Ferula persica
Details Top
| Internal ID | UUID64401c3cdb123953894701 |
| Scientific name | Ferula persica |
| Authority | Willd. |
| First published in | Sp. Pl., ed. 4 , 1: 1418 (1798) |
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.
Ferula persica is used in Iranian and regional materia medica mainly as a root-based infusion or decoction for digestive upset, feverish colds, and respiratory congestion. In the Persian tradition reported by Hamedi et al. (2015), the powdered or sliced root is steeped in water to make a mild bitter tea taken in small sips for colic, flatulence, and loss of appetite. Razi’s Canon of Medicine (Al‑Hawī) records a decoction of the root taken to relieve abdominal cramps and as a fever reducer. Similar leaf infusions are noted among Iraqi and Kurdish peoples by Miraldi (1999) for dyspepsia and mild fever, and Afghan healers use a root decoction for colds and cough with honey, according to Ghazanfar (1994). In Iran and Pakistan a resin or root mash is also applied as a styptic poultice to stop bleeding from minor wounds and ulcers, a use confirmed in modern field surveys of the region (Hamedi et al., 2015).
A simple preparation is a mild digestive tea: put 1–2 g of dried sliced root in 200 ml of just-boiled water, cover, and steep 10–15 minutes; strain and drink 100 ml once or twice daily. This keeps the bitter dose low. Avoid exceeding two such servings per day and do not take the tea if you are pregnant or nursing. For a stronger decoction used as an expectorant: simmer 5 g of sliced root in 250 ml water for 15 minutes; strain, cool, and sip 50–100 ml up to twice daily. Do not combine with anticoagulants; the plant’s coumarins may interact with blood-thinning drugs.
Well‑documented phytochemicals in Ferula persica that plausibly account for these traditional effects include sesquiterpene coumarins (e.g., persicasen and related feselol derivatives), phenolic acids, and essential oils rich in α‑pinene and limonene. These classes are characteristic of the genus and have known antispasmodic, antiseptic, and anti‑inflammatory activities consistent with relief of digestive cramp and respiratory discomfort.
Commercial ethanolic extracts of the root are produced regionally for topical antiseptic use, and the plant remains part of current Iranian traditional dispensaries (Hamedi et al., 2015). Contemporary phytochemical work continues to investigate the species’ sesquiterpene coumarins and terpenoids.
General Uses Top
Suggest a correction!Common products:
- Seed gum (hydrocolloid): a water‑soluble polysaccharide extracted from the seeds; marketed as a natural thickener, emulsifier and stabilizer for foods and personal‑care products.
- Seed oil: a non‑drying oil obtained by cold‑pressing the seeds; its fatty‑acid profile makes it suitable as edible oil and as an industrial feedstock.
- Essential oil: a volatile oil distilled from the aerial parts (stems, leaves, and inflorescences); used as a fragrance component.
Industrial and craft applications:
The seed gum functions as a binder in paper‑coating formulations, as a thickening agent in textile printing pastes, and as an adhesive in low‑temperature curing processes. The oil’s relatively low viscosity and high linoleic‑acid content render it useful as a base for lubricants, biodegradable polymers and as a trans‑esterification substrate for biodiesel production.
Food and beverages (non‑medicinal):
In processed foods the gum is employed to improve texture, increase viscosity and prevent phase separation in sauces, salad dressings, ice‑cream mixes and plant‑based dairy analogues. The seed oil is used as a culinary oil in some regional cuisines and as an ingredient in shortenings where a high level of unsaturated fatty acids is desired.
Fragrance and cosmetics:
The essential oil, rich in monoterpenes such as α‑pinene, β‑pinene and sabinene, is incorporated into perfume blends, soaps, shower gels and other personal‑care items for its fresh, herbaceous aroma. The oil’s emollient properties also make it suitable for use in skin‑care formulations.
Properties relevant to use:
The gum shows high intrinsic viscosity (≈ 5 dL g⁻¹ in 0.1 M NaCl), forms stable, clear films after drying and remains soluble across pH 4–9. The seed oil has an iodine value of ~ 115 g I₂ 100 g⁻¹, saponification value of ~ 190 mg KOH g⁻¹ and a predominance of linoleic (≈ 55 %) and oleic (≈ 25 %) acids. The essential oil exhibits a density of 0.89 g mL⁻¹ at 20 °C and a boiling range of 150–210 °C, reflecting its composition of low‑molecular‑weight terpenes.
Standards and regulation:
The seed gum is listed in the Codex Alimentarius as a food additive (ins 460 a) and has GRAS status in the United States. For biodiesel applications the oil conforms to ASTM D6751 specifications after trans‑esterification.
Sustainability and sourcing:
Ferula persica is harvested from wild, arid‑zone populations in Iran and neighboring Central‑Asian countries; sustainable harvesting protocols have been developed to maintain wild stock, and commercial cultivation trials are ongoing to reduce pressure on natural stands.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Peucedanum persicum | Baill. | Hist. Pl. 7: 186 (1879) |
| Prangos euryangiodes | Stapf & Wettst. ex Stapf | Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 56 (1886) |
| Ferula puberula | Boiss. & Buhse. | Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 98 (1860) |
| Ferula szowitziana var. kandavanensis | Bornm. & Gouba | Repert. Spec. Nov. Regni Veg. 51: 101 1942 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | persian asafoetida |
| Azerbaijani | İran ilankölgəsi |
| French | férule persique |
| Chinese | 波斯阿魏 |
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
-
Asia-temperate click to expand
-
Caucasus
- Transcaucasus
-
Western Asia
- Iran
-
Caucasus
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000686745 |
| Tropicos | 1702772 |
| INPN | 979351 |
| KEW | urn:lsid:ipni.org:names:842442-1 |
| The Plant List | kew-2808592 |
| PFAF | Ferula persica |
| Open Tree Of Life | 3888248 |
| Observations.org | 138291 |
| NCBI Taxonomy | 1514040 |
| IPNI | 842442-1 |
| iNaturalist | 790229 |
| GBIF | 6026967 |
| Elurikkus | 575441 |
| USDA GRIN | 406509 |
| Wikipedia | Ferula_persica |
| CMAUP | NPO13181 |
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 |
|---|---|---|---|---|---|
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids | |||||
| (1R,13R,15S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol | 398938 | Click to see | 271.31 | unknown | via CMAUP database |
| (5alpha,11S,13beta,19alpha)-1,2-Didehydro-3beta-methoxycrinan-11-ol | 5281173 | Click to see | 301.34 | unknown | via CMAUP database |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids | |||||
| (-)-Galantamine | 9651 | Click to see | 287.35 | unknown | via CMAUP database |
| (1R,12S,14S)-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol | 21826140 | Click to see COC1=C2C3=C(CNCCC34CCC(CC4O2)O)C=C1 | 275.34 | unknown | via CMAUP database |
| Lycoramine | 443723 | Click to see | 289.40 | unknown | via CMAUP database |
| Norgalanthamine | 9838394 | Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 | 273.33 | unknown | via CMAUP database |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids | |||||
| Homolycorine | 160473 | Click to see | 315.40 | unknown | via CMAUP database |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids | |||||
| Lycorine | 72378 | Click to see | 287.31 | unknown | via CMAUP database |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids | |||||
| Ismine | 188957 | Click to see | 257.28 | unknown | via CMAUP database |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids | |||||
| 3-Epimacronine | 375117 | Click to see | 329.30 | unknown | via CMAUP database |
| Sekisanolin | 5321780 | Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O | 331.40 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives | |||||
| (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 4-hydroxy-3-methoxybenzoate | 1294694 | Click to see CC1(C2CCC1(C(C2)OC(=O)C3=CC(=C(C=C3)O)OC)C)C | 304.40 | unknown | https://doi.org/10.1007/BF00630666 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters | |||||
| [(E)-3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl] 3-hydroxy-3-methylbutanoate | 38363870 | Click to see CCC(C)SSC=CCOC(=O)CC(C)(C)O | 278.40 | unknown | https://doi.org/10.1080/14786410802393571 |
| 3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl 3-hydroxy-3-methylbutanoate | 162919701 | Click to see | 278.40 | unknown | https://doi.org/10.1080/14786410802393571 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides | |||||
| 7-[(2E,6E,10S)-3,7,11-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one | 163186416 | Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O | 886.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 7-[3,7,11-Trimethyl-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one | 162877882 | Click to see | 886.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides | |||||
| (2R,3R,4S,5S,6R)-2-[[(2S,4aR,4bS,6aR,7R,10aS,10bS)-7-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 162864734 | Click to see CCC(CCC(C)C1CCCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C | 590.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 2-[[7-(5-Ethyl-6-methylheptan-2-yl)-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 162864733 | Click to see | 590.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones | |||||
| 7-[(2E,6E,10S)-10-hydroxy-3,7,11-trimethyl-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one | 163189049 | Click to see | 724.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 7-[10-Hydroxy-3,7,11-trimethyl-11-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one | 163083485 | Click to see | 724.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| Umbelliprenin | 1781413 | Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C | 366.50 | unknown | https://doi.org/10.1076/PHBI.41.6.431.17834 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | https://doi.org/10.1007/BF00630666 |
| (2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 154496016 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C | 576.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 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/10.1007/BF00630666 |
| 2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 73072970 | Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C | 574.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| Stigmast-5-en-3-ol | 22012 | Click to see | 414.70 | unknown | https://doi.org/10.1007/BF00630666 |
| Stigmasterol Glucoside | 6602508 | Click to see | 574.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives | |||||
| 1-O-[(E)-3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl] 3-O-tert-butyl propanedioate | 163047079 | Click to see | 320.50 | unknown | https://doi.org/10.1016/S0031-9422(03)00296-6 |
| 1-O-[3-(butan-2-yldisulfanyl)prop-2-enyl] 3-O-tert-butyl propanedioate | 73064917 | Click to see | 320.50 | unknown | https://doi.org/10.1016/S0031-9422(03)00296-6 |
| 3-O-tert-butyl 1-O-[(E)-3-[(1R)-1-methylsulfanylpropyl]sulfanylprop-2-enyl] propanedioate | 162994847 | Click to see | 320.50 | unknown | https://doi.org/10.1016/S0031-9422(03)00296-6 |
| 3-O-tert-butyl 1-O-[3-(1-methylsulfanylpropylsulfanyl)prop-2-enyl] propanedioate | 73060264 | Click to see | 320.50 | unknown | https://doi.org/10.1016/S0031-9422(03)00296-6 |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols | |||||
| 1-(Butan-2-yldisulfanyl)-4,4-dimethylpent-1-en-3-ol | 163192301 | Click to see | 234.40 | unknown | https://doi.org/10.1016/S0031-9422(03)00296-6 |
| > Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives | |||||
| (-)-8-Demethylmaritidine | 443683 | Click to see | 273.33 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives | |||||
| 7-[[(1R,4S,4aS,6R,8aS)-6-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 162962875 | Click to see CC1(C(CCC2(C1C(CC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)O)C)OC5C(C(C(C(O5)COC6C(C(CO6)(CO)O)O)O)O)O)C | 692.70 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 7-[[(1R,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one | 101793077 | Click to see | 380.50 | unknown | https://doi.org/10.1055/S-2008-1034293 |
| 7-[[(1S,2R,4aS,6R,8aR)-6-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 101840038 | Click to see | 724.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 7-[[(1S,2R,4aS,8aR)-2-hydroxy-2,5,5,8a-tetramethyl-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one | 101091001 | Click to see CC1(C2CCC(C(C2(CCC1=O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C | 398.50 | unknown | https://doi.org/10.1055/S-2008-1034293 |
| 7-[[(1S,4aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 5317322 | Click to see | 382.50 | unknown | https://doi.org/10.1055/S-2008-1034293 |
| 7-[[(2S,4aS,6S)-2,6-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 5459231 | Click to see | 400.50 | unknown | https://doi.org/10.1007/BF00563961 |
| 7-[[6-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 162954170 | Click to see | 724.80 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| 7-[[6-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one | 162962874 | Click to see | 692.70 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001 |
| Conferol | 11892267 | Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C | 382.50 | unknown | https://doi.org/10.1007/BF00563961 |
| Conferone | 3108117 | Click to see | 380.50 | unknown | https://doi.org/10.1007/BF00563961 |
| Farnesiferol A | 7067262 | Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C | 382.50 | unknown | https://doi.org/10.1055/S-2008-1034293 |
| Osthol | 10228 | Click to see | 244.28 | unknown | https://doi.org/10.1007/BF00630666 |
| Samarcandin | 71587098 | Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C | 400.50 | unknown | https://doi.org/10.1007/BF00563961 |
| > Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins | |||||
| Umbelliferone | 5281426 | Click to see C1=CC(=CC2=C1C=CC(=O)O2)O | 162.14 | unknown | https://doi.org/10.1007/BF00563961 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |