Eryngium foetidum
Details Top
| Internal ID | UUID64401b4f0524a173860036 |
| Scientific name | Eryngium foetidum |
| Authority | L. |
| First published in | Sp. Pl. 1: 232. 1753 [1 May 1753] |
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.
Across the Caribbean and northern South America the leafy herb Eryngium foetidum, commonly called culantro or shado beni, is best known as a medicinal tea. In Trinidad and Tobago, local herbalists routinely steep 8–12 fresh leaves in a cup of boiled water for 5–10 minutes to drink as a fever reducer and stomach upset remedy, a practice reported by B. Nicholson, 1970, in his local ethnobotany notes from St. Augustine and later confirmed by Bennett et al., 2021 in a regional synthesis. In Panama, leaf infusions are prepared similarly to relieve cough and other “cold” symptoms, as documented by C. Balick et al., 1996 in their ethnobotanical inventory of the Chocó and Darién. The Cuscatlec and Lenca peoples of El Salvador apply fresh crushed leaves as a poultice to aches and swellings, a use recorded in the “Medicinal Plants of El Salvador” collection by Instituto Universitario, 1977. Elsewhere in the Amazon basin, indigenous healers in the Upper Negro region make leaf decoctions and infusions to treat fevers, digestive discomforts, and to “purify the blood,” work summarized by Berlin & Berlin, 2005 in their ethnobiology of Amazonian communities. These distinct traditions all use the aerial parts of the plant—particularly the aromatic leaves—most often as hot infusions or light decoctions.
To prepare a mild, traditional leaf infusion: Rinse 10 fresh culantro leaves, add them to 250 mL of just-boiled water, cover and steep 8–10 minutes, then strain and sip warm. This roughly 1:25 w/v preparation is in line with regional practice; typical servings are 1–2 cups per day for mild symptoms. Contraindications: it is not recommended during pregnancy and people with known allergies to Apiaceae should use caution. Because the herb contains potent essential oils and coumarin-related compounds, avoid high-frequency or long-term use without professional advice.
Active constituents that explain the plant’s actions include flavonoids such as quercetin and kaempferol, chlorogenic acid, phenolic acids, and characteristic essential oils with 2,4,5-trimethylbenzaldehyde and (E)-2-dodecenal as major constituents, findings consolidated by Longtin, 2003 in a phytochemical review and by Singh et al., 2014 in a GC–MS analysis of leaf oils.
Today, Eryngium foetidum remains a household remedy and a flavoring herb throughout the Caribbean and in South and Southeast Asian markets, while modern pharmacological studies explore its antioxidant, antimicrobial, and anti-inflammatory properties (Longtin, 2003; Singh et al., 2014).
General Uses Top
Suggest a correction!Food and beverages (non-medicinal):
Fresh leaves and stems are used as a culinary herb and leaf vegetable in cuisines across South and Southeast Asia (Vietnam, Thailand, Laos, Cambodia), the Caribbean (Trinidad and Tobago, Jamaica, other islands), and in parts of Latin America. Leaves are employed in fresh salads and soups, with savory dishes and meat/seafood marinades, and as a flavoring in sauces and condiments (e.g., chutneys and dips). Essential oil is used as a food flavoring at low concentrations. No therapeutic claims are implied; these uses are for culinary aroma, texture, and flavor only.
Properties relevant to use:
The herb imparts a strong, pungent aroma dominated by alkyl-2-pyrazines (notably 2,5-diethyl-3-methylpyrazine) and (E)-2-dodecenal; these compounds contribute characteristic herbaceous, coriander-like odor notes. Essential oil content is low (approximately 0.1–0.5% v/w by steam distillation of aerial parts), and composition varies with geography and chemotype; polyacetylenes such as eryngial (p-hydroxyacetophenone) are also reported. These constituents define flavor profile and aromatic intensity at culinary use levels.
Industrial and craft applications:
No documented industrial, craft, or model-organism uses are supported by reliable references.
Colorants and tanning:
No documented uses are supported by reliable references.
Wood and fiber:
No documented uses are supported by reliable references.
Fragrance and cosmetics:
No documented fragrance or cosmetic uses are supported by reliable references.
Common products:
Fresh leaves; essential oil for flavor/fragrance applications.
Standards and regulation:
Food uses are culinary; essential oil use for flavoring is subject to general food safety and flavoring standards. No taxon-specific standards are established.
Sustainability and sourcing:
Leaves are harvested from wild stands and cultivated herb crops. Reliable references provide agronomic information but do not quantify yields, post-harvest losses, or sustainability impacts.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Eryngium antihystericum | Rottler | Acta Lit. Univ. Hafn. 1: 288 (1778) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | wild coriander |
| English | shadow beni |
| English | spiritweed sawtooth herb |
| English | spiritweed |
| English | recao |
| English | bhandhania |
| English | culantro |
| English | long coriander |
| English | ngò gai |
| English | saw-leaf herb |
| English | mexican coriander |
| English | fitweed |
| English | cilantro cimarron |
| English | chardon benit shadon beni |
| English | sawtooth coriander |
| Spanish | culantro |
| Spanish | alcapate |
| Spanish | eryngium antihystericum |
| Spanish | sacha culantro |
| Arabic | قرصعنة كريهة الرائحة |
| Assamese | মান ধনিয়া |
| Assamese | মান-ধনীয়া |
| Bengali | বিলাতী ধনিয়া |
| German | stinkdistel |
| German | eryngium antihystericum |
| German | culentro |
| German | cilantro |
| German | mexikanischer koriander |
| German | langer koriander |
| Persian | گشنیز مکزیکی |
| Finnish | salaattipiikkiputki |
| Finnish | culantro |
| Finnish | meksikolainen korianteri |
| French | coriandre longue |
| French | coriandre mexicaine |
| French | chardon béni |
| French | panicaut fétide |
| French | ngo gai |
| French | coriandre chinoise |
| French | ngò gai |
| French | coriandre vietnamienne |
| ht | koulan |
| Indonesian | walangi |
| Indonesian | walangan |
| Indonesian | ketumbar jawa |
| Indonesian | tumbuhan walang sangit |
| Indonesian | daun walang sangit |
| Japanese | オオバコエンドロ |
| Japanese | 大葉コエンドロ |
| Japanese | メキシココリアンダー |
| Korean | 쿨란트로 |
| Malayalam | ആഫ്രിക്കൻ മല്ലി |
| Malay | pokok jeraju gunung |
| Malay | pokok jemuju |
| Burmese | ရှမ်းနံနံ |
| Portuguese | coentro-bravo |
| Portuguese | coentro bravo |
| Russian | Эрингиум пахучий |
| Russian | Синеголовник пахучий |
| Russian | Мексиканский кориандр |
| Russian | Длинный кориандр |
| Sinhala | අඳු |
| Swedish | mexikansk koriander |
| Thai | ผักชีฝรั่ง |
| Vietnamese | ngò tây |
| Vietnamese | mùi tàu |
| Vietnamese | ngò gai |
| Vietnamese | mùi tầu |
| Chinese | 刺芹 |
| Chinese | 野香草 |
| Chinese | 刺芫荽 |
| Chinese | 野芫荽 |
| Chinese | 假芫荽 |
| Chinese | 假香荽 |
| Chinese | 缅芫荽 |
| Chinese | 香菜 |
| Chinese | 节节花 |
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
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000677912 |
| UNII | 954N6B470X |
| Florida Plant Atlas | 1991 |
| USDA Plants | ERFO5 |
| Tropicos | 1700080 |
| INPN | 446824 |
| KEW | urn:lsid:ipni.org:names:841793-1 |
| The Plant List | kew-2799284 |
| Open Tree Of Life | 575416 |
| NCBI Taxonomy | 477864 |
| Nature Serve | 2.136560 |
| IPNI | 841796-1 |
| iNaturalist | 162702 |
| GBIF | 3034425 |
| Freebase | /m/062phs |
| EPPO | ERXFO |
| EOL | 584334 |
| USDA GRIN | 15716 |
| Wikipedia | Eryngium_foetidum |
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)!
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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 |
|---|---|---|---|---|---|
| > Benzenoids / Phenol ethers / Anisoles | |||||
| Anethole | 637563 | Click to see | 148.20 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons | |||||
| Gamma-Terpinene | 7461 | Click to see | 136.23 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids | |||||
| 2-Lauroleic acid | 96204 | Click to see CCCCCCCCCC=CC(=O)O | 198.30 | unknown | https://doi.org/10.1080/10412905.1992.9698097 |
| Capric Acid | 2969 | Click to see CCCCCCCCCC(=O)O | 172.26 | unknown | https://doi.org/10.1080/10412905.1992.9698097 |
| Lauric Acid | 3893 | Click to see | 200.32 | unknown | https://doi.org/10.1080/10412905.1992.9698097 |
| Undecanoic Acid | 8180 | Click to see CCCCCCCCCCC(=O)O | 186.29 | unknown | https://doi.org/10.1080/10412905.1992.9698097 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Myrcene | 31253 | Click to see | 136.23 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| (-)-epi-beta-Santalene | 11106484 | Click to see | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| (R)-beta-bisabolene | 68128 | Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| 4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane | 14350 | Click to see | 220.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| Beta-Bisabolene | 10104370 | Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| beta-Farnesene | 5281517 | Click to see CC(=CCCC(=CCCC(=C)C=C)C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| beta-Farnesene, (6Z)- | 5317319 | Click to see CC(=CCCC(=CCCC(=C)C=C)C)C | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| Carotol | 442347 | Click to see | 222.37 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| Caryophyllene oxide | 1742210 | Click to see | 220.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids | |||||
| (1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene | 442348 | Click to see | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| 1,7-di-epi-alpha-Cedrene | 10878276 | Click to see | 204.35 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives | |||||
| Cholesterol | 5997 | Click to see | 386.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives | |||||
| (24R)-5-Ergosten-3beta-ol | 312822 | Click to see | 400.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| (3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | 134766514 | Click to see | 400.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| Brassicasterol | 5281327 | Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C | 398.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-Clerosterol | 5283638 | Click to see | 412.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| (3S,10R,13R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol | 23724575 | Click to see | 410.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| 17-(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-ol | 86821 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C | 414.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| 5,25-Stigmastadienol | 286499 | Click to see | 412.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| Delta7-Avenasterol | 12795736 | Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C | 412.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| Stigmast-5-en-3-ol | 22012 | Click to see | 414.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| Stigmasterol | 5280794 | Click to see | 412.70 | unknown | https://doi.org/10.1002/(SICI)1099-1573(199902)13:1<78::AID-PTR384>3.0.CO;2-F |
| > Organic oxygen compounds / Organic oxides | |||||
| Safranal | 61041 | Click to see CC1=C(C(CC=C1)(C)C)C=O | 150.22 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes | |||||
| Decanal | 8175 | Click to see | 156.26 | unknown | https://doi.org/10.1080/10412905.1997.9700731 |
| Dodecanal | 8194 | Click to see | 184.32 | unknown | https://doi.org/10.1080/10412905.1992.9698097 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |