Examples of using Aromatization in English and their translations into Thai
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Process called aromatization.
Resist aromatization therefore impossible to develop gynecomastia.
Advantages of Ultrasonic Aromatization.
It acts to slow aromatization conversion into estrogen.
Among them include aromatase inhibitors, which can help reduce the estrogen-like side effects caused by aromatization.
Because there is no aromatization, gynecomastia is also not an issue.
Structurally, it is Dianabol with an added chlorine at the -4 position, which has the predictable advantage of preventing aromatization.
And like all testosterone drugs, the effects of aromatization are likely as well.
Though the risk of aromatization is reduced, estrogenic-like side effects can occur.
Esiclene(formebolone) is reputed to have very low androgenic properties, meaning that it resists aromatization or conversion of testosterone into estrogen.
Aromatization related to the compound with a very limited amount of water retention experienced by most.
Testosterone Acetate is also converted by aromatization to estradiol in peripheral tissue.
No aromatization: The steroid doesn't turn into estrogen hence no muscle cells will be burned.
Androgens are responsible for the development of secondary sex male characteristics, but they do convert from testosterone into estrogen, in a process known as aromatization.
With lower doses, the potential for aromatization when using Boldenone acetate is less than other anabolic androgenic steroids.
Many prohormones available start out as a testosterone-like substance in the body, but then eventually turn into estrogen through a process called aromatization.
At safe dosage levels, however, the potential for aromatization results in a relatively low risk for negative side effects including water retention.
Aromatization- Though estrogenic side effects like gynecomastia may seem anything but mild, they are easy enough to mitigate by using an aromatase inhibitor like Arimidex during your cycle. This is a requirement.
Deca Durabolin(and Nandrolone in general) doesnt produce many estrogenic or androgenic side effects.This is because Deca Durabolin has a very low rate of aromatization(conversion to estrogen via the aromatase enzyme), roughly equal to 20% the rate of Testosterone.
As stated earlier, Methylstenbolone is derived from DHT, for users this means that aromatization is virtually impossible, so it does not convert to an estrogenic metabolite or have any affinity for the progesterone receptor, so estrogen mediated side effects should be virtually non-existent.
Nandrolone has a modest inclination for estrogen conversion, counted on to be just approximately twenty percent of that seen with testosterone. It is because while the liver could commute nandrolone to estradiol, in next more activist sites of steroid aromatization specified fatty tissue nandrolone is far more closed to this action.
Halodrol produces zero aromatization, as a result you can expect to be free from estrogenic side effects(those due to increases in estrogen estradiol, progesterone or progestin) which generally include increased water retention, body fat gain, and gyno due to the testosterone to estrogen ratio imbalance.
Why? One explanation is found in the drug's metabolism. Specifically, Boldenone metabolizes to an anti-aromatase inhibitor known as 1,4 dienedone. This could certainly explain why Boldenone, despite it relatively high rate of aromatization, does not deliver anywhere near the estrogenic punch that its aromatization rate implies.
Boldenone is associated with mild sides- low aromatization, conversion to estrogen is approx 50% comparing to testosterone. Water retention is mild, comparable to deca but much less than with test. There's some risk of developing gynocomastia for estrogen-sensitive athletes when high dosages used. All of these could be easily cured by using tamoxifen or clomiphene, stronger antiaromatisers are not needed.
Nandrolone has a low tendency for estrogen conversion, estimated to be only about 20% of that seen with testosterone.516 This is because while the liver can convert nandrolone to estradiol, in other more active sites of steroid aromatization such as adipose tissue nandrolone is far less open to this process.517 Consequently, estrogen-related side effects are a much lower concern with this drug than with testosterone.
Even with a high rate of aromatization, propionate did not cause gyno as often as other testosterone esters. Users who realize this normally did so due to less frequent injections: Not due to some special quality of the drug. I liked propionate because an increase in IGF-1 was common during liver deactivation. Also because use could be discontinued at the first sign of overt side effects thus allowing the chemical to no longer be the cause after 2-3 days post-discontinuance.
Andarine(S4), unlike many androgens, does not convert to dihydrotestosterone(DHT) and it does not aromatize. Aromatization refers to the conversion of testosterone to estrogen. This makes S4 a bit more appealing on a functional basis compared to other androgenic compounds as negative DHT and Estradiol effects cannot occur with this compound. In fact, S4 has been shown to block DHT from binding to the prostate receptor sites.