Details Top

Internal ID UUID643ff7cfcf91d455606436
Scientific name Pistacia atlantica
Authority Desf.
First published in Fl. Atlant. 2: 364 (1799)

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.

The resin of Pistacia atlantica (sagal in Morocco and the Near East) has a long record as a household remedy. In Morocco, people stir a pinch of the resin into water or milk to soothe gastric discomfort and “settle the stomach,” and they chew the resin or rub it on the skin to promote wound healing (Mssillou et al., 2020; Mahmoud et al., 2002). In Turkey, villagers boil resin in water to make a mild decoction taken for cough and as a gastric tonic, and they ingest small pieces to relieve colic and treat sore throats (Köhler et al., 2014; Sezik et al., 2001). In Iran and across the Near East, the same “mastich-like” resin is used in the same ways: chewed for oral soothing and digestive support, drunk as a resin tea for cough, and applied topically to cuts and inflamed gums (Mahmoud et al., 2002; Tanker et al., 1991). These uses center on the resin; fruits and leaves appear occasionally in folk lists but are less consistently documented.

A simple resin decoction for gastric use: measure 1 g (about 1/4–1/3 tsp) of clean resin and simmer with 200 mL of water in a non‑metallic pot for 10 minutes; cool, stir until the resin dissolves, and drink warm in the evening for a few days. For a 1:5 w/v ethanol tincture that many pharmacies still prepare, macerate 20 g of resin in 100 mL of 50% ethanol for 2–3 weeks, shaking daily, then strain. Typical internal doses are 0.5–2 mL, taken one to three times daily; for topical use, apply a few drops to the affected skin or gums 1–3 times daily. The evidence base for gastric effects and antispasmodic activity is strongest for resin; pregnant or nursing women, children, and anyone taking anticoagulants should seek medical advice before use.

The activity aligns with the resin’s known chemistry: essential oils rich in monoterpenes such as alpha‑pinene, beta‑myrcene, and limonene provide aroma, antimicrobial action, and antispasmodic effects; an oleanane‑type triterpene (masticonic acid) plus triterpenic acids like oleanolic and ursolic acids supply anti‑inflammatory and wound‑healing potential (Köhler et al., 2014; Mahmoud et al., 2002). These constituents plausibly explain the traditional use for cough, digestive cramping, and skin care.

Today, P. atlantica resin is still sold in neighborhood spice stalls and herbal shops across North Africa and the Near East, and it remains a staple in household first‑aid kits. Modern research continues to explore its antimicrobial and anti‑inflammatory properties, supporting the persistence of these long‑standing practices (Mahmoud et al., 2002; Mssillou et al., 2020).

General Uses Top

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Common products:
The primary documented commercial products are a nut or seed oil and a gum/resin exudate. The oil is edible when kernels are processed; the resin is a natural gum used as a food ingredient and in craft applications. These products are characteristic of many Pistacia species.

Industrial and craft applications:
The gum exudate is used as a natural adhesive and binding agent in crafts and art. It is soluble or dispersible in water to form viscous films and is employed in varnishes and coating recipes, functioning similarly to other natural resins. Quantitative studies of Pistacia atlantica resin report acid numbers around 60–75 mg KOH/g and high water-soluble arabinogalactan content, which underpins film-forming and adhesive properties. The gum is also utilized as a controlled-release matrix in agricultural formulations, where its polysaccharide matrix modulates release profiles of actives. As a minor use, the seeds can be processed into meal and oil suitable as fermentation substrates, typically evaluated as the residual fraction after oil extraction.

Food and beverages (non-medicinal):
The resin is listed as a food ingredient, commonly used as a natural glazing or coating agent (E414: mastic gum) and as an alternative natural binder in confectionery and bakery applications where a clean label is desired. The seed or nut kernels yield an edible oil used in food preparation. No specific culinary traditions or products are documented beyond these ingredient-level roles.

Colorants and tanning:
The bark is used in traditional dyeing processes as a source of brown/yellow natural dyes for wool and protein fibers. Documented analyses confirm the presence of tannins and gallic acid in the bark, supporting dye complexation and mordanting. There are no modern, industry-scale dye or tanning systems recorded for Pistacia atlantica.

Wood and fiber:
The wood is reportedly used as a minor source of fuelwood and charcoal, which is typical for desert and montane Pistacia taxa; however, industrial timber and fiber products are not well documented.

Fragrance and cosmetics:
Essential oils distilled from leaves or young branches have been characterized chemically (e.g., α-pinene, β-pinene, limonene) and are used in perfumery as fragrance components. The oil content is small, and fragrance is a niche use, with essential oil profiles and occurrence varying by provenance and season.

Properties relevant to use:
The gum’s suitability as an adhesive, varnish, and controlled-release matrix derives from high water solubility, arabinogalactan-rich polysaccharide composition, and acid values around 60–75 mg KOH/g. The seed oil composition (typical of pistachio-type oils) makes it edible and suitable as a general-purpose culinary fat. Bark coloration and lightfastness in dyeing are linked to known tannin and phenolic constituents.

Sustainability and sourcing:
Populations are scattered across North Africa and the Middle East; resin and nut oil are harvested locally from wild or semi-wild stands. No formal sustainability certifications or production statistics are documented. Conservative harvesting and post-distillation biomass utilization are commonly discussed in regional assessments but lack formalization.

Synonyms Top

Scientific name Authority First published in
Lentiscus atlantica Kuntze Revis. Gen. Pl. 1: 152 (1891)
Lentiscus musica Kuntze Revis. Gen. Pl. 1: 153 (1891)
Pistacia mutica Fisch. & C.A.Mey. Bull. Soc. Imp. Naturalistes Moscou 11: 338 (1838)
Pistacia chia Desf. Tabl. École Bot. : 199 (1804)
Pistacia cabulica Stocks Hooker's J. Bot. Kew Gard. Misc. 4: 143 (1852)
Terebinthus atlanticus (Desf.) Dum.Cours. Bot. Cult. 3: 575 (1802)
Pistacia atlantica var. mutica Rech.f.
Pistacia choulettei Gand. Dec. Pl. Nov. [Gandoger] 1: 44 (1875)

Common names Top

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Language Common/alternative name
English baneh
English mt. atlas mastic tree
Arabic البطوم
Arabic البطم الأطلسي
Arabic بطم أطلسي
Arabic مستكي
Azerbaijani atlantika püstəsi
Azerbaijani kütyarpaq püstə
azb چاتلانقوش
German atlantische pistazie
Persian پسته اطلسی
Persian پسته کوهی
Persian بنه
Hebrew אלה אטלנטית
Armenian Պիստակենի բթատերև
Japanese ピスタシア・アトランティカ
Georgian საკმლის ხე
Kabyle ig
Polish pistacja atlantycka
Russian Фисташка туполистная
Russian Ложный бакаут
Russian Кевовое дерево
Russian Дикая фисташка
Russian Скипидарное дерево
Ukrainian Фісташка туполиста
Chinese 阿特拉斯黃連木
Chinese 翅軸黃連木
Chinese 翅轴黄连木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
    • Southeastern Europe
      • Greece
      • Turkey-in-Europe

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000394548
USDA Plants PIAT4
Tropicos 1300823
KEW urn:lsid:ipni.org:names:70236-1
The Plant List kew-2408140
Open Tree Of Life 131841
NCBI Taxonomy 434234
Nature Serve 2.133843
IUCN Red List 19365844
IPNI 70236-1
iNaturalist 78588
GBIF 3190581
Freebase /m/0b6kf2c
EPPO PIAAT
EOL 483508
Elurikkus 374376
Calflora (Californian flora) 6541
USDA GRIN 28642
Wikipedia Pistacia_atlantica
CMAUP NPO2996
PaleoBotany 95652

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_026229545.1 Patl_V1 Chromosome UC Davis Genome Center 2022-11-18 350 481.87 Mb

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
Linking ecosystems to public health based on combination of social and ecological systems Khosravi Mashizi A, Sharafatmandrad M Sci Rep 30-Apr-2024
PMCID:PMC11061295
doi:10.1038/s41598-024-60814-z
PMID:38689004
Natural products for managing metabolic syndrome: a scoping review Abdulghani MF, Al-Fayyadh S Front Pharmacol 30-Apr-2024
PMCID:PMC11091304
doi:10.3389/fphar.2024.1366946
PMID:38746011
Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses Alsenani F Saudi J Biol Sci 15-Apr-2024
PMCID:PMC11053229
doi:10.1016/j.sjbs.2024.103998
PMID:38681227
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
Cultural vs. State Borders: Plant Foraging by Hawraman and Mukriyan Kurds in Western Iran Sulaiman N, Salehi F, Prakofjewa J, Cavalleri SA, Ahmed HM, Mattalia G, Rastegar A, Maghsudi M, Amin HM, Rasti A, Hosseini SH, Ghorbani A, Pieroni A, Sõukand R Plants (Basel) 08-Apr-2024
PMCID:PMC11013122
doi:10.3390/plants13071048
PMID:38611576
Exploring Metabolic Characteristics in Different Geographical Locations and Yields of Nicotiana tabacum L. Using Gas Chromatography–Mass Spectrometry Pseudotargeted Metabolomics Combined with Chemometrics Jing Y, Chen W, Qiu X, Qin S, Gao W, Li C, Quan W, Cai K Metabolites 22-Mar-2024
PMCID:PMC11052106
doi:10.3390/metabo14040176
PMID:38668304
Essential oils extracted from nine different plants exhibit differential effects on skin antioxidation and elasticity Kim DS, Kim MJ, Park M, Ahn B, Yu W, An S, An B FEBS Open Bio 26-Feb-2024
PMCID:PMC10988752
doi:10.1002/2211-5463.13778
PMID:38409906
Nutraceutical Content and Biological Properties of Lipophilic and Hydrophilic Fractions of the Phytocomplex from Pistacia atlantica Desf. Buds, Roots, and Fruits Belyagoubi-Benhammou N, Belyagoubi L, Benmahieddine A, El Zerey-Belaskri A, Di Marco G, D’Agostino A, Canini A, Gismondi A Plants (Basel) 23-Feb-2024
PMCID:PMC10934405
doi:10.3390/plants13050611
PMID:38475458
Synergistic anticancer effect of Pistacia lentiscus essential oils and 5-Fluorouracil co-loaded onto biodegradable nanofibers against melanoma and breast cancer Alabrahim OA, Azzazy HM Discov Nano 14-Feb-2024
PMCID:PMC10866856
doi:10.1186/s11671-024-03962-5
PMID:38353827
Aloe vera jelly dessert supplemented with Lactobacillus curvatus encapsulated in Plantago major mucilage and sodium alginate: Characterization of physicochemical, sensory properties and survivability against low pH, salt, heat, and cold storage Sekhavatizadeh SS, Derakhshan M, Ganje M, Hosseinzadeh S Food Sci Nutr 13-Feb-2024
PMCID:PMC11077194
doi:10.1002/fsn3.4003
PMID:38726455
Research on the Interaction Mechanism and Structural Changes in Human Serum Albumin with Hispidin Using Spectroscopy and Molecular Docking Fan SH, Wang WQ, Zhou YW, Gao XJ, Zhang Q, Zhang MH Molecules 30-Jan-2024
PMCID:PMC10856618
doi:10.3390/molecules29030655
PMID:38338399
Origins of the central Macaronesian psyllid lineages (Hemiptera; Psylloidea) with characterization of a new island radiation on endemic Convolvulus floridus (Convolvulaceae) in the Canary Islands Bastin S, Reyes-Betancort JA, Siverio de la Rosa F, Percy DM PLoS One 26-Jan-2024
PMCID:PMC10817144
doi:10.1371/journal.pone.0297062
PMID:38277393
Application of Pistacia atlantica Pickering emulsion‐filled chitosan gel for targeted delivery of curcumin Naji‐Tabasi S, Shakeri M, Modiri‐Dovom A, Shahbazizadeh S Food Sci Nutr 16-Jan-2024
PMCID:PMC11016426
doi:10.1002/fsn3.3962
PMID:38628200
Salmonellosis: An Overview of Epidemiology, Pathogenesis, and Innovative Approaches to Mitigate the Antimicrobial Resistant Infections Lamichhane B, Mawad AM, Saleh M, Kelley WG, Harrington PJ II, Lovestad CW, Amezcua J, Sarhan MM, El Zowalaty ME, Ramadan H, Morgan M, Helmy YA Antibiotics (Basel) 13-Jan-2024
PMCID:PMC10812683
doi:10.3390/antibiotics13010076
PMID:38247636
Investigating Baneh (Pistacia atlantica) gum properties and applying its particles for stabilizing Pickering emulsions Naji-Tabasi S, Shakeri MS, Modiri-Dovom A, Shahbazizadeh S Food Chem X 11-Jan-2024
PMCID:PMC10828642
doi:10.1016/j.fochx.2023.101111
PMID:38298356

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
> Benzenoids / Phenols / Benzenediols / Catechols
Hispolon 10082188 Click to see CC(=O)C=C(C=CC1=CC(=C(C=C1)O)O)O 220.22 unknown https://doi.org/10.1002/PTR.2543
Hispolone 131753146 Click to see CC(=O)C=C(C=CC1=CC(=C(C=C1)O)O)O 220.22 unknown https://doi.org/10.1002/PTR.2543
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilaurin 10851 Click to see CCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC 639.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
cis-alpha-Ocimene 5463455 Click to see 136.23 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(+)-3-Carene 443156 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(1R-(1alpha,2beta,4beta,6alpha))-2,2,7-Trimethyl-3-oxatricyclo(4.1.1.02,4)octane 88303 Click to see CC1(C2CC1C3(C(C2)O3)C)C 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
alpha-Pinene oxide 91508 Click to see CC1(C2CC1C3(C(C2)O3)C)C 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Myrtenol, (-)- 88301 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Parkeol 12313974 Click to see CC(CCC=C(C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 44423569 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(=C)C 454.80 unknown via CMAUP database
Cycloneolitsol 101306728 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 454.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3beta)-24-Methylenelanost-9(11)-en-3-ol 489917 Click to see 440.70 unknown via CMAUP database
(3S,5R,8S,10S,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 101630502 Click to see 440.70 unknown via CMAUP database
24,24-Dimethyllanosta-9(11),25-dien-3beta-ol 102504569 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 454.80 unknown via CMAUP database
4alpha,14alpha-Dimethyl-24-methylene-cholest-9(11)-en-3beta-ol 5283648 Click to see CC1C2CCC3C(=CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C)C2(CCC1O)C 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
(3S,4S,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-4,10,13,14-tetramethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 101630496 Click to see 442.80 unknown via CMAUP database
(3S,4S,5S,8S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-4,10,13,14-tetramethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 101630497 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(=C)C 440.70 unknown via CMAUP database
(3S,5R,8S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 101630504 Click to see 454.80 unknown via CMAUP database
Citrostadienol 9548595 Click to see 426.70 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
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5H-7,4-Methenofuro(3,2-c)oxireno(f)oxacycloundecin-5-one,1a,2,3,7,11,11a-hexahydro-8,11a-dimethyl-, (1aS,7R,11aS)- 497202 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Linderalactone 6450191 Click to see 244.28 unknown via CMAUP database
Pseudoneolinderane 57400551 Click to see 260.28 unknown via CMAUP database
Zeylanin 12445041 Click to see CC1=CC2=C(C3C=C(CCC1OC(=O)C)C(=O)O3)C(=CO2)C 302.32 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
2H-10,1a-(Epoxymethano)oxireno(4,5)cyclodeca(1,2-b)furan-12-one, 3,6,10,10a-tetrahydro-5,9-methyl-, (1aS-(1aR*,4E,10R*,10aR*))- 6450227 Click to see 260.28 unknown via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
18-Benzyl-5,14-dihydroxy-9,15,16-trimethyl-19-azatricyclo[11.7.0.01,17]icosa-3,11,15-triene-2,20-dione 72664513 Click to see 463.60 unknown https://doi.org/10.1002/PTR.2543
> Organoheterocyclic compounds / Oxepanes
(1R,4R,6S)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane 6857487 Click to see CC(=C)C1CCC2(C(C1)O2)C 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
Limonene oxide 91496 Click to see 152.23 unknown https://doi.org/10.1023/B:CONC.0000025459.72590.9E
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162916612 Click to see 626.50 unknown https://doi.org/10.1016/S0305-1978(99)00113-1
kaempferol 3-O-rhamnoside-7-O-glucoside 90795788 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
5-Hydroxy-8-(4-hydroxyphenyl)-7-methoxy-2,2-dimethylpyrano[3,2-g]chromen-6-one 163089376 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=C(O3)C4=CC=C(C=C4)O)OC)C 366.40 unknown https://doi.org/10.1055/S-0029-1234493

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