Mgm and 7 Ban

[Boofy416]

With these substances being temporarily schedule 1 tomorrow is anyone able to take over in place of the popular online vendors? The regular places act legally and I'm sure tons of people haven't been able to stock up for the upcoming months. It's a great opportunity for someone to step in. I should be good for a few weeks but then I'll be looking for some myself so if anyone knows anyone that can get it or if there's a thread somewhere else please point me to it!

 

[Deepnorth]

I am still slightly confused why anyone would prefer emgeem with legit mags pharma are still reachable. The side effects seem to be unworth it. Now I will say…. Until now as a back up it had its place. I do wish I understood the help of SR17 but I’m late on the draw there too. Can someone with more knowledge explain how SR reduces T levels or is a good option with emgeem. Is it to avoid T levels going through the roof? Sorry if this is already greatly explained elsewhere. Also sorry my bold text kicked in lol.

I imagine though something will take the place of MIT (emgeem) quickly.

 

[baberuth]

I am still slightly confused why anyone would prefer emgeem with legit mags pharma are still reachable. The side effects seem to be unworth it. Now I will say…. Until now as a back up it had its place. I do wish I understood the help of SR17 but I’m late on the draw there too. Can someone with more knowledge explain how SR reduces T levels or is a good option with emgeem. Is it to avoid T levels going through the roof? Sorry if this is already greatly explained elsewhere. Also sorry my bold text kicked in lol.

I imagine though something will take the place of MIT (emgeem) quickly.

I'm gonna quote something I wrote in a reply to a completely different question:

"The subjective effects of mu opioid agonists are sundry, and some of these effects are linked to different pathways of mu opioid agonism. SR-17018 preferentially stimulates G protein signaling pathways. (The mu opioid receptor is a G protein coupled receptor or GCPR.) In GCPRs, agonism induces a cascade of intracellular effects - essentially a growing chain reaction (more or less) that leads to the ultimate results you feel. What's different about SR-17018? It achieves what was just described while largely ignoring beta-arrestin recruitment. Beta-arrestin is involved in desensitization to GCPR agonism and receptor internalization, among other things. This is presumably why SR-17018 yields some opioid effects (namely analgesia) without others (notably euphoria and the accruing of tolerance, at least relative to traditional opioids)."

Not a biochemist or anything so take with a grain of salt. Feel free to follow up with questions if anything is unclear!