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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:- Rhynchosia pyramidalis     PPD ID:- PPD-ID24_5


COMPOUND/COMMON NAME:- genistein
CAS ID
N/A
INCHI KEY
TZBJGXHYKVUXJN-UHFFFAOYSA-N
MOLECULAR WEIGHT
270.24
MOLECULAR FORMULA
C15H10O5
MOLECULAR MASS
270.240
BIOLOGICAL SOURCE
Rhynchosia pyramidalis
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
Isoflavonoids
NLRP3 DOCKING SCORE(Kcal/mol)
-7.044
CANONICAL SMILES   O=c1c(-c2ccc(O)cc2)coc2cc(O)cc(O)c12
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   Yes
SYNONYMS
genistein, 446-72-0, Prunetol, 4',5,7-Trihydroxyisoflavone, Genisterin, Genisteol, Sophoricol, 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one, 5,7,4'-Trihydroxyisoflavone, Bonistein, Genestein, Differenol A, NPI 031L, 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one, 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one, 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-, C.I. 75610, SIPI 807-1, MFCD00016952, NSC 36586, CCRIS 7675, 4',5, 7-Trihydroxyisoflavone, NSC36586, EINECS 207-174-9, UNII-DH2M523P0H, NSC-36586, Genistein [USAN], BRN 0263823, DH2M523P0H, NPI-031L, 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone, Genistein (Standard), DTXSID5022308, ISOFLAVONE, 4',5,7-TRIHYDROXY-, CHEBI:28088, HSDB 7475, BIO-300, SIPI-807-1, CHEMBL44, FW-635I-2, Bio 300, MLS000738127, DTXCID002308, GEN, 5-18-04-00594 (Beilstein Handbook Reference), Genistein (USAN), NCGC00015479-09, GENISTEIN (MART.), GENISTEIN [MART.], GENISTEIN (USP-RS), GENISTEIN [USP-RS], 5,7-dihydroxy-3-(4-hydroxyphenyl)-chromen-4-one, 690224-00-1, CAS-446-72-0, Lactoferrin-genistein, SR-01000075498, Genistein?, STO514, PTI G4660, PTI-G4660, SIPI-9764-I, 3kgt, 3kgu, Genistein, 8, Genistein,(S), PTI-G 4660, Genistein (GEN), TNP00151, Spectrum_000320, Tocris-1110, 1x7r, 2qa8, Genistein 85% HPLC, GENISTEIN [INN], SpecPlus_000305, GENISTEIN [MI], GENISTEIN [HSDB], Spectrum2_000638, Spectrum3_000678, Spectrum4_001543, Spectrum5_000106, Lopac-G-6649, 4',7-Trihydroxyisoflavone, MolMap_000022, UPCMLD-DP096, G 6649, GENISTEIN [WHO-DD], Isoflavone,5,7-trihydroxy-, Lopac0_000520, Oprea1_224620, Oprea1_437815, SCHEMBL19166, BSPBio_002375, KBioGR_002006, KBioGR_002564, KBioSS_000800, KBioSS_002573, NPI031L, SPECTRUM210296, BIDD:ER0113, DivK1c_006401, Genistein, analytical standard, TEMPO HOT FLASH RELIEF, SPBio_000636, 4',5,7-trihydroxy-Isoflavone, GTPL2826, MEGxp0_000568, 4,5,7-Trihydroxy Iso-Flavone, UPCMLD-DP096:001, ACon1_001065, BDBM19459, C.I. 75610(ChemID), cid_5280961, KBio1_001345, KBio2_000800, KBio2_002564, KBio2_003368, KBio2_005132, KBio2_005936, KBio2_007700, KBio3_001595, KBio3_003042, CHEBI: 28088, cMAP_000086, Bio1_000445, Bio1_000934, Bio1_001423, HMS2271K09, HMS3261H21, HMS3267K14, HMS3412I13, HMS3428M01, HMS3649B22, HMS3654D17, HMS3676I13, HMS3742I07, ALBB-015886, BCP07581, Tox21_110161, Tox21_201428, Tox21_300585, Tox21_500520, AC-472, BBL010484, CCG-38551, HB2775, HY-14596R, LMPK12050218, s1342, STK801619, WHO 11073, AKOS001590147, Tox21_110161_1, CS-1534, DB01645, KS-5128, LP00520, SB17235, SDCCGSBI-0050503.P003, SMP1_000133, Genistein; 4',5,7-Trihydroxyisoflavone, NCGC00015479-01, NCGC00015479-02, NCGC00015479-04, NCGC00015479-05, NCGC00015479-06, NCGC00015479-07, NCGC00015479-08, NCGC00015479-10, NCGC00015479-11, NCGC00015479-12, NCGC00015479-13, NCGC00015479-14, NCGC00015479-15, NCGC00015479-16, NCGC00015479-17, NCGC00015479-18, NCGC00015479-19, NCGC00015479-20, NCGC00015479-38, NCGC00025005-01, NCGC00025005-02, NCGC00025005-03, NCGC00025005-04, NCGC00025005-05, NCGC00025005-06, NCGC00025005-07, NCGC00169711-01, NCGC00169711-02, NCGC00254275-01, NCGC00258979-01, NCGC00261205-01, 1ST40142, HY-14596, NCI60_003369, SMR000112580, SY050124, CS-0694819, EU-0100520, G0272, GENISTEIN (CONSTITUENT OF RED CLOVER), NS00009870, SW203763-2, C06563, D11680, EN300-210743, G-2535, Genistein, synthetic, >=98% (HPLC), powder, K00046, US8552057, 2, AB00052696_09, AB00052696_12, GENISTEIN (CONSTITUENT OF SOY ISOFLAVONES), Q415957, GENISTEIN (CONSTITUENT OF RED CLOVER) [DSC], Genistein, primary pharmaceutical reference standard, Q-100484, SR-01000075498-1, SR-01000075498-3, SR-01000075498-6, BRD-K43797669-001-02-3, BRD-K43797669-001-03-1, BRD-K43797669-001-10-6, BRD-K43797669-001-28-8, BRD-K43797669-001-29-6, BRD-K43797669-001-30-4, Genistein, from Glycine max (soybean), ~98% (HPLC), SR-01000075498-10, F0001-2388, GENISTEIN (CONSTITUENT OF SOY ISOFLAVONES) [DSC], 4H-1-Benzopyran-4-one,7-dihydroxy-3-(4-hydroxyphenyl)-, 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4 H-1-benzopyran-4-one, Genistein, United States Pharmacopeia (USP) Reference Standard, 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-(ChemID), Genistein, Pharmaceutical Secondary Standard; Certified Reference Material
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