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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 |
HFPZCAJZSCWRBC-UHFFFAOYSA-N |
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MOLECULAR WEIGHT |
134.22 |
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MOLECULAR FORMULA |
C10H14 |
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MOLECULAR MASS |
134.222 |
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BIOLOGICAL SOURCE |
Sassafras albidum |
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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 |
Prenol lipids |
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NLRP3 DOCKING SCORE(Kcal/mol) |
-4.845 |
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CANONICAL SMILES Cc1ccc(C(C)C)cc1
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BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES
No
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SYNONYMS |
P-CYMENE, 4-Isopropyltoluene, 99-87-6, p-Isopropyltoluene, Dolcymene, Para-cymene, p-Cymol, Paracymene, 1-Isopropyl-4-methylbenzene, Camphogen, p-Methylcumene, 4-Cymene, 2-p-Tolylpropane, Cymol, CYMENE, Benzene, 1-methyl-4-(1-methylethyl)-, p-Methylisopropylbenzene, Paracymol, 1-Methyl-4-isopropylbenzene, p-Cimene, 4-Isopropyl-1-methylbenzene, Cumene, p-methyl-, 4-Methylisopropylbenzene, 1-Methyl-4-(1-methylethyl)benzene, p-methyl cumene, p-Isopropylmethylbenzene, 4-Methyl-1-isopropylbenzene, Cymene, p-, Benzene, 1-isopropyl-4-methyl-, Isopropyltoluene, 1-methyl-4-(propan-2-yl)benzene, 4-Isopropyltoluol, FEMA No. 2356, 4-Isopropylbenzyl radical, 4-methyl isopropylbenzene, 1-methyl-4-propan-2-ylbenzene, 4-Cymol, NSC 4162, HSDB 5128, Methyl-4-(1-methylethyl)benzene, 4-methyl-1-(propan-2-yl)benzene, EINECS 202-796-7, UNII-1G1C8T1N7Q, 1-isopropyl-4-methyl-Benzene, 1G1C8T1N7Q, DTXSID3026645, CHEBI:28768, AI3-02272, NSC-4162, MFCD00008893, p-Mentha-1,3,5-triene, DTXCID006645, EC 202-796-7, 1-Methyl-4-(1-methylethyl)-benzene, CYMENE (MART.), CYMENE [MART.], BENZENE,1-ISOPROPYL,4-METHYL P-CYMENE, 4939-75-7, para cymene, CAS-99-87-6, isopropyltoluol, p-methyl-Cumene, 4-lsopropyltoluene, MML, p-Cymene, 99%, p-Cymene [UN2046] [Flammable liquid], p-Cymene [UN2046] [Flammable liquid], Carvacrol derivative, 8, p-Methylisopropyl benzene, P- Isopropylmethylbenzene, P-CYMENE [FHFI], P-CYMENE [HSDB], P-CYMENE [FCC], P-CYMENE [MI], bmse000503, P-CYMENE [WHO-DD], p-Cymene, analytical standard, 1-Methyl-4-isopropyl benzene, p-Cymene, >=97%, FG, CHEMBL442915, NSC4162, BDBM248165, benzene, 1-methyl-4-methylethyl-, WLN: 1Y1 & R D1, 1-(1-methylethyl)-4-methylbenzene, Tox21_201932, Tox21_300338, s5598, AKOS000121521, Benzene, 1-methyl-4(1-methylethyl)-, CCG-266123, LMPR0102090014, p-Isopropyltoluene, analytical standard, USEPA/OPP Pesticide Code: 122103, NCGC00247998-01, NCGC00247998-02, NCGC00254425-01, NCGC00259481-01, AC-34132, AS-11012, NS00005157, S0664, EN300-21455, C06575, Q284072, W-100013, p-Cymene, certified reference material, TraceCERT(R), F8889-6466, Z104497772, InChI=1/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H |
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