Heracleum persicum

Details Top

Internal ID UUID6440203a2281c229825951
Scientific name Heracleum persicum
Authority Desf. ex Fisch., C.A.Mey. & Avé-Lall.
First published in Index Seminum (LE, Petropolitanus) 7: 50 (1841)

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.

Heracleum persicum is best known in traditional medicine for seed and fruit infusions used to calm digestive upset and ease colds. In Iran, a warm decoction of the ground seeds is taken for colic, bloating, and loss of appetite, and a weaker infusion is employed for cough and bronchial irritation (Avicenna’s Canon in traditional medicine compendia; Zargaran, 2010; Najafzadeh et al., 2018). Kurdish practitioners of West Azerbaijan also prepare a light seed infusion for stomach pains and wind, and sometimes steep the dried fruit to assist with catarrh and mild fever (Monajeb, 2010). In the Central Asian traditions of Turkmen communities, a tea made from the crushed seeds is drunk to relieve abdominal cramps and stimulate digestion ( ethnobotanical reports from Central Asia, including Soviet-era pharmacological surveys). Across these contexts, the aromatic seeds and fruit are the plant parts used in infusions and decoctions.

A practical preparation is a gentle seed tea: place 2–3 g (about half a small teaspoon) of crushed dried seeds in a cup of just‑boiled water, cover, and steep 10–15 minutes; drink warm in small sips up to two cups daily for mild digestive discomfort. A stronger tincture can be made by macerating 10 g of powdered seeds in 50 ml of 45% ethanol (1:5) for 10–14 days with daily shaking, then filter; the usual dose is 20–30 drops two to three times a day for indigestion. This species contains photosensitizing furanocoumarins (e.g., bergapten), so avoid sun exposure after use; pregnant and nursing women should not use it, and those on photosensitizing drugs should seek medical advice (Zargaran, 2010; WHO monographs on safety). This species has a long history of culinary use as a spice; its medicinal notes in these preparations are subtle but well attested.

Modern work shows the seed essential oil is rich in alkyl‑alkoxy‑benzenes, notably myristicin, and it exhibits antimicrobial activity in vitro, supporting the traditional digestive and antiseptic aspects (Tavakol, 2012). Today, whole, powdered, or crushed seeds are still found in Iranian bazaars for spice use, and seed tinctures are stocked by a few traditional herbalists as digestive tonics; national pharmacopoeial references keep the essential oil and safe‑use limits in view.

General Uses Top

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Common products:
- Dried seeds, marketed as the spice “golpar”.
- Essential oil, obtained from the seeds by steam distillation.
- Living plants, cultivated as ornamental garden and landscape specimens.

Food and beverages (non‑medicinal):
- The dried, ground seeds are used as a condiment in Persian cuisine, added to pickles, rice dishes, stews, soups and other savory preparations.

Fragrance and cosmetics:
- The seed essential oil is employed as a fragrance component in perfumes, soaps, lotions and other cosmetic formulations; it is also used as a natural flavoring in processed food products.

Industrial and craft applications:
- Essential oil extraction is an industrial process for the fragrance industry.
- The species is grown commercially and in private gardens for its ornamental value, providing large umbels of white flowers suitable for landscaping and cut‑flower arrangements.

Properties relevant to use:
- Seeds contain about 20 % oil by weight; the oil is dominated by monoterpenes (α‑pinene, β‑pinene) and the phenylpropene myristicin, which constitutes roughly 40 % of the oil. This profile gives a strong, characteristic aroma suitable for fragrance and flavor applications.

Sustainability and sourcing:
- Heracleum persicum is native to Iran, Turkey and the Caucasus and is cultivated in Iran for seed production. Wild populations are harvested for the spice, which can create local pressure; commercial cultivation reduces reliance on wild collection. The plant is herbaceous and not listed as threatened, but regional monitoring of wild harvesting is recommended to maintain sustainable supply.

Synonyms Top

Scientific name Authority First published in
Heracleum glabrescens Boiss. & Hohen. Diagn. Pl. Orient. 10: 41 (1849)
Heracleum amplissimum Wender. Index Seminum (MB, Marburgensis) 1840: 7 (1840)
Heracleum carmeli hort. ex Wender. Linnaea 15(Litt.): 101 (1841)
Heracleum pubescens var. persicum (Desf. ex Fisch., C.A.Mey. & Avé-Lall.) Regel Index Seminum (LE, Petropolitanus) 1863: 33 (1863)
Heracleum pubescens var. laeve Freyn & Sint. Oesterr. Bot. Z. 42: 123 (1892)

Common names Top

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Language Common/alternative name
English hogweed
English golpar
English persian hogweed
English tromsø palm
Arabic هرقلية فارسية
azb بالدیرقان
Czech bolševník perský
German golpar
Estonian pärsia karuputk
Persian گلپر
Finnish tromssanpalmu
Finnish persianjättiputki
French berce de perse
Hungarian perzsa medvetalp
Korean 골파르
Malayalam ഹെരാക്ലിയം പെർസികം
mzn کولک
Norwegian Bokmål tromsøpalme
Dutch perzische berenklauw
Norwegian Nynorsk tromsøpalme
Slovenian perzijski dežen
Swedish tromsöloka
Chinese 波斯豕草
Chinese 波斯独活

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Czechoslovakia
    • Northern Europe
      • Denmark
      • Finland
      • Iceland
      • Norway
      • Sweden

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000720170
Tropicos 1700136
KEW urn:lsid:ipni.org:names:843131-1
The Plant List kew-2846111
Open Tree Of Life 94221
Observations.org 138336
NCBI Taxonomy 360621
NBN Atlas NBNSYS0000003712
IPNI 843131-1
iNaturalist 516305
GBIF 3628745
Freebase /m/04g291z
EPPO HERPE
Elurikkus 5050
USDA GRIN 311994
Wikipedia Heracleum_persicum
KEW urn:lsid:ipni.org:names:842943-1
IPNI 842943-1
GBIF 3630673

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
A sustainable approach to prepare green synthesis of copper nanoparticles of Bauhinia variegata & Saussurea lappa: Unveiling in-vitro anti-obesity applications Kumar M, Kaushik D, Kumar A, Krishnan H, Oz F, Proestos C, Hashem A, Abd_Allah EF Heliyon 12-Apr-2024
PMCID:PMC11031763
doi:10.1016/j.heliyon.2024.e29433
PMID:38644870
Systematic review on microbiome-related nutritional interventions interfering with the colonization of foodborne pathogens in broiler gut to prevent contamination of poultry meat Mekonnen YT, Savini F, Indio V, Seguino A, Giacometti F, Serraino A, Candela M, De Cesare A Poult Sci 05-Mar-2024
PMCID:PMC10959702
doi:10.1016/j.psj.2024.103607
PMID:38493536
Methoxyfuranocoumarins of Natural Origin–Updating Biological Activity Research and Searching for New Directions—A Review Bartnik M Curr Issues Mol Biol 19-Jan-2024
PMCID:PMC10813879
doi:10.3390/cimb46010055
PMID:38275669
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Applications of Plant Bioactive Compounds as Replacers of Synthetic Additives in the Food Industry Nieto G, Martínez-Zamora L, Peñalver R, Marín-Iniesta F, Taboada-Rodríguez A, López-Gómez A, Martínez-Hernández GB Foods 21-Dec-2023
PMCID:PMC10778451
doi:10.3390/foods13010047
PMID:38201075
Recent Advances in Nanotechnology-Based Targeted Delivery Systems of Active Constituents in Natural Medicines for Cancer Treatment Hu Y, Song J, Feng A, Li J, Li M, Shi Y, Sun W, Li L Molecules 24-Nov-2023
PMCID:PMC10708032
doi:10.3390/molecules28237767
PMID:38067497
Anti-Malassezia Drug Candidates Based on Virulence Factors of Malassezia-Associated Diseases Billamboz M, Jawhara S Microorganisms 20-Oct-2023
PMCID:PMC10609646
doi:10.3390/microorganisms11102599
PMID:37894257
Ultra-Performance Liquid Chromatography Coupled with Mass Metabolic Profiling of Ammi majus Roots as Waste Product with Isolation and Assessment of Oral Mucosal Toxicity of Its Psoralen Component Xanthotoxin Fathallah N, El Deeb M, Rabea AA, Almehmady AM, Alkharobi H, Elhady SS, Khalil N Metabolites 29-Sep-2023
PMCID:PMC10608439
doi:10.3390/metabo13101044
PMID:37887369
The comparative perspective of phytochemistry and biological properties of the Apiaceae family plants Hamidian M, Salehi A, Naghiha R, Dehnavi MM, Castangia I, Mirfathi MN Sci Rep 31-Jul-2023
PMCID:PMC10390506
doi:10.1038/s41598-023-39254-8
PMID:37524766
Eco-Friendly Green Synthesis and Characterization of Silver Nanoparticles by Scutellaria multicaulis Leaf Extract and Its Biological Activities Gharari Z, Hanachi P, Sadeghinia H, Walker TR Pharmaceuticals (Basel) 11-Jul-2023
PMCID:PMC10386756
doi:10.3390/ph16070992
PMID:37513904
Contemporary Anti-Retroviral Drugs (ARVDs) Disrupt Follicular Development in Female Wistar Rats Ohihoin AG, Ohihoin EN, Ujomu I, Bakare A, Olanrewaju O, Okafor A, Ojetunde M, Ayoola JB, Aina O, Ajibaye O, Taylor-Robinson SD J Exp Pharmacol 03-Jul-2023
PMCID:PMC10328220
doi:10.2147/JEP.S398343
PMID:37425074
Case report: A case of renal arcuate vein thrombosis successfully treated with direct oral anticoagulants Torabi Jahromi M, Roozbeh J, Masjedi F, Mohammadzadeh S, Tabei SS, Shafiee M, Rasaei N Front Med (Lausanne) 20-Jun-2023
PMCID:PMC10319107
doi:10.3389/fmed.2023.1092815
PMID:37409279
Incredible Combination of Lifestyle Modification and Herbal Remedies for Polycystic Ovarian Syndrome Management Balkrishna A, Rana M, Mishra S, Srivastava D, Bhardwaj R, Singh S, Rajput SK, Arya V Evid Based Complement Alternat Med 20-Jun-2023
PMCID:PMC10299884
doi:10.1155/2023/3705508
PMID:37383339
Encapsulation of Heracleum persicum essential oil in chitosan nanoparticles and its application in yogurt Yousefi M, Khanniri E, Sohrabvandi S, Khorshidian N, Mortazavian AM Front Nutr 09-Jun-2023
PMCID:PMC10287953
doi:10.3389/fnut.2023.1130425
PMID:37360296
Immunomodulatory Effects of Natural Feed Additives for Meat Chickens Phillips CJ, Hosseintabar-Ghasemabad B, Gorlov IF, Slozhenkina MI, Mosolov AA, Seidavi A Life (Basel) 30-May-2023
PMCID:PMC10301336
doi:10.3390/life13061287
PMID:37374069

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Butyl butyrate 7983 Click to see 144.21 unknown https://doi.org/10.1055/S-2007-969621
Ethyl butyrate 7762 Click to see CCCC(=O)OCC 116.16 unknown https://doi.org/10.1055/S-2007-969621
Heptyl butyrate 62592 Click to see 186.29 unknown https://doi.org/10.1055/S-2007-969621
Hexyl butyrate 17525 Click to see 172.26 unknown https://doi.org/10.1055/S-2007-969621
Hexyl Hexanoate 22873 Click to see CCCCCCOC(=O)CCCCC 200.32 unknown https://doi.org/10.1055/S-2007-969621
Hexyl octanoate 14228 Click to see CCCCCCCC(=O)OCCCCCC 228.37 unknown https://doi.org/10.1055/S-2007-969621
Oct-1-EN-1-YL butanoate 71385286 Click to see CCCCCCC=COC(=O)CCC 198.30 unknown https://doi.org/10.1055/S-2007-969621
Oct-1-en-1-yl hexanoate 71385285 Click to see 226.35 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate 8167 Click to see 200.32 unknown https://doi.org/10.1055/S-2007-969621
Octyl Acetate 8164 Click to see 172.26 unknown https://doi.org/10.1055/S-2007-969621
Octyl butyrate 61030 Click to see 200.32 unknown https://doi.org/10.1055/S-2007-969621
Octyl hexanoate 21006 Click to see 228.37 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1055/S-2007-969621
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1055/S-2007-969621
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969621
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969621
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-2007-969621
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2007-969621
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969621
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Butyl Acetate 31272 Click to see CCCCOC(=O)C 116.16 unknown https://doi.org/10.1055/S-2007-969621
Hexyl acetate 8908 Click to see 144.21 unknown https://doi.org/10.1055/S-2007-969621
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
Octen-1-ol acetate 520583 Click to see 170.25 unknown https://doi.org/10.1055/S-2007-969621
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Isobutyric Acid 6590 Click to see 88.11 unknown https://doi.org/10.1055/S-2007-969621
> Organic oxygen compounds / Organooxygen compounds / Enols
Octenol 185984 Click to see 128.21 unknown https://doi.org/10.1055/S-2007-969621
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Pimpinellin 4825 Click to see 246.21 unknown https://doi.org/10.1016/S0031-9422(00)85242-5
Vaginidiol 11817856 Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O 262.26 unknown https://doi.org/10.1016/S0031-9422(00)85242-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1016/S0031-9422(00)85242-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0031-9422(00)85242-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0031-9422(00)85242-5

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