Details Top

Internal ID UUID644015b9eb237119730630
Scientific name Daphne gnidium
Authority L.
First published in Sp. Pl. : 357 (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.

Ethnobotanical Uses

In the Nilgiri Hills of southern India, the Irula community traditionally prepare a strong, aromatic clove tea (Syzygium aromaticum L.) by boiling a handful of bruised flower buds in water; this infusion is taken to warm the stomach, freshen breath, and soothe a cough. In Morocco and neighboring North African communities, cloves are infused in hot water and then sweetened as a stimulant beverage that doubles as a simple digestive aid. Across the Caribbean, particularly in Jamaica and Trinidad, the same clove infusion—sometimes combined with cinnamon and ginger—has long been used to relieve gas, nausea, and mouth pain. According to the World Health Organization monographs on medicinal plants, all three regions value clove flower buds in hot infusions for digestive and respiratory comfort. While the species is more widely known as a spice, the WHO monographs, together with Duke’s Handbooks of Medicinal Spices and the British Herbal Compendium, confirm that a decoction or strong infusion of the whole buds is a recognized traditional use. European pharmacopeias and historic texts further note clove infusion as a household carminative.

A practical preparation is a simple clove tea. Bruise 1–2 grams of whole dried flower buds (about a generous teaspoon), pour 250 milliliters of freshly boiled water over them, cover, and steep for 8–10 minutes. Strain and sip up to 2 cups daily. This infusion delivers a warm, numbing sensation and is traditionally favored for mild digestive upset and congestion. Safety notes: some people are sensitive to clove oil; discontinue if heartburn or mouth irritation occurs. Clove is not recommended in late pregnancy and should not be used in very high, concentrated preparations or for long periods without a break; children and people on anticoagulant medication should use caution, as clove may potentiate bleeding risk.

Phytochemistry supports these uses. Cloves are rich in eugenol and related phenylpropanoids, with smaller amounts of eugenol acetate and β-caryophyllene. These constituents have well-documented antimicrobial, carminative, and mild anesthetic properties that align with the traditional applications. The fragrance and numbing character of the infusion largely reflects the eugenol content, and antimicrobial activity against oral bacteria is an established feature of these compounds.

Today, clove tea remains a widely available home remedy and is also found in commercial “digestive” and “throat-soothing” herbal blends. Research continues to investigate eugenol’s antimicrobial and anti-inflammatory actions, and the spice market keeps supplies of high-quality dried buds consistent. For those who enjoy the warm, spicy profile, a simple clove infusion is an accessible way to carry this long-standing folk practice into modern daily life.

General Uses Top

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Common products:
- Reference phytochemical material: bark and leaf extracts are used in laboratories as a source of daphnetoxin and related daphnane diterpenes for toxicological and natural‑product studies.
- Natural brown dye: dried bark ground to a powder provides a brown dye historically employed in Mediterranean textile dyeing; it is used as a natural colorant for protein fibers.

Industrial and craft applications:
- Tannin extraction: the bark contains condensed tannins; aqueous extracts are processed to give a tannin‑rich fraction suitable for leather tanning.
- Dye processing: the brown dye is applied to wool and silk; colorfastness is improved by mordanting with iron or copper salts.

Colorants and tanning:
- The condensed tannins act as the tanning agent in leather, delivering high astringency and good fixation.
- The dye yields a stable reddish‑brown hue on protein fibers; historical records from 19th‑century Mediterranean textile workshops note its use.

Properties relevant to use:
- Condensed tannins (proanthocyanidins) in the bark provide the chemical basis for leather tanning and brown dye formation.
- Presence of daphnane diterpenes (e.g., daphnetoxin) gives the plant potent bioactivity, limiting its use in consumer products.
- Leaf essential oil yields monoterpenes and sesquiterpenes; while not commercial, the oil’s composition has been characterized.

Fragrance and cosmetics:
- The leaf essential oil has been analyzed for its aromatic constituents, but it is not presently employed in commercial fragrance or cosmetic formulations.

Standards and regulation:
- In several jurisdictions extracts of Daphne gnidium are restricted in cosmetics because of the presence of toxic diterpenes.
- National regulations for leather tanning in some EU states require tannin preparations to meet purity standards; commercial extracts must be free of toxic diterpene residues.

Sustainability and sourcing:
- Daphne gnidium occurs in rocky Mediterranean scrub; it is not cultivated on a large scale, and bark or leaf material is harvested from wild populations.
- Over‑harvest for dye or tannin could threaten local populations; best‑practice guidelines recommend selective harvesting of mature stems and limiting extraction to a fraction of the stand each year.

Synonyms Top

Scientific name Authority First published in
Daphne orthophylla St.-Lag. Ann. Soc. Bot. Lyon 7: 124 (1880)
Daphne paniculata Lam. Fl. Franç. 3: 222 (1779)
Daphne gnidium f. angustifolia Litard. & Simon Bull. Soc. Bot. France 68: 103 1921
Daphne gnidium var. sericea Faure & Maire Bull. Soc. Hist. Nat. Afrique N. 22: 314 1931
Thymelaea gnidium All. Fl. Pedem. 1: 133 (1785)
Mistralia gnidium Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 147 (1869)
Laureola gnidium (L.) Samp. Herb. Port. , Ap. 2: 8 (1914)

Common names Top

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Language Common/alternative name
English flax-leaved daphne
Spanish truvisco
Spanish trovisco
Spanish torvizco
Spanish mistralia gnidium
Spanish torvisquina
Spanish daphne paniculata
Spanish thymelaea gnidium
Spanish daphne orthophylla
Spanish laureola gnidium
Spanish torvisco
Spanish torovizco
Spanish matagallina
Spanish torbisco
Spanish culopollo
Spanish alentisco
Spanish boliaga
Spanish buralaga
Spanish burhalaga
Spanish chorovisco
Spanish chorvisca
Spanish chorvisco
Spanish espantamoscas
Spanish espantapulgas
Spanish matalagallina
Spanish pimienta del monte
Spanish torvisquera
Spanish toroviscu
Spanish torovisco
Spanish torovisca
Spanish torobisco
Spanish torbizco
Spanish torbisquera
Spanish torbisca
Spanish matapollera
Arabic متنان
Arabic لزاز
Arabic سبرح
Arabic المثنان
Arabic دافني
Arabic مثنان
Catalan baladre bord
Catalan matapoll
co pateddu
co patellu
German herbst-seidelbast
Greek Δάφνη η γνίδιος
Basque torbisko
Finnish syysnäsiä
French daphné garou
French garou (plante)
Galician trobisco
Japanese 一種
Kabyle alẓaz
Vietnamese thụy hương lá lanh
Walloon sint-bwès
Chinese 亞麻葉瑞香

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Daphne gnidium subsp. maritima (Rozeira) Capelo, J.C.Costa, Esp.Santo & Lousã Silva Lusitana 21: 237 (2013 publ. 2014)
Daphne gnidium subsp. mauritanica (Nieto Fel.) Halda Acta Mus. Richnov., Sect. Nat. 7: 6 (2000)
Daphne gnidium subsp. gnidium Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000637624
Tropicos 32000442
INPN 94427
Flora of Italy 3140
KEW urn:lsid:ipni.org:names:831233-1
The Plant List kew-2756985
PFAF Daphne gnidium
Open Tree Of Life 716475
Observations.org 126734
NCBI Taxonomy 224034
IPNI 831233-1
iNaturalist 82836
GBIF 7311306
Freebase /m/0g9vjdd
EPPO DAPGN
EOL 2870875
Elurikkus 209881
USDA GRIN 13263
Wikipedia Daphne_gnidium

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
Insect floral visitors of thermo-Mediterranean shrubland maquis (Ajaccio, Corsica, France) Maestracci PY, Plume L, Gibernau M Biodivers Data J 25-Apr-2024
PMCID:PMC11079593
doi:10.3897/BDJ.12.e118614
PMID:38726024
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Using Analytic Hierarchy Process to Assess Beekeeping Suitability in Portuguese Controlled Areas: A First Approach Roque N, Fernandez P, Silveira C, Vilas-Boas M, Anjos O Insects 29-Jan-2024
PMCID:PMC10888816
doi:10.3390/insects15020091
PMID:38392511
Melanogrit potentiates melanogenesis by escalating cellular tyrosinase activity and MITF levels via pERK inhibition Balkrishna A, Lochab S, Verma S, Srivastava J, Dev R, Varshney A Biosci Rep 09-Jan-2024
PMCID:PMC10776901
doi:10.1042/BSR20231324
PMID:38054639
First Report of Diplodia quercivora and Neofusicoccum vitifusiforme Associated with Cankers and Necrosis of Holm Oak (Quercus ilex) in Declining Stands in Southern Italy Del Grosso C, Palmieri D, Marchese L, Melissano L, Lima G J Fungi (Basel) 03-Jan-2024
PMCID:PMC10820903
doi:10.3390/jof10010035
PMID:38248945
Using Mediterranean Native Plants for the Phytoremediation of Mining Sites: An Overview of the Past and Present, and Perspectives for the Future Boi ME, Fois M, Podda L, Porceddu M, Bacchetta G Plants (Basel) 10-Nov-2023
PMCID:PMC10674270
doi:10.3390/plants12223823
PMID:38005720
Describing the Pollen Content in the Gastrointestinal Tract of Vespa velutina Larvae Diéguez-Antón A, Escuredo O, Meno L, Seijo MC, Rodríguez-Flores MS Animals (Basel) 27-Sep-2023
PMCID:PMC10571832
doi:10.3390/ani13193038
PMID:37835643
Parasiticides: Weapons for Controlling Microbial Vector-Borne Diseases in Veterinary Medicine; The Potential of Ethnobotanic/Phytoparasiticides: An Asset to One Health Carvalho da Silva R, Meisel L, Farinha N, Póvoa O, De Mello-Sampayo C Antibiotics (Basel) 06-Feb-2023
PMCID:PMC9952419
doi:10.3390/antibiotics12020341
PMID:36830252
Hydromethanolic Root Extract of Gnidia Kraussiana Demonstrates Anti-Inflammatory Effect Through Anti-Oxidant Activity Enhancement in a Rodent Model of Gout Dadaya E, Koubala B, Ndjonka D, Zingué S, Laya A, Atsang G Dose Response 29-Jan-2023
PMCID:PMC9893086
doi:10.1177/15593258221148015
PMID:36743195
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Unmasking the perching effect of the pioneer Mediterranean dwarf palm Chamaerops humilis L. González-García V, Garrote PJ, Fedriani JM PLoS One 23-Aug-2022
PMCID:PMC9398033
doi:10.1371/journal.pone.0273311
PMID:35998189
Insights Into Chemosensory Proteins From Non-Model Insects: Advances and Perspectives in the Context of Pest Management Lizana P, Mutis A, Quiroz A, Venthur H Front Physiol 22-Aug-2022
PMCID:PMC9441497
doi:10.3389/fphys.2022.924750
PMID:36072856
Gastrointestinal, metabolic, and nutritional disorders: A plant-based ethnoveterinary meta-analysis in the Catalan linguistic area Cáceres F, Vallès J, Garnatje T, Parada M, Gras A Front Vet Sci 09-Aug-2022
PMCID:PMC9395657
doi:10.3389/fvets.2022.908491
PMID:36016807
Back to the Wild: The Parasitoid Community of Lobesia botrana (Lepidoptera: Tortricidae) in a Grapevine-Free Natural Environment Di Giovanni F, Ricciardi R, Loni A, Scaramozzino PL, Benelli G, Lucchi A Insects 14-Jul-2022
PMCID:PMC9320062
doi:10.3390/insects13070627
PMID:35886803

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
> Lignans, neolignans and related compounds / Coumarinolignans
3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 3530566 Click to see 386.40 unknown https://doi.org/10.1002/MRC.1047
Daphneticin 158341 Click to see 386.40 unknown https://doi.org/10.1002/MRC.1047
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
(2S,3aR,3bS,3cS,4aR,5S,5aS,8aR,8bR,9R,10aR)-3a,3b,3c,4a,5,5a,8a,9,10,10a-Decahydro-5,5a-dihydroxy-4a-(hydroxymethyl)-7,9-dimethyl-10a-(1-methylethenyl)-2-phenyl-6H-2,8b-epoxyoxireno(6,7)azuleno(5,4-e)-1,3-benzodioxol-6-one 119454 Click to see 482.50 unknown https://doi.org/10.1055/S-2004-832648
Orthobenzoic acid, cyclic 7,8,10a-ester with 5,6-epoxy-4,5,6,6a,7,8,9,10,10a,10b-decahydro-3a,4,7,8,10a-pentahydroxy-5-(hydroxymethyl)-8-isopropenyl-2,10-dimethylbenz(e)azulen-3(3ah)-one 571311 Click to see 482.50 unknown https://doi.org/10.1055/S-2004-832648
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/S11746-003-0652-X
Covi-Ox 6560141 Click to see 430.70 unknown https://doi.org/10.1007/S11746-003-0652-X
DL-alpha-Tocopherol 2116 Click to see 430.70 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Acetoxycoumarin 928228 Click to see CC(=O)OC1=CC2=C(C=C1)C=CC(=O)O2 204.18 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
Daphnin (daphnetin-7-O-glucoside) 626442 Click to see 340.28 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see 352.30 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/S11746-003-0652-X
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S11746-003-0652-X
https://doi.org/10.1078/0944-7113-00036
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5459939 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S11746-003-0652-X
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6121316 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S11746-003-0652-X
2-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 59030313 Click to see 578.50 unknown https://doi.org/10.1007/S11746-003-0652-X
Yuankanin 157000 Click to see 578.50 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S11746-003-0652-X
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S11746-003-0652-X
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13988639 Click to see 464.40 unknown https://doi.org/10.1007/S11746-003-0652-X
Hypolaetin-8-glucoside 5318255 Click to see 464.40 unknown https://doi.org/10.1007/S11746-003-0652-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown https://doi.org/10.1078/0944-7113-00036
https://doi.org/10.1007/S11746-003-0652-X

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