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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.
Compound Summary
PLANT NAME:- Turnera diffusa PPD ID:-
PPD-ID36_91
COMPOUND/COMMON NAME:- benzyl tiglate
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CAS ID |
N/A |
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INCHI KEY |
QRGSTISKDZCDHV-XCVCLJGOSA-N |
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MOLECULAR WEIGHT |
190.24 |
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MOLECULAR FORMULA |
C12H14O2 |
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MOLECULAR MASS |
190.242 |
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BIOLOGICAL SOURCE |
Turnera diffusa |
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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 |
Benzene and substituted derivatives |
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NLRP3 DOCKING SCORE(Kcal/mol) |
-5.71 |
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CANONICAL SMILES C/C=C(\C)C(=O)OCc1ccccc1
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BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES
No
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SYNONYMS |
Benzyl tiglate, 37526-88-8, Tiglic Acid Benzyl Ester, (E)-Benzyl 2-methylbut-2-enoate, benzyl (E)-2-methylbut-2-enoate, Benzyl trans-2,3-dimethylacrylate, Benzyl trans-2-methyl-2-butenoate, Benzyl 2-methylcrotonate, 2-Butenoic acid, 2-methyl-, phenylmethyl ester, (2E)-, Benzyl 2-methyl-2-butenoate, Benzyl trans-2-methylcrotonate, FEMA No. 3330, 2-Butenoic acid, 2-methyl-, phenylmethyl ester, (E)-, benzyl (2E)-2-methylbut-2-enoate, 67UEP899RR, DTXSID3047130, NSC-69098, trans-2-Butenoic acid, 2-methyl-, phenylmethyl ester, 2-Butenoic acid, 2-methyl-, phenylmethyl ester, (E)-benzyl tiglate, UNII-67UEP899RR, (2E)-2-Methyl-2-butenoic Acid Phenylmethyl Ester; Benzyl Tiglate; NSC 69098, Benzyl (E)-2-methyl-2-butenoate, EINECS 253-544-8, EINECS 266-880-5, MFCD00017279, NSC 69098, Phenylmethyl 2-methyl-2-butenoate, (E)-, AI3-05784, Benzyl tiglate, AldrichCPR, BENZYL TIGLATE [FHFI], SCHEMBL873995, SCHEMBL873996, BENZYL TIGLATE, (E)-, CHEMBL3186295, DTXCID1027130, CHEBI:187225, (E)-benzyl 2-methyl-2-butenoate, NSC69098, Tox21_302648, AKOS025296168, Benzyl (2E)-2-methyl-2-butenoate #, (E)-Phenylmethyl 2-methyl-2-butenoate, NCGC00256881-01, LS-14071, trans-2-Butenoic acid, phenylmethyl ester, CAS-37526-88-8, B3348, BENZYL 2-METHYL-2-BUTENOATE, (E)-, NS00012012, D78437, 2-Methyl-phenylmethyl ester(2E)-2-Butenoic acid, W-106529, Benzyl tiglate stabilized with 0.1% alpha-tocopherol, Q27264164 |
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