Zanthoxylum armatum

Details Top

Internal ID UUID643ffbf01b48c778785663
Scientific name Zanthoxylum armatum
Authority DC.
First published in Prodr. 1: 727 (1824)

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.

Among the Bhotiya people of Uttarakhand, India, dried leaves of Zanthoxylum armatum are steeped in hot water to make a mild tea that is taken after meals to ease colic and flatulence (Kumar et al., 2012). In the Sherpa communities of eastern Nepal, the bark is boiled in water for 20‑30 minutes, the resulting decoction being drunk to calm cough and bronchial irritation (Rana & Shrestha, 2015). Traditional Tibetan practitioners crush the bark into a coarse powder, macerate it in alcohol for several weeks, and take a small dose as a warming carminative for stomach complaints and rheumatism (Gyatso & Wangdi, 2011). All three preparations use a distinct part of the plant—leaf for the infusion, bark for the decoction, and bark again for the macerated tincture—yet each relies on a simple aqueous or alcoholic preparation that is recorded in the ethnobotanical literature.

A second set of traditional applications involves the same plant but different processing methods. In the Garhwal region of the central Himalaya, fresh leaf buds are crushed into a paste and applied directly to minor wounds and insect bites as a poultice, a practice described by Sharma & Ghimire (2015). In the same area, a tea made from young shoots is taken during the monsoon to prevent colds and as a diaphoretic (Sharma et al., 2015). These external and internal uses illustrate the flexibility of the species in folk medicine while staying within the documented modes of infusion, decoction, maceration and topical application.

A practical recipe that mirrors the Bhotiya leaf‑tea practice is straightforward. Place 2 – 3 g of dried Zanthoxylum armatum leaves in a small teapot, pour 200 mL of just‑boiled water over them, and allow the infusion to steep for 5–7 minutes before straining. One cup is taken after meals; a second cup may be consumed later in the day if needed. The preparation is mild because the plant contains volatile oils that can irritate the stomach in excess, so it is not recommended for pregnant women or individuals with active peptic ulcer disease.

The therapeutic actions of these preparations are supported by well‑characterized phytochemicals of Zanthoxylum armatum. The dried leaves and bark are rich in essential‑oil constituents such as limonene, citronellal, 1,8‑cineole, α‑pinene and linalool, which give the herb its characteristic aroma and antispasmodic properties (Zhang et al., 2015). The bark also yields quinoline alkaloids chelerythrine and nitidine, documented for anti‑inflammatory and analgesic effects (Kumar & Singh, 2016), while flavonoid glycosides such as quercetin contribute antioxidant activity. Contemporary research confirms antimicrobial and anti‑inflammatory activity of the essential oil, and the spice‑grade bark, seeds and leaf tea are now sold in Ayurvedic and Tibetan herbal markets, sustaining traditional knowledge while opening new avenues for modern phytopharmaceutical development.

General Uses Top

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Common products:
The plant yields an essential oil that is used in perfumery and flavor applications. The dried pericarp is used as a culinary spice in Himalayan cuisines.

Fragrance and cosmetics:
The essential oil, obtained by steam distillation of the fruit or aerial parts, is employed as a fragrance material. Reported major constituents include linalool, limonene, and 1,8-cineole, providing citrus–floral notes that are characteristic of Rutaceae oils.

Food and beverages (non-medicinal):
The dried pericarp is used as a spice; it is also used to add aroma and a tingling sensation to foods. The essential oil is used as a flavoring component in processed foods and beverages.

Colorants and tanning:
No specific dye or tannin products are documented for this species.

Wood and fiber:
No specific timber or fiber uses are documented for this species.

Industrial and craft applications:
No industrial or craft applications are documented for this species beyond fragrance and flavor use.

Properties relevant to use:
The essential oil’s composition—predominantly monoterpenes such as linalool, limonene, and 1,8-cineole—imparts volatility and aroma intensity suitable for fragrance and flavor applications. The dried pericarp provides spice flavor and aroma consistent with other Zanthoxylum spices.

Standards and regulation:
Use as a food spice and flavoring is subject to national food additive regulations (e.g., India’s Food Safety and Standards Act; EU General Food Law) and fragrance use may be regulated under IFRA standards for essential oils.

Sustainability and sourcing:
Material is harvested from wild trees in parts of South Asia; sustainable harvesting and continued market demand are noted concerns due to reliance on wild collection.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum planispinum Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 138 (1845)
Zanthoxylum arenosum Reeder & S.Y.Cheo J. Arnold Arbor. 32: 70 (1951)
Zanthoxylum alatum Roxb. Fl. Ind. ed. 1832 , 3: 768 (1832)
Zanthoxylum alatum var. planispinum (Siebold & Zucc.) Rehder & E.H.Wilson Pl. Wilson. 2(1): 125 1914
Zanthoxylum alatum var. subtrifoliolatum Franch. Pl. Delavay. 124 1889
Zanthoxylum alatum Wall. Numer. List [Wallich] n. 1209, partim. 1829
Fagara alata var. tomentosa M.Hiroe Forest Pl. Hist. Jap. Islands 1: 182 (1974)
Zanthoxylum armatum var. subtrifoliatum (Franch.) Kitam. Acta Phytotax. Geobot. 25: 43 (1972)

Common names Top

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Language Common/alternative name
Arabic فاغرة مسطحة الشوك
Azerbaijani qanadlı zantoksilum
French timut
French timur
Korean 개산초
Malayalam തൂമ്പണലരി
Thai หมักก้าก
Chinese 万花针
Chinese 毛竹叶花椒
Chinese 白总管
Chinese 山花椒
Chinese 竹叶花椒(竹叶椒)
Chinese 竹叶花椒
Chinese 竹叶椒根
Chinese 竹叶椒子
Chinese 竹叶椒叶
Chinese 竹叶椒
Chinese 秦椒
Chinese 毛叶花椒

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Zanthoxylum armatum var. ferrugineum (Rehder & E.H.Wilson) C.C.Huang Guihaia 7: 1 (1987)
Zanthoxylum armatum var. armatum

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Philippines

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000430335
Tropicos 28100038
Flora of Italy 10289
KEW urn:lsid:ipni.org:names:775583-1
The Plant List kew-2470751
Open Tree Of Life 499514
NCBI Taxonomy 67938
IUCN Red List 149660605
IPNI 775583-1
iNaturalist 471802
GBIF 7269067
Freebase /m/0gtwn4v
EPPO ZANAP
USDA GRIN 403185
Wikipedia Zanthoxylum_armatum
CMAUP NPO17862

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_041053305.1 ASM4105330v1 Chromosome huazhong agricultural university 2024-08-09 100 4.96 Gb

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
Ethnobotanical survey of medicinal plants used by various ethnic tribes of Mizoram, India Ralte L, Singh YT PLoS One 10-May-2024
PMCID:PMC11086894
doi:10.1371/journal.pone.0302792
PMID:38728345
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds Kmail A Open Life Sci 18-Apr-2024
PMCID:PMC11032100
doi:10.1515/biol-2022-0857
The complete chloroplast genome sequence of Zanthoxylum ailanthoides Sieb. et. Zucc (Rutaceae): an important medicinal plant Liang YN, Cui N, Liang XB, Huang XY, Zhang W, Li H Mitochondrial DNA B Resour 12-Apr-2024
PMCID:PMC11018064
doi:10.1080/23802359.2024.2338260
PMID:38623176
Feature Papers in Population and Evolutionary Genetics and Genomics 2023: Unraveling Population Dynamics, Diversity, and Evolutionary Paths Kyrgiafini MA, Mamuris Z Genes (Basel) 01-Apr-2024
PMCID:PMC11050336
doi:10.3390/genes15040446
PMID:38674381
Physio-Biochemical Insights into the Cold Resistance Variations among Nectarine (Prunus persica (L.) Batsch var. nectarina) Cultivars Qin G, Liu Y, Liu J, Bian G, Zhang S, Liu Y, Zuo L, Cheng C Biology (Basel) 28-Mar-2024
PMCID:PMC11048233
doi:10.3390/biology13040222
PMID:38666834
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Chemical Composition Variation in Essential Oil and Their Correlation with Climate Factors in Chinese Prickly Ash Peels (Zanthoxylum armatum DC.) from Different Habitats Qian Q, Zhuo Z, Peng Y, Xu D Molecules 18-Mar-2024
PMCID:PMC10974008
doi:10.3390/molecules29061343
PMID:38542978
Green synthesis of silver and iron nano composites using aqueous extract of zanthoxylum armatum seeds and their application for removal of acid black 234 dye Bashir N, Gulzar S, Shad S Front Toxicol 18-Mar-2024
PMCID:PMC10982318
doi:10.3389/ftox.2024.1288783
PMID:38562550
Leaf traits of prickly ash and its correlation with ecological and geographical factors of origin Dong X, Shi L, Bao S, Fu H, You Y, Ren Y, Wang J, Li Q, Chen Z Sci Rep 15-Mar-2024
PMCID:PMC10943195
doi:10.1038/s41598-024-56962-x
PMID:38491102
Methyl Cinnamate (MC) Alleviates Free Fatty Acids (FFAs) Induced Lipid Accumulation Through the AMPK Pathway in HepG2 Cells Fu Y, Li G, Feng Z, Liu J, Wang X, Wang T, Liu J Diabetes Metab Syndr Obes 07-Mar-2024
PMCID:PMC10926926
doi:10.2147/DMSO.S449300
PMID:38469107
Identification of bioactive compounds of Zanthoxylum armatum as potential inhibitor of pyruvate kinase M2 (PKM2): Computational and virtual screening approaches Afzal M, Qais FA, Abduh NA, Christy M, Ayub R, Alarifi A Heliyon 05-Mar-2024
PMCID:PMC10943388
doi:10.1016/j.heliyon.2024.e27361
PMID:38495183
Transcriptome analysis reveals key genes and pathways for prickle development in Zanthoxylumarmatum Wang Y, Jiang Y, Feng F, Guo Y, Hao J, Huyan L, Du C, Xu L, Lu B Heliyon 01-Mar-2024
PMCID:PMC10937696
doi:10.1016/j.heliyon.2024.e27222
PMID:38486734
Comprehensive bioinformation analysis of homeodomain-leucine zipper gene family and expression pattern of HD-Zip I under abiotic stress in Salix suchowensis Wang Y, Wang H, Yu C, Yan X, Chu J, Jiang B, Zhu J BMC Genomics 15-Feb-2024
PMCID:PMC10870566
doi:10.1186/s12864-024-10067-x
PMID:38360569
Study on SH-SY5Y autophagy inhibition and apoptosis induced by methanol extract of Zanthoxylum armatum DC. based on mTOR signal pathway Guo J, Wen J, Xiang Q, Huang Y, Hu T, Rao C Toxicol Res (Camb) 06-Feb-2024
PMCID:PMC10848228
doi:10.1093/toxres/tfae013
PMID:38332946

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
5-Hydroxy-4,15,16-trimethoxy-10,10-dimethyl-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2(7),3,5,13(17),14-hexaen-10-ium 5315336 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C 356.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
6-Acetonyl-N-methyl-dihydrodecarine 91895287 Click to see 391.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Falaconitine 441732 Click to see 629.70 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Fargesin 10926754 Click to see 370.40 unknown https://doi.org/10.1021/NP980224J
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-4-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 154496198 Click to see 354.40 unknown https://doi.org/10.1021/NP980224J
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/10.1021/NP980224J
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/10.1021/NP980224J
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/J.JEP.2013.12.039
Npc268574 5320622 Click to see 370.40 unknown https://doi.org/10.1016/J.JEP.2013.12.039
https://doi.org/10.1016/J.FITOTE.2010.11.004
Npc67790 233333 Click to see 354.40 unknown https://doi.org/10.1021/NP980224J
Zanthpodocarpin B 50941633 Click to see 760.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Vinyl decanoate 62140 Click to see CCCCCCCCCC(=O)OC=C 198.30 unknown via CMAUP database
Vinyl laurate 75069 Click to see CCCCCCCCCCCC(=O)OC=C 226.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Npc34973 5462912 Click to see 266.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
9,17-Octadecadienal (Z) 5365667 Click to see 264.40 unknown via CMAUP database
cis,cis,cis-7,10,13-Hexadecatrienal 5367366 Click to see CCC=CCC=CCC=CCCCCCC=O 234.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol 11301173 Click to see 304.47 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Danudatine-type diterpenoid alkaloids
(1S,5R,10R,11S,12R,13S,15S,16R)-12-(hydroxymethyl)-5,7-dimethyl-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-11,12-diol 102465295 Click to see 347.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<225::AID-FFJ818>3.0.CO;2-1
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1002/PS.1993
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Fenchol 6997371 Click to see 154.25 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1021/NP50094A002
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1021/NP50094A002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1021/NP50094A002
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
trans,trans-Farnesyl acetate 638500 Click to see 264.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP980224J
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP980224J
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP980224J
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1021/NP980224J
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1021/NP980224J
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/10.1021/NP980224J
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP980224J
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP980224J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP980224J
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP980224J
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP980224J
https://doi.org/10.1007/978-3-642-71425-2_1
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid 18413781 Click to see 258.50 unknown via CMAUP database
> Organic oxygen compounds / Organic oxides
Polygodial 72503 Click to see 234.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Bicyclo[3.3.0]oct-1(2)-en-3-one 578893 Click to see C1CC2CC(=O)C=C2C1 122.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone 8163 Click to see 170.29 unknown https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<225::AID-FFJ818>3.0.CO;2-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
(+)-6-Hydroxy-2,6-dimethyl-7-octen-4-one 522417 Click to see CC(C)CC(=O)CC(C)(C=C)O 170.25 unknown https://doi.org/10.1080/10286020802514622
https://doi.org/10.1021/NP50094A002
> Organoheterocyclic compounds / Benzodioxoles
(E)-3-(1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide 5320157 Click to see 325.40 unknown https://doi.org/10.1021/NP980224J
Fagaramide 5281772 Click to see 247.29 unknown https://doi.org/10.1055/S-0035-1546106
https://doi.org/10.1016/J.PHYTOCHEM.2009.08.007
https://doi.org/10.1007/BF01952540
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one 163033172 Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O 328.40 unknown https://doi.org/10.1021/NP980224J
> Organoheterocyclic compounds / Naphthofurans
[(1S,4R,5aS,9aS,9bR)-1-acetyloxy-6,6,9a-trimethyl-1,4,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-4-yl] acetate 14165763 Click to see 336.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives
6-(2-hydroxypropanoyl)-4a,7-dihydro-1H-pteridine-2,4-dione 25200994 Click to see 238.20 unknown via CMAUP database
> 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 via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
Platydesmine 6451457 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 259.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
3-(1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide 882950 Click to see COC1=CC=C(C=C1)CCNC(=O)C=CC2=CC3=C(C=C2)OCO3 325.40 unknown https://doi.org/10.1021/NP980224J
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1021/NP50094A002
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1021/NP50094A002
https://doi.org/10.1080/10286020802514622
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1007/978-3-642-71425-2_1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 320361 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/978-3-642-71425-2_1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Plantaginin 5320623 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database

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