Posts made by jamezb46

A lot of us are interested in using transdermal/oral/sublingual steroids to get performance enhancing effects or pro-libido and pro-masculinizing effects.

So, what do you think about a methylated androsterone formulation? In theory it would convert to methyl-DHT, which would stay in the body longer than would its base metabolite, bioidentical DHT. It should also convert to methyl-androstanediol, which shares many of the calming effects of allopregnenalone and would again remain in the body for longer due to the methylation.

I don’t think any of the metabolites of methyl-androsterone would be hepatotoxic, either. That is because the hepatotoxicity of the methylated androgens is likely due to the methylated estrogens that the androgens are metabolized into. But since neither Androsterone nor its metabolites can be easily turned into estrogen, I don’t think this is a concern.

Lastly, I recall that Haidut posted a study showing that androsterone and DHEA in a 50-50 to 25-75 ratio were capable of completely re-masculinizing castrated rats. So, if the methylated androsterone ever gets produced, perhaps running it with IdeaLabs Pansterone would be the ultimate pro-masculinizing stack.

@bio3nergetic Can I have the bottle lol

@Santosh do you mean 80% DMSO 20% Ethanol by volume or by weight?

@noodlecat59 Interesting concern. What I will say is that if it is, none of the studies looking at Bemitil mentioned it or any other serious adverse effects.

Bemitil is relatively metabolsim resistant, meaning that it stays in the body (particularly the brain) unchanged for long periods of time.

That is why it is recommended to use it only about once a week at a dose of about 500-750 mg before exertion.

To answer your concern directly, I would be inclined to say that the Bromide ion would only become problematic if it were liberated from the parent Bemitil compound at some step in the drug's metabolism or if it otherwise occured to a sufficently great extent in the body.

I'm just not aware of that occuring, and in the absence of evidence that it does occur and in the presence of its powerful ergogenic effects, I would opt to experiment with it before intense training sessions for a performance boost and discontinue permaturely if I felt the need to.

@Kilgore

My pleasure. Mildronate is a Latvian drug that inhibits carnitine synthesis and competitively inhibits carnitine transport proteins in the mitochondria. It therefore forces your cells to utilize glucose oxidation for their energy supply.

As a consequence, you get less cytotoxic products of incomplete beta-oxidation that build up during exertion, as your cells rely on Glucose oxidation and glycolysis to a much greater extent.

While running mildronate, it is advisable to use 250-1000mg per day

You do, however, need to cycle. 3 weeks on a weeks off is a typical course.

@TexugoDoMel

How do you get CO2 in? Do you just do bag breathing?

@Beach-Stud

If you’re talking about a low fat diet and increasing GO, look no further than Mildronate.

You can try cycling it 3 weeks in 3 weeks off. Stuff will improve your endurance like crazy and squeeze every drop of glucose from your blood into those juicy muscle cells.

I’m planning on adding Bemitil and Emoxypine to my preworkout stack, and really want to include methylene blue (as IdeaLabs Oxidal) as well.

Also included in my stack are:

Beta-alanine
Oral ATP
Agmatine Sulfate
Magnesium
Niacinamide

I might add in some injectable l-carnitine and/or Amino Asylum’s Super Shredder as well on my more pump focused days.

According to the Oxidal thread on the RP forum, due to Methylene Blue’s reversible binding to MAO-A, dietary tyramine should be reduced. I, like many others into Ray’s work, eat cheese daily (with most meals, in fact) and use whey protein and eat bananas and chocolate and dry fruits, etc. all of which contain tyramine.

So, my questions are:

1. do people find the tyramine interaction to be serious, and if so how much time is needed between high tyramine food consumption and taking the methylene blue (ideally there would be a scientific paper looking at how MB affects dietary tyramine metabolism)

2. what have people’s experiences been like taking MB PWO?

@basebolt

Perhaps it would be worth looking into eye drops with NAD+? You would try dissolving raw NAD+ powder into a super saturated yet eye safe solution, and putting a few drops in each eye.

Benefits would be felt in the brain the quickest, due to law of locality.

Yo.

Figured I’d post this question here first, because the RP community tends to be pretty knowledgeable about this kind of stuff, and there’s no way I’m giving my hard earned money to Charles the Bald on a monthly basis (lol)

What I’m looking for is an exhaustive list (preferable) or at least examples of AAS that have the following property:

1. Resistant to Aromatase enzyme
2. Subject to 5AR
3. 5A reductant is more anabolic than the original

For example, Trenbolone would not qualify, as dihydrotrenbolone is not more anabolic than Trenbolone.

Peace