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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:- Osteophloeum platyspermum     PPD ID:- PPD-ID31_5


COMPOUND/COMMON NAME:- 3-hydroxy-8,9-methylenedioxypterocarpan; (6ar,12ar)-form 
CAS ID
2035-15-6
INCHI KEY
HUKSJTUUSUGIDC-UHFFFAOYSA-N
MOLECULAR WEIGHT
284.27
MOLECULAR FORMULA
C16H12O5
MOLECULAR MASS
284.267
BIOLOGICAL SOURCE
Osteophloeum platyspermum
DATA SOURCE
Dictionary of Natural Product. http://dnp.chemnetbase.com. .; Bennett, Bradey & Alarcon, Rocio. (1994). Osteophloeum platyspermum and Virola duckei (Myristicaceae): Newly reported as hallucinogens from Amazonian Ecuador. Economic Botany. 48. 152-158. 10.1007/BF02908205.
CHEMICAL CLASS OF COMPOUND
Isoflavonoids
NLRP3 DOCKING SCORE(Kcal/mol)
-5.985
CANONICAL SMILES   Oc1ccc2c(c1)OCC1c3cc4c(cc3OC21)OCO4
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   No
SYNONYMS
Maackiain, 19908-48-6, 3-hydroxy-8,9-methylenedioxypterocarpane, CHEBI:73029, NSC629152, 6a,12a-dihydro-6H-[1,3]dioxolo[5,6][1]benzofuro[3,2-c]chromen-3-ol, 5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-ol, DL-aackiain, Spectrum_000238, SpecPlus_000557, Spectrum2_001925, Spectrum3_000231, Spectrum4_001528, Spectrum5_000036, BSPBio_001901, KBioGR_001936, KBioSS_000718, SPECTRUM201654, DivK1c_006653, SPBio_001929, CHEMBL239047, SCHEMBL12810278, ACon1_001470, KBio1_001597, KBio2_000718, KBio2_003286, KBio2_005854, KBio3_001401, HUKSJTUUSUGIDC-UHFFFAOYSA-N, CCG-38492, AKOS015909127, NSC-629152, NCGC00095514-01, NCGC00095514-02, NCGC00095514-03, NS00015825, NS00067877, NS00115975, BRD-A95445494-001-03-7, Q27140245, 6a,12a-Dihydro-6H-(1,3)dioxolo(5,6)benzofuro(3,2-c)chromen-3-ol, 6a,12a-Dihydro-6H-[1,3]dioxolo[4',5':5,6][1]benzofuro[3,2-c]chromen-3-ol, 6a,12a-Dihydro-6H-[1,3]dioxolo[4',5':5,6][1]benzofuro[3,2-c]chromen-3-ol #, cis-6a,12a-Dihydro-6H-[1,3]dioxolo[4',5':5,6]benzofuro[3,2-c]chromen-3-ol, {6H-[1,3]Dioxolo[5,6]benzofuro[3,} {2-c][1]benzopyran-3-ol,6a,12a-dihydro-,} (6aR-cis)- (CA INDEX NAME), 5,7,11,19-tetraoxapentacyclo[10.8.0.0(2),(1)?.0?,?.0(1)(3),(1)?]icosa-2(10),3,8,13,15,17-hexaen-16-ol, 6H-[1,6]benzofuro[3,2-c][1]benzopyran-3-ol,6a,12a-dihydro-, (6aR-cis)- (CA INDEX NAME)
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