AAS Androgenic to Anabolic ChartResults 1 to 7 of 7. Corticosteroid injection low back pain, just go over to Steroid dot com. Androgeniv the steroid anabolic androgenic chart when the majority of steroid research was undertaken, before steroids became a dirty word, the goal of the researchers was to develop steroids steroid anabolic androgenic chart could increase muscle mass in cancer patients, burn victims, those with wasting diseases etc. They were trying to develop steroids that were anabolic without being androgenic. Of course medical science has pesky moral objections to testing unknown substances on human test subjects even though oxymetholone pubchem days gymrats are willing to queue round the block to take the latest untested designer steroid compoundsso a system of testing was developed on rats.
Steroid Effectiveness Chart - jmhw.info
Results 1 to 12 of Anabolic ratio and Androgenic ratio chart. This is a really nice chart, Liquidex. It may need a little explanation for people that are new to this sort of thing: In very simple terms, a high anabolic number means that the compound is very effective with like cell growth getting swole.
A high anrogenic number means that the compund will promote virilization, or the development of masculine characteristics deep voice, body hair etc. Compounds with a high ratio of androgenic to an anabolic effects are the drug of choice in androgen-replacement therapy TRT , whereas compounds with a reduced androgenic: Want to see something crazy? Have a look at the values for Metribolone above.
I believe one of our new sponsors actually carries this. Originally Posted by GSRacer. Metribolone methyltrienolone Androgenic 6,, Anabolic 12,, Standard Methyltestosterone oral Chemical Names 17alpha-methylbetahydroxyestra-4,9,trieneone 17alpha-methyl-trenbolone Estrogenic Activity none Progestational Activity no data available Description: Methyltrienolone is one of the strongest oral anabolic steroids ever produced.
This agent is a derivative of trenbolone trienolone , which has been c alpha alkylated to allow for oral administration. This modification has created a steroid that is significantly stronger than its non-methylated cousin.
Its potency has been measured to be anywhere from times greater than that of methyltestosterone, with greater dissociation between anabolic and androgenic effects. Its potency is only matched by its relative toxicity, however, which has limited its modern use to that of laboratory research only.
Methyltrienolone was first described in In spite of its high relative activity, however, methyltrienolone has seen very limited use in humans. It was used clinically during the late 's and early '70's, most notably in the treatment of advanced breast cancer. Such application was not long lived, however, as more realistic evaluations of the drug's toxicity soon led to its abandonment in human medicine. By the mid's, methyltrienolone was becoming an accepted standard in non-human research studies, particularly those pertaining to the study of the androgen receptor activity.
For this purpose the agent is very well suited. Its sheer potency and resistance to serum-binding proteins makes it an excellent in-vitro receptor-binding standard to compare other agents to.
Being so resistant to metabolism, active methyltrienolone metabolites are also not going to greatly interfere with the results of most experiments. Body tissues can metabolize most steroids fairly easily, which means that even incubation studies can be complicated with the question of what is causing a particular effect, the steroid or one of its unidentified metabolites.
This is much less of an issue with methyltrienolone. Today, methyltrienolone remains an agent of research use only. Methyltrienolone is not available as a commercial agent. Methyltrienolone is a modified form of nandrolone. The resulting steroid is significantly more potent than its nandrolone base, and displays a much longer half-life and lower affinity for serum-binding proteins in comparison.
Methyltrienolone chemically differs from trenbolone only by the addition of a methyl group at c This alteration changes the activity of methyltrienolone considerably, however, such that this agent should not simply be considered an oral form of trenbolone.
Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability. For maximum utilization, methyltrienolone should be taken on an empty stomach. Methyltrienolone is no longer used in clinical medicine due to an unacceptable level of hepatotoxicity. This agent is generally not recommended for physique-or performance-enhancing purposes for the same reason. Those absolutely insisting on its use need to take its level of liver toxicity very seriously.
At the very least, routine blood tests should be conducted to ensure the agent is not imparting damage. Drug duration should also be very limited, preferably to 4 weeks of use or less. The relative potency of methyltrienolone is extremely high, requiring doses as little as. Its effective and tolerable range is usually considered to be. Dianabol-type doses of mg daily are completely unthinkable, and should never be attempted. Again, this is an extremely toxic steroid, and all good advice would say to avoid it.
Anyone of the many commercially available steroids would be much safer choices. This agent is not recommended for women for physique-or performance-enhancing purposes due to its extremely strong toxicity and tendency to produce virilizing side effects. Anabolics 9th ed , Metribolone methyltrienolone pp. Anabolic ratio and Androgenic ratio chart Nice.
Where can I find this. I want to bathe in it. Metribolone is where Captain America came from. Originally Posted by babyhulk. I've never seen it, guess i'm barking up the wrong tree. You can go further with Dimethyltrienolone.. Differs from methyltrienolone by the addition of a 7-methyl group.
A few highlights to paint a picture for ya "the main function of the addition of a 7-methyl group is to reduce binding to serum proteins like SHGB Sex Hormone Binding Globulin , increasing the percentage of free active steroid in the blood. This agent is very similar in structure to Metribolone methyltrienolone , which was determined to be not only extremely potent, but also the most hepatotoxic steroid ever developed at the time of its testing. I came across one that had it in a blend I would imagine that if you had any concerns about using Halotestin then you may want to avoid something like this I dont know even if I came across one I dont think I will ever touch it.
Effects described on liver here sound very scary. Just good old anadrol and dbol are good with meh. Test to NPP Ratio. By RoidsR4m3 in forum Anabolic Steroids.