KitchenChemist
Greenlighter
- Joined
- Apr 19, 2011
- Messages
- 18
I have long been a fan of Kratom - a tree of the Rubiaceae family of the scientific name Mitragyna speciosa. This tree contains the psychoactive alkaloid Mitragynine and 7-Hydroxymitragynine, which both funtion as powerful mu-Opioid receptor agonists.
Kratom reminds me of high dose hydrocodone or low - moderate dose oxycodone, as it is rather stimulatory, though, this may be due to other adrenergic alkaloids in the tree, rather than the principal opioid alkaloids.
The opioid alkaloids contained in Kratom are as follows:
Another synthetic anaolugue, known as 7-Acetoxymitragynine occurs as follows:
Both 7-Hydroxymitragynine and 7-Acetoxymitragynine seem to be much more potent than Mitragynine itself. However, I have known people who have obtained pure samples of both 7-Hydroxymitragynine and 7-Acetoxymitragynine from chemical suppliers, and state that they do not provide much of an IV rush, and are not much more actively intravenously rather than orally.
What I am wondering is if any of the advanced chemists here can shed any light on which chemical derivatives of these compounds may make it more IV active. I am also wondering if anyone knows of any other chemical substitutions of these compounds that may also be psychoactive, either orall, IM, or IV.
Paging seiko..
Hanks for any help that you can provide!
Kratom reminds me of high dose hydrocodone or low - moderate dose oxycodone, as it is rather stimulatory, though, this may be due to other adrenergic alkaloids in the tree, rather than the principal opioid alkaloids.
The opioid alkaloids contained in Kratom are as follows:


Another synthetic anaolugue, known as 7-Acetoxymitragynine occurs as follows:

Both 7-Hydroxymitragynine and 7-Acetoxymitragynine seem to be much more potent than Mitragynine itself. However, I have known people who have obtained pure samples of both 7-Hydroxymitragynine and 7-Acetoxymitragynine from chemical suppliers, and state that they do not provide much of an IV rush, and are not much more actively intravenously rather than orally.
What I am wondering is if any of the advanced chemists here can shed any light on which chemical derivatives of these compounds may make it more IV active. I am also wondering if anyone knows of any other chemical substitutions of these compounds that may also be psychoactive, either orall, IM, or IV.
Paging seiko..
Hanks for any help that you can provide!