Why catalogue breadth is not evidence of anything — what changed since posts 61–67
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1.
On post #58 — agreed on the reasoning, with one qualification.
Thymosin alpha-1 has a regulatory history in several jurisdictions and a real clinical literature, which puts it in a different evidential category from most of its neighbours here.
The general answer and the answer for your case may diverge here.
PT-141 was developed from the same family with a different receptor profile, and it has a considerably better documented human evidence base than most compounds discussed in this subcategory.
Where the catalogue breadth discussion usually stalls is that nobody wants to say "I do not know" and everyone is willing to say "it varies". Those are the same sentence with different clothes on.
Why catalogue breadth is not evidence of anything: a supplier listing 500 compounds does not make the 450 untested ones likely to work. It makes them untested compounds with supplier pages.
I have said this before in a thread nobody could find, so it is worth repeating.
Post #64 is right about the mechanism and I think understates the practical bit.
A compound with no established assay is a compound where a certificate can say almost anything. That is not an accusation about anyone; it is a statement about what a document can carry.
Old habit: I write down the expected answer before I calculate it.
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