This is intended as a suggestion for investigating hydroxytryptamine potential releasing agents.
I list molecules, which are considered being neither reuptake transporter inhibitors, nor reuptake transporter inverters.
The recursive correspondence between their chemical terminations and their clinical pharmacology is impressive: any carboxyl-R-amine or carboxamide (acetamide) seem behaving in similar way! The model may be possibly generalized comparing the behaviour of any primary amine?
I tried closing my eyes, but the reality made me keep them wide open again...
This is just a sample:
http://www.ncbi.nlm.nih.gov/pubmed/9776325 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1572811/ http://www.ncbi.nlm.nih.gov/pubmed/22735246
http://www.ncbi.nlm.nih.gov/pubmed/21414089
The FDA provides with warnings (about effects which may be explained with a serotonin release model together with ion channels block): http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm100190.htm
I hope someone has the resources to do a systemic linking to the scientific publications; there is already laboratory documentation available.
carboxyl-R-amines
- glycine methionine serine and probably most of the biogenic amino acids or primary amines
- baclofen gabapentin phenibut pregabalin vigabatrin
- procaine procainamide
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carboxamides
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