5-氟二甲基色胺

**5-氟二甲基色胺**
识别信息
	IUPAC命名法 2-(5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine; ;
CAS号	22120-36-1
PubChem CID	2762738;
ChemSpider	2043436 ;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID30376407 ;
化学信息
化学式	C12H15FN2
摩尔质量	206.26 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
	SMILES CN(C)CCC1=CNC2=C1C=C(C=C2)F;
	InChI InChI=1S/C12H15FN2/c1-15(2)6-5-9-8-14-12-4-3-10(13)7-11(9)12/h3-4,7-8,14H,5-6H2,1-2H3 ; Key:BXYDWQABVPBLBU-UHFFFAOYSA-N ;

5-氟-N,N-二甲基色胺（英語：5-Fluoro-N,N-dimethyltryptamine，简称5-fluoro-DMT，5-氟二甲基色胺）是一种色胺衍生物，类似于5-溴二甲基色胺和5-甲氧基二甲基色胺。二甲基色胺的氟取代对其与5-HT_2A/C受体的亲和性影响不大，但6-氟二乙基色胺对5-HT_2A受体的激动性几乎无效，而4-氟-5-甲基二甲基色胺却是5-HT_1A受体的强激动剂^[1]^[2]。

参考文献[编辑]

^ Blair, JB; Kurrasch-Orbaugh, D; Marona-Lewicka, D; Cumbay, MG; Watts, VJ; Barker, EL; Nichols, DE. Effect of ring fluorination on the pharmacology of hallucinogenic tryptamines. Journal of Medicinal Chemistry. 2000, 43 (24): 4701–10. PMID 11101361. doi:10.1021/jm000339w.
^ Rabin, RA; Regina, M; Doat, M; Winter, JC. 5-HT2A receptor-stimulated phosphoinositide hydrolysis in the stimulus effects of hallucinogens. Pharmacology, Biochemistry, and Behavior. 2002, 72 (1–2): 29–37. PMID 11900766. doi:10.1016/S0091-3057(01)00720-1.

外部链接[编辑]

6-Fluoro-DET（页面存档备份，存于互联网档案馆）

[1] Blair, JB; Kurrasch-Orbaugh, D; Marona-Lewicka, D; Cumbay, MG; Watts, VJ; Barker, EL; Nichols, DE. Effect of ring fluorination on the pharmacology of hallucinogenic tryptamines. Journal of Medicinal Chemistry. 2000, 43 (24): 4701–10. PMID 11101361. doi:10.1021/jm000339w.

[2] Rabin, RA; Regina, M; Doat, M; Winter, JC. 5-HT2A receptor-stimulated phosphoinositide hydrolysis in the stimulus effects of hallucinogens. Pharmacology, Biochemistry, and Behavior. 2002, 72 (1–2): 29–37. PMID 11900766. doi:10.1016/S0091-3057(01)00720-1.

[1]

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