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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:- Juniperus recurva PPD ID:-
PPD-ID19_88
COMPOUND/COMMON NAME:- Nerolidol
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CAS ID |
N/A |
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INCHI KEY |
FQTLCLSUCSAZDY-SDNWHVSQSA-N |
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MOLECULAR WEIGHT |
222.37 |
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MOLECULAR FORMULA |
C15H26O |
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MOLECULAR MASS |
222.372 |
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BIOLOGICAL SOURCE |
Juniperus recurva |
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DATA SOURCE |
Vivek-Ananth, R. P., Mohanraj, K., Sahoo, A. K., & Samal, A. (2023). IMPPAT 2.0: An Enhanced and Expanded Phytochemical Atlas of Indian Medicinal Plants. ACS omega, 8(9), 8827–8845. https://doi.org/10.1021/acsomega.3c00156 | ||
CHEMICAL CLASS OF COMPOUND |
Prenol lipids |
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NLRP3 DOCKING SCORE(Kcal/mol) |
-3.244 |
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CANONICAL SMILES C=CC(C)(O)CC/C=C(\C)CCC=C(C)C
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BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES
No
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SYNONYMS |
NEROLIDOL, trans-Nerolidol, 7212-44-4, 40716-66-3, 3,7,11-Trimethyldodeca-1,6,10-trien-3-ol, (6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol, (E)-3,7,11-Trimethyldodeca-1,6,10-trien-3-ol, 3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, Nerolidol trans-form, FCI 119b, Stirrup, 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (6E)-, (+)-Nerolidol, (6E)-nerolidol, 3-Hydroxy-3,7,11-trimethyl-1,6,10-dodecatriene, (E)-nerolidol, FG5V0N8P2H, 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, DTXSID2040783, Methylvinylhomogeranyl carbinol, (3s)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol, FEMA No. 2772, NCGC00095837-01, (.+/-.)-Nerolidol, EINECS 230-597-5, MFCD00008911, EPA Pesticide Chemical Code 128910, BRN 1724135, UNII-QR6IP857S6, trans nerolidol, AI3-10519, CCRIS 7678, 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (E)-, Nerolidol (E), EC 230-597-5, 3,7,11-Trimethyl-1,6,10-dodecatriene-3-ol, 3-01-00-02042 (Beilstein Handbook Reference), CHEBI:7524, DTXCID602247, QR6IP857S6, UNII-FG5V0N8P2H, FEMA 2772, E-Nerolidol, .beta.-Nerolidol, .alpha.-Nerolidol, EINECS 255-053-4, Spectrum5_000460, .+/-.-trans-Nerolidol, NEROLIDOL, TRANS-, Nerolidol (cis and trans), (6E)-(+/-)-nerolidol, BSPBio_002958, CHEMBL25424, SCHEMBL114136, SPECTRUM1502251, DTXCID0020783, CHEBI:141283, NEROLIDOL TRANS-FORM [MI], HY-N1944, HY-N6635, Tox21_111527, Tox21_301382, trans-Nerolidol, analytical standard, BBL018508, CCG-38883, s5345, STL193540, AKOS015902890, AKOS025310880, SDCCGMLS-0066709.P001, NEROLIDOL, (6E)-(+/-)-, NCGC00095837-02, NCGC00095837-03, NCGC00255198-01, 1ST40226, 35944-21-9, AS-16074, AS-75500, DA-56113, CAS-7212-44-4, 1ST168607, CAS-40716-66-3, CS-0018255, CS-0044197, N0454, NS00004499, Q415421, SR-05000002467, Q-201460, SR-05000002467-1, W-110939, (6E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, trans-3,7,11-trimethyl-dodeca-1,6,10-trien-3-ol, trans-Nerolidol, primary pharmaceutical reference standard, (E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, trans-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol |
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