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维基百科

5-AcO-DMT

5-AcO-DMT5-乙酰氧基-N,N-二甲基色胺,英語:5-acetoxy-N,N-dimethyltryptamine 或称为:O-乙酰基蟾毒色胺,O-Acetylbufotenine,5-acetoxy-DMT,bufotenine acetate)是一种色胺衍生物,化学式为C14H18N2O2,可通过血脑屏障,并代谢为蟾毒色胺[1][2][3]

O-Acetylbufotenine
臨床資料
其他名稱3-(2-(dimethylamino)ethyl)-1H-indol-5-yl acetate; 5-Acetoxy-DMT; 5-Acetoxy-N,N-dimethyltryptamine; 5-AcO-DMT; 3-(2-(Dimethylamino)ethyl]-1H-indol-5-yl acetate
识别信息
  • [3-[2-(dimethylamino)ethyl]-1H-indol-5-yl] acetate
CAS号16977-50-7  Y
PubChem CID
  • 15480709
ChemSpider
  • 23194786
ChEMBL
  • ChEMBL111000
化学信息
化学式C14H18N2O2
摩尔质量246.31 g·mol−1
3D模型(JSmol英语JSmol
  • 交互式图像
  • CC(=O)OC1=CC2=C(C=C1)NC=C2CCN(C)C
  • InChI=1S/C14H18N2O2/c1-10(17)18-12-4-5-14-13(8-12)11(9-15-14)6-7-16(2)3/h4-5,8-9,15H,6-7H2,1-3H3
  • Key:BZFGYTBVFYYKOK-UHFFFAOYSA-N

参考文献 编辑

  1. ^ Shulgin & Shulgin. TiHKAL #19. 5-HO-DMT. [2023-11-03]. (原始内容于2023-11-03). 
  2. ^ Gessner PK, Dankova JB. Brain Bufotenine from Administered Acetylbufotenine: Comparison of Its Tremorgenic Activity with That of N,N-Dimethyltryptamine and 5-Methoxy-N,N-Dimethyltryptamine.. Pharmacologist. January 1975, 17 (2): 259. 
  3. ^ Winter JC, Amorosi DJ, Rice KC, Cheng K, Yu AM. Stimulus control by 5-methoxy-N,N-dimethyltryptamine in wild-type and CYP2D6-humanized mice. Pharmacology, Biochemistry, and Behavior. September 2011, 99 (3): 311–5. PMC 3129464 . PMID 21624387. doi:10.1016/j.pbb.2011.05.015. 

外部链接 编辑

乙酰氧基, 二甲基色胺, 英語, acetoxy, dimethyltryptamine, 或称为, 乙酰基蟾毒色胺, acetylbufotenine, acetoxy, bufotenine, acetate, 是一种色胺衍生物, 化学式为c14h18n2o2, 可通过血脑屏障, 并代谢为蟾毒色胺, acetylbufotenine臨床資料其他名稱3, dimethylamino, ethyl, indol, acetate, acetoxy, acetoxy, dimethyltryptamine, dime. 5 AcO DMT 5 乙酰氧基 N N 二甲基色胺 英語 5 acetoxy N N dimethyltryptamine 或称为 O 乙酰基蟾毒色胺 O Acetylbufotenine 5 acetoxy DMT bufotenine acetate 是一种色胺衍生物 化学式为C14H18N2O2 可通过血脑屏障 并代谢为蟾毒色胺 1 2 3 O Acetylbufotenine臨床資料其他名稱3 2 dimethylamino ethyl 1H indol 5 yl acetate 5 Acetoxy DMT 5 Acetoxy N N dimethyltryptamine 5 AcO DMT 3 2 Dimethylamino ethyl 1H indol 5 yl acetate识别信息IUPAC命名法 3 2 dimethylamino ethyl 1H indol 5 yl acetateCAS号16977 50 7 YPubChem CID15480709ChemSpider23194786ChEMBLChEMBL111000化学信息化学式C 14H 18N 2O 2摩尔质量246 31 g mol 13D模型 JSmol 英语 JSmol 交互式图像SMILES CC O OC1 CC2 C C C1 NC C2CCN C CInChI InChI 1S C14H18N2O2 c1 10 17 18 12 4 5 14 13 8 12 11 9 15 14 6 7 16 2 3 h4 5 8 9 15H 6 7H2 1 3H3Key BZFGYTBVFYYKOK UHFFFAOYSA N参考文献 编辑 Shulgin amp Shulgin TiHKAL 19 5 HO DMT 2023 11 03 原始内容存档于2023 11 03 Gessner PK Dankova JB Brain Bufotenine from Administered Acetylbufotenine Comparison of Its Tremorgenic Activity with That of N N Dimethyltryptamine and 5 Methoxy N N Dimethyltryptamine Pharmacologist January 1975 17 2 259 Winter JC Amorosi DJ Rice KC Cheng K Yu AM Stimulus control by 5 methoxy N N dimethyltryptamine in wild type and CYP2D6 humanized mice Pharmacology Biochemistry and Behavior September 2011 99 3 311 5 PMC 3129464 nbsp PMID 21624387 doi 10 1016 j pbb 2011 05 015 外部链接 编辑 取自 https zh wikipedia org w index php title 5 AcO DMT amp oldid 79677978, 维基百科,wiki,书籍,书籍,图书馆,

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