sandiegopopla.blogg.se - Is a type of drug that induces a soothing

PMID 11888573.For ratings, users were asked how effective they found the medicine while considering positive/adverse effects and ease of use (1 = not effective, 10 = most effective).Īctivity is based on recent site visitor activity relative to other medications in the list. Neurochemical, therapeutic and adverse effects". Implications for the development of novel antidepressants with a short onset of action". "Effects of 5-HT-releasing agents on the extracellullar hippocampal 5-HT of rats.

Scorza C, Silveira R, Nichols DE, Reyes-Parada M (July 1999).

"The Effect of Selective Serotonin Releasing Agents in the Chronic Mild Stress Model of Depression in Rats".

Marona-Lewicka D, Nichols DE (December 1997).

Nichols DE, Marona-Lewicka D, Huang X, Johnson MP (1993).

N-Ethyl-5-trifluoromethyl-2-aminoindane (ETAI).

6,7-Methylenedioxy-N-methyl-2-aminotetralin (MDMAT).

6,7-Methylenedioxy-2-aminotetralin (MDAT).

5,6-Methylenedioxy- N-methyl-2-aminoindane (MDMAI).

5,6-Methylenedioxy-2-aminoindane (MDAI).

5-(2-Aminopropyl)-2,3-dihydrobenzofuran (5-APDB).

3,4-Ethylenedioxy- N-methylamphetamine (EDMA).

3-Methyl-4,5-methylenedioxyamphetamine (5-Methyl-MDA).

2-Methyl-3,4-methylenedioxyamphetamine (2-Methyl-MDA).

Carbamazepine (Equetro, Epitol, and many other variations).Levofenfluramine ( enantiomer of fenfluramine).Indeloxazine (Elen, Noin) (non-selective discontinued).Flucetorex (related to chlorphentermine never marketed).Etolorex ( prodrug of chlorphentermine never marketed).Dexfenfluramine (Redux) ( enantiomer of fenfluramine).

Cloforex (Oberex) ( prodrug of chlorphentermine).Chlorphentermine (Apsedon, Desopimon, Lucofen).Indeloxazine is an SRA and norepinephrine reuptake inhibitor that was formerly used as an antidepressant, nootropic, and neuroprotective. They have since been discontinued and are now encountered solely as recreational drugs. αET and αMT, also tryptamines, are SNDRAs and non-selective serotonin receptor agonists that were originally thought to be monoamine oxidase inhibitors and were formerly used as antidepressants. These drugs are serotonergic psychedelics, which is a consequence of their ability to activate the 5-HT 2A receptor. Many tryptamines, such as DMT, DET, DPT, DiPT, psilocin, and bufotenin, are SRAs as well as non-selective serotonin receptor agonists. The designer drug 4-methylaminorex, which is an SNDRA and 5-HT 2B agonist, has been reported to cause this effect as well. This side effect has been attributed to their additional action of potent agonism of the 5-HT 2B receptor. Fenfluramine, chlorphentermine, and aminorex, which are also amphetamines and relatives, were formerly used as appetite suppressants but were discontinued due to concerns of cardiac valvulopathy. They act as serotonin-norepinephrine-dopamine releasing agents (SNDRAs) and also agonize serotonin receptors such as those in the 5-HT 2 subfamily. Amphetamines like MDMA, MDEA, MDA, and MBDB, among other relatives (see MDxx), are recreational drugs termed entactogens.