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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:- Juglans regia     PPD ID:- PPD-ID48_329


COMPOUND/COMMON NAME:- p-coumaric-acid
CAS ID
N/A
INCHI KEY
NGSWKAQJJWESNS-ZZXKWVIFSA-N
MOLECULAR WEIGHT
164.16
MOLECULAR FORMULA
C9H8O3
MOLECULAR MASS
164.160
BIOLOGICAL SOURCE
Juglans regia
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
Cinnamic acids and derivatives
NLRP3 DOCKING SCORE(Kcal/mol)
-4.865
CANONICAL SMILES   O=C(O)/C=C/c1ccc(O)cc1
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   No
SYNONYMS
p-coumaric acid, 4-Hydroxycinnamic acid, 501-98-4, p-Hydroxycinnamic acid, trans-4-Hydroxycinnamic acid, 4-Coumaric acid, trans-p-Coumaric acid, 7400-08-0, p-Cumaric acid, Naringeninic acid, p-Hydroxy-cinnamic acid, Para-Coumaric acid, Hydroxycinnamic acid, (E)-p-Coumaric acid, trans-4-coumaric acid, 3-(4-hydroxyphenyl)acrylic acid, trans-p-Coumarinic acid, (E)-3-(4-Hydroxyphenyl)acrylic acid, Cinnamic acid, p-hydroxy-, (E)-p-Hydroxycinnamic acid, 4'-hydroxycinnamic acid, trans-p-Hydroxycinnamic acid, 2-propenoic acid, 3-(4-hydroxyphenyl)-, (2E)-, p-Hydroxyphenylacrylic acid, (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid, 3-(4-Hydroxyphenyl)-2-propenoic acid, 4-coumarate, Cinnamic acid, p-hydroxy-, (E)-, trans-p-Hydroxycinnamate, 2-Propenoic acid, 3-(4-hydroxyphenyl)-, (E)-3-(4-Hydroxyphenyl)-2-propenoic acid, (E)-3-(4-hydroxyphenyl)prop-2-enoic acid, 4-Hydroxycinnamate, (2E)-3-(4-hydroxyphenyl)acrylic acid, beta-(4-Hydroxyphenyl)acrylic acid, trans-4-hydroxycinnamate, UNII-IBS9D1EU3J, IBS9D1EU3J, EINECS 231-000-0, Para coumaric acid, MFCD00004399, NSC 59260, 3-(4-hydroxyphenyl)prop-2-enoic acid, NSC 674321, p-coumarate, 2-Propenoic acid, 3-(4-hydroxyphenyl)-, (E)-, BRN 2207381, BRN 2207383, CHEBI:32374, ORISTAR PCA, parahydroxycinnamic acid, NSC-59260, NSC-674321, 4-hydroxy cinnamic acid, CHEMBL66879, PARA HYDROXYCINNAMIC ACID, beta-[4-Hydroxyphenyl]acrylic acid, 0-10-00-00297 (Beilstein Handbook Reference), 4-10-00-01005 (Beilstein Handbook Reference), NSC674321, trans-p-coumarate, 3-(4-hydroxyphenyl)acrylate, .beta.-[4-Hydroxyphenyl]acrylic acid, trans-HPPA, (E)-4-hydroxycinnamic acid, (E)-3-[4-hydroxyphenyl]-2-propenoic acid, 4-coumaric acid, (E)-isomer, 4-Hydroxycinnamicacid, trans-p-Cumaric Acid, 4-Hydroxycinamic acid, .BETA.-(4-HYDROXYPHENYL)ACRYLIC ACID, 2-Propenoic acid, 3-(4-hydroxyphenyl)-, (Z)-, CHEBI:36090, hydroxycinnamate, Para coumarate, p-coumaric-acid, Para-Coumarate, p-Cumarate, naringeninic-acid, p-Hydroxycinnamate, 4qem, Coumaric acid, p-, 4'-Hydroxycinnamate, 4-Hydroxy cinnamate, p-Coumaric acid,trans, p-Coumaric acid 98%, 4f8j, p-Coumaric acid, trans, 4-Hydroxyphenylpropenoate, (2E)-3-(4-Hydroxyphenyl)-2-propenoic acid, trans-3-(4'-hydroxyphenyl)-2-propenoic acid, bmse000150, bmse000591, bmse010208, trans-4-HydroxycinnamicAcid, b-[4-Hydroxyphenyl]acrylate, SCHEMBL39106, p-hydroxycinnamic acid (M4), MLS001066419, p-Hydroxycinnamic acid, trans, P-COUMARIC ACID [MI], beta-[4-Hydroxyphenyl]acrylate, BDBM4374, GTPL5787, b-[4-Hydroxyphenyl]acrylic acid, trans-p-HydroxyzimtsA currencyure, DTXSID30901076, P-COUMARIC ACID [WHO-DD], HMS1409E10, 3-(4-Hydroxyphenyl)-2-propenoate, BCP22803, HY-N2391, NSC59260, STR06515, 4-HYDROXYPHENYLPROPENOIC ACID, Cinnamic acid, 4-hydroxy-, trans-, AC7957, BBL012226, CK2547, s4759, s9564, STL163567, AKOS000120685, BCP9001042, CCG-266309, CS-W020394, DB04066, propenoic acid, 3-(4-hydroxyphenyl)-, p-Coumaric acid, >=98.0% (HPLC), (E)-3-(4-hydroxyphenyl)prop-2-enoate, NCGC00246974-01, 1ST40051, 50940-26-6, AC-10318, AC-34130, AC-34133, AS-12000, BP-13278, SMR000112201, (E)-3-(4-hydroxyphenyl)prop-2-enoicacid, trans-p-Coumaric acid, analytical standard, NS00068187, EN300-17292, C00811, Q99374, (2E)-3-(4-Hydroxyphenyl)-2-propenoic acid #, Dehydroepiandrosterone-[D6] (CertiMass solution), AE-562/40414679, p-Coumaric acid (synonym: p-Hydroxycinnamic acid), trans-p-Coumaric acid 1000 microg/mL in Acetone, Q-100560, W-104438, BRD-K87122641-001-08-1, BRD-K87122641-001-10-7, Z56911963, 0C1BFF2D-2CF7-4FC1-9F76-3268C2C7F783, F2191-0188, p-Coumaric acid, primary pharmaceutical reference standard, InChI=1/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/b6-3
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