Stealth500
Member
How many prompts did this take?I’m prepared for being roasted for the AI slop, but it basically hit all the marks.
Follow along with the video below to see how to install our site as a web app on your home screen.
Note: This feature may not be available in some browsers.
How many prompts did this take?I’m prepared for being roasted for the AI slop, but it basically hit all the marks.
You should be able to get it with one whack if you pay for the service lolHow many prompts did this take?
Looking forward to the great @Ghoul's response haha“Ghoul, let’s apply a forensic level of precision to this particular strand of your argument—the notion that zinc-induced “strings” in a UGL rhGH vial represent amyloid fibrils capable of seeding beta-amyloid (Aβ) plaques, thereby precipitating Wrangel7’s symptoms into an Alzheimer’s trajectory. You’ve leaned heavily on that 2016 Scientific Reports paper to imply a mechanistic bridge, but a closer examination reveals this as a categorical error, not a causal chain. We’ll unpack it systematically, because conflating growth hormone (GH) fibrils with Aβ is like equating a firecracker to a thermonuclear device: superficial similarities in “explosive” potential, but worlds apart in structure, function, and consequence.
First, the identity crisis: Those zinc-facilitated structures in the study are unequivocally GH-specific fibrils, not Aβ. The paper describes them as short, curved aggregates (10–20 nm in length, per TEM imaging) formed via zinc’s coordination with GH’s histidine residues, stabilizing a dimeric or oligomeric state akin to natural pituitary storage granules. This is physiological amyloidogenesis—a benign, reversible process that enhances GH bioavailability, as corroborated in a 2022 Endocrinology review on hormone packaging. Aβ, by contrast, is a 39–42 amino acid peptide cleaved from amyloid precursor protein (APP), forming long, straight beta-sheet fibrils (hundreds of nm) that template neurotoxic plaques via prion-like templating. Sequence homology? Negligible—GH is a 191-residue helical protein; Aβ is a beta-strand fragment. No cross-seeding documented: a 2023 Journal of Alzheimer’s Disease meta-analysis on heterologous amyloids (e.g., alpha-synuclein influencing Aβ) finds no GH-Aβ interactions, let alone propagation. Your “amyloid-like” label? A semantic sleight-of-hand; not all amyloids are pathogenic, Ghoul—insulin forms them too, yet diabetics aren’t seeding plaques from their pens.
Second, the seeding fallacy: Even granting your fibrils’ existence post-reconstitution (dubious, given plasma denaturation), there’s no pathway for them to emulate Aβ’s plaque-seeding. True Aβ seeding requires conformational templating—exogenous Aβ misfolds endogenous Aβ into beta-sheets, per 2024 cryo-EM studies in Nature Structural & Molecular Biology. GH fibrils? They lack Aβ’s sticky hydrophobic core (e.g., residues 16–20 in Aβ); instead, they rely on zinc bridges that dissolve in vivo. Animal models underscore this: intracerebral Aβ injections seed plaques in APP-transgenic mice (e.g., 2025 Acta Neuropathologica Communications update), but no analogous GH experiments exist—because GH isn’t implicated in amyloid cascades. Peripheral injection? As we’ve established, it fails for Aβ absent heroic doses; for GH, it’s a non-starter. A 2024 Frontiers in Neuroscience paper on iatrogenic amyloidoses explicitly excludes recombinant proteins like rhGH, noting their monomeric purity precludes seeding. If GH fibrils seeded Aβ, we’d see signals in the 40-year rhGH pharmacovigilance data—yet FDA’s FAERS database (queried through 2025) reports zero AD linkages, versus the c-hGH outliers you cherry-pick.
Third, the temporal and symptomatic mismatch: Wrangel7’s acute fog and headaches align with GH’s direct effects—e.g., IGF-1-mediated cerebral edema or glucose swings, per 2023 Clinical Endocrinology cohorts on acromegaly analogs—not insidious plaque buildup, which incubates asymptomatically for decades (e.g., 20–30 years pre-diagnosis in AD trials). Your neuroPASC angle? Valid for BBB vulnerability, but it amplifies inflammation, not fibril smuggling. No 2024–2025 studies (PubMed-scoured) link rhGH to AD exacerbation; if anything, low-dose rhGH shows neuroprotective promise in mild cognitive impairment trials (Journal of Clinical Endocrinology & Metabolism, 2024), boosting hippocampal neurogenesis without amyloid risks.
Ghoul, your filtration advocacy stands on firmer ground—UGL impurities warrant it—but draping it in this Aβ doomsaying erodes credibility. Wrangel7’s plight merits pragmatic advice: taper the 8–14 IU, monitor IGF-1, rule out confounders via that MRI. By inflating GH fibrils into Aβ proxies, you’re not illuminating; you’re obfuscating, turning a solvable side effect into a speculative scourge. Evidence demands distinction, not conflation. Retract the amyloid alarm, refocus on facts, and perhaps Wrangel7 sharpens without the shadow of your specter. Logic, after all, is the ultimate filter.”
I’m prepared for being roasted for the AI slop, but it basically hit all the marks.
I don't pay for it. Usually would take me at least 5 or 6 to arrive at something like this, still the information is always off when you take a closer look.You should be able to get it with one whack if you pay for the service lol
And yet there's still people complaining about AI not answering medical questions geezI don't pay for it. Usually would take me at least 5 or 6 to arrive at something like this, still the information is always off when you take a closer look.
The other day I asked chat gpt about turning test base raws into test cyp raws.
later I notice the instructions said to put
"Approx. 50 liters of N,N-dimethylacetamide (DMA)"
into
"Large reaction vessel (10-15 liters capacity)"
What could go wrongAnd yet there's still people complaining about AI not answering medical questions geez![]()
Good eh? I told it to use the style of Ben Shapiro to own with facts and logicHow many prompts did this take?

I recall this, that there was no way a ugl could replicate the original tirzepitide from eli lilly because it was too complicated and that it was going to cost some extraordinary amount of money. What was the result?E.g pretending he had a friend with a access to an NMR lab test UGL tirzepatide and show it had improper structure.
There was no result, as the test was never done. He just made up a lie for some bizarre reason.I recall this, that there was no way a ugl could replicate the original tirzepitide from eli lilly because it was too complicated and that it was going to cost some extraordinary amount of money. What was the result?
If I am remembering correctly the original nuked thread was saying something about the cost being upwards of 10,000usd?There was no result, as the test was never done. He just made up a lie for some bizarre reason.
Hiccup Hell
If I am remembering correctly the original nuked thread was saying something about the cost being upwards of 10,000usd?
This was clearly fantasy, there was no proof of any of these tests. Also the things he is claiming don’t make any logical sense.There's much more going on in regards to potency and half life than peptide purity tests indicate.
It sounds like you got an exceptionally strong batch compared to what you had previously. Or maybe just fucked up in a way that caused stronger receptor binding to something inducing hiccups.
I had a conversation with a pharmaceutical scientist, and he was able to connect me with a lab that had a look at a leftover vial of QSC 30mg group buy Tirz that had tested at around 98% purity, yet 20mg doses I had been taking for months (which did work) were clearly not as strong as 15mg pharma.
Despite the dismissal of "feels", it became obvious after going back to 15mg pharma pens. While I was expecting a lessening of effect, it was so strong I ate too much for the dose, and ended up getting severe sides. The duration of appetite suppression was clearly longer than the QSC Tirz as well.
TLDR, I had a battery of tests done on that vial, which, despite a huge discount still cost $1400.
HPLC-MS showed this year old vial at ~96%+ "purity", but an NMR analysis, which I never heard of before, revealed two major problems.
One was that an expensive, hard to get ingredient in Tirz was substituted in the QSC Tirz for a cheap cosmetic ingredient, and the second was a "lipid linker" attached to the wrong part of the peptide. Doing it this way likely cut the time to manufacture the Tirz in half.
Neither is these is detectable by an HPLC-MS "purity" analysis, and among other (some potentially health harming) issues, can reduce potency and duration.
This might explain why batches of GLPs, rHGH, and other peptides can seemingly vary so much in potency despite appearing in HPLC-MS to have similar purity and dosing.
all international warehouse including "pharma grade and pct" international close till january?EU domestic stock is back.
All warehouses are operating except the international warehouse.
EU domestic stock is limited.
The international warehouse will open in January.
Thank you
I think 170$Anyone knows how much was his 310 hgh price ?
170$Anyone knows how much was his 310 hgh price ?
