Same. Never noticed this with dhb so I’m curiousDo you have any papers on the mechanism of aromatization? It'd be great to see comparisons with other AAS and what structural features increase/decrease affinity if there are any..
Same. Never noticed this with dhb so I’m curiousDo you have any papers on the mechanism of aromatization? It'd be great to see comparisons with other AAS and what structural features increase/decrease affinity if there are any..
It doesn't aromatizeLol. A few pages back guys were discussing DHB “crashing” e2 because it’s a DHT. Now it shifts to DHB potentially aromatizing. This is good stuff.
Just run it and get bloodwork. Why overthink this shit so much?
Yea cause it's the shitI didn't notice any change in my 8 week blood work from my test/ npp cycle to the current test/ npp / dhb. I expected to see higher rbc and ast alt numbers, but they were very comparable.
Not overthinking it. I know GreenAmine is a chemist of some sort and it's rare for me nowadays to be able to bounce sometimes crazy ideas and thoughts off another who's in a similar field.Lol. A few pages back guys were discussing DHB “crashing” e2 because it’s a DHT. Now it shifts to DHB potentially aromatizing. This is good stuff.
Just run it and get bloodwork. Why overthink this shit so much?
As far as my research has taken me, it seems that anadrol acts like a prohormone only, with immeasurably low binding affinity to the AR. Its primary metabolite, 17α-methyl-5α-androstane-3α,17β-diol, seems to be the primary active metabolite. Anadrol also increases the production of 17-hydroxyprogesterone, which is a progestin, so is capable of inducing/exacerbating gyno. The full mechanism is unfortunately not completely understood.Similar to anadrol causing gyno from receptor binding opposed to conversion ?
I can't think of any offhand, but I will look on SciFinder and get back to you. I'm traveling for work this week, so I may be delayed.Do you have any papers on the mechanism of aromatization? It'd be great to see comparisons with other AAS and what structural features increase/decrease affinity if there are any..
For DHB, the C1-C2 bond is already oxidized, so the H cannot be extracted in an elimination reaction, as this would form an allene, which has a linear geometry (i.e., cannot be part of a ring, unless in a high-energy transition state). The Glu residue that removes the H from C1 would probably not be in a close enough proximity in the binding site to access C4 for an elimination reaction.This is the only mechanism I can see and it's proposed by a chemist. No binding models.
Aromatization - an overview | ScienceDirect Topics
www.sciencedirect.com
Why wouldn't it be believable that the Proton on C1 gets abstracted in step 4 because c4 is already oxidized?
This is the c4 Proton abstraction I was thinking of. No geometrical constraints here.For DHB, the C1-C2 bond is already oxidized, so the H cannot be extracted in an elimination reaction, as this would form an allene, which has a linear geometry (i.e., cannot be part of a ring, unless in a high-energy transition state). The Glu residue that removes the H from C1 would probably not be in a close enough proximity in the binding site to access C4 for an elimination reaction.
Right, but what would remove it? That's why I included this:This is the c4 Proton abstraction I was thinking of. No geometrical constraints here.
To be fair, I'm not very knowledgeable about the tertiary structure of the binding site, but i don't think that it's possible at C4 simply based on the fact that DHT isn't a substrate for aromatase.The Glu residue that removes the H from C1 would probably not be in a close enough proximity in the binding site to access C4 for an elimination reaction.
This is the c4 Proton abstraction I was thinking of. No geometrical constraints here.
Right, but what would remove it? That's why I included this:
To be fair, I'm not very knowledgeable about the tertiary structure of the binding site, but i don't think that it's possible at C4 simply based on the fact that DHT isn't a substrate for aromatase.
Real-world data is just as (if not MORE) important than this theoretical shit. I greatly appreciate your valuable anecdotal data.I just take the drugs.