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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.
CAS ID |
N/A |
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INCHI KEY |
YCIMNLLNPGFGHC-UHFFFAOYSA-N |
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MOLECULAR WEIGHT |
110.11 |
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MOLECULAR FORMULA |
C6H6O2 |
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MOLECULAR MASS |
110.112 |
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BIOLOGICAL SOURCE |
Anadenanthera peregrina |
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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 |
Phenols |
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NLRP3 DOCKING SCORE(Kcal/mol) |
-5.111 |
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CANONICAL SMILES Oc1ccccc1O
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BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES
Yes
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SYNONYMS |
pyrocatechol, catechol, 120-80-9, 1,2-dihydroxybenzene, 1,2-benzenediol, benzene-1,2-diol, pyrocatechin, 2-hydroxyphenol, o-Benzenediol, o-Dihydroxybenzene, o-Dioxybenzene, o-Hydroquinone, o-Hydroxyphenol, Phthalhydroquinone, Pyrocatechine, o-Phenylenediol, Oxyphenic acid, Fouramine PCH, benzenediol, Durafur developer C, Pelagol Grey C, Catechin (phenol), Fourrine 68, Benzene, o-dihydroxy-, Catechol (phenol), o-Diphenol, C.I. Oxidation Base 26, Pyrokatechin, Pyrokatechol, Katechol, ortho-Dihydroxybenzene, NCI-C55856, NSC 1573, C.I. 76500, MFCD00002188, Catechol-pyrocatechol, 12385-08-9, DTXSID3020257, LF3AJ089DQ, CHEMBL280998, CHEBI:18135, NSC-1573, ortho-Hydroxyphenol, CAQ, 1,?2-?Benzenediol, ortho-Benzenediol, ortho-Dioxybenzene, ortho-Hydroquinone, Katechol [Czech], ortho-Phenylenediol, Pyrocatechinic acid, 26982-53-6, DTXCID30257, Pyrokatechin [Czech], Pyrokatechol [Czech], Benzene-1,2-diol (Pyrocatechol), CI Oxidation Base 26, Phthalic alcohol, CAS-120-80-9, SMR000326660, CCRIS 741, HSDB 1436, EINECS 204-427-5, UNII-LF3AJ089DQ, BRN 0471401, Oxyphenate, CI 76500, Kachin, ortho-diphenol, benzene diol, ortho-Quinol, AI3-03995, 4oow, alpha-hydroxyphenol, o-dihydroxy-benzene, 1,a2-aBenzenediol, phenol derivative, 2, 3fw4, 4k7i, CATECHOL [HSDB], CATECHOL [IARC], Pyrocatechol, >=99%, CATECHOL [VANDF], Lopac-C-9510, PYROCATECHOL [MI], WLN: QR BQ, bmse000385, EC 204-427-5, 1,2-Dihydroxybenzene, XI, 1,2-Benzenediol; Catechol, Lopac0_000280, SCHEMBL18351, MLS002153385, MLS002303022, BIDD:ER0327, Pyrocatechinic acidPyrocatechol, Pyrocatechol, p.a., 99.0%, BDBM26188, Durafur Developer CFouramine PCH, NSC1573, HMS2233A17, HMS3260H22, HMS3373K16, Tox21_202317, Tox21_300153, Tox21_500280, s6305, STK398651, AKOS000119002, CCG-204375, DB02232, LP00280, SDCCGSBI-0050268.P002, NCGC00015283-01, NCGC00015283-02, NCGC00015283-03, NCGC00015283-04, NCGC00015283-05, NCGC00015283-06, NCGC00015283-07, NCGC00015283-08, NCGC00015283-10, NCGC00091262-01, NCGC00091262-02, NCGC00091262-03, NCGC00253952-01, NCGC00259866-01, NCGC00260965-01, AC-34196, BP-21156, BS-20054, Catechol (Pyrocatechol; Benzene-1,2-diol), DB-003770, C.I.-76500, EU-0100280, NS00007130, P0317, P0567, EN300-19426, C 9510, C00090, C01785, D91943, 1,2-Dihydroxybenzene, ReagentPlus(R), >=99%, Pyrocatechol, purified by sublimation, >=99.5%, A804599, AB-131/40235236, Q282440, SR-01000075791, SR-01000075791-1, W-109068, 1,2-Dihydroxybenzene 1000 microg/mL in Dichloromethane, F0001-0332, Pyrocatechol, certified reference material, TraceCERT(R), Z104473810, InChI=1/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8, Pyrocatechol, plant cell culture tested, BioReagent, >=99%, powder, 2H-1-Benzopyran-3,5,7-triol, 2-(3,4-dihydroxyphenyl)-3,4-dihydro-,(2R-trans)- |
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