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  Psychoactive Plant Database - Neuroactive Phytochemical Collection





Worldwide, there are plants known as psychoactive plants that naturally contain psychedelic active components. They have a high concentration of neuroprotective substances that can interact with the nervous system to produce psychedelic effects. Despite these plants' hazardous potential, recreational use of them is on the rise because of their psychoactive properties. Early neuroscience studies relied heavily on psychoactive plants and plant natural products (NPs), and both recreational and hazardous NPs have contributed significantly to the understanding of almost all neurotransmitter systems. Worldwide, there are many plants that contain psychoactive properties, and people have been using them for ages. Psychoactive plant compounds may significantly alter how people perceive the world.

 

 

1. Clemastine. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. 2024 Aug 15. Small occasional doses of clemastine are acceptable during breastfeeding. Larger doses or more prolonged use may cause drowsiness and other effects in the infant or decrease the milk supply, particularly in combination with a sympathomimetic such as pseudoephedrine or before lactation is well established. Single bedtime doses after the last feeding of the day may be adequate for many women and will minimize any effects of the drug. The nonsedating antihistamines are preferred alternatives. PMID: 30000667 2. Pest Manag Sci. 2024 Nov;80(11):5648-5655. doi: 10.1002/ps.8281. Epub 2024 Jul 11. Repellency, toxicity, and physiological actions of low molecular weight basic amines in mosquitoes. Yang L(1)(2), Demares F(1)(3), Norris EJ(4), Bloomquist JR(1). Author information: (1)Emerging Pathogens Institute, Entomology and Nematology Department, University of Florida, Gainesville, FL, USA. (2)Corteva Agriscience, Shanghai, China. (3)CEFE, University of Montpellier, CNRS, EPHE, IRD, Montpellier, France. (4)Center for Medical, Agricultural, and Veterinary Entomology, United States Department of Agriculture, Agricultural Research Service, Gainesville, FL, USA. BACKGROUND: This study investigated the behavioral responses and toxicity of three basic amines: 1-methylpiperazine, 1-methylpyrrolidine, and triethylamine (TEA), compounds suggested previously to be anosmic in vapor exposures to caged mosquitoes. RESULTS: These compounds showed repellency of Aedes aegypti mosquitoes, followed by flightlessness, knockdown, and paralysis, all increasing with exposure time and dosage. Electrophysiological experiments showed a blocking effect on nerve discharge of the Drosophila melanogaster larval central nervous system (CNS) with little evidence of hyperexcitation. Blockage of voltage-gated (Kv2) potassium channel currents under patch clamp occurred at similar concentrations. Involvement of K+ channels in the action of basic amines was supported by behavior and CNS recordings of a Shaker Kv1 mutant exposed to TEA, where instead of blockage, a hyperexcitation of nerve firing was observed. Experiments on cockroach leg mechanoreceptors demonstrated neuronal excitation and on mosquito antennae strong electroantennogram (EAG) signals with an augmentation of blank air responses after a single puff of basic amine. CONCLUSIONS: The neurophysiological effects of basic amines are consistent with K+ channel block, whereas the antennal EAG response was not obviously associated with anosmia. The low-dose effects of basic amines appear to be repellency and bradykinesia. Overall, the findings provide key insights into the mechanisms underlying the biological activity of basic amines. © 2024 Society of Chemical Industry. © 2024 Society of Chemical Industry. DOI: 10.1002/ps.8281 PMID: 38993039 [Indexed for MEDLINE] 3. Inorg Chem. 2024 Apr 29;63(17):7966-7972. doi: 10.1021/acs.inorgchem.4c00986. Epub 2024 Apr 15. Three-Step Ferroelastic Transitions from Hexagonal to Triclinic Phases in a Hybrid Perovskite: (1-Fluoromethyl-1-methylpyrrolidine)[CdCl(3)]. Chen S(1), Han DC(1), Ye L(1), Zhang WX(1). Author information: (1)MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou 510275, China. Hybrid ferroelastic crystals have emerged as a hot research topic in recent years owing to their prospective applications in piezoelectric sensors, mechanical switches, and optoelectronic devices. Nevertheless, most of the documented materials exhibit one-step or two-step ferroelastic phase transition(s), and those with multistep ferroelastic transitions are extremely scarce. We present a new hexagonal molecular perovskite based on a fluoro-substituted flexible cyclic ammonium cation, (1-fluoromethyl-1-methylpyrrolidine)[CdCl3] (1), undergoing unusual three-step ferroelastic phase transitions from hexagonal paraelastic phase to orthorhombic, monoclinic, and triclinic ferroelastic phases at 388, 376, and 311 K, respectively, with Aizu notation of 6/mmmFmmm, mmmF2/m, and 2/mF-1, featuring spontaneous strain of 0.002, 0.023, and 0.110, respectively. Furthermore, variable-temperature single-crystal diffraction reveals that the phase-transition mechanism in 1 principally originates from intriguing dynamic change of organic cations and synchronous displacement of inorganic chains. This scarce instance of multistep hybrid ferroelastic provides important clues for finding advanced ferroelastic materials. DOI: 10.1021/acs.inorgchem.4c00986 PMID: 38620044 4. ChemSusChem. 2021 Nov 19;14(22):5021-5031. doi: 10.1002/cssc.202101446. Epub 2021 Oct 18. Conductivity and Stability Properties of Anion Exchange Membranes: Cation Effect and Backbone Effect. Han J(1), Song W(1), Cheng X(1), Cheng Q(2), Zhang Y(1), Liu C(1), Zhou X(1), Ren Z(1), Hu M(3), Ning T(3), Xiao L(3), Zhuang L(3). Author information: (1)School of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan, 430023, P. R. China. (2)Early Warning Simulation Training Center, People's Liberation Army Air Force Early Warning Academy, Wuhan, 430019, P. R. China. (3)College of Chemistry and Molecular Sciences Hubei Key Lab of Electrochemical Power Sources, Wuhan University, Wuhan, 430072, P. R. China. The rise of heterocycle cations, a new class of stable cations, has fueled faster growth of research interest in heterocycle cation-attached anion exchange membranes (AEMs). However, once cations are grafted onto backbones, the effect of backbones on properties of AEMs must also be taken into account. In order to comprehensively study the influence of cations effect and backbones effect on AEMs performance, a series of AEMs were prepared by grafting spacer cations, heterocycles cations, and aromatic cations onto brominated poly(2,6-dimethyl-1,4-phenylene oxide) (BPPO) or poly(vinylbenzyl chloride) (PVB) backbones, respectively. Spacer cation [trimethylamine (TMA), N,N-dimethylethylamine (DMEA)]-attached AEMs showed general ion transportation and stability behaviors, but exhibited high cationic reaction efficiency. Heterocycle cation [1-methylpyrrolidine (MPY), 1-methylpiperidine (MPrD)]-attached AEMs showed excellent chemical stability, but their ion conduction properties were unimpressive. Aromatic cation [1-methylimidazole (MeIm), N,N-dimethylaniline (DMAni)]-attached AEMs exhibited superior ionic conductivity, while their poor cations stabilities hindered the application of the membranes. Besides, it was found that PVB-based AEMs had excellent backbone stability, but BPPO-based AEMs exhibited higher OH- conductivity and cation stability than those of the same cations grafted PVB-based AEMs due to their higher water uptake (WU). For example, the ionic conductivities (ICs) of BPPO-TMA and PVB-TMA at 80 °C were 53.1 and 38.3 mS cm-1 , and their WU was 152.3 and 95.1 %, respectively. After the stability test, the IC losses of BPPO-TMA and PVB-TMA were 21.4 and 32.2 %, respectively. The result demonstrated that the conductivity and stability properties of the AEMs could be enhanced by increasing the WU of the membranes. These findings allowed the matching of cations to the appropriate backbones and reasonable modification of the AEM structure. In addition, these results helped to fundamentally understand the influence of cation effect and backbone effect on AEM performance. © 2021 Wiley-VCH GmbH. DOI: 10.1002/cssc.202101446 PMID: 34498428 5. Carbohydr Polym. 2021 Mar 1;255:117375. doi: 10.1016/j.carbpol.2020.117375. Epub 2020 Nov 10. Influence of ionic liquid-like cationic pendants composition in cellulose based polyelectrolytes on membrane-based CO(2) separation. Nikolaeva D(1), Verachtert K(2), Azcune I(3), Jansen JC(4), Vankelecom IFJ(2). Author information: (1)Membrane Technology Group (MTG), cMACS, Faculty Bio-science Engineering, Celestijnenlaan 200F, 3001 Leuven, Belgium; UCLouvain - IMMC, Materials & Process Engineering, Place Sainte Barbe 2, 1348 Louvain-la-Neuve, Belgium. Electronic address: daria.nikolaeva@uclouvain.be. (2)Membrane Technology Group (MTG), cMACS, Faculty Bio-science Engineering, Celestijnenlaan 200F, 3001 Leuven, Belgium. (3)Fundación CIDETEC, Paseo Miramon 196, 20014 Donostia, San Sebastian, Spain. (4)Institute on Membrane Technology (ITM-CNR), Via P. Bucci 17/C, 87036 Rende (CS), Italy. Cellulose acetate (CA) is an attractive membrane polymer for CO2 capture market. However, its low CO2 permeability hampers its application as part of a membrane for most relevant types of CO2 containing feeds. This work investigates the enhancement of CA separation performance by incorporating ionic liquid-like pendants (1-methylimidazol, 1-methylpyrrolidine, and 2-hydroxyethyldimethylamine (HEDMA) on the CA backbone. These CA-based polyelectrolytes (PEs), synthesised by covalent grafting of cationic pendants with anion metathesis, were characterised by NMR, FTIR, DSC/TGA, and processed into thin-film composite membranes. The membrane performance in CO2/N2 mixed-gas permeation experiments shows a decrease in CO2 and N2 permeability and an initial decrease and then gradual increase in CO2/N2 selectivity with increasing HEDMA content. The amount of HEDMA attached to the CA backbone determines overall separation process in bifunctional PEs. This indicates that the hydroxy-substituted cationic pendants alter interactions between PEs network and permeating CO2 molecules, suggesting possibilities for further improvements. Copyright © 2020 Elsevier Ltd. All rights reserved. DOI: 10.1016/j.carbpol.2020.117375 PMID: 33436206