| 词条 | 25C-NBOH |
| 释义 |
| Verifiedfields = | verifiedrevid = | IUPAC_name = 2-({[2-(4-chloro-2,5-dimethoxyphenyl)ethyl]amino}methyl)phenol | image = NBOH-2CC_structure.png | tradename = | CAS_number_Ref = | CAS_number = 1391488-16-6 | PubChem = | ChemSpiderID_Ref = | ChemSpiderID = 58191432 | C=17 | H=20 | Cl=1 | N=1 | O=3 | molecular_weight = 321.80 g/mol | smiles = COc1cc(Cl)c(OC)cc1CCNCc2ccccc2O | StdInChI_Ref = | StdInChI = 1S/C17H20ClNO3/c1-21-16-10-14(18)17(22-2)9-12(16)7-8-19-11-13-5-3-4-6-15(13)20/h3-6,9-10,19-20H,7-8,11H2,1-2H3 | StdInChIKey_Ref = | StdInChIKey = VHWXICYYQMMZCW-UHFFFAOYSA-N }}25-C-NBOH (2C-C-NBOH, NBOH-2CC) is a derivative of the phenethylamine derived hallucinogen 2C-C which has been sold as a designer drug. It has similar serotonin receptor affinity to the better-known compound 25C-NBOMe.[1][2] Analogues and derivatives{{2C-C analogues and derivatives}}LegalityUnited Kingdom{{N-benzylphenethylamine-Legality-United Kingdom}}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. ^Martin Hansen PhD. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain. University of Copenhagen, 2011. 4 : 25-NB (psychedelics)|Chloroarenes|Designer drugs|Serotonin receptor agonists |
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