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维基百科

25D-NBOMe

25D-NBOMe是一种含氮有机化合物,化学式为C19H25NO3,属于苯乙胺致幻剂2C-D衍生物(N-邻甲氧基苄基2C-D,缩写NBOMe-2C-D),可作为血清素受体5HT2A激动剂[2][3]

25D-NBOMe
法律規範狀態
法律規範
  • NpSG
  • Class A
  • Illegal in China and Sweden
识别信息
  • 2-(2,5-dimethoxy-4-methylphenyl)-N-(2-methoxybenzyl)ethanamine
CAS号1354632-02-2
PubChem CID
  • 118536027
ChemSpider
  • 48059920 Y
UNII
  • 7RET11HE13
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
  • DTXSID601014189
化学信息
化学式C19H25NO3
摩尔质量315.41 g·mol−1
3D模型(JSmol英语JSmol
  • 交互式图像
  • COC1=C(C=C(C(=C1)C)OC)CCNCC2=C(C=CC=C2)OC
  • InChI=1S/C19H25NO3/c1-14-11-19(23-4)15(12-18(14)22-3)9-10-20-13-16-7-5-6-8-17(16)21-2/h5-8,11-12,20H,9-10,13H2,1-4H3 Y
  • Key:UTVHBNXCFSATDB-UHFFFAOYSA-N Y

参考文献 编辑

  1. ^ Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control]. Diário Oficial da União. 2023-07-24 (2023-07-25) [2023-08-27]. (原始内容于2023-08-27) (巴西葡萄牙语). 
  2. ^ Hansen M, Phonekeo K, Paine JS, Leth-Petersen S, Begtrup M, Bräuner-Osborne H, Kristensen JL. Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists. ACS Chemical Neuroscience. March 2014, 5 (3): 243–9. PMC 3963123 . PMID 24397362. doi:10.1021/cn400216u. 
  3. ^ Hansen M. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain. (Ph.D.论文). University of Copenhagen. 2010-12-16. doi:10.13140/RG.2.2.33671.14245. 

外部链接 编辑

Template:Navbox with collapsible groups

nbome, 是一种含氮有机化合物, 化学式为c19h25no3, 属于苯乙胺类致幻剂2c, d的衍生物, 邻甲氧基苄基2c, 缩写nbome, 可作为血清素受体5ht2a的激动剂, 法律規範狀態法律規範德, npsg, class, illegal, china, sweden识别信息iupac命名法, dimethoxy, methylphenyl, methoxybenzyl, ethanaminecas号1354632, 2pubchem, cid118536027chemspider48059920, y. 25D NBOMe是一种含氮有机化合物 化学式为C19H25NO3 属于苯乙胺类致幻剂2C D的衍生物 N 邻甲氧基苄基2C D 缩写NBOMe 2C D 可作为血清素受体5HT2A的激动剂 2 3 25D NBOMe法律規範狀態法律規範德 NpSG 英 Class A Illegal in China and Sweden识别信息IUPAC命名法 2 2 5 dimethoxy 4 methylphenyl N 2 methoxybenzyl ethanamineCAS号1354632 02 2PubChem CID118536027ChemSpider48059920 YUNII7RET11HE13CompTox Dashboard 英语 CompTox Chemicals Dashboard EPA DTXSID601014189化学信息化学式C 19H 25N O 3摩尔质量315 41 g mol 13D模型 JSmol 英语 JSmol 交互式图像SMILES COC1 C C C C C1 C OC CCNCC2 C C CC C2 OCInChI InChI 1S C19H25NO3 c1 14 11 19 23 4 15 12 18 14 22 3 9 10 20 13 16 7 5 6 8 17 16 21 2 h5 8 11 12 20H 9 10 13H2 1 4H3 YKey UTVHBNXCFSATDB UHFFFAOYSA N Y参考文献 编辑 Anvisa RDC Nº 804 Listas de Substancias Entorpecentes Psicotropicas Precursoras e Outras sob Controle Especial Collegiate Board Resolution No 804 Lists of Narcotic Psychotropic Precursor and Other Substances under Special Control Diario Oficial da Uniao 2023 07 24 2023 07 25 2023 08 27 原始内容存档于2023 08 27 巴西葡萄牙语 请检查 publication date 中的日期值 帮助 Hansen M Phonekeo K Paine JS Leth Petersen S Begtrup M Brauner Osborne H Kristensen JL Synthesis and structure activity relationships of N benzyl phenethylamines as 5 HT2A 2C agonists ACS Chemical Neuroscience March 2014 5 3 243 9 PMC 3963123 nbsp PMID 24397362 doi 10 1021 cn400216u Hansen M Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain Ph D 论文 University of Copenhagen 2010 12 16 doi 10 13140 RG 2 2 33671 14245 外部链接 编辑Template Navbox with collapsible groups 取自 https zh wikipedia org w index php title 25D NBOMe amp oldid 79809989, 维基百科,wiki,书籍,书籍,图书馆,

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