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

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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

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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*

Subspecies (abbr. subsp./ssp.) Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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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!
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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Promising Antileishmanial Activity of Micromeria nervosa Essential Oil: In Vitro and In Silico Studies Essid R, Kefi S, Damergi B, Abid G, Fares N, Jallouli S, Abid I, Hussein D, Tabbene O, Limam F Molecules 19-Apr-2024
PMCID:PMC11055018
doi:10.3390/molecules29081876
PMID:38675696
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Fabrication and characterization of gold nanoparticles using alginate: In vitro and in vivo assessment of its administration effects with swimming exercise on diabetic rats Hashemzadeh V, Hashemzadeh A, Mohebbati R, Arefi RG, Yazdi ME Open Life Sci 17-Apr-2024
PMCID:PMC11032099
doi:10.1515/biol-2022-0869
Improving Lead Phytoremediation Using Endophytic Bacteria Isolated from the Pioneer Plant Ageratina adenophora (Spreng.) from a Mining Area Li Q, Yao S, Wen H, Li W, Jin L, Huang X Toxics 16-Apr-2024
PMCID:PMC11054004
doi:10.3390/toxics12040291
PMID:38668514
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Antimicrobial and Cytotoxic Effect of Positively Charged Nanosilver-Coated Silk Sutures Monroy Caltzonci DA, Rasu Chettiar AD, Ibarra VC, Marasamy L, Loredo-Tovías M, Acosta-Torres LS, Manisekaran R ACS Omega 08-Apr-2024
PMCID:PMC11025086
doi:10.1021/acsomega.4c01257
PMID:38645349
Molecular modelling and anticholinesterase activity of the essential oil from three chemotypes of Lippia alba (Mill.) N.E.Br. ex Britton & P. Wilson (Verbenaceae) Silva Júnior AQ, Rodrigues GD, Alcântara de Sousa K, Maduro Bouillet LE, Bianchi dos Santos G, de Sousa Barroso A, Veras Mourão RH Heliyon 03-Apr-2024
PMCID:PMC11031784
doi:10.1016/j.heliyon.2024.e29063
Soil Nitrogen and Flooding Intensity Determine the Trade-Off between Leaf and Root Traits of Riparian Plant Species Zou H, Wang W, Huang J, Li X, Ma M, Wu S, Zhao C Plants (Basel) 29-Mar-2024
PMCID:PMC11013260
doi:10.3390/plants13070978
PMID:38611507
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
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
Analysis of Primary and Secondary Metabolites, Physical Properties, Antioxidant and Antidiabetic Activities, and Chemical Composition of Rosmarinus officinalis Essential Oils under Differential Water Stress Conditions Laftouhi A, Mahraz MA, Hmamou A, Assouguem A, Ullah R, Bari A, Lahlali R, Ercisli S, Kaur S, Idrissi AM, Eloutassi N, Rais Z, Taleb A, Taleb M ACS Omega 22-Mar-2024
PMCID:PMC11007863
doi:10.1021/acsomega.4c00653
PMID:38617605
Effects of Seven Plant Essential Oils on the Growth, Development and Feeding Behavior of the Wingless Aphis gossypii Glover Wang X, Zhang Y, Yuan H, Lu Y Plants (Basel) 22-Mar-2024
PMCID:PMC11013612
doi:10.3390/plants13070916
PMID:38611446
Variation in traditional knowledge of culturally important macromycete species among three indigenous communities of Oaxaca, Mexico López-García A, Gómez-Hernández M, Gándara E J Ethnobiol Ethnomed 22-Mar-2024
PMCID:PMC10958891
doi:10.1186/s13002-024-00679-8
PMID:38519986
Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 12-Mar-2024
PMCID:PMC10969124
doi:10.3390/foods13060858
PMID:38540848

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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