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

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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

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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

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-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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S Sci Rep 10-May-2024
PMCID:PMC11087530
doi:10.1038/s41598-024-61428-1
PMID:38730080
Salicylic Acid and Water Stress: Effects on Morphophysiology and Essential Oil Profile of Eryngium foetidum dos Santos SK, Gomes DD, Soares VD, Dantas EF, de Oliveira AF, Gusmão MH, de Matos EM, Souza T, Viccini LF, Grazul RM, Henschel JM, Batista DS Metabolites 21-Apr-2024
PMCID:PMC11052287
doi:10.3390/metabo14040241
PMID:38668369
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
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
The first complete chloroplast genome sequence of Pentaphragma spicatum Merr. (Pentaphragmataceae) and phylogenetic analysis Cheng Z, Yu BN, Huang XY, Bin ZJ, Liu SZ, Chi ZJ Mitochondrial DNA B Resour 12-Dec-2023
PMCID:PMC10776070
doi:10.1080/23802359.2023.2290339
PMID:38196793
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E PeerJ 07-Nov-2023
PMCID:PMC10637247
doi:10.7717/peerj.16231
PMID:37953791
Patterns of use of wild food plants by Brazilian local communities: systematic review and meta-analysis Gomes LC, Medeiros PM, Prata AP J Ethnobiol Ethnomed 25-Oct-2023
PMCID:PMC10601232
doi:10.1186/s13002-023-00619-y
PMID:37880767
The presence of wild edible plants and determinants influencing their harvest, consumption, and conservation in south eastern Bhutan Bajgai RC, Bajgai Y, Johnson SB PLoS One 10-Oct-2023
PMCID:PMC10564141
doi:10.1371/journal.pone.0285936
PMID:37816046
Complete chloroplast of four Sanicula taxa (Apiaceae) endemic to China: lights into genome structure, comparative analysis, and phylogenetic relationships Li H, Wu M, Lai Q, Zhou W, Song C BMC Plant Biol 21-Sep-2023
PMCID:PMC10512634
doi:10.1186/s12870-023-04447-w
PMID:37730528
Water stress and exogenous carnitine on growth and essential oil profile of Eryngium foetidum L. dos Santos SK, da Silva Gomes D, de Oliveira AF, Silva AM, de Moura VS, Gusmão MH, de Matos EM, Viccini LF, Grazul RM, Henschel JM, Batista DS 3 Biotech 02-Sep-2023
PMCID:PMC10475002
doi:10.1007/s13205-023-03757-y
PMID:37667775
Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods Li M, Li M, Wang L, Li M, Wei J Molecules 27-May-2023
PMCID:PMC10254214
doi:10.3390/molecules28114384
PMID:37298861
Choice Modeling for the Commercial Cultivation of Underutilized Aromatic Plants for Producing Mosquito Repellents: Targeting Rural Sector Income Generation Munugoda KD, Talagala TS, Subasinghe SM, Hettiarachchi DS, Cooray AT Econ Bot 25-May-2023
PMCID:PMC10211285
doi:10.1007/s12231-023-09573-y
PMID:37359047
Extracts of Eryngium foetidum Leaves from the Amazonia Were Efficient Scavengers of ROS and RNS Leitão DD, Barbosa-Carvalho AP, de Siqueira FC, Sousa RP, Lopes AS, Chisté RC Antioxidants (Basel) 18-May-2023
PMCID:PMC10215176
doi:10.3390/antiox12051112
PMID:37237978

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

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