| 词条 | 25CN-NBOMe |
| 释义 |
| IUPAC_name = 2,5-Dimethoxy-4-(2-(2-methoxybenzylamino)ethyl)benzonitrile | image = 25CN-NBOMe.svg | width = 200 | tradename = | CAS_number = 1354632-16-8 | PubChem = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 58191430 | C=19 | H=22 | N=2 | O=3 | molecular_weight = 326.39 g/mol | smiles = N#CC1=CC(OC)=C(CCNCC2=C(OC)C=CC=C2)C=C1OC | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C19H22N2O3/c1-22-17-7-5-4-6-15(17)13-21-9-8-14-10-19(24-3)16(12-20)11-18(14)23-2/h4-7,10-11,21H,8-9,13H2,1-3H3 | StdInChIKey = QBJWOIWLBRLGKZ-UHFFFAOYSA-N | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} }}25CN-NBOMe (2C-CN-NBOMe, NBOMe-2C-CN) is a derivative of the phenethylamine 2C-CN. It acts in a similar manner to related compounds such as 25I-NBOMe, which are potent agonists at the 5HT2A receptor.[1][2] LegalityUnited Kingdom{{N-benzylphenethylamine-Legality-United Kingdom}}See also
References1. ^{{Cite journal | last1 = Hansen | first1 = M. | last2 = Phonekeo | first2 = K. | last3 = Paine | first3 = J. S. | last4 = Leth-Petersen | first4 = S. | last5 = Begtrup | first5 = M. | last6 = Bräuner-Osborne | first6 = H. | last7 = Kristensen | first7 = J. L. | doi = 10.1021/cn400216u | title = Synthesis and Structure-Activity Relationships of N-Benzyl Phenethylamines as 5-HT2A/2C Agonists | journal = ACS Chemical Neuroscience | volume = 5 | issue = 3 | pages = 243–9 | year = 2014 | pmid = 24397362| pmc = 3963123}} {{Hallucinogens}}{{Serotonin receptor modulators}}{{Phenethylamines}}{{hallucinogen-stub}}2. ^Hansen, M. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain. PhD Thesis, University of Copenhagen, 2011. 1 : 25-NB (psychedelics) |
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