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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_332


COMPOUND/COMMON NAME:- plumbagin
CAS ID
N/A
INCHI KEY
VCMMXZQDRFWYSE-UHFFFAOYSA-N
MOLECULAR WEIGHT
188.18
MOLECULAR FORMULA
C11H8O3
MOLECULAR MASS
188.182
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
Naphthalenes
NLRP3 DOCKING SCORE(Kcal/mol)
-5.068
CANONICAL SMILES   CC1=CC(=O)c2c(O)cccc2C1=O
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   Yes
SYNONYMS
Plumbagin, 481-42-5, 5-hydroxy-2-methylnaphthalene-1,4-dione, 5-Hydroxy-2-methyl-1,4-naphthoquinone, Plumbagine, 2-Methyljuglone, Plumbaein, Plumbagone, 5-Hydroxy-2-methyl-1,4-naphthalenedione, 1,4-Naphthalenedione, 5-hydroxy-2-methyl-, 5-Hydroxy-2-methyl-[1,4]naphthoquinone, 2-Methyl-5-hydroxy-1,4-naphthoquinone, NSC 236613, NSC 688284, 5-hydroxy-2-methyl-1,4-dihydronaphthalene-1,4-dione, YAS4TBQ4OQ, MFCD00001682, NSC-236613, NSC-688284, CHEBI:8273, CHEMBL295316, PCUR-101, 1,4-NAPHTHOQUINONE, 5-HYDROXY-2-METHYL-, NSC236613, NSC688284, 5-Hydroxy-2-methyl-naphthalene-1,4-dione, CCRIS 6671, SR-05000002263, UNII-YAS4TBQ4OQ, EINECS 207-569-6, BRN 1870475, Pumbagin, AI3-38055, 5-Hydroxy-2-methylnaphthoquinone, Plumbagin [WHO-DD], ST069355, PLUMBAGIN [MI], RTK1, 1, 5-hydroxy-2-methyl-, SCHEMBL34186, BSPBio_002546, 4-08-00-02376 (Beilstein Handbook Reference), Plumbagin from Plumbago indica, SPECTRUM1505129, GTPL7003, DTXSID8075413, ACon1_001611, HMS3870L13, WLN: L66 BV EVJ C1 GQ, HY-N1497, BDBM50012070, s4777, STL564479, AKOS015969699, CCG-208032, CCG-208410, NCGC00094567-01, NCGC00094567-02, NCGC00094567-03, NCGC00094567-04, NCGC00094567-05, NCGC00094567-06, BP-25404, NCI60_001904, PS-11338, 1ST177647, DB-051524, CS-0017042, NS00031768, P1139, 5- HYDROXY,2-METHYL-1,4-NAPHTOQUINONE, AP-782/41885488, A1-00788, Q2550553, SR-05000002263-2, SR-05000002263-3, W-202844, BRD-K36137799-001-02-4, BRD-K36137799-001-03-2, InChI=1/C11H8O3/c1-6-5-9(13)10-7(11(6)14)3-2-4-8(10)12/h2-5,12H,1H, Plumbagin2-Methyljuglone; 5-hydroxy-2-methylnaphthalene-1,4-dione; 5-Hydroxy-2-methyl-1,4-naphthoquinone
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