5-AcO-DMT

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] acetate; ;
CAS号	16977-50-7
PubChem CID	15480709;
ChemSpider	23194786;
ChEMBL	ChEMBL111000;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID701345666 ;
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;
	SMILES CC(=O)OC1=CC2=C(C=C1)NC=C2CCN(C)C;
	InChI 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]

参考文献

^ 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.

外部链接

[1] Shulgin & Shulgin. TiHKAL #19. 5-HO-DMT. [2023-11-03]. （原始内容存档于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.

[pmid21624387-3] 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.

[1]

[2]

[3]