RedLeader
Bluelight Crew
Just read up on rilmazafone and avizafone, being prodrugs of the benzodiazopine variety. At first, it was in attempt to make a complete list of water-soluable (i.e. injectable) benzos, and through such I came across these.
Seeing as they are metabolized into active benzos once in the body, but don't cause any direct effect on benzo receptors (from Wiki on the former):
I wonder how this would affect physical addiction. I cannot really seem to find any literature on this - how a benzodiazopine prodrug would contrast with more typical benzos when it comes to a tolerance and withdrawal symptoms. It's mainly curiosity, but has anybody ever looked into these drugs before, or prodrugs of the benzo variety in research? Or sampled?
I understand that fosazepam was engineered to be a (good) water-soluble derivative of diazepam, but why the need for a pro-diazepam as well? If it has nothing to do with dependency, why would such be administered as compared to alternatives?
Seeing as they are metabolized into active benzos once in the body, but don't cause any direct effect on benzo receptors (from Wiki on the former):
SourceRilmazafone has no effects on benzodiazepine receptors itself, but once inside the body is metabolised by aminopeptidase enzymes in the small intestine to form the active benzodiazepine 8-chloro-6-(2-chlorophenyl)-N,N-dimethyl-4H-1,2,4-triazolo [1,5-a] [1,4]benzodiazepine-2-carboxamide.
I wonder how this would affect physical addiction. I cannot really seem to find any literature on this - how a benzodiazopine prodrug would contrast with more typical benzos when it comes to a tolerance and withdrawal symptoms. It's mainly curiosity, but has anybody ever looked into these drugs before, or prodrugs of the benzo variety in research? Or sampled?
I understand that fosazepam was engineered to be a (good) water-soluble derivative of diazepam, but why the need for a pro-diazepam as well? If it has nothing to do with dependency, why would such be administered as compared to alternatives?
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