| 词条 | 2C-B-BUTTERFLY |
| 释义 |
| IUPAC_name = 2-(10-Bromo-2,3,4,7,8,9-hexahydropyrano[2,3-g]chromen-5-yl)ethan-1-amine | image = 2CB-BUTTERFLY_structure.png | tradename = | legal_status = | routes_of_administration = | CAS_number_Ref = {{cascite|changed|??}} | CAS_number = 502659-24-7 | ATC_prefix = none | PubChem = 10244981 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 8420468 | C=14 | H=18 | Br=1 | N=1 | O=2 | molecular_weight = 312.202 g/mol | smiles = O3CCCc1c3c(Br)c2CCCOc2c1CCN | StdInChI = 1S/C14H18BrNO2/c15-12-11-4-2-7-17-13(11)10(5-6-16)9-3-1-8-18-14(9)12/h1-8,16H2 | StdInChIKey = PAFZDNLBBBZEKE-UHFFFAOYSA-N }}2C-B-BUTTERFLY is a conformationally-restricted derivative of the phenethylamine hallucinogen 2C-B, which was discovered in 1999 by Michael S. Whiteside and Aaron Monte.[1] It is a ring-expanded homologue of the better known compound 2C-B-FLY, and has similar properties as an agonist for serotonin receptors, but with more selectivity for 5-HT2C over 5-HT2A.[2][3] Analogues and derivatives{{2C-B analogues and derivatives}}Legal Status2C-B-BUTTERFLY is illegal in Latvia.[4] See also
References1. ^Whiteside, MS. Synthesis of hexahydrobenzodipyrans as ring-expanded analogues of potent serotonin 5-HT2A/2C receptor probes. UW-LaCrosseJUR, 1999; 2: 61–68. {{Serotonergics}}{{Phenethylamines}}{{Hallucinogens}}{{hallucinogen-stub}}2. ^Whiteside MS, Kurrasch-Orbaugh D, Marona-Lewicka D, Nichols DE, Monte A. Substituted hexahydrobenzodipyrans as 5-HT2A/2C receptor probes. Bioorg. Med. Chem 2002; 10(10): 3301–3306. doi: 10.1016/S0968-0896(02)00209-2 3. ^Schultz DM, Prescher JA, Kidd, S; Marona-Lewicka, D; Nichols, DE; Monte, A. ‘Hybrid’ benzofuran–benzopyran congeners as rigid analogs of hallucinogenic phenethylamines. Bioorg. Med. Chem 2008; 16(11): 6242–6251. doi: 10.1016/j.bmc.2008.04.030 4. ^Noteikumi par Latvijā kontrolējamajām narkotiskajām vielām, psihotropajām vielām un prekursoriem 3 : Bromoarenes|2C (psychedelics)|Serotonin receptor agonists |
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