Pistacia terebinthus

Details Top

Internal ID UUID643ff7b7a3079127093742
Scientific name Pistacia terebinthus
Authority L.
First published in Sp. Pl. : 1025 (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.

In parts of Greece and western Turkey, the hardened oleoresin (gum) of Pistacia terebinthus is chewed fresh or dissolved in warm water for digestive upset, respiratory congestion, and to clear a sore throat. Above all it is valued as an astringent and aromatic expectorant among healers of the Ottoman tradition (Dalal et al., 2013). In North Africa, especially in the Middle Atlas of Morocco, a tea made from the young leaves is given to ease bronchial irritation and short colds (Hseini et al., 2007). Among Palestinian, Jordanian and Lebanese practitioners, decoctions of the resinous gum or leaf‑rich infusions are taken to relieve coughs and “cold in the chest,” a practice noted repeatedly in ethnomedicinal surveys of the Levant (Khafagi et al., 2007). The resin has long been recorded in Western classical literature as an internal and external astringent and stimulant: for example, Dioscorides reports chewing the gum for respiratory complaints and drinking a decoction of the resin for bronchial irritation ( Dioscorides, 1st century CE ).

For practical preparation, a simple 1:5 (w:v) tincture of the resin is the most straightforward traditional recipe. Measure 20 grams of finely powdered gum resin and place it in a clean amber jar. Add 100 milliliters of 45% ethanol (neutral grain spirit works well), seal, and shake daily for 2–3 weeks in a cool, dark place. Filter through fine cloth and store in a dark bottle. A typical dose is 2–3 milliliters up to three times a day, kept for short courses only. Do not use the tincture or the gum during pregnancy or while breastfeeding; it is not recommended for children, and people with allergies to Anacardiaceae or mastication‑stimulating resins should avoid it.

The resin is rich in essential‑oil terpenoids such as α‑pinene, limonene, β‑caryophyllene and verbenone, with high levels of polymeric terebinthone‑type diterpenes that give it its strong astringency. These constituents are well documented in species‑level chemical analyses of Pistacia terebinthus resin and plausibly account for its astringent, antimicrobial and mild expectorant effects (Speranza et al., 2005). Small amounts of flavonoids such as myricetin glycosides and gallotannins in the leaves complement the resin’s astringency and align with the tea’s short‑term use for colds.

Modern relevance: while this tree still appears as a “wild resin” in Mediterranean herbal and specialty markets, the bulk of commercial terebinth resin now comes from Pistacia lentiscus (mastic). Research on Pistacia terebinthus remains active, with ongoing phytochemical profiling and pharmacological studies to validate its traditional aromatic and astringent uses (Dalal et al., 2013).

General Uses Top

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Common products:
The species yields an oleoresin known as terebinth or Chian turpentine. It is harvested by tapping the trunk and consists of an essential oil fraction (turpentine) and a non-volatile rosin fraction. The resin is sold for technical and craft use rather than food.

Industrial and craft applications:
Terebinth resin functions as a natural varnish and coating medium. When the turpentine solvent evaporates, the rosin component hardens to form a protective film used on wood and as a traditional spirit varnish. The rosin fraction is a brittle, glassy material with high acid value, suitable as a solid resin in varnish and coating systems. The oleoresin also serves as an adhesive and is used in some small-object woodworking and icon painting as a varnish binder.

Colorants and tanning:
Although pistachio species are rich in tannins, the specific literature for Pistacia terebinthus does not document its use in leather tanning or natural dyeing; those applications are therefore not recorded here.

Fragrance and cosmetics:
The essential oil from the oleoresin is used as a fragrance ingredient in perfumery and as a flavoring agent. Its volatile profile includes monoterpenes such as alpha-pinene; however, it is processed primarily for technical resin use rather than as a cosmetic emollient.

Properties relevant to use:
The oleoresin is a two-phase system: a volatile turpentine fraction responsible for solvency and a non-volatile rosin fraction that forms the film. The rosin has high acid value and resin hardness, enabling it to function as a solid resin in varnishes and adhesives after solvent evaporation. These characteristics are well established in the resin literature and are consistent with the behavior of pine-type oleoresins generally used in technical applications.

Standards and regulation:
Materials derived from terebinth resin are used as natural base materials and may be subject to general regulations for natural resins and turpentine-type substances in industrial and fragrance applications, including safety and labeling requirements. Specific harmonized standards for this exact product type are not documented in the references consulted.

Sustainability and sourcing:
The resin is obtained by tapping wild or cultivated trees. Sustainable harvesting involves selective incision and controlled frequency to maintain tree health; overexploitation can impair vitality. Information on yields, sap flow, and comparative sustainability across regions is not provided in the sources consulted.

Synonyms Top

Scientific name Authority First published in
Lentiscus terebinthus Kuntze Revis. Gen. Pl. 1: 153 (1891)
Lentiscus vulgaris Garsault Fig. Pl. Med. 1: t. 87. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 63. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 784.
Pistacia palaestina Boiss. Diagn. Pl. Orient. 9: 1 (1849)
Pistacia terebinthina St.-Lag. Ann. Soc. Bot. Lyon vii. (1880) 132.
Terebinthus vulgaris Dum.Cours. Bot. Cult. , ed. 2, 6: 222 (1811)
Terebinthus communis Dum.Cours. Bot. Cult. 3: 575.1802
Pistacia crassifolia Salisb. Prodr. Stirp. Chap. Allerton 172 (1796)
Pistacia terebinthus subsp. palaestina (Boiss.) Engl.

Common names Top

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Language Common/alternative name
English cyprus turpentine
English terebinth
English turpentine tree
Spanish cornicabra
Spanish albotin
Spanish albotín
Spanish arbol de nuestra senora
Spanish arbol de nuestra señora
Spanish Árbol de nuestra senora
Spanish Árbol de nuestra señora
Spanish arbol trementino
Spanish Árbol trementino
Spanish cabra coja
Spanish cabracoja
Spanish cabracorna
Spanish cabricuerno
Spanish caricuerno
Spanish charnera
Spanish charneta
Spanish colneta
Spanish cornicabre
Spanish cornicabro
Spanish cornita
Spanish descornacabras
Spanish escuernicabra
Spanish granillo cornicabra
Spanish higuera silvestre
Spanish jedisco
Spanish lentisco albar
Spanish noguerola
Spanish quemaculo
Spanish terebinto
Spanish tornalobo
Spanish trementina de kios
Spanish valvarija
an sarrampuz
Arabic بطم تربنتيني
Arabic بطم
Arabic بطم ساقس
Azerbaijani terebint püstəsi
azb داغ پوستهسی
Bulgarian кукуч
Catalan cornicabra
Catalan noguerola
Catalan arbre de pi
Catalan arbre de trementina
Catalan noguereta
Catalan terebint
Czech Řečík palestinský
Czech terebint
Czech řečík terebintový
German terpentinpistazie
German terpentinpistazien
German terpentin-pistazie
Greek Κοκκορεβυθιά
Greek Τραμιθιά
Greek Τριμιθιά
Greek Τερέβινθος
Esperanto terebintarbo
Basque ahuntzadar
Persian پسته کوهی
Finnish tärpättipistaasi
French pistachier terebinthe
French térébinthe
French pistachier térébinthe
Irish tuirpintín
Irish crann tuirpintín
Irish teiribint
Galician terebinto
Hebrew אלת טרבינת
Croatian smrdljika
Upper Sorbian terpentinowa pistacija
io terebinto
Italian terebinto
Japanese トクノウコウ
Japanese テレビンノキ
Kabyle hejji
ku kezwan
ku Şengîlî
Macedonian смрдлика
mwl fedigueira
mwl fedieira
Norwegian Bokmål terpentintre
Dutch terebint
Dutch terpentijnboom
oc petelin
Polish drzewo terpentynowe
Polish terebint
Polish pistacja terpentynowa
Portuguese cornalheira
Portuguese terebinto
Russian Теревинф
Russian Фисташка терпентинная
Russian Терпентинное дерево
Serbo-Croatian smrdljika
Slovenian terebint
Swedish terebint
Turkish melengiç
Turkish menengiç
Ukrainian Терпентинне дерево
Chinese 笃耨香
Chinese 圓柄黃連木
Chinese 圆柄黄连木

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
  • Asia-temperate
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • 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-0000393769
USDA Plants PITE10
Tropicos 50319302
INPN 113748
KEW urn:lsid:ipni.org:names:70274-1
The Plant List kew-2407017
Open Tree Of Life 131831
Observations.org 147470
NCBI Taxonomy 434238
IUCN Red List 20678342
IPNI 70274-1
iNaturalist 81870
GBIF 3190580
Freebase /m/07260j
EPPO PIATE
EOL 396429
Elurikkus 374375
Calflora (Californian flora) 12780
USDA GRIN 28653
Wikipedia Pistacia_terebinthus

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
Effect of Pistacia Terebinthus (terebinth) resin extract on aggressive breast cancer cells Fırat K, Nisari M, Metin İ, Fırat YY, Karatoprak GŞ, Hamurcu Z Toxicol Res (Camb) 24-Mar-2024
PMCID:PMC10962014
doi:10.1093/toxres/tfae046
PMID:38533180
Chemical Composition Variation in Essential Oil and Their Correlation with Climate Factors in Chinese Prickly Ash Peels (Zanthoxylum armatum DC.) from Different Habitats Qian Q, Zhuo Z, Peng Y, Xu D Molecules 18-Mar-2024
PMCID:PMC10974008
doi:10.3390/molecules29061343
PMID:38542978
Growth form, regeneration mode, and vegetation type explain leaf trait variability at the species and community levels in Mediterranean woody vegetation Tüfekcioğlu İ, Tavşanoğlu Ç Ecol Evol 11-Mar-2024
PMCID:PMC10927360
doi:10.1002/ece3.11145
PMID:38469041
Modern and traditional cooking methods affect the antioxidant activity and phenolic compounds content of Trachystemon Orientalis (L.) G. Don Demirel Ozbek Y, Saral O, Turker PF PLoS One 23-Feb-2024
PMCID:PMC10890727
doi:10.1371/journal.pone.0299037
PMID:38394328
Multi-scale datasets for monitoring Mediterranean oak forests from optical remote sensing during the SENTHYMED/MEDOAK experiment in the north of Montpellier (France) Adeline K, Féret JB, Clenet H, Limousin JM, Ourcival JM, Mouillot F, Alleaume S, Jolivot A, Briottet X, Bidel L, Aria E, Defossez A, Gaubert T, Giffard-Carlet J, Kempf J, Longepierre D, Lopez F, Miraglio T, Vigouroux J, Debue M Data Brief 13-Feb-2024
PMCID:PMC10884421
doi:10.1016/j.dib.2024.110185
PMID:38406250
Effect of apricot kernel seed extract on biophysical properties of chitosan film for packaging applications Saied M, Ward A, Hamieda SF Sci Rep 10-Feb-2024
PMCID:PMC10858884
doi:10.1038/s41598-024-53397-2
PMID:38341481
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Advances in the characterisation and identification of mastic (Pistacia sp.) resin in archaeological samples by GC-QToF-MS Tamburini D, Fulcher K, Briggs L, von Aderkas N, Pulak C, Stacey R RSC Adv 02-Jan-2024
PMCID:PMC10759165
doi:10.1039/d3ra06651g
PMID:38174260
Further Improvement Based on Traditional Nanocapsule Preparation Methods: A Review Zhou Y, Wang P, Wan F, Zhu L, Wang Z, Fan G, Wang P, Luo H, Liao S, Yang Y, Chen S, Zhang J Nanomaterials (Basel) 12-Dec-2023
PMCID:PMC10745493
doi:10.3390/nano13243125
PMID:38133022
First Detection of Cryptosporidium parvum in the Endemic Cyprus Mouflon (Ovis gmelini ophion) Hasapis KA, Charalambidou I, Schou C, O’Dowd Phanis C, Kazamia S, Kassinis N, Hadjisterkotis E, Karanis P Acta Parasitol 08-Dec-2023
PMCID:PMC11001731
doi:10.1007/s11686-023-00747-1
PMID:38062227
Development and characterization of antioxidant bilayer film based on poly lactic acid-bitter vetch (Vicia ervilia) seed protein incorporated with Pistacia terebinthus extract for active food packaging Dodange S, Shekarchizadeh H, Kadivar M Curr Res Food Sci 05-Oct-2023
PMCID:PMC10582362
doi:10.1016/j.crfs.2023.100613
PMID:37860146
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Harnessing the Bioactive Potential of Limonium spathulatum (Desf.) Kuntze: Insights into Enzyme Inhibition and Phytochemical Profile Youssef S, Custódio L, Rodrigues MJ, Pereira CG, Calhelha RC, Jekő J, Cziáky Z, Ben Hamed K Plants (Basel) 26-Sep-2023
PMCID:PMC10574883
doi:10.3390/plants12193391
PMID:37836131
Mediterranean Plants with Antimicrobial Activity against Staphylococcus aureus, a Meta-Analysis for Green Veterinary Pharmacology Applications Oppedisano F, De Fazio R, Gugliandolo E, Crupi R, Palma E, Abbas Raza SH, Tilocca B, Merola C, Piras C, Britti D Microorganisms 09-Sep-2023
PMCID:PMC10534841
doi:10.3390/microorganisms11092264
PMID:37764109
Effect of Encapsulation Techniques on Aroma Retention of Pistacia terebinthus L. Fruit Oil: Spray Drying, Spray Freeze Drying, and Freeze Drying Yaman DM, Koçak Yanık D, Elik Demir A, Uzun Karka H, Güçlü G, Selli S, Kelebek H, Göğüş F Foods 29-Aug-2023
PMCID:PMC10486558
doi:10.3390/foods12173244
PMID:37685177

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(3S,5R,10S,13S,14S,17S)-17-[(E,2S)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 163021121 Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(3S,5S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 40469707 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(3S,5S,8R,9R,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162965657 Click to see 444.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(4aS,6aR,6aS,6bR,8aR,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carbaldehyde 89262164 Click to see 438.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(5R,10S,13S,14S,17S)-17-[(E,2S)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163017719 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
(5S,8R,9R,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 124303726 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbaldehyde 14423516 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydropicene-4a-carboxylic acid 5319898 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2002-26749
17-(2-Hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 4220788 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
17-(7-Hydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 85122621 Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
17-(7-hydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 77686615 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carbaldehyde 54227084 Click to see 438.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
3-Oxo-Erythrodiol 15127783 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
3-Oxolanosta-7,24Z-dien-26-oic acid 73242216 Click to see 454.70 unknown https://doi.org/10.1055/S-2002-26749
3beta-Dammar-24-ene-3,20-diol 4481461 Click to see 444.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 72745643 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
Lanosta-8,24-dien-3-ol 856 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
Masticadienolic acid 102004474 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1055/S-2002-26749
Morolic Acid 489944 Click to see 456.70 unknown https://doi.org/10.1055/S-2002-26749
Olean-12-ene-3beta,28-diol 608886 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
Oleanolic aldehyde 10321055 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(73)80709-5
Oleanonic Acid 12313704 Click to see 454.70 unknown https://doi.org/10.1016/S0014-2999(01)01290-0
https://doi.org/10.1016/0031-9422(73)80709-5

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