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

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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

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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

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Investigation of physio-mechanical, antioxidant and antimicrobial properties of starch–zinc oxide nanoparticles active films reinforced with Ferula gummosa Boiss essential oil Sarhadi H, Shahdadi F, Salehi Sardoei A, Hatami M, Ghorbanpour M Sci Rep 09-Mar-2024
PMCID:PMC10925051
doi:10.1038/s41598-024-56062-w
PMID:38461344
Intensification of extraction process through IVDV pretreatment from Eryngium creticum leaves and stems: Maximizing yields and assessing biological activities Hammoud M, Debs E, van den Broek LA, Rajha HN, Safi C, van Erven G, Maroun RG, Chokr A, Rammal H, Louka N Heliyon 08-Mar-2024
PMCID:PMC10951497
doi:10.1016/j.heliyon.2024.e27431
PMID:38509897
Unveiling Morphine: A Rapid and Selective Fluorescence Sensor for Forensic and Medical Analysis Boroujerdi R, Butt A, Paul R, Majumder S Sensors (Basel) 07-Mar-2024
PMCID:PMC10974434
doi:10.3390/s24061722
PMID:38543983
Combined Effects of Zein Nanofiber Coating Containing Laurel (Laurus nobilis) and Air Fryer Cooking on Quality Properties of Fish Fillets during Cold Storage Ceylan Z, Meral R, Alav A, Torusdağ GB, Bildik F, Altay F ACS Omega 14-Feb-2024
PMCID:PMC10905579
doi:10.1021/acsomega.3c06318
PMID:38434834
Habitat potential modelling and the effect of climate change on the current and future distribution of three Thymus species in Iran using MaxEnt Hosseini N, Ghorbanpour M, Mostafavi H Sci Rep 13-Feb-2024
PMCID:PMC10864348
doi:10.1038/s41598-024-53405-5
PMID:38351276
Progress of nanopreparation technology applied to volatile oil drug delivery systems Ye ZW, Yang QY, Lin QH, Liu XX, Li FQ, Xuan HD, Bai YY, Huang YP, Wang L, Wang F Heliyon 08-Jan-2024
PMCID:PMC10825498
doi:10.1016/j.heliyon.2024.e24302
PMID:38293491
Efficient extraction of oleoresin from Ferula gummosa roots by natural deep eutectic solvent and its structure and chemical characterizations Radmard J, Mohamadi Sani A, Arianfar A, Mahmoodzadeh Vaziri B Sci Rep 02-Jan-2024
PMCID:PMC10762197
doi:10.1038/s41598-023-46198-6
PMID:38167968
Comparison effects of Ferula gummosa essential oil and Beta-pinene Alginate nanoparticles on human melanoma and breast cancer cells proliferation and apoptotic index in short term normobaric hyperoxic model Osanloo M, Pishamad S, ghanbariasad A, Zarenezhad E, Alipanah M, Alipanah H BMC Complement Med Ther 28-Nov-2023
PMCID:PMC10683214
doi:10.1186/s12906-023-04266-4
PMID:38017466
Immunosuppressive effect of Plantago major on the innate immunity of Galleria mellonella Kaya S PeerJ 22-Sep-2023
PMCID:PMC10519203
doi:10.7717/peerj.15982
PMID:37753175
Characterization of Portulaca oleracea Whole Plant: Evaluating Antioxidant, Anticancer, Antibacterial, and Antiviral Activities and Application as Quality Enhancer in Yogurt Al-Quwaie DA, Allohibi A, Aljadani M, Alghamdi AM, Alharbi AA, Baty RS, Qahl SH, Saleh O, Shakak AO, Alqahtani FS, Khalil OS, El-Saadony MT, Saad AM Molecules 03-Aug-2023
PMCID:PMC10421184
doi:10.3390/molecules28155859
PMID:37570829
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
Encapsulation of probiotic Lactobacillus acidophilus ATCC 4356 in alginate–galbanum (Ferula Gummosa Boiss) gum microspheres and evaluation of the survival in simulated gastrointestinal conditions in probiotic Tahini halva Sekhavatizadeh SS, Afrasiabi F, Montaseri Z Braz J Microbiol 29-Jul-2023
PMCID:PMC10485199
doi:10.1007/s42770-023-01074-3
PMID:37515666
The Impact of Acute Low-Dose Gamma Irradiation on Biomass Accumulation and Secondary Metabolites Production in Cotinus coggygria Scop. and Fragaria × ananassa Duch. Red Callus Cultures Ciocan AG, Maximilian C, Mitoi EM, Moldovan RC, Neguț D, Iuga CA, Helepciuc FE, Holobiuc I, Radu M, Vassu Dimov T, Cogălniceanu G Metabolites 28-Jul-2023
PMCID:PMC10456250
doi:10.3390/metabo13080894
PMID:37623838
Review of potential spermatogenic and aphrodisiac effects of the Ferula genus Bagheri SM, Shieh A, Ghalenoei JA, Yadegari M, Alborzi N Clin Exp Reprod Med 28-Jul-2023
PMCID:PMC10477414
doi:10.5653/cerm.2023.05995
PMID:37643827
Recent Advances in the Discovery of Plant-Derived Antimicrobial Natural Products to Combat Antimicrobial Resistant Pathogens: Insights from 2018–2022 Woo S, Marquez L, Crandall W, Risener C, Quave CL Nat Prod Rep 19-Jul-2023
PMCID:PMC10472255
doi:10.1039/d2np00090c
PMID:37439502

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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

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