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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.

 

Compound Summary

 

PLANT NAME:- Sassafras albidum     PPD ID:- PPD-ID28_126


COMPOUND/COMMON NAME:- 4-allyl-2,6-dimethoxyphenol
CAS ID
N/A
INCHI KEY
FWMPKHMKIJDEMJ-UHFFFAOYSA-N
MOLECULAR WEIGHT
194.23
MOLECULAR FORMULA
C11H14O3
MOLECULAR MASS
194.230
BIOLOGICAL SOURCE
Sassafras albidum
DATA SOURCE
Afendi, F. M., Okada, T., Yamazaki, M., Hirai-Morita, A., Nakamura, Y., Nakamura, K., Ikeda, S., Takahashi, H., Altaf-Ul-Amin, M., Darusman, L. K., Saito, K., & Kanaya, S. (2012). KNApSAcK family databases: integrated metabolite-plant species databases for multifaceted plant research. Plant & cell physiology, 53(2), e1. https://doi.org/10.1093/pcp/pcr165
CHEMICAL CLASS OF COMPOUND
Phenols
NLRP3 DOCKING SCORE(Kcal/mol)
-4.226
CANONICAL SMILES   C=CCc1cc(OC)c(O)c(OC)c1
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   N/A
SYNONYMS
4-Allyl-2,6-dimethoxyphenol, 6627-88-9, Methoxyeugenol, 2,6-dimethoxy-4-prop-2-enylphenol, 4-Allylsyringol, 2,6-Dimethoxychavicol, Phenol, 2,6-dimethoxy-4-(2-propenyl)-, Phenol, 4-allyl-2,6-dimethoxy-, 2,6-Dimethoxy-4-allylphenol, 4-Allyl-2,6-dimetoxyphenol, 4-Hydroxy-3,5-dimethoxyallylbenzene, FEMA No. 3655, CHEBI:86562, 6-methoxyeugenol, UNII-8VF00YWP89, 2,6-dimethoxy-4-(2-propenyl)phenol, 8VF00YWP89, EINECS 229-600-2, NSC 16953, NSC 60246, NSC-16953, NSC-60246, Phenol, 4-(2-propenyl)-2,6-dimethoxy, 2,6-dimethoxy-4-(prop-2-en-1-yl)phenol, AI3-23057, Phenol,2,6-dimethoxy-4-(2-propen-1-yl)-, 4-(2-PROPENYL)SYRINGOL, DTXSID30216470, CHAVICOL, 2,6-DIMETHOXY-, Phenol,6-dimethoxy-, 4-ALLYL-2,6-DIMETHOXYPHENOL [FHFI], PHENOL, 2,6-DIMETHOXY-4-(2-PROPEN-1-YL)-, 4-(2-Propenyl)-2,6-dimethoxyphenol (4-allylsyringol), Phenol,6-dimethoxy-4-(2-propenyl)-, MFCD00008655, bmse010054, SCHEMBL293977, 4-allyl-2,6-dimethoxy-phenol, CHEMBL2059292, DTXCID30138961, NSC16953, NSC60246, 4-Allyl-2,6-dimethoxyphenol, 8CI, BDBM50242963, 4-(2-Propenyl)-2,6-dimethoxyphenol, AKOS015888171, 2,6-dimethoxy-4-(2-propenyl)-phenol, 2,6-Dimethoxy-4-(2-propenyl) phenol, 4-Allyl-2,6-dimethoxyphenol, >=95%, Phenol, 4-allyl-2,6-dimethoxy-(8CI), AS-36789, BP-10517, Phenol, 4-allyl-2,6-dimethoxy- (8CI), DB-054902, 2,6-Dimethoxy-4-(2-propenyl)phenol, 9CI, 4-Allyl-2,6-dimethoxyphenol, >=95%, FG, CS-0158007, NS00022639, Phenol, 2,6-dimethoxy-4-(2-propenyl)-(9CI), Phenol, 2,6-dimethoxy-4-(2-propenyl)- (9CI), Q27159248
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