Gigantine
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| IUPAC name
6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinolin-5-ol
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| Other names
1,2-Dimethyl-5-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline
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3D model (JSmol)
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| Properties | |
| C13H19NO3 | |
| Molar mass | 237.299 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Template:Chembox Footer/trackingTemplate:Short description
Gigantine is a tetrahydroisoquinoline alkaloid found in Carnegiea gigantea and other related cactus species.[1][2] It was first discovered along with macromerine in 1967.[3] Gigantine is found in significant quantities in many mescaline-containing cactus species, but it is unclear whether it contributes to their psychoactive effects.[1] The compound has been suspected to be hallucinogenic based on animal studies in cats and monkeys, but has not been evaluated in humans.[4][3]
See also
References
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- ^ a b Page Module:Citation/CS1/styles.css has no content.Shulgin, Alexander Theodore; Perry, Wendy E. (2002). The Simple Plant Isoquinolines. Transform Press. ISBN 978-0-9630096-2-3. OCLC 51006569. OL 8521520M.
- ^ Page Module:Citation/CS1/styles.css has no content.Bruhn JG, Lundström J (1976). "Alkaloids of Carnegiea gigantea. Arizonine, a new tetrahydroisoquinoline alkaloid". Lloydia. 39 (4): 197–203. PMID 957908.
- ^ a b Page Module:Citation/CS1/styles.css has no content.Hodgkins JE, Brown SD, Massingill JL (April 1967). "Two new alkaloids in cacti". Tetrahedron Lett. 8 (14): 1321–1324. doi:10.1016/s0040-4039(00)90694-4. PMID 6044211.
Synthetic d,l-macromerine, natural macromerine and natural gigantine are physiologically active. Both alkaloids caused hallucinogenic reactions when tested on squirrel monkeys and cats (macromerine; 20 mg/kilo-I.P., hallucinogenic; gigantine, 20 mg/kilo-I.P., lethal; 5 mg/kilo-I.P., hallucinogenic).14 Macromerine shows "anti" adrenaline results in the turtle heart.15 [...] REFERENCES [...] (14) We wish to thank Dr. E. S. Barratt, Director, Behavioral Science Lab., Department of Neurology and Psychiatry, University of Texas Medical Branch, Galveston, Texas, for obtaining the physiological data. (15) We wish to thank S. Eppstein, M.D., for his interpretation of the E.K.G.'s and Professor E. W. Gardner of T.C.U. for assistance in obtaining the [...]
- ^ Page Module:Citation/CS1/styles.css has no content.Keeper Trout & friends (2013). Trout's Notes on The Cactus Alkaloids Nomenclature, Physical properties, Pharmacology & Occurrences (Sacred Cacti Fourth Edition, Part C: Cactus Chemistry: Section 1) (PDF). Mydriatic Productions/Better Days Publishing.
Suspected hallucinogen based on animal studies. Claimed to be hallucinogenic in monkeys and cats at 5 mg./ kg./ip.; Hodgkins et al. 1967. Apparently lacking any human evaluation. Fatal in monkeys and cats at 20 mg/kg/ip. Hodgkins et al. 1967.
External links
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