O -Acetylbufotenine临床资料 其他名称 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 ChemSpider ChEMBL 化学信息 化学式 C 14 H 18 N 2 O 2 摩尔质量 246.31 g·mol−1 3D模型(JSmol )
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
5-AcO-DMT (5-乙酰氧基-N ,N -二甲基色胺 ,英语: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C14 H18 N2 O2 ,可通过血脑屏障 ,并代谢为蟾毒色胺 。[1] [2] [3]
参考文献 [ 编辑 ]
^ Shulgin & 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 . PMID 21624387 . doi:10.1016/j.pbb.2011.05.015 .
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