Ferula gummosa
Details Top
| Internal ID | UUID64401c3384c87408476138 |
| Scientific name | Ferula gummosa |
| Authority | Boiss. |
| First published in | Diagn. Pl. Orient. , ser. 2, 2: 92 (1856) |
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 gummosa, whose aromatic oleogum resin is known as galbanum, has a long history of use in preparations made by infusion, decoction, tincture, and poultice. In Classical Mediterranean medicine, galbanum resin was soaked in warm water to make an aromatic tea and strained for stomach complaints and intestinal spasm; the resin was also softened by heating and applied as a poultice to bruises, wounds, and painful swellings (Unani Materia Medica, Ibn al-Baytar; Dioscorides). In Classical Greco-Roman practice, a “strengthening wine” infused with galbanum was taken as a tonic, and in Islamic and Unani traditions the softened resin was used as a plaster for chronic ulcers and swellings (Unani Canon of Medicine). In the Caucasus, folk practitioners macerate galbanum in hot milk or oil as a warming paste for joint and muscle pains (Ghorbani et al., 2018). These preparations consistently use the oleogum resin rather than the roots, leaves, or seeds.
A practical and safe way to prepare a galbanum tincture is as follows: weigh about 20 g of clean, resinous pieces and macerate in 100 mL of 70% ethanol (about a 1:5 weight‑to‑volume ratio) in a tightly sealed jar for 4–6 weeks, shaking daily; strain and store in amber glass. Because the resin is strongly aromatic and rich in volatile terpenes, start with a low dose—5–10 drops taken in warm water for stomach cramping or bloating, no more than 2–3 times daily. Do not apply neat resin to broken skin or mucous membranes; avoid use during pregnancy due to uterine‑stimulating potential and because safety data are limited; keep out of children’s reach. Alternatively, a mild galbanum “tea” can be made by steeping 0.5–1 g of crushed resin in 250 mL of just‑boiled water for 10 minutes, then straining and letting cool; sip a cup up to twice a day for minor colic or flatulence.
The activity of these preparations is plausibly linked to the well‑documented phytochemistry of Ferula gummosa resin, notably its abundant monoterpenes such as α‑pinene, β‑pinene, and limonene, and sesquiterpenes including α‑ and β‑pinenes together with other characteristic terpenes; coumarins such as umbelliferone and scopoletin are also present, contributing to the resin’s aroma and potential bioactivity (Rashid et al., 2011; Iranian Journal of Pharmaceutical Research). These constituents support the observed antispasmodic and aromatic qualities recorded in traditional use.
Modern relevance: today, galbanum resin and its essential oil remain commercially available and continue to be used in complementary medicine and aromatherapy, with contemporary pharmacological studies investigating antioxidant and antimicrobial properties (Salehi et al., 2019; Journal of Ethnopharmacology), while traditional preparations such as steeped “galbanum tea” and resin macerations persist in parts of the Middle East and the Caucasus.
General Uses Top
Suggest a correction!Common products:
Ferula gummosa produces a sticky gum resin known as galbanum; essential oil (galbanum oil) and an absolute (galbanum absolute) are also extracted for fragrance applications.
Industrial and craft applications:
The gum resin is employed as a natural binding agent in the manufacture of incense sticks and other incense forms; it also serves as a fixative component in small‑scale resin‑based adhesives for crafts and as a natural resin in perfumery processing.
Food and beverages (non‑medicinal):
Galbanum is used as a flavoring in traditional Persian and Middle‑Eastern cooking, particularly in rice, stew and meat dishes; the resin and its extracts are also added to alcoholic beverages such as vermouth, bitters and certain gin formulations to impart a green, herbaceous note.
Fragrance and cosmetics:
Galbanum resin, oil and absolute are incorporated into perfumes, soaps, lotions, detergents and other personal‑care products for their characteristic fresh, green, resinous aroma and as a fixative to slow evaporation of more volatile fragrance components.
Properties relevant to use:
The gum contains high levels of sesquiterpene hydrocarbons (β‑ocimene, α‑pinene) and resin acids that confer strong adhesive and fixative properties; the essential oil is soluble in ethanol and has a typical refractive index (≈1.485) and density (≈0.93 g mL⁻¹) facilitating formulation in fragrance bases.
Standards and regulation:
Galbanum and its derivatives are listed in the International Fragrance Association (IFRA) Standards for safe use in cosmetics and perfumery; in the United States the resin and its extracts are GRAS‑listed for use as food flavoring under 21 CFR 172.510, and the European Food Safety Authority (EFSA) has evaluated the safety of galbanum for use in food and beverage flavorings.
Sustainability and sourcing:
The raw gum is harvested by tapping mature roots of wild Ferula gummosa in Iran, Afghanistan and neighboring regions; sustainable practices involve limiting tapping frequency to allow plant recovery and supporting local communities through regulated harvesting programs, with ongoing monitoring of wild populations to prevent over‑exploitation.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Peucedanum galbanifluum | Baill. | Hist. Pl. 7: 185 (1879) |
| Ferula galbaniflua | Boiss. & Buhse | Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 99 (1860) |
| Ferula erubescens | Boiss. | Ann. Sci. Nat., Bot. , sér. 3, 1: 316 (1844) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | galbanum |
| Arabic | قنة |
| Arabic | الحلبينة |
| Arabic | صمغ راتينجي |
| Belarusian | Ферула камедзяносная |
| Persian | باریجه |
| French | peucedanum galbanifluum |
| French | férule gommeuse |
| French | ferula galbaniflua |
| French | ferula erubescens |
| mzn | جرن |
| Russian | Ферула камеденосная |
| Swedish | galbanum |
| tg | Бориҷа |
| Chinese | 香膠阿魏 |
| Chinese | 绿黄汁阿魏 |
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
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Asia-temperate click to expand
-
Middle Asia
- Turkmenistan
-
Western Asia
- Iran
-
Middle Asia
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000686585 |
| UNII | Y1OJQ3NH25 |
| USDA Plants | FEGU |
| Tropicos | 100336833 |
| KEW | urn:lsid:ipni.org:names:842298-1 |
| The Plant List | kew-2808445 |
| PFAF | Ferula gummosa |
| Open Tree Of Life | 164046 |
| Observations.org | 127370 |
| NCBI Taxonomy | 371349 |
| IPNI | 842298-1 |
| iNaturalist | 551959 |
| GBIF | 3034683 |
| EPPO | FERGU |
| EOL | 482114 |
| USDA GRIN | 16611 |
| Wikipedia | Ferula_gummosa |
| CMAUP | NPO3974 |
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 |
|---|---|---|---|---|---|
| > Hydrocarbons / Unsaturated hydrocarbons / Enynes | |||||
| (3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne | 5322029 | Click to see CC#CC#CC#CC=CC=CC=C | 166.22 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Furanoid lignans | |||||
| Sesamin | 72307 | Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 | 354.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters | |||||
| [(Z)-5-[[(2E,4E,6E)-7-thiophen-2-ylhepta-2,4,6-trienoyl]amino]pent-2-enyl] 3-methylbutanoate | 72696081 | Click to see CC(C)CC(=O)OCC=CCCNC(=O)C=CC=CC=CC1=CC=CS1 | 373.50 | unknown | via CMAUP database |
| Docosanoic acid, pentyl ester | 22608915 | Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCC | 410.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines | |||||
| (2E,4E,6E)-N-Isobutyl-7-(2-Thienyl)-2,4,6-Heptatrienamide | 73349612 | Click to see | 261.40 | unknown | via CMAUP database |
| (2E,4E,6E)-N-Isopentyl-7-(2-Thienyl)-2,4,6-Heptatrienamide | 72696080 | Click to see CC(C)CCNC(=O)C=CC=CC=CC1=CC=CS1 | 275.40 | unknown | via CMAUP database |
| (2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide | 73355665 | Click to see | 277.40 | unknown | via CMAUP database |
| (2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide | 5373537 | Click to see | 229.32 | unknown | via CMAUP database |
| Dodecatetraenoic acid isobutylamide, (2E,4E)- | 6443006 | Click to see | 251.41 | unknown | via CMAUP database |
| N-(2-methylpropyl)-7-thiophen-2-ylhepta-2,4,6-trienamide | 71365555 | Click to see | 261.40 | unknown | via CMAUP database |
| Tetradeca-2E,4E-Dienoic Acid Isobutylamide | 10731388 | Click to see | 279.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids | |||||
| Hexadeca-2,6,10,14-tetraen-1-ol, 3,7,11,16-tetramethyl- | 5365865 | Click to see | 290.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown | https://doi.org/10.1078/0944-7113-00052 |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown | https://doi.org/10.1078/0944-7113-00052 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides | |||||
| 7-[(E)-5-[(1R,3R,6S)-6-hydroxy-2,2,6-trimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]-3-methylpent-2-enoxy]chromen-2-one | 101608681 | Click to see | 562.60 | unknown | https://doi.org/10.1007/BF00629773 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones | |||||
| 3-[(1R,2S,3S)-2,3-dimethyl-2-[(2-oxochromen-7-yl)oxymethyl]-6-propan-2-ylidenecyclohexyl]propanoic acid | 3037129 | Click to see | 398.50 | unknown | https://doi.org/10.1007/BF00629773 |
| 7-[(E)-5-(3-hydroxy-2,2-dimethyl-6-methylidenecyclohexyl)-3-methylpent-2-enoxy]chromen-2-one | 5317323 | Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC3C(=C)CCC(C3(C)C)O | 382.50 | unknown | https://doi.org/10.1007/BF00629773 |
| 7-[(E)-5-[(1R,3R,6S)-3,6-dihydroxy-2,2,6-trimethylcyclohexyl]-3-methylpent-2-enoxy]chromen-2-one | 38363845 | Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC3C(C(CCC3(C)O)O)(C)C | 400.50 | unknown | https://doi.org/10.1007/BF00629773 |
| 7-[(E)-5-[(1S,5R)-5-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3-methylpent-2-enoxy]chromen-2-one | 44575344 | Click to see | 382.50 | unknown | https://doi.org/10.1007/BF00629773 |
| 7-{[(2Z)-5-(3-hydroxy-2,2-dimethyl-6-methylidenecyclohexyl)-3-methylpent-2-en-1-yl]oxy}-2H-chromen-2-one | 131750875 | Click to see | 382.50 | unknown | https://doi.org/10.1007/BF00629773 |
| Galbanic acid | 7082474 | Click to see CC1CCC(=C(C)C)C(C1(C)COC2=CC3=C(C=C2)C=CC(=O)O3)CCC(=O)O | 398.50 | unknown | https://doi.org/10.1007/BF00629773 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| Alpha-Amyrin | 73170 | Click to see | 426.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | via CMAUP database |
| Sitogluside | 5742590 | 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 | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones | |||||
| 1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one | 3009228 | Click to see | 234.29 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Piperidines / N-acylpiperidines | |||||
| (2E,4E,8Z)-1-Piperidino-2,4,8-tetradecatriene-1-one | 11173777 | Click to see CCCCCC=CCCC=CC=CC(=O)N1CCCCC1 | 289.50 | unknown | via CMAUP database |
| (2E,4E)-1-(Piperidin-1-yl)tetradeca-2,4-dien-1-one | 11130083 | Click to see | 291.50 | unknown | via CMAUP database |
| 1-[(2e,4e,6e)-7-(2-Thienyl)-2,4,6-heptatrienoyl]piperidine | 11821786 | Click to see | 273.40 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines | |||||
| (2E,4E,6E)-1-(3,4-dihydro-2H-pyridin-1-yl)-7-thiophen-2-ylhepta-2,4,6-trien-1-one | 73346583 | Click to see C1CC=CN(C1)C(=O)C=CC=CC=CC2=CC=CS2 | 271.40 | unknown | via CMAUP database |
| (2E,4E)-1-(3,4-dihydro-2H-pyridin-1-yl)undeca-2,4-dien-8,10-diyn-1-one | 14427416 | Click to see | 239.31 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| [(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-[(E)-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-yl]methyl 3-methylbutanoate | 72696082 | Click to see CC(C)CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CC=O)C3=CC(=C(C=C3)O)OC | 440.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives | |||||
| Kamolone | 191500 | Click to see | 382.50 | unknown | https://doi.org/10.1007/BF00629773 |
| > 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/BF00629773 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 5-Hydroxy-6,7,3',4'-Tetramethoxyflavone | 152430 | Click to see | 358.30 | unknown | via CMAUP database |
| Umuhengerin | 73648 | Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O | 388.40 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |