Phendimetrazine

Fazidinium bromide Fenoterol hydrobromide Folic acid Halothane Ifenprodil tartrate Ketamine HCI Mema ntine Metaproterenol Norfenefrine Oxaflozane HCI Phendimetrazine tartrate Phentermine HCI Procarbazine HCI Promegestone Pyrovalerone HCI Sulfacytine Sulfalene Trioxsalen N-8romoacetamide Fluazacort... 

C17H21NO2 60725-36-2) see Nefopam a-[/V-(2-hydroxyethyl)methylamino]propiophenone (C 2H,7N02) see Phendimetrazine l-(2-hydroxyethyl)-4-(2-methylbenzyl)piperazine (C13H20N2O 40004-66-8) see Chlorbenzoxamine [2K-[2a(7f )3P(7t )]]-3-(l-hydroxyethyl)-Y-methyl-p,4-di-oxo-2-azetidinebutanoic acid (4-nitropheiiyl)methyl ester (C,7H2oN207 90822-23-4) see Meropenem... 

CjH,NO I09-8J-I) see Cafaminol Mianserin Nefopam Phendimetrazine Rosiglitazone Tofenacin Xantinol nicolinate... 

Ci)H f 0 93-55-0) see Amfeprainone Dextropropoxyphene Eprazinone Mephenytoin Phendimetrazine Phenmetrazine Phenylpropanolamine Tamoxifen... 

Chemical Structures. Figure 1 shows the chemical structures for 14 phenylethylamine compounds. Nine of these compounds are used clinically as anorectics (ii-amphetamine, phentermine, diethylpropion, phenmetrazine, phendimetrazine, clotermine, chlorphentermine, benzphetamine, and fenfluramine). Four of these compounds are not approved for clinical use and are reported to have hallucinogenic properties (MDA, PMA, DOM, and DOET). The final compound ( /-ephedrine) is used clinically for bronchial muscle relaxation, cardiovascular, and mydriatic effects. Figure 2 shows the chemical structure for MDMA, the methyl analog of MDA. MDMA is not approved for clinical use and has been reported to produce both LSD-like and cocaine-like effects. 

Figure 3 presents the mean levels of self-infusion for the 14 phenylethyl-amines shown in figure 1. Of all the drugs tested, injection rates were... 

Phendimetrazine (Prelu2, Bontril, Plegine) Short-term use 70-105... 

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