Triptamina (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Triptamina" in Indonesian language version.

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  • Shulgin A (1997). Tihkal: The Continuation. Transform Press. #53. T. ISBN 978-0-9630096-9-2. Diakses tanggal 17 Agustus 2024. (with 250 mg, intravenously) "Tryptamine was infused intravenously over a period of up to 7.5 minutes. Physical changes included an increases in blood pressure, in the amplitude of the patellar reflex, and in pupillary diameter. The subjective changes are not unlike those seen with small doses of LSD. A point-by-point comparison between the tryptamine and LSD syndromes reveals a close similarity which is consistent with the hypothesis that tryptamine and LSD have a common mode of action."{{cite book}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)
  • Kametani T, Takano S, Hibino S, Takeshita M (1972). "Studies on the Syntheses of Heterocyclic Compounds. Part CDLXXXI 1 . A Simple Preparation of Tryptamine". Synthesis. 1972 (9): 475. doi:10.1055/s-1972-21902. ISSN 0039-7881. Tryptamine was first synthesized by means of Fischer indole cyclization of the phenylhydrazone of 4-aminobutyraldehyde2. Later, Majima and Hoshino3 prepared it by reduction of indol-3-yl-acetonitrile which was derived from the reaction of indol-3-yl-magnesium iodide with chloroacetonitrile. These methods have been superseded by the preparative sequence involving gramine methiodide4, and by the synthesis via indol-3-yl-glyoxylamides5,6. Other methods are the lithium aluminum hydride reduction of either 3-(2-nitroethyl)-indole7 or 3-(2-nitrovinyl)-indole8. A synthesis by the reaction of indolylmagnesium bromide with ethylene imine was also reported9. However, these methods require expensive materials and numerous steps. Now we wish to report an inexpensive one-step preparation of tryptamine from L-tryptophan (1). [...] 2. A. J. Evins, J. Chem. Soc. 99, 270 (1911).

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  • "Tryptamine". pubchem.ncbi.nlm.nih.gov. Diakses tanggal 2020-12-01.
  • "Tryptamine". PubChem. Diakses tanggal 7 November 2024.{{cite web}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)

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  • Dale HH (1958). "Arthur James Ewins, 1882-1958" (PDF). Biographical Memoirs of Fellows of the Royal Society (4): 81–91. doi:10.1098/rsbm.1958.0007. Promotion to the staff brought Ewins into more immediate collaboration in research with Laidlaw and myself. As the Bibliography again shows, he was promptly at work with Laidlaw on the isolation of a previously unknown member of the series of the proteinogenous amines—3β-aminoethyl-indole, indole-ethylamine, or tryptamine, the amine formed by the decarboxylation of tryptophane; and Ewins proceeded to produce this base also by an artificial synthesis. I have sometimes thought, during the past few years, that Laidlaw's largely forgotten description, at that early date, of its physiological actions may, at some points, have anticipated the discovery of the actions of the nearly related 5-hydroxy-tryptamine, the natural occurrence and activities of which have recently excited so rapid a growth of attention.

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  • "PDSP Database". UNC (dalam bahasa Zulu). Diakses tanggal 7 November 2024.{{cite web}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)

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