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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:- Turnera diffusa     PPD ID:- PPD-ID36_79


COMPOUND/COMMON NAME:- p-cymen-8-ol
CAS ID
N/A
INCHI KEY
XLPDVYGDNRIQFV-UHFFFAOYSA-N
MOLECULAR WEIGHT
150.22
MOLECULAR FORMULA
C10H14O
MOLECULAR MASS
150.221
BIOLOGICAL SOURCE
Turnera diffusa
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
Benzene and substituted derivatives
NLRP3 DOCKING SCORE(Kcal/mol)
-5.315
CANONICAL SMILES   Cc1ccc(C(C)(C)O)cc1
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   No
SYNONYMS
2-(4-methylphenyl)propan-2-ol, 1197-01-9, p-Cymen-8-ol, 8-Hydroxy-p-cymene, Dimethyl-p-tolyl carbinol, 2-(4-Methylphenyl)-2-propanol, Cymen-8-ol, p-, 2-p-Tolyl-2-propanol, Benzenemethanol, alpha,alpha,4-trimethyl-, FEMA No. 3242, 1-Methyl-4-(1-hydroxy-1-methylethyl)benzene, 2-(P-Methylphenyl)-2-propanol, P-CYMENE-8-OL, para-Cymen-8-ol, p,alpha,alpha-Trimethylbenzyl alcohol, alpha,alpha,4-Trimethylbenzyl alcohol, p-Cymenol-8, alpha,alpha,4-Trimethylbenzenemethanol, 1-Methyl-4-(alpha-hydroxyisopropyl)benzene, 2-p-tolylpropan-2-ol, Benzenemethanol, .alpha.,.alpha.,4-trimethyl-, 6TFS69V5BW, DTXSID0024890, NSC-361057, 2-(p-tolyl)propan-2-ol, cherry propanol, 2-?(4-?Methylphenyl)?propan-?2-?ol, EINECS 214-817-7, UNII-6TFS69V5BW, NSC 361057, Trimethylbenzyl alcohol, P,alpha,alpha-, AI3-00732, p-Cymenol, 8-p-cymenol, P-Cymen-alpha-ol, a-Hydroxy-p-cymene, Cimen-8-ol, Cymen-8-ol, NSC361057, p-Cymen-.alpha.-ol, Dimethyl-p-tolylcarbinol, p-(Hydroxyisopropyl)toluene, laquo Rhoraquo -Cymene-8-ol, SCHEMBL858049, DTXCID704890, CHEMBL3186822, p-Mentha-1,3,5-trien-8-ol, XLPDVYGDNRIQFV-UHFFFAOYSA-, CHEBI:167408, 2-(4-methylphenyl) propan-2-ol, Tox21_302135, a,a,4-Trimethylbenzenemethanol, 9CI, a,a,4-Trimethylbenzyl alcohol, 8CI, AKOS009996535, alpha,alpha,4-Trimethyl-Benzenemethanol, 1,1-dimethyl-2-(4-methylphenyl)ethanol, NCGC00255334-01, AS-61419, CAS-1197-01-9, DB-012809, CS-0206670, NS00013253, 1-Methyl-4-(.alpha.-hydroxyisopropyl)benzene, D86508, .ALPHA.,.ALPHA.,4-TRIMETHYLBENZYL ALCOHOL, p,alpha,alpha-Trimethylbenzyl alcohol, >=95%, FG, Q27265496, P,.ALPHA.,.ALPHA.-TRIMETHYLBENZYL ALCOHOL [FHFI], InChI=1/C10H14O/c1-8-4-6-9(7-5-8)10(2,3)11/h4-7,11H,1-3H3
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