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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_21


COMPOUND/COMMON NAME:- imp
CAS ID
N/A
INCHI KEY
GRSZFWQUAKGDAV-KQYNXXCUSA-N
MOLECULAR WEIGHT
348.21
MOLECULAR FORMULA
C10H13N4O8P
MOLECULAR MASS
348.208
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
Purine nucleotides
NLRP3 DOCKING SCORE(Kcal/mol)
-7.384
CANONICAL SMILES   O=c1[nH]cnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   N/A
SYNONYMS
Inosinic acid, 5'-inosinic acid, 131-99-7, inosine 5'-monophosphate, inosine monophosphate, 5'-IMP, 5'-inosinate, IMP, inosine 5'-phosphate, INOSINE-5'-MONOPHOSPHATE, 5'-inosine monophosphate, Inosine-5'-monophosphoric acid, Inosine 5'-Monophosphoric acid, BRN 0630517, UNII-TAO7US05G5, Cytosine inosinate, EINECS 205-045-1, TAO7US05G5, ribosylhypoxanthine monophosphate, CHEBI:17202, Inosine 5'-(dihydrogen phosphate), 30918-54-8, 2'-inosine-5'-monophosphate, INOSINIC ACID, 5'-, hypoxanthosine 5'-monophosphate, INS NO.630, INS-630, inosinate, I-5'-P, CID 5280323, E-630, HYPOXANTHINE RIBOSIDE-5-PHOSPHORIC ACID, [(2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate, Acid, Inosinic, [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-hydroxypurin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate, {[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-6,9-dihydro-3H-purin-9-yl)oxolan-2-yl]methoxy}phosphonic acid, inosinsaure, inosine phosphate, 1yfz, 5'-aInosinic acid, 1g9s, 1qk4, 1z6d, 5'-IMP; IMP; Inosine 5'-(dihydrogen phosphate), Inosine 5' monophosphate, [3h]inosine monophosphate, bmse000175, INOSINIC ACID [MI], SCHEMBL19255, ((2R,3S,4R,5R)-3,4-Dihydroxy-5-(6-hydroxy-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl dihydrogen phosphate, GTPL5124, CHEMBL1207374, BDBM19254, DTXSID80948097, 1p17, 1p19, Inosine-5'-(dihydrogen phosphate), CYTOSINE INOSINATE [WHO-DD], MFCD00066754, STL564942, AKOS015896456, AKOS015918470, AKOS030494380, DB04566, AS-56817, HY-108213, CS-0027540, NS00014854, C00130, F81515, A1-01972, W-108320, Q27074273, BB128E2C-BC89-4360-B0A0-190DDF5C0B57, I-5 inverted exclamation marka-P IMP Inosinic Acid;IMP, [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)oxolan-2-yl]methyl dihydrogen, [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)tetrahydrofuran-2-yl]methyl dihydrogen phosphate, {[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-6,9-dihydro-1H-purin-9-yl)oxolan-2-yl]methoxy}phosphonic acid, 25249-22-3
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