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Mescaline: all studies

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Research

ChemInform Abstract: Dihydrobenzofuran Analogues of Hallucinogens. Part 4. Mescaline Derivatives.

ChemInform January 6, 1998 Aaron Monte, Steve R. Waldman, Danuta Marona‐lewicka et al.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Dihydrobenzofuran Analogues of Hallucinogens. 4. Mescaline Derivatives

Journal of Medicinal Chemistry September 1, 1997 Aaron Monte, Steve R. Waldman, Danuta Marona‐lewicka et al. 89 citations

Dihydrobenzofuran and tetrahydrobenzodifuran functionalities were employed as conformationally restricted bioisosteres of the aromatic methoxy groups in the prototypical hallucinogen, mescaline (1). Thus, 4-(2-aminoethyl)-6,7-dimethoxy-2,3-dihydrobenzofuran hydrochloride (8) and 1-(8-methoxy-2,3,5,6-tetrahydrobenzo[1,2-b:5,4-b']difuran-4-yl)-2- aminoethane hydrochloride (9) were prepared and...

Determination of Mescaline in Hallucinogenic Cactaceae by Ion-Interaction HPLC.

Analytical Letters October 1, 1996 M. C. Gennaro, E. Gioannini, D. Giacosa et al. 12 citations

Abstract An ion-interaction HPLC method is developed for the determination of mescaline in some Cactaceae species, namely Gymnocactus beguinii, Echinocactus polycephalus, Coriphanta radians, Coriphanta scolymoides, Coriphanta palmeri, Lophophora williamsii and Trichocereus pachanoi. Mescaline is characterized by hallucinogenic properties and can be prescribed as a psychodrug. The method makes...

DOI: 10.1080/00032719608002260 (opens in new tab) Mescaline Cactus Aqueous solution Detection limit +1

The Higher Powers: Fred M. Smith and the Peyote Ceremonies

Dialogue: A Journal of Mormon Thought December 1, 1995 Shelby M. Barnes

Frederick Madison Smith was third president and prophet of the Reorganized Church of Jesus Christ of Latter Day Saints.Son of Joseph III and grandson of Joseph the Martyr, Fred M., as he was generally known, came to lead the Reorganization in 1915.Smith was a highly educated man interested in the relationship between science and religion.His interest led him to experiment with the religious...

3,4,5-Trimethoxyphenylacetaldehyde, an Intermediate Metabolite of Mescaline, Is a Substrate for Microsomal Aldehyde Oxygenase in the Mouse Liver.

Biological and Pharmaceutical Bulletin 1995 Kenji Watanabe, Yuichiro Kayano, Tatsuo Matsunaga et al. 9 citations

3,4,5-Trimethoxyphenylacetaldehyde, an intermediate metabolite of mescaline, was oxidized to 3,4,5-trimethoxyphenylacetic acid by mouse hepatic microsomes. The reaction was NADPH-dependent, and inhibited by SKF 525-A, metyrapone and disulfiram. A P450 isozyme in mouse hepatic microsomes, P450 MUT-2 (CYP2C29), catalyzed the reaction (0.96 nmol/min/nmol P450) in which NADPH and NADPH-cytochrome c...

DOI: 10.1248/bpb.18.696 (opens in new tab) Mescaline Microsome Metabolite Cytochrome p450 +7

Effects of mescaline and some of its analogs on cholinergic neuromuscular transmission

Neuropharmacology February 1, 1993 Emmanuel Ghansah, Prapaporn Kopsombut, M A Maleque et al. 22 citations

Mescaline (3,4,5-trimethoxyphenylethylamine; MES) and its analogs, anhalinine (ANH) and methylenemescaline trimer (MMT) were investigated, using sciatic-sartorius preparations of the frog and cortical tissue from the rat. The effects of MES and its analogs were examined with respect to muscle twitch, resting membrane potential and nicotinic receptor binding. Mescaline and its analogs (10-100...

DOI: 10.1016/0028-3908(93)90097-m (opens in new tab) Mescaline Neuromuscular transmission Nicotinic agonist Cholinergic +5

Mescaline-induced psychopathological, neuropsychological, and neurometabolic effects in normal subjects: experimental psychosis as a tool for psychiatric research.

Biological Psychiatry December 1, 1992 L. Hermle, M. Fünfgeld, G. Oepen et al. 185 citations

The psychological, neuropsychological, and neurometabolic effects of the hallucinogenic agent mescaline were investigated in 12 normal men who were volunteers. Mescaline produced an acute psychotic state 3 1/2-4 hr after drug intake, as measured by the Brief Psychiatric Rating Scale (BPRS) and Paranoid Depression Scale (PDS). The Assessment of Altered States of Consciousness (APZ) questionnaire...

Nootropic Candidates Inhibit Head-Twitches Induced by Mescaline in Mice

The Japanese Journal of Pharmacology 1992 Tsuneyuki Yamamoto, Masuo Ohno, Shin‐ichi Yatsugi et al. 1 citation

The effects of various nootropic candidates on mescaline-induced head-twitches were studied in mice. The number of head-twitches induced by mescaline (100 mg/kg, s.c.) was significantly reduced by idebenone (32 and 100 mg/kg, i.p.), minaprine (0.32–10 mg/kg, p.o.) and nebracetam (100 mg/kg, p.o.). Cholinesterase inhibitors such as tetrahydroaminoacridine (1 and 10 mg/kg, p.o.), NIK-247 (10 and...

DOI: 10.1016/s0021-5198(19)35545-3 (opens in new tab) Mescaline Physostigmine Nootropic Pharmacology +8

Nootropic Candidates Inhibit Head-Twitches Induced by Mescaline in Mice.

The Japanese Journal of Pharmacology 1992 Tsuneyuki Yamamoto, Masuo Ohno, Shin‐ichi Yatsugi et al. 7 citations

The effects of various nootropic candidates on mescaline-induced head-twitches were studied in mice. The number of head-twitches induced by mescaline (100 mg/kg, s.c.) was significantly reduced by idebenone (32 and 100 mg/kg, i.p.), minaprine (0.32-10 mg/kg, p.o.) and nebracetam (100 mg/kg, p.o.). Cholinesterase inhibitors such as tetrahydroaminoacridine (1 and 10 mg/kg, p.o.), NIK-247 (10 and...

DOI: 10.1254/jjp.59.419 (opens in new tab) Mescaline Physostigmine Pharmacology Nootropic +5

ChemInform Abstract: Tris‐N,N′,N′′‐(3′,4′,5′‐trimethoxyphenethyl)‐1,3,5‐hexahydrotriazine, a Methylenemescaline Trimer: Characterization and Selective Cyclization to Anhalinine Under Non‐Aqueous Conditions.

ChemInform January 9, 1990 Linda A. Chrisey, A. Brossi

Abstract Cyclocondensation of mescaline (I) with aqueous formaldehyde (II) gives the 1,3,5‐hexahydrotriazine (III) which undergoes ring cleavage and recyclization upon treatment with hydrochlorid acid, producing a mixture of mescaline (I) and anhalinine hydrochloride (IV).