore are probably only important when levels are very high (as can be seen with certain single-nucleotide polymorphisms [SNPs] of CYP1A1). These metabolites can be measured in the blood or urine to ensure that levels are low before starting I3C or DIM.
Take one (1) capsule three (3) times daily in divided doses with food.