Meyers-Riggs, B. Biosynthesis of 4-substituted tryptamine derivatives. countyourculture, countyourculture: rational exploration of the underground, 17 Feb 2012.
Meyers-Riggs, B. Grid biosynthesis of psilocybin. countyourculture, countyourculture: rational exploration of the underground, 5 Dec 2011.
Fricke, J; Lenz, C; Wick, J; Blei, F; Hoffmeister, D. Production options for psilocybin: Making of the magic. Chem. Eur. J., 18 Jan 2019, 25 (4), 897–903. 1.8 MB. https://doi.org/10.1002/chem.201802758 #5
Chadeayne, AR; Pham, DNK; Golen, JA; Manke, DR. Norpsilocin: Freebase and fumarate salt. Acta Crystallogr. E, 1 Apr 2020, 76 (4), 589–593. 931 kB. https://doi.org/10.1107/S2056989020004077 #Norpsilocin NMR,other
Lenz, C; Wick, J; Hoffmeister, D. Identification of ω-N-methyl-4-hydroxytryptamine (Norpsilocin) as a Psilocybe natural product. J. Nat. Prod., 27 Oct 2017, 80 (10), 2835–2838. 1.1 MB. https://doi.org/10.1021/acs.jnatprod.7b00407 #Norpsilocin LC,MS,NMR
Milne, N; Thomsen, P; Knudsen, NM; Rubaszka, P; Kristensen, M; Borodina, I. Metabolic engineering of Saccharomyces cerevisiae for the de novo production of psilocybin and related tryptamine derivatives. Metab. Eng., 1 Jul 2020, 60, 25–36. 2.4 MB. https://doi.org/10.1016/j.ymben.2019.12.007 #Norpsilocin LC,MS
Blei, F; Dörner, S; Fricke, J; Baldeweg, F; Trottmann, F; Komor, A; Meyer, F; Hertweck, C; Hoffmeister, D. Simultaneous production of psilocybin and a cocktail of β-carboline monoamine oxidase inhibitors in “magic” mushrooms. Chem. Eur. J., 13 Jan 2020, 26 (3), 729–734. 1.2 MB. https://doi.org/10.1002/chem.201904363 #norpsilocin LC,MS,UV,other
Sherwood, AM; Halberstadt, AL; Klein, AK; McCorvy, JD; Kaylo, KW; Kargbo, RB; Meisenheimer, P. Synthesis and biological evaluation of tryptamines found in hallucinogenic mushrooms: norbaeocystin, baeocystin, norpsilocin, and aeruginascin. J. Nat. Prod., 28 Feb 2020, 83 (2), 461–467. 3.8 MB. https://doi.org/10.1021/acs.jnatprod.9b01061 #6 LC,MS,NMR
Lenz, C; Dörner, S; Trottmann, F; Hertweck, C; Sherwood, A; Hoffmeister, D. Assessment of bioactivity‐modulating pseudo‐ring formation in psilocin and related tryptamines. ChemBioChem, 28 Apr 2022, 23 (13), e202200183. 3.2 MB. https://doi.org/10.1002/cbic.202200183 #4 NMR
Glatfelter, GC; Pottie, E; Partilla, JS; Sherwood, AM; Kaylo, K; Pham, DNK; Naeem, M; Sammeta, VR; DeBoer, S; Golen, JA; Hulley, EB; Stove, CP; Chadeayne, AR; Manke, DR; Baumann, MH. Structure–activity relationships for psilocybin, baeocystin, aeruginascin, and related analogues to produce pharmacological effects in mice. ACS Pharmacol. Transl. Sci., 11 Nov 2022, 5 (11), 1181–1196. 4.8 MB. https://doi.org/10.1021/acsptsci.2c00177 #Norpsilocin MS,NMR,other