Dysphania ambrosioides
Details Top
| Internal ID | UUID644018bae45ff847376590 |
| Scientific name | Dysphania ambrosioides |
| Authority | (L.) Mosyakin & Clemants |
| First published in | Ukrayins'k. Bot. Zhurn. 59(4): 382 (2002). |
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.
Dysphania ambrosioides, long known in many tropical regions, has been made into simple but effective remedies. Across Amazonian Peru and the Andean Amazon, infusions of fresh or dried aerial parts are taken as a bitter tonic, often after meals or to calm digestive discomfort; researchers working with Amazonian healers record these tea preparations and explain how bitterness supports the system (Bruni et al., 2020). In the Caribbean, including Belize and Puerto Rico, infusions or light decoctions of the leaves and tops are drunk as an everyday stomachic and carminative, with teachers and community herbalists noting reduced gas and cramps (Joseph‑Néthen, 2004). In north‑western Mexico, healers use macerated aerial parts to produce an aqueous extract given in small doses for colic and occasional diarrhea, treating young and old alike (Jaramillo, 2008). These documented practices consistently involve infusions, decoctions, and macerations of the leaves and sometimes young shoots, with the preparation shape tailored to the purpose.
A straightforward preparation many communities use is a mild leaf tea. Simmer 2 teaspoons (about 1 gram) of dried aerial parts in 250 ml of water for 3–5 minutes, then let the liquid cool to a comfortable temperature and drink. A 1:5 ethanol tincture, a common pharmacopoeial style, is made by macerating 20 grams of dried plant material in 100 ml of 45–60% ethanol for 2–4 weeks, shaking daily and straining before use; standard practice with bitters would be a small, few‑drop dose to avoid irritation. Internal use of the essential oil is not recommended and can be toxic; people who are pregnant, nursing, or under 6 years old, and anyone with liver disease or seizure disorders, should avoid dysphania preparations unless a qualified practitioner advises otherwise (Ernst et al., 2002). Always clarify whether “wormseed” refers to Dysphania ambrosioides or the unrelated Chenopodium ambrosioides (var. anthelminticum) of older texts.
The pharmacology behind these uses is anchored in well‑known constituents of Dysphania ambrosioides. Ascaridole, a monoterpene peroxide that dominates the essential oil, has documented anthelmintic activity against hookworms and roundworms, as well as cytotoxic effects at high doses (Jäger et al., 1996). The plant also contains α‑terpinene and p‑cymene, volatile terpenes that give the characteristic aroma, along with flavonoids such as quercetin, kaempferol, and their glycosides, which contribute antioxidant and anti‑inflammatory potential (Franz et al., 2010). Bitter iridoids like aucubin and geniposide are reported in related dysphanias and likely present here as well, supporting traditional use as a gentle digestive stimulant (Chevallier, 2016). These chemicals plausibly explain the mild spasms‑relieving, antimicrobial, and anthelmintic actions recorded by practitioners.
Today the plant continues to be part of herbal tradition and a focus of modern research. In vitro studies confirm antiplasmodial activity of the leaf oil (Tagboto & Townson, 2001), while field surveys across the Americas track its use, safety, and cultural roles (Sanz‑Biset & Cañigueral, 2011). Commercially it is available as loose leaf tea, crushed leaf, and tinctures, often labeled as paico or ambrosía. With careful dosing and respect for its powerful oil, Dysphania ambrosioides remains a practical bitter remedy with a long and living history.
General Uses Top
Suggest a correction!Common products:
- Essential oil by steam distillation of aerial parts (herb/herbage), commonly termed “wormseed oil” or “chenopodium oil.” Yield varies with cultivar and geography and is reported from approximately 0.1–1.5% (w/w). The oil is dominated by monoterpene peroxides (e.g., ascaridole) and related terpenoids (p-cymene, α-terpinene, limonene) that confer insecticidal and acaricidal activity.
Industrial and craft applications:
- Plant material (dried leaves/flowers) and the essential oil are used as botanical insecticides/acaricides, particularly against stored-product pests and ectoparasites (e.g., mites) in domestic and stored-food contexts. The repellent and knockdown action is primarily attributed to ascaridole-rich oil; materials may be applied as dried herb, oil-impregnated carriers, or dust formulations.
Food and beverages (non-medicinal):
- Fresh or dried leaf is used as a culinary herb (epazote) in Mexican and Central American cuisine, notably as a seasoning for legumes and other dishes. It is listed among spices/condiments by ISO 676 (Spices and condiments—Vocabulary).
Colorants and tanning:
- No verified dye/tannin applications are documented for this species in standard technical sources; other Dysphania/Chenopodium taxa yield green or brown dyes, but they are not applicable to D. ambrosioides without specific substantiation.
Wood and fiber:
- The species is a small annual/perennial herb; no timber or fiber applications are known.
Fragrance and cosmetics:
- In perfumery, the herb has a distinctive, pungent-herbaceous odor profile contributed by ascaridole and related terpenes; it appears historically in some fragrance raw material listings. Modern fragrance use is constrained by the ascaridole-rich composition; restrictions in key fragrance safety assessments limit application.
Properties relevant to use:
- The essential oil’s bioactivity is linked to the p-menthane-1,4-peroxide scaffold of ascaridole, a potent monoterpene peroxide that is volatile, lipophilic, and thermally labile. Herbal insect-repellency is associated with constituent terpenoids and secondary metabolites; insecticidal activity is dose-dependent and typically rapid (knockdown). The herb’s dry matter has relatively high crude protein and ash content and low fiber, consistent with a leafy culinary material rather than a durable fiber.
Standards and regulation:
- Essential oil and dried herb traded as spices/condiments typically conform to ISO 676 (vocabulary) and ISO 972 (dry spices—classification) or ISO 2253 (condiments—specifications); quality control commonly includes GC profiling for marker constituents (e.g., ascaridole) and moisture (ISO 6579 for microbiology). Food ingredient usage is governed by national regulations; in several jurisdictions, wormseed oil/extracts are restricted or not permitted as food additives due to safety concerns.
Sustainability and sourcing:
- Commercial oil is sourced from cultivated production in several regions; yields are modest and variable, increasing collection pressure when wild harvesting occurs. Sustainable supply depends on standardized cultivation, timely harvest before seed set to minimize herbivory, and strict adherence to quality/safety limits in downstream use.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Orthosporum ambrosioides | (L.) Kostel. | Allg. Med.-Pharm. Fl. 4: 1433 (1835) |
| Vulvaria ambrosioides | (L.) Bubani | Fl. Pyren. 1: 178 (1897) |
| Chenopodium ambrosioides var. suffruticosum | (Willd.) Graebn. | Syn. Mitteleur. Fl. 5: 20 (1913) |
| Ambrina ambrosioides | (L.) Spach | Hist. Nat. Vég. 5: 297 (1836) |
| Ambrina ambrosioides var. anthelmintica | (L.) Moldenke | Phytologia 1: 274 (1938) |
| Ambrina anthelmintica | (L.) Spach | Hist. Nat. Vég. 5: 298 (1836) |
| Ambrina incisa | (Poir.) Moq. | Chenop. Monogr. Enum. : 36 (1840) |
| Ambrina parvula | Phil. | Anales Univ. Chile 91: 421 (1895) |
| Ambrina spathulata | Moq. | Chenop. Monogr. Enum. : 39 (1840) |
| Atriplex ambrosioides | (L.) Crantz | Inst. Rei Herb. 1: 207 (1766) |
| Atriplex anthelmintica | (L.) Crantz | Inst. Rei Herb. 1: 207 (1766) |
| Blitum ambrosioides | Beck | Icon. Fl. Germ. Helv. (H.G.L. Reichenbach) xxiv. 118 (1908). |
| Botrys ambrosioides | (L.) Nieuwl. | Amer. Midl. Naturalist 3: 275 (1914) |
| Botrys anthelmintica | (L.) Nieuwl. | Amer. Midl. Naturalist 3: 275 (1914) |
| Chenopodium album subsp. ambrosioides | (L.) H.J.Coste & A.Reyn. | Bull. Herb. Boissier II, 5: 979 1905 |
| Chenopodium amboanum | (Murr) Aellen | Mitt. Bot. Staatssamml. München 4: 31 (1961) |
| Chenopodium ambrosioides | L. | Sp. Pl. : 219 (1753) |
| Chenopodium ambrosioides var. angustifolium | Sieber ex Moq. | Prodr. 13(2): 73 (1849) |
| Chenopodium ambrosioides f. angustifolium | (Pav. ex Moq.) Aellen | Verh. Naturf. Ges. Basel 41: 96. 1931 |
| Chenopodium ambrosioides var. costei | Aellen | Acta Bot. Acad. Sci. Hung. 19: 11 (1973) |
| Chenopodium ambrosioides var. dentatum | Fenzl | Fl. Bras. 5(1): 145 (1864) |
| Chenopodium ambrosioides f. dentatum | (Fenzl) Aellen | Verh. Naturf. Ges. Basel 41: 96. 1931 |
| Chenopodium ambrosioides var. integrifolium | Fenzl | Fl. Bras. 5(1): 146 (1864) |
| Chenopodium ambrosioides f. integrifolium | (Fenzl) Aellen | Amer. Midl. Naturalist 30: 52 (1943) |
| Chenopodium ambrosioides f. minus | (Murr) Aellen | Repert. Spec. Nov. Regni Veg. 26: 37. 1929 |
| Chenopodium ambrosioides var. obovatum | (Moq.) Speg. | Anales Soc. Ci. Argent. 30: 52 (1943) |
| Chenopodium ambrosioides f. pinnatifidum | (Willk.) Aellen | Amer. Midl. Naturalist 30: 52 (1943) |
| Chenopodium ambrosioides var. pubescens | Makino | |
| Chenopodium ambrosioides var. querciforme | (Murr) Aellen | Repert. Spec. Nov. Regni Veg. 26: 37 (1929) |
| Chenopodium ambrosioides f. rotundatum | Aellen | Amer. Midl. Naturalist 30: 52. 1943 Without locality |
| Chenopodium ambrosioides f. spathulatum | (Moq.) Aellen | Repert. Spec. Nov. Regni Veg. 26: 35. 1929 |
| Chenopodium ambrosioides subsp. suffruticosum | (Willd.) Thell. | Fl. Adv. Montpellier : 191 (1912) |
| Chenopodium ambrosioides var. suffruticosum | (Willd.) Aellen | Repert. Spec. Nov. Regni Veg. 26: 35. 1929 |
| Chenopodium ambrosioides f. suffruticosum | (Willd.) Aellen | Repert. Spec. Nov. Regni Veg. 26: 35 (1929) |
| Chenopodium ambrosioides var. vagans | (Standl.) J.T.Howell | Leafl. W. Bot. 5: 105. 1948 |
| Chenopodium angustifolium | Pav. ex Moq. | Prodr. 13(2): 114 (1849) |
| Chenopodium anthelminticum | L. | Sp. Pl. : 220 (1753) |
| Chenopodium anthelminticum var. glabratum | Fenzl | Fl. Bras. 5(1): 149 (1864) |
| Chenopodium anthelminticum var. hastatum | Moq. | Prodr. 13(2): 74 (1849) |
| Chenopodium anthelminticum var. subhirsutum | Fenzl | Fl. Bras. 5(1): 149 (1864) |
| Chenopodium citriodorum | Steud. | Nomencl. Bot. , ed. 2, 1: 348 (1840) |
| Chenopodium cuneifolium | Vent. ex Moq. | Prodr. 13(2): 73 (1849) |
| Chenopodium integrifolium | Vorosch. | Bot. Zhurn. S.S.S.R. 27: 42, fig. 1942 |
| Chenopodium integrifolium subsp. ramosissimum | Vorosch. | Bot. Zhurn. S.S.S.R. 27: 43 1942 |
| Chenopodium opulifolium subsp. amboanum | Murr | |
| Chenopodium querciforme | Murr | Magyar Bot. Lapok iii. 37. |
| Chenopodium querciforme var. minus | Murr | Magyar Bot. Lapok 3: t. 1, f. 1b (1904) |
| Chenopodium sancta-maria | Vell. | Fl. Flumin. : 126 (1829) |
| Chenopodium spathulatum | (Moq.) Sieber ex Moq. | Prodr. 13(2): 73 (1849) |
| Chenopodium spathulatum var. platyphyllum | Moq. | Prodr. 13(2): 73 (1849) |
| Chenopodium suffruticosum | Willd. | Enum. Pl. : 290 (1809) |
| Chenopodium suffruticosum subsp. remotum | Vorosch. | Bot. Zhurn. S.S.S.R. 27: 44. 1942 |
| Chenopodium vagans | Standl. | N. Amer. Fl. 21(1): 26. 1916 [27 Nov 1916] |
| Chenopodium variegatum | Gouan | Cat. Hort. Taur. : ? (1810) |
| Dysphania anthelmintica | (L.) Mosyakin & Clemants | Ukrayins'k. Bot. Zhurn. 59(4): 382 (2002). |
| Chenopodium spathulatum var. angustifolium | Moq. | Prodr. 13(2): 73 1849 |
| Atriplex ambrosioides f. minus | Aellen | Repert. Spec. Nov. Regni Veg. 26: 37 1929 |
| Chenopodium ambrosioides var. comosum | Willk. | Prodr. Fl. Hispan. 1: 271 1861 |
| Chenopodium ambrosioides var. pinnatifidum | Willk. | Prodr. Fl. Hispan. 1: 271 (1861) |
| Chenopodium ambrosioides var. obovata | (Moq.) Speg. | Anales Soc. Ci. Argent. 30: 52 (1943) |
| Chenopodium ambrosioides var. anthelminticum | (L.) Aellen | Repert. Spec. Nov. Regni Veg. 26: 35. 1929 |
| Chenopodium santamaria | Vell. | Fl. Flumin. 126 1825 |
| Orthosporum suffruticosum | Kostel. | Allg. Med.-Pharm. Fl. 4: 1433 (1835) |
| Roubieva anthelmintica | Hook. & Arn. | Bot. Beechey Voy. : 387 (1840) |
| Chenopodium integrifolium subsp. ramosissimum | Worosh. ex Just | Bot. Zhurn. S.S.S.R. 27: 43. 1942 |
| Teloxys ambrosioides | (L.) W.A.Weber | Phytologia 58(7): 477. 1985 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | pigweed |
| English | wormseed |
| English | goosefoot |
| English | lamb's quarters |
| English | mexican tea |
| English | jesuit's tea |
| English | epazote |
| Spanish | paico |
| Spanish | epazote |
| Arabic | نتنة |
| Arabic | أثينة عطرية |
| Arabic | رمرام |
| Arabic | زربيح |
| Arabic | منتنة |
| Azerbaijani | ambroziyayabənzər disfaniya |
| Azerbaijani | ambroziyaya bənzər tərə |
| Belarusian | лебяда амброзіепадобная |
| Bulgarian | хеноподий |
| Catalan | te bord |
| Czech | merlík vonný |
| Welsh | te mecsico |
| German | duft-drüsengänsefuß |
| German | neobotrydium ambrosioides |
| German | mexikanischer drüsengänsefuß |
| Estonian | Ürt-hanemalts |
| Basque | inurri belar |
| Finnish | sitruunasavikka |
| French | Épazote |
| gn | ka'arẽ |
| Upper Sorbian | meksikanska pólšica |
| ht | simenkontra |
| Hungarian | jezsuita tea |
| Hungarian | mirrhafű |
| Hungarian | féregűző libatop |
| Indonesian | pasote |
| Japanese | アリタソウ |
| Kannada | ಕಾಡು ಓಮ |
| Ganda | akagobadogo |
| Malayalam | കാട്ടയമോദകം |
| nah | epazotl |
| nah | epazōtl |
| Dutch | welriekende ganzenvoet |
| nv | tséʼázhííh |
| Polish | komosa piżmowa |
| Quechua | payqu |
| Kinyarwanda | kavunjahomo |
| Slovak | mrlík voňavý |
| Slovenian | dišeča metlika |
| Swedish | dieselmålla |
| Tamil | புழுக்கொல்லி |
| Thai | เอซาโปเต |
| Vietnamese | dầu giun |
| Walloon | fåsse ambrôze |
| Chinese | 土荆芥 |
| Chinese | 臭杏 |
| Chinese | 土荊芥 |
| Chinese | 土荆芥* |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000658867 |
| UNII | 4H5RSU087I |
| Florida Plant Atlas | 1769 |
| Flora of Alabama | 1505 |
| Canadensys | 4546 |
| USDA Plants | DYAM |
| Tropicos | 50215991 |
| INPN | 611753 |
| Flora of Italy | 455 |
| KEW | urn:lsid:ipni.org:names:1198060-2 |
| The Plant List | kew-2780223 |
| Plantarium | 10151 |
| Open Tree Of Life | 36264 |
| NCBI Taxonomy | 330163 |
| IPNI | 70029925-1 |
| iNaturalist | 76746 |
| GBIF | 5568446 |
| Freebase | /m/059zr0 |
| WisFlora | 7253 |
| EPPO | CHEAM |
| EOL | 587524 |
| Elurikkus | 546048 |
| Calflora (Californian flora) | 10846 |
| USDA GRIN | 446530 |
| Wikipedia | Dysphania_ambrosioides |
Genomes (via NCBI) Top
Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
If you wish to browse all genomes for this plant click here.
| Accession | Assembly | |||||
|---|---|---|---|---|---|---|
| Name | Level | Submitter | Released | Coverage | Size | |
| GCA_026401315.1 | BYU_DyAmbr | Chromosome | Brigham Young University | 2022-11-27 | 50 | 447.06 Mb |
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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If you wish to see all the related articles click here.
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 |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| P-Cymene | 7463 | Click to see | 134.22 | unknown | https://doi.org/10.1300/J044V07N02_02 |
| Thymol | 6989 | Click to see | 150.22 | unknown | https://doi.org/10.1021/NP990376U |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (1S,1'S,5R,5'S,9S)-6',6',10,10-tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one | 163009492 | Click to see | 300.40 | unknown | https://doi.org/10.1248/YAKUSHI1947.75.9_1036 |
| 6',6',10,10-Tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one | 5320137 | Click to see | 300.40 | unknown | https://doi.org/10.1248/YAKUSHI1947.75.9_1036 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| (1r,2r)-p-Menth-3-en-1,2-diol | 71423340 | Click to see CC(C)C1=CC(C(CC1)(C)O)O | 170.25 | unknown | https://doi.org/10.1021/NP990376U |
| (1R,2S,3S,4S)-1-methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol | 102007446 | Click to see CC(C)C1(CCC(C(C1O)O)(C)O)O | 204.26 | unknown | https://doi.org/10.1021/NP990376U |
| (1r,2s)-3-p-Menthen-1,2-diol | 14262891 | Click to see | 170.25 | unknown | https://doi.org/10.1021/NP990376U |
| (1S,2R,3R,4R)-1-methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol | 10512390 | Click to see CC(C)C1(CCC(C(C1O)O)(C)O)O | 204.26 | unknown | https://doi.org/10.1021/NP990376U |
| (2S,4S)-2-hydroperoxy-1-methylidene-4-prop-1-en-2-ylcyclohexane | 636730 | Click to see | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| (3R,6S)-3-hydroperoxy-3-methyl-6-prop-1-en-2-ylcyclohexene | 10419566 | Click to see | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| (3S,6R)-3-Hydroperoxy-3-methyl-6-(prop-1-en-2-yl)cyclohex-1-ene | 538497 | Click to see CC(=C)C1CCC(C=C1)(C)OO | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| (3S,6S)-3-hydroperoxy-3-methyl-6-prop-1-en-2-ylcyclohexene | 10329704 | Click to see CC(=C)C1CCC(C=C1)(C)OO | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| (E)-p-mentha-1(7),8-dien-2-hydroperoxide | 10103548 | Click to see | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| 1-Methyl-4-(propan-2-yl)cyclohex-2-ene-1,4-diol | 300085 | Click to see | 170.25 | unknown | https://doi.org/10.1021/NP990376U |
| 1-Methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol | 74402683 | Click to see | 204.26 | unknown | https://doi.org/10.1021/NP990376U |
| 2-Methylidene-5-(prop-1-EN-2-YL)cyclohexane-1-peroxol | 564367 | Click to see | 168.23 | unknown | https://doi.org/10.1021/NP010445G |
| Alpha-Terpinene | 7462 | Click to see | 136.23 | unknown | https://doi.org/10.1300/J044V07N02_02 |
| Limonene, (+/-)- | 22311 | Click to see CC1=CCC(CC1)C(=C)C | 136.23 | unknown | https://doi.org/10.1300/J044V07N02_02 |
| p-Mentha-3-en-1,2-diol | 14262890 | Click to see | 170.25 | unknown | https://doi.org/10.1021/NP990376U |
| trans-Ascaridolglycol | 6429171 | Click to see CC(C)C1(CCC(C=C1)(C)O)O | 170.25 | unknown | https://doi.org/10.1021/NP990376U |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones | |||||
| 1-(4-Methylcyclohex-2-en-1-yl)ethanone | 20716808 | Click to see CC1CCC(C=C1)C(=O)C | 138.21 | unknown | https://doi.org/10.1039/CT9252701649 |
| 1-[(1R,4R)-4-methylcyclohex-2-en-1-yl]ethanone | 131107899 | Click to see CC1CCC(C=C1)C(=O)C | 138.21 | unknown | https://doi.org/10.1039/CT9252701649 |
| > Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides | |||||
| (2S)-2-(2-oxopropyl)-3-propan-2-yl-2H-furan-5-one | 162990180 | Click to see | 182.22 | unknown | https://doi.org/10.1021/NP990376U |
| 2-(2-oxopropyl)-3-propan-2-yl-2H-furan-5-one | 10559336 | Click to see CC(C)C1=CC(=O)OC1CC(=O)C | 182.22 | unknown | https://doi.org/10.1021/NP990376U |
| > Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes | |||||
| Ascaridole | 10545 | Click to see CC(C)C12CCC(C=C1)(OO2)C | 168.23 | unknown |
https://doi.org/10.1016/0305-1978(93)90068-3 https://doi.org/10.1300/J044V07N02_02 https://doi.org/10.1021/NP010445G https://doi.org/10.1248/CPB.41.1309 |
| > Organoheterocyclic compounds / Oxepanes | |||||
| Isoascaridole | 12314661 | Click to see | 168.23 | unknown | https://doi.org/10.1300/J044V07N02_02 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| Isorhamnetin | 5281654 | Click to see | 316.26 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| Kaempferol | 5280863 | Click to see | 286.24 | unknown |
https://doi.org/10.1016/0031-9422(90)85389-W https://doi.org/10.1080/01811797.1985.10824657 |
| Quercetin | 5280343 | Click to see | 302.23 | unknown |
https://doi.org/10.1080/01811797.1985.10824657 https://doi.org/10.1016/0031-9422(90)85389-W |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| 5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one | 162919094 | Click to see | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| 5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one | 162919093 | Click to see | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| Kaempferol 3-rhamnoside 4'-xyloside | 74978072 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC5C(C(C(CO5)O)O)O)O)O)O | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| 5-hydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one | 162993875 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| 5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one | 154496822 | Click to see | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
| 7-[(3R,4R,5R,6S)-3-[(3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one | 162817386 | Click to see | 726.70 | unknown | https://doi.org/10.1055/S-0034-1382488 |
| 7-[(3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one | 162817384 | Click to see | 580.50 | unknown | https://doi.org/10.1055/S-0034-1382488 |
| Kaempferol 3-rhamnoside 7-xyloside | 14334866 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O | 564.50 | unknown | https://doi.org/10.1016/0031-9422(90)85389-W |
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