Is there any other than MK & GW?
Thanks
Thanks
Sorry, I knew that. Silly me.Anything hormonal is going to need to be followed by a pct. I'm sure you know but mk and gw are not sarms and are not hormonal.
The most common sarms right now are osta, lgd, rad140, and s4 which all require a pct. By definition, a sarm interacts with the androgen receptor which can negatively impact the hpta. The only true difference in sarms and traditional aas is the fact that sarms are selective by nature and only interact with the androgen receptors in bone and muscle tissue. Hpta impact is lessened by this but suppression is still a concern.Sorry, I knew that. Silly me.
Anything else these companies release? I notice alot of compounds I've never heard of from companies like Focused Nutrition EU.
SARMS aside, any other compounds like MK/GW?The most common sarms right now are osta, lgd, rad140, and s4 which all require a pct. By definition, a sarm interacts with the androgen receptor which can negatively impact the hpta. The only true difference in sarms and traditional aas is the fact that sarms are selective by nature and only interact with the androgen receptors in bone and muscle tissue. Hpta impact is lessened by this but suppression is still a concern.
Imo not much else has come out that proves to be effective that I've seen.SARMS aside, any other compounds like MK/GW?
Dammit. My mate did GW and noticed nothing.Imo not much else has come out that proves to be effective that I've seen.
What are they? Will tell you what I know.Dammit. My mate did GW and noticed nothing.
It's just focused nutrition had some interesting new products and Ivr never heard of them.
SR 9099What are they? Will tell you what I know.
I didn't say it was, I mentioned other compounds I wasn't aware of. Topic is a bit off, totally forgot half of these aren't SARMS when I created it.yk-11 isn't a Sarm either..
Need standard serm pctDrop body fat. I've read conflicting information on you need/don't need PCT for S4. Trying to verify which one is correct.
https://www.ncbi.nlm.nih.gov/pubmed/23995658The myogenic differentiation of C2C12 myoblast cells is induced by the novel androgen receptor (AR) partial agonist, (17α,20E)-17,20-[(1-methoxyethylidene)bis-(oxy)]-3-oxo-19-norpregna-4,20-diene-21-carboxylic acid methyl ester (YK11), as well as by dihydrotestosterone (DHT). YK11 is a selective androgen receptor modulator (SARM), which activates AR without the N/C interaction. In this study, we further investigated the mechanism by which YK11 induces myogenic differentiation of C2C12 cells. The induction of key myogenic regulatory factors (MRFs), such as myogenic differentiation factor (MyoD), myogenic factor 5 (Myf5) and myogenin, was more significant in the presence of YK11 than in the presence of DHT. YK11 treatment of C2C12 cells, but not DHT, induced the expression of follistatin (Fst), and the YK11-mediated myogenic differentiation was reversed by anti-Fst antibody. These results suggest that the induction of Fst is important for the anabolic effect of YK11.
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