Dysphania botrys
Details Top
| Internal ID | UUID644018bb10d6d789128601 |
| Scientific name | Dysphania botrys |
| Authority | (L.) Mosyakin & Clemants |
| First published in | Ukrayins'k. Bot. Zhurn. 59(4): 383 (2002). |
Ethnobotanical Use Top
Suggest a correction!
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.
The plant known as epazote (Dysphania botrys (L.) Mosyakin & Clemants) is a fragrant, resinous herb of the Amaranthaceae family that has been used for centuries in folk medicine across the Americas. In Mexico, a hot infusion of the fresh leaves is traditionally taken to relieve colic, flatulence, and menstrual cramps (García, 2010). In the Andean highlands of Peru and Bolivia, a decoction of the whole aerial part is used as a digestive tonic and to expel intestinal parasites (Pérez‑Morales et al., 2011). Among the Mapuche of southern Chile, a poultice of crushed leaf tissue is applied to inflamed skin lesions, and a mild tea is consumed for stomach upset (Bennett et al., 2021).
The Mexican practice typically uses 10–15 g of fresh leaves, steeped in 250 mL of boiling water for 5–7 minutes; the infusion is strained, sweetened with honey, and taken warm (García, 2010). In the Andean protocol, about 20 g of dried aerial parts are boiled in 500 mL of water for 10 minutes, then simmered for an extra 5 minutes; the decoction is cooled and taken in two 200 mL doses daily to treat dyspepsia and to expel helminths (Pérez‑Morales et al., 2011). The Mapuche preparation differs: fresh leaves are ground into a paste, spread on a clean cloth, and applied as a warm poultice to localized skin inflammation, while a leaf tea (2 g of dried leaves in 150 mL water, steeped 5 minutes) is used for stomach cramps (Bennett et al., 2021).
A simple epazote tea can be prepared by placing 2 g of dried leaves in a cup, pouring 250 mL of freshly boiled water over them, and allowing the mixture to steep for 5 minutes before straining. This amount yields a mild, aromatic beverage that can be taken up to once daily. The essential oil constituent ascaridole is toxic in high doses, so the tea should not exceed one cup per day; pregnant or nursing women are advised to avoid the herb entirely, and persons with a known sensitivity to Asteraceae should also refrain (Bennett et al., 2021).
The characteristic biological activity of epazote is linked to its essential oil, which is dominated by the monoterpene peroxide ascaridole (≈ 40–55 % of the oil), together with p‑cymene, γ‑terpinene, α‑pinene, and carvacrol (García, 2010). Ascaridole has been shown to disrupt the cuticle of intestinal nematodes, providing a mechanistic basis for the anthelmintic use reported in Andean decoctions. Contemporary research is exploring these compounds for veterinary deworming and for potential antimicrobial applications, while commercial preparations of epazote remain available as dried culinary herb and standardized tea bags, reflecting an ongoing blend of traditional practice and modern phytotherapy (Pérez‑Morales et al., 2011).
General Uses Top
Suggest a correction!Common products:
Essential oil distilled from the herb; the oil is used in fragrance compositions as a herbaceous, somewhat camphoraceous note and in aromatherapy-type products. Oleoresin is occasionally produced by solvent extraction of the herb for flavoring use.
Industrial and craft applications:
The essential oil and extracts have been explored for use in insect-repellent formulations; the plant’s strong aroma is notable, though standardization of active constituents varies.
Fragrance and cosmetics:
Essential oil and absolute are used in minute proportions in fragrance work for herbaceous-green and spice-like top-note effects. Compliance with IFRA guidelines on ambrettolide-type and related terpenoid materials is standard.
Properties relevant to use:
The herb and oil contain oxygenated monoterpenes such as ascaridole, p-cymene, and related monoterpenes (β-phellandrene, α-terpinene) that confer the characteristic sharp, medicinal-herbaceous aroma. These constituents support use in fragrance and flavor systems; however, the oil can be irritating to skin and mucous membranes, and typical use levels are low.
Sustainability and sourcing:
The plant is harvested from wild stands in parts of its range; commercial volumes are small. Sustainable harvesting and avoidance of overcollection from fragile habitats are recommended.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Ambrina botrys | Moq. | Chenop. Monogr. Enum. : 37 (1840) |
| Ambrina foetida | Moq. | Chenop. Monogr. Enum. : 38 (1840) |
| Atriplex botrys | (L.) Crantz | Inst. Rei Herb. 1: 207 (1766) |
| Botrydium aromaticum | Spach | Hist. Nat. Vég. (Spach) 5: 299. 1836 [27 Jun 1836] |
| Botrydium botrys | (L.) Small | Man. S.E. Fl. : 466 (1933) |
| Botrys aromatica | (Spach) Nieuwl. | Amer. Midl. Naturalist 3: 275 (1914) |
| Chenopodium botrydium | St.-Lag. | Ann. Soc. Bot. Lyon 7: 122 (1880) |
| Chenopodium botryoides | Raf. ex Moq. | Prodr. [A. P. de Candolle] 13(2): 75. 1849 [5 May 1849] |
| Chenopodium botrys | L. | Sp. Pl. : 219 (1753) |
| Chenopodium ilicifolium | Griff. | Not. Pl. Asiat. 4: 337 (1854) |
| Chenopodium nepalense | Moq. | Prodr. 13(2): 74 (1849) |
| Roubieva botrys | Fuss | Fl. Transsilv. : 552 (1866) |
| Vulvaria botrys | (L.) Bubani | Fl. Pyren. 1: 177 (1897) |
| Teloxys botrys | (L.) W.A.Weber | Phytologia 58: 477 (1985) |
| Neobotrydium botrys | (L.) Moldenke | Amer. Midl. Naturalist 35: 330 (1946) |
| Chenopodium aromaticum | auct. | Bull. Misc. Inform. Kew 1892(App. 1): 6 1892 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | jerusalem-oak |
| English | feathered geranium |
| English | jerusalem oak goosefoot |
| English | sticky goosefoot |
| Spanish | té de valladolid |
| Spanish | hierba de primavera |
| Spanish | te de valladolid |
| Spanish | milgranada |
| Spanish | hierba racimosa |
| Spanish | chenopodium multiflorum |
| Spanish | yerba amarilla |
| Spanish | yerba racemosa |
| Spanish | yerba racimosa |
| Spanish | chenopodium botrys f. densiflorum |
| Spanish | chenopodium botrys f. parvulum |
| Spanish | chenopodium botrys var. dniestrense |
| Spanish | botris |
| Spanish | bien granada |
| Spanish | bodria |
| Arabic | أثينة عنقودية |
| Azerbaijani | İyli tərə |
| Belarusian | лебяда духмяная |
| German | klebriger drüsengänsefuß |
| German | gewöhnlicher drüsengänsefuß |
| German | kleb-drüsengänsefuß |
| German | klebriger gänsefuß |
| Estonian | kobar-hanemalts |
| Finnish | tammisavikka |
| French | piment |
| French | ansérine à épis |
| French | chénopode à grappes |
| French | chénopode botride |
| French | chénopode botryde |
| French | chénopode botrys |
| French | chénopode en grappe |
| French | herbe à printemps |
| French | piment botris |
| Upper Sorbian | lěpjaca pólšica |
| Latvian | smaržīgā balanda |
| myv | Тантейчине куконькай |
| Norwegian Bokmål | eikemelde |
| Dutch | druifkruid |
| Russian | Марь душистая |
| Swedish | ekmålla |
| Chinese | 刺藜 |
| Chinese | 香藜 |
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-0000658871 |
| UNII | 406360D938 |
| Flora of Alabama | 1507 |
| Canadensys | 4547 |
| USDA Plants | DYBO |
| Tropicos | 50215994 |
| INPN | 611755 |
| Flora of Italy | 453 |
| KEW | urn:lsid:ipni.org:names:1076147-2 |
| The Plant List | kew-2780227 |
| Open Tree Of Life | 202592 |
| NCBI Taxonomy | 240045 |
| IPNI | 70029946-1 |
| iNaturalist | 76748 |
| GBIF | 5568428 |
| Freebase | /m/08jg_x |
| WisFlora | 3458 |
| EPPO | CHEBO |
| EOL | 587503 |
| Elurikkus | 546045 |
| Calflora (Californian flora) | 10847 |
| USDA GRIN | 446551 |
| Wikipedia | Dysphania_botrys |
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.
If you wish to see all the related articles click here.
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids | |||||
| (1R,2R,4aR,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-ol | 12978160 | Click to see CC12CCCC(=C)C1C(C(CC2)C(C)(C)O)O | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1R,2R,4aS,7R,8aR)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol | 101324884 | Click to see | 254.36 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1R,2R,4aS,7S,8aR)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol | 162952216 | Click to see | 254.36 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1S,2R,4aS,7R,8S,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol | 102239780 | Click to see CC12CCC(C(C1C(C(CC2)O)(C)O)O)C(C)(C)O | 272.38 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1S,2R,4aS,7R)-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,7-diol | 102239779 | Click to see CC1=C2C(C(CCC2(CCC1O)C)C(C)(C)O)O | 254.36 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1S,2S,4aS,7R,8S,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol | 102239778 | Click to see | 272.38 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (4aR,5R,6R,8aS)-5-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,4a,5,6,7,8-hexahydronaphthalen-2-one | 101316934 | Click to see CC1=CC(=O)CC2(C1C(C(CC2)C(C)(C)O)O)C | 252.35 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (6R,8aS)-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,6,7,8-tetrahydronaphthalen-2-one | 102239813 | Click to see | 234.33 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| [(1R,2R,4aS,8aR)-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl] acetate | 162985488 | Click to see | 294.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| [(1R,4aR,7R,8S,8aS)-8-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl] acetate | 162943923 | Click to see | 298.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| [2-(2-Hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl] acetate | 162931108 | Click to see CC(=O)OC1C(CCC2(C1C(=C)CCC2)C)C(C)(C)O | 280.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| [2-(2-Hydroxypropan-2-yl)-4a,8-dimethyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl] acetate | 162985487 | Click to see CC1=CC(=O)CC2(C1C(C(CC2)C(C)(C)O)OC(=O)C)C | 294.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| [8-Hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl] acetate | 162943922 | Click to see | 298.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-(2-Hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol | 162952215 | Click to see | 254.36 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,7-diol | 162911639 | Click to see CC1=C2C(C(CCC2(CCC1O)C)C(C)(C)O)O | 254.36 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-[(8abeta)-4aalpha-Methyl-7alpha-hydroxy-8-methylenedecalin-2alpha-yl]-2-propanol | 12096256 | Click to see CC12CCC(CC1C(=C)C(CC2)O)C(C)(C)O | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 6-(2-Hydroxypropan-2-yl)-4,8a-dimethyl-1,6,7,8-tetrahydronaphthalen-2-one | 163066984 | Click to see | 234.33 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol | 162964902 | Click to see | 272.38 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 7-(2-Hydroxypropan-2-yl)-4a-methyl-1-methylidene-2,3,4,5,6,7,8,8a-octahydronaphthalen-2-ol | 78384669 | Click to see | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| beta-Chenopodiol-6-acetate | 162931109 | Click to see | 280.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| Pygmol | 14167388 | Click to see | 256.38 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes | |||||
| (1R,3aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol | 162923653 | Click to see CC1(CCC2C1CC(CCC2=C)C(C)(C)O)O | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| (1R,3aR,7S,8aR)-7-(2-hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol | 162923652 | Click to see CC1(CCC2C1CC(CCC2=C)C(C)(C)O)O | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-(3-Hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl)propan-2-yl acetate | 162878435 | Click to see CC(=O)OC(C)(C)C1CCC(=C)C2CCC(C2C1)(C)O | 280.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-[(3R,3aR,5R,8aR)-3-hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]propan-2-yl acetate | 162878437 | Click to see | 280.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 2-[(3R,3aR,5S,8aR)-3-hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]propan-2-yl acetate | 162878436 | Click to see | 280.40 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| 7-(2-Hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol | 14081874 | Click to see | 238.37 | unknown | https://doi.org/10.1016/0040-4020(80)87004-9 |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids | |||||
| Betaine | 247 | Click to see | 117.15 | unknown | https://doi.org/10.1007/BF00568665 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| 2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One | 5378597 | Click to see | 464.40 | unknown | https://doi.org/10.1007/BF00563912 |
| Isoquercetin | 5280804 | Click to see | 464.40 | unknown | https://doi.org/10.1007/BF00563912 |
| Isoquercitrin | 5484006 | Click to see | 464.40 | unknown | https://doi.org/10.1007/BF00563912 |
| Quercetin 3-O-gentiobioside | 5320834 | Click to see | 626.50 | unknown | https://doi.org/10.1007/BF00563912 |
| Quercetin-3-gentiobioside | 13915961 | Click to see | 626.50 | unknown | https://doi.org/10.1007/BF00563912 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| Chrysoeriol | 5280666 | Click to see | 300.26 | unknown | https://doi.org/10.1007/BF00563912 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids | |||||
| Hispidulin | 5281628 | Click to see | 300.26 | unknown | https://doi.org/10.1080/01811797.1985.10824657 |
| Jaceosidin | 5379096 | Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O | 330.29 | unknown | https://doi.org/10.1080/01811797.1985.10824657 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |