5-htp Mdai

The chemical structure of the MDAI is illicit drug MDA, but group chain alpha-methyl amphetamine page to the benzene nucleus forced an Indane ring system, substantially modify its properties pharmacological indirectly derived amino alkyl. MDAI can occur 3-(4-3, Metilendioxifenil) propionic acid. in chloride acid converted and then heated to 5, to produce 6-Metilendiossi-1 - Indanone. Treatment of Amyl nitrite with Indanone in methanol with permitted HC1 Hydroxyimino ketone. It is reduced to 2-aminoindan, after a previous Nichols edition discussed a DOM method, a similar role. Family drug MDMA produced in the body and therefore its effects through multiple mechanisms of action of three different characters who are trained animals, usually respond: marked a signal with stimulants such as methamphetamine, a bunch of hallucinogenic drugs such as LSD and DOM and an Empatogeno signal, caused by medications such as MDAI and MBDB. These drugs cause reactions in animals, appropriate drugs that is trained to detect the effects of MDMA, but no responses in animals, produce the targeted to treat stimulants or hallucinogens trained. Because of serotonin in the brains of the release, but have little effect on levels of dopamine or noradrenaline have these connections, produce Empathogenic effects but without stimulating, 5-htp mdai rather a little sedative action. Atypische Antipsychotika (p). EJ. (, Amperozide, Aripiprazole, Asenapina, Carpipramine, Clocapramine, Blonanserin, Clorotepine, Clozapina, Fluperlapine, Gevotroline, Melperon, Iloperidone, Mosapramine, Olanzapina, palipéridone, Risperidone, Quetiapina, Sertindolo, Zicronapine, Ziprasidone, Zotepin). . . . . .