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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_26


COMPOUND/COMMON NAME:- paraxanthine
CAS ID
N/A
INCHI KEY
QUNWUDVFRNGTCO-UHFFFAOYSA-N
MOLECULAR WEIGHT
180.16
MOLECULAR FORMULA
C7H8N4O2
MOLECULAR MASS
180.167
BIOLOGICAL SOURCE
Paullinia cupana
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
Imidazopyrimidines
NLRP3 DOCKING SCORE(Kcal/mol)
-5.748
CANONICAL SMILES   Cn1c(=O)[nH]c2ncn(C)c2c1=O
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   N/A
SYNONYMS
paraxanthine, 1,7-Dimethylxanthine, 611-59-6, p-Xanthine, 1,7-Dimethyl-1H-purine-2,6(3H,7H)-dione, 1H-Purine-2,6-dione, 3,7-dihydro-1,7-dimethyl-, 1,7-dimethyl-3H-purine-2,6-dione, Xanthine, 1,7-dimethyl-, Caffeine Impurity F, 3,7-Dihydro-1,7-dimethyl-1H-purine-2,6-dione, 1,7-dimethyl-Xanthine, 1,7-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione, MFCD00005727, 1,7-Dimethyl-3,7-dihydro-1H-purine-2,6-dione, NSC-400018, CHEMBL1158, DTXSID2052281, CHEBI:25858, Q3565Y41V7, EINECS 210-271-9, NSC 400018, BRN 0197907, UNII-Q3565Y41V7, 2,6-Dihydroxy-1,7-dimethylpurine, PXT, 1,7-Dimethyl-1H-purine-2,6-dione, Paraxanthine(72%), Spectrum2_001733, Spectrum3_000774, Spectrum4_001207, Spectrum5_001506, Lopac-D-5385, Lopac0_000389, BSPBio_002448, KBioGR_001614, 5-26-13-00554 (Beilstein Handbook Reference), MLS000859929, DivK1c_000081, SCHEMBL232702, SPECTRUM2300170, SPBio_001806, SCHEMBL4651937, DTXCID2030853, HMS500E03, KBio1_000081, KBio3_001668, 1,7-Dimethylxanthine/Paraxanthine, NINDS_000081, HMS2231K19, HMS3261M19, HMS3370A12, 6-hydroxy-1,7-dimethylpurin-2-one, Tox21_303803, Tox21_500389, BDBM50042210, CCG-39489, NSC400018, Paraxanthine (1,7-Dimethylxanthine), 1,7-Dimethylxanthine, ~98%, solid, AKOS015913484, CS-W017214, HY-W016498, LP00389, SDCCGSBI-0050376.P003, IDI1_000081, NCGC00015347-01, NCGC00015347-02, NCGC00015347-03, NCGC00015347-04, NCGC00015347-05, NCGC00015347-06, NCGC00015347-07, NCGC00015347-09, NCGC00093817-01, NCGC00093817-02, NCGC00093817-03, NCGC00093817-04, NCGC00261074-01, NCGC00357087-01, AS-64037, CAFFEINE IMPURITY F [EP IMPURITY], CAS-611-59-6, SMR000326790, DB-005072, Eur J Pharmacol 179: 295 (1990), 1H-Purine-2, 3,7-dihydro-1,7-dimethyl-, D5696, EU-0100389, NS00010640, purine-2,6(1H,3H)-dione, 1,7-dimethyl-, D 5385, D94772, EN300-1666036, A853055, Q419223, SR-01000075184, 1,7-Dimethyl-3,7-dihydro-1H-purine-2,6-dione #, 1,7-Dimethylxanthine 100 microg/mL in Acetonitrile, SR-01000075184-1, BRD-K24084088-001-02-2, BRD-K24084088-001-06-3, BRD-K24084088-001-11-3, CAFFEINE MONOHYDRATE IMPURITY F [EP IMPURITY], Z1255430986, 1,7-Dimethyl-3,7-dihydro-1H-purine-2,6-dione (Paraxanthine; 1,7-Dimethylxanthine), 1,7-DIMETHYL-3,7-DIHYDRO- 1H-PURINE-2,6-DIONE (Caffeine Impurity F), Pharmaceutical Secondary Standard; Certified Reference Material, InChI=1/C7H8N4O2/c1-10-3-8-5-4(10)6(12)11(2)7(13)9-5/h3H,1-2H3,(H,9,13
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