Psychotridine
Chemical compound
- none
- 3-methyl-5,8b-bis[3-methyl-5-(3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl)-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole
- 52617-25-1
- 171175
- 149650
- Interactive image
- CN1CCC2(C1NC1=CC=CC=C21)C1=CC=CC2=C1NC1N(C)CCC21C1=CC=CC2=C1NC1N(C)CCC21C12CCN(C)C1NC1=C2C=CC=C1C12CCN(C)C1NC1=CC=CC=C21
Psychotridine is an alkaloid found in some species of the genus Psychotria, namely Psychotria colorata,[1] but also Psychotria forsteriana,[2] Psychotria lyciiflora,[3] Psychotria oleoides,[3] and Psychotria beccarioides.[4] Psychotridine has analgesic effects and dose-dependently inhibits dizocilpine binding to cortical membranes in vitro, suggesting that it acts as a non-competitive NMDA receptor antagonist.[1]
See also
- Hodgkinsine
References
- ^ a b Amador TA, Verotta L, Nunes DS, Elisabetsky E (May 2001). "Involvement of NMDA receptors in the analgesic properties of psychotridine". Phytomedicine. 8 (3): 202–206. doi:10.1078/0944-7113-00025. PMID 11417913.
- ^ Beretz A, Roth-Georger A, Corre G, Kuballa B, Anton R, Cazenave JP (August 1985). "Polyindolinic Alkaloids from Psychotria forsteriana. Potent Inhibitors of the Aggregation of Human Platelets". Planta Medica. 51 (4): 300–303. doi:10.1055/s-2007-969496. PMID 17340518. S2CID 12146923.
- ^ a b Jannic V, Guéritte F, Laprévote O, Serani L, Martin MT, Sévenet T, Potier P (June 1999). "Pyrrolidinoindoline alkaloids from Psychotria oleoides and Psychotria lyciiflora". Journal of Natural Products. 62 (6): 838–843. doi:10.1021/np9805387. PMID 10395499.
- ^ Hart N, Johns S, Lamberton J, Summons R (1974). "Psychotridine, a C55H62N10 alkaloid from Psychotria beccarioides (Rubiaceae)". Australian Journal of Chemistry. 27 (3): 639–646. doi:10.1071/ch9740639.
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modulators
| Calcium blockers |
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| Sodium blockers |
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| Potassium openers |
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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