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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.
CAS ID |
N/A |
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INCHI KEY |
KCDXJAYRVLXPFO-UHFFFAOYSA-N |
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MOLECULAR WEIGHT |
182.17 |
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MOLECULAR FORMULA |
C9H10O4 |
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MOLECULAR MASS |
182.175 |
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BIOLOGICAL SOURCE |
Juglans regia |
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DATA SOURCE |
U.S. Department of Agriculture, Agricultural Research Service. 1992-2016. Dr. Duke's Phytochemical and Ethnobotanical Databases. Home Page, http://phytochem.nal.usda.gov/ http://dx.doi.org/10.15482/USDA.ADC/1239279 | ||
CHEMICAL CLASS OF COMPOUND |
Phenols |
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NLRP3 DOCKING SCORE(Kcal/mol) |
-4.203 |
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CANONICAL SMILES COc1cc(C=O)cc(OC)c1O
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BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES
No
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SYNONYMS |
SYRINGALDEHYDE, 134-96-3, 4-Hydroxy-3,5-dimethoxybenzaldehyde, 3,5-Dimethoxy-4-hydroxybenzaldehyde, Syringic aldehyde, Syringylaldehyde, Syringealdehyde, Benzaldehyde, 4-hydroxy-3,5-dimethoxy-, Gallaldehyde 3,5-dimethyl ether, 3,5-Dimethoxy-4-hydroxybenzene carbonal, Springaldehyde, Cedar aldehyde, 4-hydroxy-3,5-dimethoxy-benzaldehyde, Benzaldehyde, 3,5-dimethoxy-4-hydroxy-, MFCD00006943, NSC 41153, Syringe aldehyde, AI3-28796, EINECS 205-167-5, UNII-2ZR01KTT21, 4-Hydroksy-3,5-dwumetoksybenzaldehyd, 4-Hydroksy-3,5-dwumetoksybenzaldehyd [Polish], BRN 0784514, 2ZR01KTT21, CHEBI:67380, NSC-41153, SYRINGALDEHYDE [MI], DTXSID2059643, FEMA NO. 4049, 2,6-DIMETHOXY-4-FORMYLPHENOL, 4-FORMYL-2,6-DIMETHOXYPHENOL, 3,5-dimethoxy-4-oxidanyl-benzaldehyde, 4-HYDROXY-3,5-DIMETHOXYBENZALDEHYDE [FHFI], syringaldehye, not relevant, 4-Formylsyringol, 3,5-Dimethoxy-4-Hydroxy-Benzaldehyde, Syringaldehyde, 98%, bmse000595, bmse010204, SCHEMBL150376, Gallaldehyde 3,5dimethyl ether, Syringaldehyde, >=98%, FG, CHEMBL225303, Syringaldehyde (3,5-Dimethoxy-4-hydroxybenzaldehyde), 3,5Dimethoxy4hydroxybenzaldehyde, 4Hydroxy3,5dimethoxybenzaldehyde, DTXCID6034182, 86220_FLUKA, 4Hydroksy3,5dwumetoksybenzaldehyd, VND3207, 4-H-3,5-DMBA, Syringaldehyde, analytical standard, Benzaldehyde, 3,5dimethoxy4hydroxy, Benzaldehyde, 4hydroxy3,5dimethoxy, HY-N1390, NSC41153, STR09162, 3,5Dimethoxy4hydroxybenzene carbonal, AC7930, BBL023037, Benzaldehyde,5-dimethoxy-4-hydroxy-, s4765, STK801968, ZINC00152926, 4-hydroxy-3,5-dimethoxy benzaldehyde, 3,5-Dimethoxy-4-hydroxy benzaldehyde, AKOS000119539, AC-7993, CCG-266448, BP-12551, DA-67881, SY014703, CS-0016810, D0635, NS00020999, EN300-21558, Syringaldehyde, Vetec(TM) reagent grade, 98%, AP-065/41884112, Q411695, W-108274, F2190-0619, Z104501688, IJV |
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