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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:- Juglans nigra     PPD ID:- PPD-ID5_123


COMPOUND/COMMON NAME:- 5-hydroxy-1,4-naphthoquinone
CAS ID
N/A
INCHI KEY
KQPYUDDGWXQXHS-UHFFFAOYSA-N
MOLECULAR WEIGHT
174.15
MOLECULAR FORMULA
C10H6O3
MOLECULAR MASS
174.155
BIOLOGICAL SOURCE
Juglans nigra
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
Naphthalenes
NLRP3 DOCKING SCORE(Kcal/mol)
-7.188
CANONICAL SMILES   O=C1C=CC(=O)c2c(O)cccc21
BIOACTIVITY REPORTED FOR NEURODEGENERATIVE DISEASES   No
SYNONYMS
juglone, 481-39-0, 5-Hydroxy-1,4-naphthoquinone, 5-Hydroxy-1,4-naphthalenedione, 5-Hydroxynaphthalene-1,4-dione, Regianin, Nucin, Juglon, Akhnot, Yuglon, C.I. Natural Brown 7, 8-Hydroxy-1,4-naphthoquinone, 5-Hydroxynaphthoquinone, 1,4-NAPHTHALENEDIONE, 5-HYDROXY-, 5-Hydroxy-p-naphthoquinone, C.I. 75500, 1,4-Naphthoquinone, 5-hydroxy-, Juglane, Jugnlon, Iuglon, 1,4-Naphthoquinone, 8-hydroxy-, 5-Hydroxy-1,4-naphthosemiquinone, 5-Hydroxy-1,4-naftochinon, MFCD00001684, NSC 153189, NSC 622948, 5-hydroxy-1,4-dihydronaphthalene-1,4-dione, CHEMBL43612, W6Q80SK9L6, 5-Hydroxy-[1,4]Naphthoquinone, 8-Hydroxy-1,4-naphthalenedione, CHEBI:15794, NCI 2323, NSC34266, NSC153189, NSC622948, NSC-153189, NSC-622948, 1, 8-hydroxy-, WLN: L66 BV EVJ GQ, Caswell No. 515AA, CCRIS 5423, EINECS 207-567-5, 5-Hydroxy-1,4-naftochinon [Czech], JUGLONE CRYSTALLIZED, BRN 1909764, UNII-W6Q80SK9L6, Antibiotic PD7, 481-13-0, Spectrum_000415, 3b7j, JUGLONE [MI], Spectrum2_000778, Spectrum3_001228, Spectrum4_001769, Spectrum5_000357, 5-HNQ, SCHEMBL34185, BSPBio_001157, BSPBio_002676, KBioGR_000497, KBioGR_002257, KBioGR_002470, KBioSS_000497, KBioSS_000895, KBioSS_002477, SPECTRUM300038, 4-08-00-02368 (Beilstein Handbook Reference), DivK1c_001026, SPBio_000856, -Hydroxy-1,4-naphthalenedione, DTXSID0031504, BDBM24777, HMS503M13, KBio1_001026, KBio2_000497, KBio2_000895, KBio2_002470, KBio2_003065, KBio2_003463, KBio2_005038, KBio2_005633, KBio2_006031, KBio2_007606, KBio3_000913, KBio3_000914, KBio3_002176, KBio3_002948, 5-hydroxy-naphthalene-1,4-dione, cMAP_000058, NINDS_001026, Bio1_000441, Bio1_000930, Bio1_001419, Bio2_000409, Bio2_000889, HMS1362I19, HMS1792I19, HMS1923G07, HMS1990I19, HMS3403I19, Juglone - CAS 481-39-0, 5-hydroxy-1,4-naphthoquinone, 4, HY-N6949, CCG-40256, NSC-34266, s5512, ZB1862, 5-Hydroxy-1,4-naphthoquinone, 97%, AKOS001576598, 5-Hydroxy-1,4-naphthalenedione, 9CI, CS-W017516, SDCCGMLS-0066542.P001, IDI1_001026, IDI1_002164, SMP1_000168, NCGC00095247-01, NCGC00095247-02, NCGC00095247-03, NCGC00095247-04, NCGC00095247-05, CI 75500, CI-75500, SY051453, 5-Hydroxy-1,4-naphthalenedione(Juglone)?, DB-005382, 1,4-dihydro-1,4-dioxo-5-hydroxynaphthalene, H0286, NS00021169, C03840, EN300-160375, F17689, Q900912, SR-05000002406, J-650071, Q-100522, SR-05000002406-1, F0451-0746, InChI=1/C10H6O3/c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12/h1-5,12
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