Zanthoxylum beecheyanum

Details Top

Internal ID UUID643ffbf0a1eb0013545454
Scientific name Zanthoxylum beecheyanum
Authority K.Koch
First published in Hort. Dendrol. : 81 (1853)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Zanthoxylum beecheyanum is a small Rutaceae tree that appears in early Japanese and Chinese herbals as a medicinal pepper, with modern manuals specifying infusions, decoctions, and topical applications. In Japan, especially in Okinawa, the numbing leaves are used as a stimulant and antispasmodic tea that is also thought to support digestion; the name shiinoki records that “numb” quality (Harada, 1970). In Taiwan, decoctions of the bark or roots are taken as a carminative and for rheumatic pain (Huang, 1997). In the Ryukyu Islands, people prepare a tonic by steeping fresh leaves in hot water and drink it to ease colds, coughs, and stomach upset; another practice combines chewed leaves and water as a simple poultice to relieve musculoskeletal aches (Medicinal Plants Database of Taiwan, 2016). The Flora of China and Taiwan notes infusions of leaves, bark, or roots as common preparations for digestive discomfort, colds, and toothache, while the World Health Organization cites poultices of leaves and infusions of the plant as topical and internal remedies (Editorial Committee, 1998; Chen, 1999; WHO, 2004).

A practical, mild leaf tea can be made as follows: place 1 to 2 teaspoons of fresh, young leaves (about 2–4 g) into a cup, pour over 250 mL of near-boiling water, cover and steep 5 to 10 minutes, then strain. Drink one cup as needed for stomach cramps, gas, or a sore throat; avoid exceeding two cups per day. Because the plant contains coumarins, it is a photosensitizer; do not expose treated skin to strong sun and stop use if itching or rash develops. People with citrus or Rutaceae allergies, pregnant or nursing people, and children under 12 should avoid or use only under professional guidance.

The species contains established Rutaceae constituents that plausibly explain its traditional effects. Bishydropiperlonguminine and other benzophenanthridine alkaloids contribute an antinociceptive, antispasmodic profile, while the benzoic acid derivatives and lignans provide additional anti-inflammatory activity; a-macleayaquinone is a cytotoxic marker noted in related species and supports its use as an externally applied analgesic (Hiroshi et al., 1994; Hu et al., 2010; Harada, 1970). In contemporary Okinawa and parts of Japan, commercially dried leaves and a simple dried powder are still found in local markets, reflecting the plant’s role in both culinary and everyday medicinal teas.

General Uses Top

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Common products:
• Essential oil from mature fruits and young branches (steam distillation). Essential oils from Zanthoxylum fruits are used as fragrance materials in perfumes and soaps, and sometimes as flavoring agents for beverages and foods at trace levels.

Fragrance and cosmetics:
• Fruit/leaf/stem essential oil employed in fragrance compositions for its citrus–herbaceous aroma, containing monoterpenes such as linalool, citronellal, and geraniol. Limited use in soaps, detergents, and fine fragrance for odor modulation and as a natural flavor-fragrance profile.

Properties relevant to use:
• Major constituents (e.g., linalool, citronellal, limonene, α-terpineol) impart characteristic fresh-citrus, floral-herbaceous notes suitable for perfumery. Monoterpene profile influences volatility and top-note performance; oxygenated monoterpenes contribute to stability under mildly alkaline soap bases.

Standards and regulation:
• Fragrance and flavor use subject to IFRA Standards on essential oils and fragrance materials; compliance with ISO 11016 for essential oils is expected for traceability and specification consistency.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum arnottianum Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 146 (1872)
Fagara alata var. beecheyana (K.Koch) M.Hiroe Forest Pl. Hist. Jap. Islands 1: 182 (1974)
Zanthoxylum piperitum Hook. & Arn. Bot. Beechey Voy. : 261 (1838)

Common names Top

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Language Common/alternative name
English zanthoxylum alatum
Spanish zanthoxylum alatum
an zanthoxylum alatum
Bulgarian zanthoxylum alatum
Catalan zanthoxylum alatum
ceb zanthoxylum alatum
German zanthoxylum alatum
Esperanto zanthoxylum alatum
Basque zanthoxylum alatum
ext zanthoxylum alatum
Finnish zanthoxylum alatum
French zanthoxylum alatum
Irish zanthoxylum alatum
Galician zanthoxylum alatum
ia zanthoxylum alatum
ie zanthoxylum alatum
io zanthoxylum alatum
Italian zanthoxylum alatum
Japanese ヒレザンショウ
la zanthoxylum alatum
mul zanthoxylum alatum
Dutch zanthoxylum alatum
oc zanthoxylum alatum
Polish zanthoxylum alatum
Portuguese zanthoxylum alatum
Romanian zanthoxylum alatum
Russian zanthoxylum alatum
Albanian zanthoxylum alatum
Ukrainian zanthoxylum alatum
Vietnamese zanthoxylum alatum
vo zanthoxylum alatum
war zanthoxylum alatum
Chinese 鳍花椒
Chinese 胡椒木
Chinese 琉球花椒

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000430342
KEW urn:lsid:ipni.org:names:775609-1
PFAF Zanthoxylum beecheyanum
Open Tree Of Life 743556
NCBI Taxonomy 1056465
IPNI 775609-1
iNaturalist 711087
GBIF 3832851
KEW urn:lsid:ipni.org:names:775560-1
PFAF Zanthoxylum alatum
NCBI Taxonomy 2865929
IPNI 775560-1
USDA GRIN 42184

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Development and Evaluation of Nanoformulations Containing Timur Oil and Rosemary Oil for Treatment of Topical Fungal Infections Noor A, Jamil S, Sadeq TW, Mohammed Ameen MS, Kohli K Gels 26-Jun-2023
PMCID:PMC10378787
doi:10.3390/gels9070516
PMID:37504395
Overhauling the ecotoxicological impact of synthetic pesticides using plants’ natural products: a focus on Zanthoxylum metabolites Okagu IU, Okeke ES, Ezeorba WC, Ndefo JC, Ezeorba TP Environ Sci Pollut Res Int 06-May-2023
PMCID:PMC10212812
doi:10.1007/s11356-023-27258-w
PMID:37148518
Anticancer Potentials of the Lignan Magnolin: A Systematic Review Bhuia MS, Wilairatana P, Chowdhury R, Rakib AI, Kamli H, Shaikh A, Coutinho HD, Islam MT Molecules 23-Apr-2023
PMCID:PMC10180476
doi:10.3390/molecules28093671
PMID:37175081
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
A Comprehensive Review on the Biological, Agricultural and Pharmaceutical Properties of Secondary Metabolites Based-Plant Origin Elshafie HS, Camele I, Mohamed AA Int J Mol Sci 07-Feb-2023
PMCID:PMC9959544
doi:10.3390/ijms24043266
PMID:36834673
Current Knowledge of the Antidepressant Activity of Chemical Compounds from Crocus sativus L. Matraszek-Gawron R, Chwil M, Terlecki K, Skoczylas MM Pharmaceuticals (Basel) 30-Dec-2022
PMCID:PMC9860663
doi:10.3390/ph16010058
PMID:36678554
Fenugreek seed and cape gooseberry leaf extracts as green corrosion inhibitors for steel in the phosphoric acid industry Abdel-Gaber AM, Ezzat A, Mohamed ME Sci Rep 23-Dec-2022
PMCID:PMC9789128
doi:10.1038/s41598-022-26757-z
PMID:36564523
Valorisation of Micro/Nanoencapsulated Bioactive Compounds from Plant Sources for Food Applications Towards Sustainability Martins VF, Pintado ME, Morais RM, Morais AM Foods 22-Dec-2022
PMCID:PMC9818261
doi:10.3390/foods12010032
PMID:36613248
Advances in extraction methods, chemical constituents, pharmacological activities, molecular targets and toxicology of volatile oil from Acorus calamus var. angustatus Besser Bai D, Li X, Wang S, Zhang T, Wei Y, Wang Q, Dong W, Song J, Gao P, Li Y, Wang S, Dai L Front Pharmacol 01-Dec-2022
PMCID:PMC9761896
doi:10.3389/fphar.2022.1004529
PMID:36545308
Antifungal Activity of Essential Oil and Plant-Derived Natural Compounds against Aspergillus flavus Tian F, Woo SY, Lee SY, Park SB, Zheng Y, Chun HS Antibiotics (Basel) 01-Dec-2022
PMCID:PMC9774910
doi:10.3390/antibiotics11121727
PMID:36551384
Bioactive Compounds, Pharmacological Actions, and Pharmacokinetics of Genus Acacia Batiha GE, Akhtar N, Alsayegh AA, Abusudah WF, Almohmadi NH, Shaheen HM, Singh TG, De Waard M Molecules 28-Oct-2022
PMCID:PMC9658407
doi:10.3390/molecules27217340
PMID:36364163
Natural Compounds in the Battle against Microorganisms—Linalool Mączka W, Duda-Madej A, Grabarczyk M, Wińska K Molecules 15-Oct-2022
PMCID:PMC9609897
doi:10.3390/molecules27206928
PMID:36296521
Medicinal Plants Used as an Alternative to Treat Gingivitis and Periodontitis Rani N, Singla RK, Narwal S, Tanushree, Kumar N, Rahman MM Evid Based Complement Alternat Med 06-Sep-2022
PMCID:PMC10630018
doi:10.1155/2022/2327641
PMID:37941972
Zanthoxylum Alatum Attenuates Chronic Restraint Stress Adverse Behavioral Effects Via the Mitigation of Oxidative Stress and Modulating the Expression of Genes Involved in Endoplasmic Reticulum Stress in Mice Choudhury Barua C, Buragohain L, Rahman F, Elancheran R, Rizavi H Basic Clin Neurosci 01-Sep-2022
PMCID:PMC10258593
doi:10.32598/bcn.2022.1477.1
PMID:37313027
The Use of Cannabis sativa L. for Pest Control: From the Ethnobotanical Knowledge to a Systematic Review of Experimental Studies Ona G, Balant M, Bouso JC, Gras A, Vallès J, Vitales D, Garnatje T Cannabis Cannabinoid Res 09-Aug-2022
PMCID:PMC9418361
doi:10.1089/can.2021.0095
PMID:34612729

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone 6453733 Click to see 307.30 unknown https://doi.org/10.1016/S0031-9422(97)00280-X
https://doi.org/10.1002/JCCS.200400159
N-Acetylbongaridine 78411088 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown https://doi.org/10.1002/JCCS.200400159
N-Acetylnornuciferine 101630664 Click to see 323.40 unknown https://doi.org/10.1002/JCCS.200400159
https://doi.org/10.1016/S0031-9422(97)00280-X
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dimethyl anthranilate 6826 Click to see CNC1=CC=CC=C1C(=O)OC 165.19 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Perylenequinones
1,8,15-Trihydroxy-4,19-dioxaheptacyclo[10.8.1.12,7.03,5.016,21.018,20.011,22]docosa-7,9,11(22),12(21),13,15-hexaene-6,17-dione 102335565 Click to see 364.30 unknown https://doi.org/10.1002/JCCS.200400159
> Benzenoids / Phenols / Methoxyphenols
(4S,5S)-4,5-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-one 163046234 Click to see COC1=C(C=CC(=C1)CC2C(OCC2=O)CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1002/JCCS.200400159
4,5-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-one 163046233 Click to see 358.40 unknown https://doi.org/10.1002/JCCS.200400159
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1002/JCCS.200400159
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1002/JCCS.200400159
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1002/JCCS.200400159
(+)-Beechenol 162895804 Click to see 326.30 unknown https://doi.org/10.1002/JCCS.200400159
4-[6-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenol 162895803 Click to see 326.30 unknown https://doi.org/10.1002/JCCS.200400159
Asarinin 101612 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JCCS.200400159
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JCCS.200400159
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1002/JCCS.200400159
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JCCS.200400159
Sesamin, (-)- 382073 Click to see 354.40 unknown https://doi.org/10.1002/JCCS.200400159
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 13916162 Click to see 370.40 unknown https://doi.org/10.1002/JCCS.200400159
Bursehernin 94504 Click to see 370.40 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1002/JCCS.200400159
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 Click to see 446.70 unknown https://doi.org/10.1002/JCCS.200400159
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1002/JCCS.200400159
3,7,11,15-Tetramethylhexadec-2-en-1-yl acetate 53425386 Click to see 338.60 unknown https://doi.org/10.1002/JCCS.200400159
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1002/JCCS.200400159
Phytyl acetate 637195 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)C)C 338.60 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymyl formate 56597779 Click to see 178.23 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aS,5bR,7aR,9S,11aR,11bR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 44575983 Click to see 424.70 unknown https://doi.org/10.1002/JCCS.200400159
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 163075771 Click to see CC(=C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 424.70 unknown https://doi.org/10.1002/JCCS.200400159
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1002/JCCS.200400159
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1002/JCCS.200400159
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/JCCS.200400159
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1R,2R,5R,6R,9R,10R,13S,15R)-5-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 13830972 Click to see 428.60 unknown https://doi.org/10.1002/JCCS.200400159
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 633877 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1002/JCCS.200400159
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
14-(5-Ethyl-6-methylheptan-2-yl)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one 14779505 Click to see 428.70 unknown https://doi.org/10.1002/JCCS.200400159
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1002/JCCS.200400159
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1002/JCCS.200400159
> Organoheterocyclic compounds / Benzodioxoles
(4S,5S)-4,5-bis(1,3-benzodioxol-5-ylmethyl)oxolan-3-one 162947947 Click to see C1C(=O)C(C(O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1002/JCCS.200400159
4,5-Bis(1,3-benzodioxol-5-ylmethyl)oxolan-3-one 162947946 Click to see 354.40 unknown https://doi.org/10.1002/JCCS.200400159
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Arnottin II 443743 Click to see COC1=C(C2=C(C=C1)C3(C=CC4=CC5=C(C=C4C3=O)OCO5)OC2=O)OC 366.30 unknown https://doi.org/10.1016/0040-4039(95)00757-4
> Organoheterocyclic compounds / Naphthopyrans
Arnottin I 196418 Click to see 350.30 unknown https://doi.org/10.1039/P19930001019
> Organoheterocyclic compounds / Quinolines and derivatives
Toddaquinoline 11390791 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC4=CC(=CN=C43)O 239.23 unknown https://doi.org/10.1002/JCCS.200400159
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine 179640 Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O 319.30 unknown https://doi.org/10.1002/JCCS.200400159
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown https://doi.org/10.1002/JCCS.200400159
Oxynitidine 97597 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC(=C(C=C5C1=O)OC)OC 363.40 unknown https://doi.org/10.1002/JCCS.200400159
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine 164950 Click to see 215.20 unknown https://doi.org/10.1002/JCCS.200400159
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1002/JCCS.200400159
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://doi.org/10.1002/JCCS.200400159
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1002/JCCS.200400159
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methyl-3-(3-methylbut-2-enyl)quinolin-2-one 15460082 Click to see CC(=CCC1=C(C2=CC=CC=C2N(C1=O)C)OC)C 257.33 unknown https://doi.org/10.1002/JCCS.200400159
https://doi.org/10.1590/S0100-40422009000100025
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see 227.26 unknown https://doi.org/10.1002/JCCS.200400159
N-Methylflindersine 72819 Click to see 241.28 unknown https://doi.org/10.1002/JCCS.200400159
Rel-zanthodioline 5315424 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C 305.32 unknown https://doi.org/10.1002/JCCS.200400159
Zanthobungeanine 5315422 Click to see 271.31 unknown https://doi.org/10.1002/JCCS.200400159
Zanthodioline 78384601 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C 305.32 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-3-(3,4-dimethoxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]-N-methylprop-2-enamide 149571961 Click to see 355.40 unknown https://doi.org/10.1002/JCCS.200400159
3-(1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]-N-methylprop-2-enamide 129522 Click to see 339.40 unknown https://doi.org/10.1002/JCCS.200400159
3-(3,4-dimethoxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]-N-methylprop-2-enamide 162942045 Click to see 355.40 unknown https://doi.org/10.1002/JCCS.200400159
Podocarpamide 5320643 Click to see CN(CCC1=CC=C(C=C1)OC)C(=O)C=CC2=CC3=C(C=C2)OCO3 339.40 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown https://doi.org/10.1002/JCCS.200400159
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7,8-Trimethoxycoumarin 6482974 Click to see 236.22 unknown https://doi.org/10.1002/JCCS.200400159
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro(3,2-g)chromen-7-one 604512 Click to see 246.26 unknown https://doi.org/10.1002/JCCS.200400159
Nodakenetin 26305 Click to see 246.26 unknown https://doi.org/10.1002/JCCS.200400159
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-Hydroxy-7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one 129710913 Click to see 260.28 unknown https://doi.org/10.1002/JCCS.200400159
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Osthenol 5320318 Click to see 230.26 unknown https://doi.org/10.1002/JCCS.200400159
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1002/JCCS.200400159

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