haribo1
Ex-Bluelighter
- Joined
- Nov 29, 2006
- Messages
- 4,822
Although there are quite a few benzomorphans tested, to my knowledge only 4 have ever reached the market. Those are matazocine, phenazocine, pentazocine and dezocine. The skeleton has some interesting features. I cannot find an instance of a pure antagonist for starters; Pentazocine is a mixed agonist/antagonist.
What makes it interesting to me is that the X & Y substituants above can be tweeked to increase potency and agonist/antagonist ration treeked. All potencies are relative to morphine.
X
--
-Methyl is RP = 0.4
-Phenylethyl = 4
-2Thienylethyl = 16
Y
--
-OH = 1.0
-NO2 = 10
So, this very scruffy research reveals that the optimal N-substituant is 2 thienyl ethyl and the optimal substituant on the benzene ring is a nitro. This compound IS 160x morphine putting it in the class with fentanyl and such. I should add that adding a NO2 to the phenanthracine opioids (like morphine itself) doesn't increase activitity, but it IS still active.
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