5-MeO-NiPT

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5-MeO-NiPT
File:5-MeO-NIPT.svg
臨床資料
其他名稱5-Methoxy-N-isopropyltryptamine
藥物類別Serotonin receptor agonist; Serotonergic psychedelic; Hallucinogen
識別資訊
  • N-[2-(5-methoxy-1H-indol-3-yl)ethyl]propan-2-amine
CAS號109921-55-3
PubChem CID
ChemSpider
UNII
化學資訊
化學式C14H20N2O
摩爾質量232.33 g·mol−1
3D模型(JSmol
  • COc1ccc2c(c1)c(CCNC(C)C)c[nH]2
  • InChI=1S/C14H20N2O/c1-10(2)15-7-6-11-9-16-14-5-4-12(17-3)8-13(11)14/h4-5,8-10,15-16H,6-7H2,1-3H3
  • Key:QQZJNZJNPDORBO-UHFFFAOYSA-N

5-MeO-NiPT,化學名5-甲氧基-N-異丙基色胺(英語:5-methoxy-N-isopropyltryptamine)是一種含氮有機化合物,化學式C
14
H
20
N
2
O
,屬於色胺衍生物[1][2][3],是5-MeO-MiPT(5-甲氧基-N-甲基-N-異丙基色胺)、5-MeO-DiPT(5-甲氧基-N,N-二異丙基色胺)在體內的活性代謝產物[1][4]

參考文獻[編輯]

  1. ^ 1.0 1.1 Glatfelter GC, Clark AA, Cavalco NG, Landavazo A, Partilla JS, Naeem M, Golen JA, Chadeayne AR, Manke DR, Blough BE, McCorvy JD, Baumann MH. Serotonin 1A Receptors Modulate Serotonin 2A Receptor-Mediated Behavioral Effects of 5-Methoxy-N,N-dimethyltryptamine Analogs in Mice. ACS Chem Neurosci. December 2024, 15 (24): 4458–4477. PMID 39636099. doi:10.1021/acschemneuro.4c00513. 
  2. ^ Puigseslloses P, Nadal-Gratacós N, Ketsela G, Weiss N, Berzosa X, Estrada-Tejedor R, Islam MN, Holy M, Niello M, Pubill D, Camarasa J, Escubedo E, Sitte HH, López-Arnau R. Structure-activity relationships of serotonergic 5-MeO-DMT derivatives: insights into psychoactive and thermoregulatory properties. Mol Psychiatry. August 2024, 29 (8): 2346–2358. PMC 11412900可免費查閱. PMID 38486047. doi:10.1038/s41380-024-02506-8. 
  3. ^ Blough BE, Landavazo A, Decker AM, Partilla JS, Baumann MH, Rothman RB. Interaction of psychoactive tryptamines with biogenic amine transporters and serotonin receptor subtypes. Psychopharmacology (Berl). October 2014, 231 (21): 4135–4144. PMC 4194234可免費查閱. PMID 24800892. doi:10.1007/s00213-014-3557-7. 
  4. ^ Araújo AM, Carvalho F, Bastos ML, Guedes de Pinho P, Carvalho M. The hallucinogenic world of tryptamines: an updated review (PDF). Archives of Toxicology. 2015, 89 (8): 1151–1173. Bibcode:2015ArTox..89.1151A. ISSN 0340-5761. PMID 25877327. doi:10.1007/s00204-015-1513-x.