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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. Chem Biodivers. 2024 Oct 23:e202402472. doi: 10.1002/cbdv.202402472. Online ahead of print. Chemical Composition, Anti-microbial, and Cytotoxic Activities of Essential Oil from Magnolia bidoupensis Q. N. Vu leaves, an Endemic Species to the Central Highlands of Vietnam. Nguyen NV(1), Tran NNU(1), Hoang BT(1). Author information: (1)University of DaLat, Biology, 01 Phu Dong Thien Vuong, 67000, Dalat, VIET NAM. An analysis was conducted on the essential oil extracted from the leaves of Magnolia bidoupensis utilizing GC-MS, revealing thirty-three constituents that account for 98.9% of the essential oil. The main components included pogostol (22.4%), δ-selinene (16.2%), and α-amorphene (14.7%). Bioassays were then performed to evaluate the oil's biological activity. The essential oil exhibited antimicrobial activity against all tested microorganisms (six bacterial strains and one fungal strain) using the minimum inhibitory concentration (MIC) method. Additional cytotoxicity tests were conducted on KB, HepG2, MCF-7, and A549 cancer cell lines using the MTT method. The essential oil exhibited strong cytotoxic effects on all four cell lines, with IC50 values ranging from 1.37 ± 0.05 μg/mL (KB) to 2.40 ± 0.06 μg/mL (A549). © 2024 Wiley‐VCH GmbH. DOI: 10.1002/cbdv.202402472 PMID: 39441558 2. Nat Prod Res. 2023 Nov 24:1-8. doi: 10.1080/14786419.2023.2283758. Online ahead of print. Potential anti-inflammatory biomarkers from Myrtaceae essential oils revealed by untargeted metabolomics. Maiolini TCS(1), Nicácio KJ(2), Rosa W(1), Miranda DO(1), Santos MFC(3), Bueno PCP(4), Lago JHG(5), Sartorelli P(6), Dias DF(1), Chagas de Paula DA(1), Soares MG(1). Author information: (1)Chemistry Institute, Federal University of Alfenas, Alfenas, Brazil. (2)Department of Chemistry, Federal University of Mato Grosso, Cuiabá, Brazil. (3)Department of Chemistry and Physics, Center for Exact, Natural and Health Sciences, Federal University of Espírito Santo, Alegre, Brazil. (4)Leibniz Institute of Vegetable and Ornamental Crops, Department of Plant Biotic Interactions, Grossbeeren, Germany. (5)Centre of Human and Natural Sciences, Federal University of ABC, Santo André, Brazil. (6)Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of São Paulo, Diadema, Brazil. Many species from Myrtaceae have traditionally been used in traditional medicine as anti-inflammatory, antimicrobial, antidiarrheal, antioxidant and antirheumatic, besides in blood cholesterol reduction. In the present work, the anti-inflammatory activity of essential oils from eighteen Myrtaceae spp. were evaluated according to their ex-vivo anti-inflammatory activity in human blood, and the corresponding biomarkers were determined using untargeted metabolomics data and multivariate data analysis. From these studied species, six displayed anti-inflammatory activity with percentage rates of inhibition of PGE2 release above 70%. Caryophyllene oxide (1), humulene epoxide II (2), β-selinene (3), α-amorphene (4), α-selinene (5), germacrene A (6), β-bisabolene (7), α-muurolene (8), α-humulene (9), β-gurjunene (10), myrcene (11), β-elemene (12), α-cadinol (13), α-copaene (14), E-nerolidol (15) and ledol (16) were annotated as potential anti-inflammatory biomarkers. The results obtained in this study point to essential oils from species of the Myrtaceae family as a rich source of anti-inflammatory agents. DOI: 10.1080/14786419.2023.2283758 PMID: 38006221 3. Plants (Basel). 2022 Dec 22;12(1):58. doi: 10.3390/plants12010058. Bioprospecting of Helichrysum Species: Chemical Profile, Phytochemical Properties, and Antifungal Efficacy against Botrytis cinerea. Matrose NA(1)(2), Belay ZA(1), Obikeze K(2), Mokwena L(3), Caleb OJ(4)(5). Author information: (1)Post-Harvest and Agro-Processing Technologies (PHATs), Agricultural Research Council (ARC) Infruitec-Nietvoorbij, Stellenbosch 7599, South Africa. (2)School of Pharmacy, Faculty of Science, University of the Western Cape, Bellville 7535, South Africa. (3)Central Analytical Facility, Stellenbosch University, Matieland 7602, South Africa. (4)Department of Food Science, Faculty of AgriSciences, Stellenbosch University, Matieland 7602, South Africa. (5)African Institute for Postharvest Technology, Faculty of AgriSciences, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa. Variation in plant species and extraction solvents play a crucial role in the recovery of their bioactive compounds and antifungal efficacy. Thus, in this study, a comparative investigation was carried out using extraction solvents: 70% acetone and 95% ethanol to obtain crude aqueous extracts from Helichrysum odoratissimum and H. patulum. Crude aqueous extracts were screened using gas chromatography-mass spectrometry (GC-MS), to gain insight into their chemical composition. Phytochemical properties (total polyphenols (TP) and radical scavenging capacity via 2,2-diphenyl-1-picrylhydrazyl (DPPH)), and antifungal activity against Botrytis cinerea of the crude extracts were evaluated. Fungicide (Rovral® WP) and extraction solvents were used as controls. Variation in Helichrysum spp. and extraction solvent had influence on the chemical composition, phytochemicals, and antifungal activities. Metabolites such as γ-terpinene (≈0.1%), α-amorphene (≈0.6%) α-gurjunene (≈1.4%), β-selinene (2.2-3.2%), γ-gurjunene (≈3.3%), and methyl cinnamate (≈20%) were detected only in extracts of H. patulum. Crude extract of H. odoratissimum using 70% acetone had the highest TP (19.3 ± 0.76 g GA 100 g-1), and DPPH capacity (13,251.5 ± 700.55 µmol Trolox g-1) compared to H. patulum (p ≤ 0.05). Ethanolic extracts of H. patulum showed highest antifungal efficacy (≈65%) against B. cinerea (p ≤ 0.05) compared to other crude extracts. This study showed that Helichrysum spp. differ in their potential as a source for bioactive compounds and antifungal treatments/formulations. DOI: 10.3390/plants12010058 PMCID: PMC9824591 PMID: 36616185 Conflict of interest statement: The authors declare no conflict of interest. 4. Z Naturforsch C J Biosci. 2022 Sep 19;77(11-12):525-529. doi: 10.1515/znc-2022-0105. Print 2022 Nov 25. Chemical composition and anticholinesterase activity of Lepisanthes rubiginosa (Roxb.) Leenh. essential oil. Salleh WMNHW(1), Ghani NA(2)(3), Abdel-Aal AM(1)(4). Author information: (1)Department of Chemistry, Faculty of Science and Mathematics, Universiti Pendidikan Sultan Idris, 35900 Tanjung Malim, Perak, Malaysia. (2)Atta-ur-Rahman Institute for Natural Product Discovery (AuRIns), Universiti Teknologi MARA, Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor, Malaysia. (3)Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia. (4)Department of Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut, 71526, Egypt. Essential oils obtained from medicinal plants show high therapeutic potential against several types of pathologies, including Alzheimer's disease. The purpose of this work was to study the chemical composition and anticholinesterase inhibitory activity of the essential oil obtained from Lepisanthes rubiginosa leaves collected from Malaysia. Twenty-four components were identified using gas chromatography-flame ionization detection (GC-FID) and gas chromatography/mass spectrometry (GC-MS), which represent 99.5% of the essential oil. The identified major components include α-cadinol (40.0%), safrole (12.6%), α-amorphene (9.5%), (E)-isosafrole (5.0%), δ-cadinene (4.2%), and t-muurolol (4.1%). Anticholinesterase activity was assessed using Ellman method, and the essential oil demonstrated a moderate inhibitory activity against acetylcholinesterase (I%: 75.2%) and butyrylcholinesterase (I%: 70.2%) at conconcetration of 1000 μg/mL. The current study is the first to report chemical composition and anticholinesterase activity of the essential oil obtained from L. rubiginosa, which may have implications on the characterization, pharmaceutical, and therapeutic applications of Lepisanthes genus essential oils. © 2022 Walter de Gruyter GmbH, Berlin/Boston. DOI: 10.1515/znc-2022-0105 PMID: 36112782 [Indexed for MEDLINE] 5. Molecules. 2022 Mar 31;27(7):2282. doi: 10.3390/molecules27072282. Antioxidant, Antimicrobial, and Insecticidal Properties of a Chemically Characterized Essential Oil from the Leaves of Dittrichia viscosa L. Mssillou I(1), Agour A(1), Allali A(2), Saghrouchni H(3), Bourhia M(4), El Moussaoui A(5), Salamatullah AM(6), Alzahrani A(6), Aboul-Soud MAM(7), Giesy JP(8)(9)(10)(11), Lyoussi B(1), Derwich E(1)(12). Author information: (1)Laboratory of Natural Substances, Pharmacology, Environment, Modeling, Health and Quality of Life (SNAMOPEQ), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, Fez 30000, Morocco. (2)Laboratory of Plant, Animal and Agro-Industry Productions, Faculty of Sciences, University of Ibn Tofail (ITU), Kenitra 14000, Morocco. (3)Department of Biotechnology, Institute of Natural and Applied Sciences, Çukurova University, Balcalı, 01330 Adana, Turkey. (4)Laboratory of Chemistry, Biochemistry, Nutrition, and Environment, Faculty of Medicine and Pharmacy, University Hassan II, Casablanca 20000, Morocco. (5)Laboratory of Biotechnology, Environment, Agri-Food and Health, Faculty of Sciences Dhar El Mahraz, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco. (6)Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Saudi Arabia. (7)Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh 11433, Saudi Arabia. (8)Toxicology Centre, University of Saskatchewan, Saskatoon, SK S7N 5B3, Canada. (9)Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada. (10)Department of Integrative Biology, Michigan State University, East Lansing, MI 48824, USA. (11)Department of Environmental Sciences, Baylor University, Waco, TX 76798, USA. (12)Unity of GC/MS and GC, City of Innovation, Sidi Mohamed Ben Abdellah University, Fez 30000, Morocco. Since some synthetic insecticides cause damage to human health, compounds in plants can be viable alternatives to conventional synthetic pesticides. Dittrichia viscosa L. is a perennial Mediterranean plant known to possess biological activities, including insecticidal properties. The chemical composition of an essential oil (EOD) from D. viscosa, as well as its antioxidant, antimicrobial, and insecticidal effects on the cowpea weevil (Callosobruchus maculatus) were determined. Forty-one volatile compounds were identified in EOD, which accounted for 97.5% of its constituents. Bornyl acetate (41%) was a major compound, followed by borneol (9.3%), α-amorphene (6.6%), and caryophyllene oxide (5.7%). EOD exhibited significant antioxidant activity in all tests performed, with an IC50 of 1.30 ± 0.05 mg/mL in the DPPH test and an EC50 equal to 36.0 ± 2.5 mg/mL in the FRAP assay. In the phosphor-molybdenum test, EOD results ranged from 39.81 ± 0.7 to 192.1 ± 0.8 mg AAE/g E. EOD was active on E. coli (9.5 ± 0.5 mm), S. aureus (31.0 ± 1.5 mm), C. albicans (20.4 ± 0.5 mm), and S. cerevisiae (28.0 ± 1.0 mm), with MICs ranging from 0.1 mg/mL to 3.3 mg/mL. We found that 1 µL of EOD caused 97.5 ± 5.0% insect mortality after 96 h in the inhalation test and 60.0 ± 8.3% in the ingestion assay. The median lethal concentration (LC50) was 7.8 ± 0.3 μL EO/L, while the effective concentration in the ingestion test (LC50) was 15.0 ± 2.1 μL EO/L. We found that 20 µL of EOD caused a reduction of more than 91% of C. maculatus laid eggs. DOI: 10.3390/molecules27072282 PMCID: PMC9000614 PMID: 35408678 [Indexed for MEDLINE] Conflict of interest statement: The authors declare no conflict of interest.