"



  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_124


COMPOUND/COMMON NAME:- apiol
CAS ID
N/A
INCHI KEY
QQRSPHJOOXUALR-UHFFFAOYSA-N
MOLECULAR WEIGHT
222.24
MOLECULAR FORMULA
C12H14O4
MOLECULAR MASS
222.240
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
Benzodioxoles
NLRP3 DOCKING SCORE(Kcal/mol)
-4.746
CANONICAL SMILES   C=CCc1cc(OC)c2c(c1OC)OCO2
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   Yes
SYNONYMS
Apiole, 523-80-8, Apioline, Apiol, Apiole (parsley), Parsley apiole, Parsley camphor, Parsley apiol, Petersiliencampher, 5-Allyl-4,7-dimethoxy-1,3-benzodioxole, 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE, 1,3-Benzodioxole, 4,7-dimethoxy-5-(2-propenyl)-, NSC 9070, 5-Allyl-4,7-dimethoxybenzo[d][1,3]dioxole, 1-Allyl-2,5-dimethoxy-3,4-methylenedioxybenzene, APIOLUM, QQ67504PXO, 4,7-Dimethoxy-5-(2-propenyl)-1,3-benzodioxole, 5-Allyl-4,7-dimethoxy-1,3-benzodioxol, APIOLE, PARSLEY, NSC-9070, EINECS 208-349-2, BRN 0195747, UNII-QQ67504PXO, 1,3-Benzodioxole, 4,7-dimethoxy-5-(2-propen-1-yl)-, AI3-14843, BENZENE, 1-ALLYL-2,5-DIMETHOXY-3,4-(METHYLENEDIOXY)-, CHEBI:70353, NSC9070, 4,7-Dimethoxy-5-(2-propen-1-yl)-1,3-Benzodioxole, 1-Allyl-2,5-dimethoxy-3,4-(methylenedioxy)benzene, 4,7-dimethoxy-5-(prop-2-en-1-yl)-2H-1,3-benzodioxole, Camphre de Persil, Apiol1503, Spectrum_000400, APIOLE [VANDF], APIOLUM [HPUS], Spectrum2_000419, Spectrum3_001283, Spectrum4_001643, Spectrum5_001718, 4,7-dimethoxy-5-prop-2-enyl-1,3-benzodioxole, BSPBio_002885, KBioGR_002105, KBioSS_000880, SPECTRUM390001, SCHEMBL497412, SPBio_000378, APIOLE (PARSLEY) [MI], CHEMBL1560118, DTXSID4041236, KBio2_000880, KBio2_003448, KBio2_006016, KBio3_002105, CCG-39582, MFCD00047270, STK664284, 1-Allyl-2,4-(methylenedioxy)benzene, AKOS003398564, 1, 4,7-dimethoxy-5-(2-propenyl)-, ApiolineApiole (parsley); Parsley apiole, NCGC00094551-01, NCGC00094551-02, NCGC00094551-03, FS-10667, 5-allyl-4,7-dimethoxy-benzo-1,3-dioxole, 1ST179657, Benzene,5-dimethoxy-3,4-(methylenedioxy)-, DB-052116, HY-135217, 5-Allyl-4,7-dimethoxy-1,3-benzodioxole #, CS-0109902, NS00032497, WLN: T56 BO DO CHJ FO1 H2U1 IO1, G88932, Apioline; Apiol; Parsley apiole; Parsley camphor, SR-05000002460, SR-05000002460-1, 1-Allyl-2,5-dimethoxy-3, 4-(methylenedioxy)benzene, 1-Allyl-2,5-dimethoxy-3,4-(methylenedioxy)-Benzene, 4,7-dimethoxy-5-(prop-2-en-1-yl)-1,3-benzodioxole, Q21071561, 4,7-Dimethoxy-5-(2-propenyl)-1,3-benzodioxole, 9CI, 4,7-dimethoxy-5-(2-propanyl)-1,3-benzodioxole, AldrichCPR
Back