>>12452237Go to genetic database.
Look for dehydroxylaze enzyme.
If it's there, it is atleast partly.
Then you can look at psylocin metabolism in scientific directory ( pubmed ).
If it's not there look back and read this:
It's possible that it's not metabolized, benzene rings won't deconstruct it's stable, therefore probably goes fast. Therefore it starts decomposing somewhere where nitrogen is, maybe even both. I don't know enzymes very much.
You can study it by sending sample of your urine to analysis, and want to know if it's there without methanol, or ethylated or with split those parts inthere.
They can do it by GSMC. Or just ask at some company that does metabolic analysis how it will decompose.
But carbon oxide is stronger than oxid carbon, because nitrogen is more (not likely, but able, and totally not probable) able to push electron away, therefore this bound is higher volatility and having more distance and less energy invested in them. In HO-Psylocin bond, more energy is invested than in nitrogen.
