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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:- Paullinia cupana     PPD ID:- PPD-ID40_17


COMPOUND/COMMON NAME:- xanthine
CAS ID
N/A
INCHI KEY
LRFVTYWOQMYALW-UHFFFAOYSA-N
MOLECULAR WEIGHT
152.11
MOLECULAR FORMULA
C5H4N4O2
MOLECULAR MASS
152.113
BIOLOGICAL SOURCE
Paullinia cupana
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
Imidazopyrimidines
NLRP3 DOCKING SCORE(Kcal/mol)
-5.573
CANONICAL SMILES   O=c1[nH]c(=O)c2[nH]cnc2[nH]1
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   Yes
SYNONYMS
xanthine, 69-89-6, 2,6-Dihydroxypurine, 2,6-dioxopurine, 1H-Purine-2,6(3H,7H)-dione, Xanthin, Xanthic oxide, Pseudoxanthine, Isoxanthine, 1H-Purine-2,6-diol, 9H-Purine-2,6-diol, Purine-2,6-diol, 1H-Purine-2,6-dione, 3,7-dihydro-, 3,7-Dihydro-1H-purine-2,6-dione, 3,7-dihydropurine-2,6-dione, 2,6(1,3)-Purinedion, 3,9-dihydro-1H-purine-2,6-dione, 2,6-Dioxo-1,2,3,6-tetrahydropurine, 1H-Purine-2,6-dione, 3,9-dihydro-, USAF CB-17, 9H-xanthine, XAN, Purine-2(3H),6(1H)-dione, 9H-Purine-2,6-(1H,3H)-dione, Purine-2,6(1H,3H)-dione, Purine-2,6-(1H,3H)-dione, MFCD00078453, NSC 14664, EPA Pesticide Chemical Code 116900, CHEBI:17712, AI3-52268, 2,3,6,9-tetrahydro-1H-purine-2,6-dione, 7H-purine-2,6-diol, 9H-Purine-2,6(1H,3H)-dione, CHEMBL1424, 1262670-81-4, 1AVZ07U9S7, 3,9-dihydropurine-2,6-dione, NSC-14664, purine, 2,6-dihydroxy-, 1H-purine-2,6(3H,9H)-dione, Xanthine (VAN), CCRIS 994, EINECS 200-718-6, UNII-1AVZ07U9S7, Dioxopurine, Dioxypurin, xanthine (2,6-dihydroxypurine), 7H-xanthine, 2-Oxohypoxanthine, 2,6-dioxypurine, Xanthine,(S), 2,6-Dihydroxypurin, Xanthine, 98%, Purine-2,3H)-dione, Xanthine, >=99%, 2uz9, XANTHINE [MI], bmse000127, MolMap_000070, XANTHINE [WHO-DD], Xanthine, p.a., 99%, 9H-Purine-2,3H)-dione, Cambridge id 5126190, SCHEMBL4965, Xanthine (VAN) (8CI), 2,2,3,6-tetrahydropurine, Oprea1_474175, 1H,3H,7H-XANTHINE, 1H,3H,9H-XANTHINE, Xanthine, BioUltra, >=99%, GTPL4557, DTXSID4035120, 3,7-dihydro-purine-2,6-dione, 3,9-Dihydro-purine-2,6-dione, BDBM82009, CHEBI:48517, LRFVTYWOQMYALW-UHFFFAOYSA-, 2,6-Dihydroxypurine; Isoxanthine, HMS1659G11, HMS3604G12, BCP15189, CAS_1188, NSC_1188, NSC14664, 1H-purine-2,6(3H, 7H)-dione, BBL028159, BDBM50227193, STL064827, STL453051, AKOS000498219, AKOS005208756, AKOS015896921, AC-8422, CCG-266216, CS-W018105, DB02134, FS-3231, HY-W017389, SDCCGMLS-0065805.P001, CID 5280342, 2,6-Dioxo-1,2,3, 6-tetrahydropurine, NCGC00164338-01, SY030113, DB-015929, 2,3,6,7-tetrahydro-1H-purine-2,6-dione, NS00001219, S3693, X0004, EN300-18289, C00385, D71218, Q50980, X-0950, AB00171825-02, AG-670/31548007, Z57825360, 92AB342E-6550-4B2B-AD76-E75AC1C2EB45, Xanthine, >=99.5% (HPLC), purified by recrystallization, InChI=1/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11)
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