| 词条 | 2-Benzylpiperidine |
| 释义 |
| verifiedrevid = 442227725 | IUPAC_name = 2-benzylpiperidine | image = 2-Benzylpiperidine.png | image2 = 2-benzylpiperidine3d.png | tradename = | pregnancy_category = | legal_status = Uncontrolled | routes_of_administration = Oral | bioavailability = | metabolism = | elimination_half-life = | excretion = | CAS_number = 32838-55-4 | ATC_prefix = none | ATC_suffix = | PubChem = 118004 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 105447 | C=12 | H=17 | N=1 | molecular_weight = 175.27 g/mol | smiles = C1CCNC(C1)CC2=CC=CC=C2 | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C12H17N/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12/h1-3,6-7,12-13H,4-5,8-10H2 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = ITXCORRITGNIHP-UHFFFAOYSA-N }}2-Benzylpiperidine is a stimulant drug of the piperidine class. It is similar in structure to other drugs such as methylphenidate and desoxypipradrol but around one twentieth as potent, and while it boosts norepinephrine levels to around the same extent as d-amphetamine,[1] it has very little effect on dopamine levels, with its binding affinity for the dopamine transporter around 175 times lower than for the noradrenaline transporter.[2] 2-benzylpiperidine is little used as a stimulant, with its main use being as a synthetic intermediate in the manufacture of other drugs.[3][4][5] See also
References1. ^{{cite journal | last1 = Ferris | first1 = RM | last2 = Tang | first2 = FL | title = Comparison of the effects of the isomers of amphetamine, methylphenidate and deoxypipradrol on the uptake of l-3Hnorepinephrine and 3Hdopamine by synaptic vesicles from rat whole brain, striatum and hypothalamus | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 210 | issue = 3 | pages = 422–8 | year = 1979 | pmid = 39160 }} {{Stimulants}}{{Monoamine releasing agents}}{{DEFAULTSORT:Benzylpiperidine, 2-}}2. ^{{cite journal | last1 = Kim | first1 = DI | last2 = Deutsch | first2 = HM | last3 = Ye | first3 = X | last4 = Schweri | first4 = MM | title = Synthesis and pharmacology of site-specific cocaine abuse treatment agents: restricted rotation analogues of methylphenidate | journal = Journal of Medicinal Chemistry | volume = 50 | issue = 11 | pages = 2718–31 | year = 2007 | pmid = 17489581 | doi = 10.1021/jm061354p }} 3. ^{{cite journal | last1 = Ablordeppey | first1 = SY | last2 = Fischer | first2 = JB | last3 = Law | first3 = H | last4 = Glennon | first4 = RA | title = Probing the proposed phenyl-A region of the sigma-1 receptor | journal = Bioorganic & Medicinal Chemistry | volume = 10 | issue = 8 | pages = 2759–65 | year = 2002 | pmid = 12057665 | doi=10.1016/S0968-0896(02)00096-2}} 4. ^Ágai B, Proszenyák A, Tárkányi G, Vida L, Faigl F. Convenient, Benign and Scalable Synthesis of 2- and 4-Substituted Benzylpiperidines. European Journal of Organic Chemistry 2004; 17:3623-3632. {{doi|10.1002/ejoc.200400215}} 5. ^Christopher F. Bigge, John F. W. Keana, Sui Xiong Cai, Eckard Weber, Richard Woodward, Nancy C. Lan, Anthony P. Guzikowski. 2-substituted piperidine analogs and their use as subtype-selective NMDA receptor antagonists. US Patent 6124317 2 : Stimulants|Piperidines |
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