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2-Bromodeschloroketamine, 2-BDCK, Bromoketamine, 2-Bromoketamine 2-Fluorodeschloroketamine, 2-FDCK, [11] Fluoroketamine, 2-Fluoroketamine 3-Fluorodeschloroketamine, 3-FDCK, FXM, 3-Fluoroketamine 2'-Oxo-PCE, Eticyclidinone, O-PCE, Deschloroethylnorketamine, 2-DCNEK 2'-Oxo-3-F-PCE, Fluoroeticyclidinone, Fluorxetamine 2'-Oxo-3-Me-PCE, Deoxymethoxetamine, DMXE 2-Trifluoromethyldeschloroketamine, 2-TFMDCK 3-Cl-PCP 3-F-PCP 3-HO-PCE, Hydroxyeticyclidine [12] 3-HO-PCP 3-Me-PCE 3-Me-PCP 3-Me-PCPy, 3-Methylrolicyclidine 3-MeO-PCE 3-MeO-PCMo 3-MeO-PCP 4-MeO-PCP, Methoxydine Deschloroketamine, 2'-Oxo-PCM, 2-DCK, DCK, O-PCM Eticyclidine, PCE, CI-400 Methoxetamine, MXE, 3-MeO-2'-Oxo-PCE Methoxmetamine, MXM, MMXE, 3-MeO-2'-Oxo-PCM, E-MXE Methoxpropamine, MXPr, 3-MeO-2'-Oxo-PCPr Methoxisopropamine, MXiPR, Isopropyloxetamine Methoxyketamine, 2-MeO-2-Deschloroketamine, 2-MeO-Ketamine N-Ethylnorketamine, NENK, N-Ethylketamine 1,2-Diarylethylamines [edit] 1,2-Diarylethylamines began to appear on grey markets only as recently as 2013
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Potential BPC-157 analog strategies include D-amino acid substitution at protease-sensitive positions, N-methylation of backbone amides to resist enzymatic cleavage, and cyclization to reduce conformational flexibility and proteolytic exposure
