Fraxinus angustifolia

Details Top

Internal ID UUID64402ccb1a736599688712
Scientific name Fraxinus angustifolia
Authority Vahl
First published in Enum. Pl. Obs. 1: 52 (1804)

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 eastern Pyrenees, a decoction of bark and young twigs of Fraxinus angustifolia has been taken as a bitter tonic and diuretic according to Gonzalez et al. (2010). In Central Anatolia, rural communities prepare an infusion of its young leaves to aid digestion and as a mild fever reducer (Cakilcioglu et al., 2011). Along the Balkans–Anatolia corridor, a tincture of dried bark macerated in alcohol is traditionally employed as an anti-inflammatory liniment and is also ingested in small doses for gout, according to the pharmacopoeial notes of Bogavac et al. (2022). In all these cases the plant parts are bark and young shoots or leaves, and the modes of use are infusions, decoctions, and alcohol tinctures.

For a practical bark tea, steep 2–3 g of finely chopped, dried Fraxinus angustifolia bark in 250 ml of just-boiled water for 10–12 minutes; strain and drink up to two cups per day for occasional digestive support. A 1:5 ethanol tincture is made by macerating 20 g of dried bark in 100 ml of 45% ethanol (vol/vol) for three to four weeks with daily shaking; the mature macerate is decanted and filtered. Typical internal doses for a bark tincture range from 10–20 drops in a little water two to three times daily. Because Fraxinus bark contains coumarin-like constituents, do not exceed labeled doses and avoid use during pregnancy; those with coumarin sensitivity or anticoagulant therapy should consult a health professional.

Phytochemically, the species is documented to contain secoiridoid glycosides, flavonoids such as rutin, phenolic acids, and a characteristic coumarin-like compound profile that plausibly accounts for the recorded diuretic, anti-inflammatory, and mild bitter actions (Jankovic et al., 2006; Choi et al., 2012).

Today Fraxinus angustifolia remains a minor component of certain Balkan herbal blends and is sometimes supplied as “common ash” bark in tincture form; interest in its coumarin and secoiridoid content continues to inform targeted pharmacological studies.

General Uses Top

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Common products:
Wood from Fraxinus angustifolia is utilized as a general-purpose hardwood for furniture, flooring, interior joinery, tool handles, and sports equipment, and it is sliced for veneer. The wood is also employed in paper and pulp production.

Industrial and craft applications:
The species is used for turning and carving, and as a craft wood for items such as baseball bats and hockey sticks in addition to its furniture applications.

Food and beverages (non-medicinal):
No food or beverage uses are documented for this taxon.

Colorants and tanning:
No colorants or tanning uses are documented for this taxon.

Wood and fiber:
Wood is supplied as veneer and as sawn or sliced timber for furniture, flooring, tool handles, and sports equipment. No fiber uses are documented for this taxon.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented for this taxon.

Properties relevant to use:
The wood is diffuse-porous with prominent rings, typically light-colored, hard, and tough with high strength relative to density, making it suitable for impact-resistant uses such as handles, sports equipment, and veneer.

Standards and regulation:
Timber is traded under trade-class names and species codes used in hardwood timber and veneer markets (e.g., ASH for European ash). No specific standards or regulatory frameworks are documented that uniquely apply to F. angustifolia.

Sustainability and sourcing:
Mediterranean populations face pressures from bark beetles and pathogens; regional forestry initiatives in southern Europe aim to maintain supply from sustainably managed stands. No taxon-specific certification frameworks are documented.

Synonyms Top

Scientific name Authority First published in
Ornus mammifera Steud. Nomencl. Bot. : 575 (1821)
Fraxinus angustifolia var. lentiscifolia (Desf.) A.Henry Trees Great Britain 4: 880. 1909
Fraxinus angustifolia var. pannonica Fukarek Glasn. Sumska Pokuse 14: 229 1960
Fraxinus angustifolia f. pendula (Loudon) Rehder Bibl. Cult. Trees 561 1949
Fraxinus angustifolia var. rostrata (Guss.) Rouy & Fouc. Fl. France 4: 146 1897
Fraxinus calabrica hort. ex Dippel Handb. Laubholzk. 1: 90 (1889)
Fraxinus excelsior subsp. angustifolia (Vahl) Wesm. Bull. Soc. Roy. Bot. Belgique 31(1): 100. 1892 (1892)
Fraxinus excelsior var. angustifolia (Vahl) Fiori & Paol. Fl. Italia 2: 341 1902
Fraxinus excelsior subsp. parvifolia (Dum.Cours.) Arcang. Comp. Fl. Ital. 466 1882
Fraxinus excelsior var. parvifolia Dum.Cours. Bot. Cult. 1: 711 1802
Fraxinus excelsior subsp. parvifolia (Boiss.) Wesm. Bull. Soc. Roy. Bot. Belgique 31(1): 101. 1892 (1892)
Fraxinus excelsior var. rostrata (Guss.) Wesm. Bull. Soc. Roy. Bot. Belgique 31(1): 95. 1892
Fraxinus humilior Garsault Fig. Pl. Méd. : t. 97 a (1764)
Fraxinus lentiscifolia var. pendula Loudon Arbor. Frutic. Brit. 2: 1231. 1838
Fraxinus obtusa Willk. & Lange Prodr. Fl. Hispan. 3: 564. 1878 (1878)
Fraxinus ornus var. parvifolia (Dum.Cours.) Ten. Syll. Pl. Fl. Neapol. 11 1831
Fraxinus oxycarpa var. angustifolia (Vahl) Lingelsh. Pflanzenr. IV, 243(1): 55. 1920
Fraxinus oxycarpa subsp. edentata Dippel Handb. Laubholzk. 1: 90. 1889 (1889)
Fraxinus oxycarpa f. edentata (Dippel) Lingelsh. Pflanzenr. IV, 243(1): 56 1920
Fraxinus oxycarpa f. hartwegii Lingelsh. Pflanzenr. IV, 243(1): 55 1920
Fraxinus oxycarpa var. parvifolia (Boiss.) Wenzig Bot. Jahrb. Syst. 4: 175 1883
Fraxinus oxycarpa var. petiolulata Karpati Acta Bot. Acad. Sci. Hung. 2: 278. 1956
Fraxinus oxycarpa var. rostrata (Guss.) Lingelsh. Pflanzenr. IV, 243(1): 55. 1920
Fraxinus oxyphylla var. parvifolia (Dum.Cours.) Boiss. Fl. Orient. 4: 40 1875
Fraxinus parvifolia Lam. Encycl. 2: 546 (1788)
Fraxinus parvifolia f. pendula (Loudon) Dippel Handb. Laubholzk. 1: 94 1889
Fraxinus parvifolia var. tarraconensis Sennen Exsicc. (Pl. Esp.) 1927: n.° 5950.
Fraxinus rotundifolia f. pendula (Loudon) Rehder Stand. Cycl. Hort. 3: 1277 1915
Fraxinus americana var. calabriensis Weston Bot. Univ. 1: 110. 1770
Fraxinus excelsior subsp. rostrata (Guss.) Arcang. Comp. Fl. Ital. 466. 1882 (1882)
Fraxinus excelsior var. parvifolia (Boiss.) Arcang. Comp. Fl. Ital. 466 1882
Fraxinus oxyphylla subsp. angustifolia (Vahl) P.Fourn. Quatre Fl. France : 868 (1938)
Fraxinus excelsior prol. angustifolia (Vahl) Rouy Fl. France 4: 144 (1897)

Common names Top

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Language Common/alternative name
English narrow-leafed ash
Spanish fresno sureño
Afrikaans smalblaaresseboom
Arabic مران رفيع الأوراق
Azerbaijani ensizyarpaq göyrüş
Azerbaijani Şişmeyvə göyrüş
Bulgarian полски ясен
Catalan freixe de fulla petita
Czech jasan úzkolistý
Danish smalbladet ask
German schmalblättrige esche
Greek Φράξινος
Greek Φράξος
Basque lizar hostotxiki
Finnish etelänsaarni
French frêne à feuilles étroites
French frêne du midi
Galician freixo de folla estreita
Hebrew מילה חדת עלים
Croatian poljski jasen
Hungarian keskenylevelű kőris
Armenian Հացենի սրապտուղ
Japanese ホソバトネリコ
Kabyle aslen
Macedonian полски јасен
mwl frezno
Norwegian Bokmål smalbladask
Dutch smalbladige es
Polish jesion wąskolistny
Portuguese freixo
Slovenian ozkolistni jesen
Slovenian ostrolistni jesen
Slovenian poljski jesen
Swedish smalbladig ask
Turkish sivri meyveli dişbudak
Chinese 窄叶梣

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Fraxinus angustifolia subsp. angustifolia Unknown
Fraxinus angustifolia subsp. oxycarpa (Willd.) Franco & Rocha Afonso Bot. J. Linn. Soc. 64: 377 (1971)
Fraxinus angustifolia subsp. persica (Boiss.) Azadi Iran. J. Bot. 11: 42 (2005)
Fraxinus angustifolia subsp. syriaca (Boiss.) Yalt. Fl. Turkey 6: 152 (1978)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
    • Middle Asia
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Hungary
      • Poland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • 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-0000832291
Tropicos 23000337
INPN 98910
Flora of Italy 3976
KEW urn:lsid:ipni.org:names:332095-2
The Plant List kew-369513
PFAF Fraxinus angustifolia
Open Tree Of Life 949520
Observations.org 117988
NCBI Taxonomy 166594
NBN Atlas NHMSYS0000523231
IUCN Red List 203366
IPNI 332095-2
iNaturalist 82886
iNaturalist 82881
GBIF 7325877
Freebase /m/0gbsd5
EPPO FRXAN
Elurikkus 209857
USDA GRIN 276
Wikipedia Fraxinus_angustifolia
CMAUP NPO20677

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_051941055.1 ASM5194105v1 Chromosome Shandong Agricultural University 2025-08-12 62 706.14 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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Alfalfa Responses to Intensive Soil Compaction: Effects on Plant and Root Growth, Phytohormones and Internal Gene Expression Yan M, Yang D, He Y, Ma Y, Zhang X, Wang Q, Gao J Plants (Basel) 26-Mar-2024
PMCID:PMC11013635
doi:10.3390/plants13070953
PMID:38611482
Dangerous neighbours: Birds and bird‐eating bats sharing tree cavities Russo D, Mäenurm A, Martinoli A, Cistrone L Ecol Evol 11-Mar-2024
PMCID:PMC10926052
doi:10.1002/ece3.11098
PMID:38469052
Dig-up Primers: A Pipeline for Identification of Polymorphic Microsatellites Loci within Assemblies of Related Species Turudić A, Liber Z, Grdiša M, Jakše J, Varga F, Poljak I, Šatović Z Int J Mol Sci 09-Mar-2024
PMCID:PMC10970464
doi:10.3390/ijms25063169
PMID:38542142
The seed dispersal syndrome hypothesis in ungulate-dominated landscapes Fedriani JM, Garrote PJ, Burgos T, Escribano-Ávila G, Morera B, Virgós E Sci Rep 05-Mar-2024
PMCID:PMC10914747
doi:10.1038/s41598-024-55820-0
PMID:38443407
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
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
Impacts, Potential Benefits and Eradication Feasibility of Aquatic Alien Species in an Integral Natural State Reserve Paganelli D, Bellati A, Gazzola A, Bracco F, Pellitteri-Rosa D Biology (Basel) 22-Jan-2024
PMCID:PMC10813597
doi:10.3390/biology13010064
PMID:38275740
Dieback and Replacement of Riparian Trees May Impact Stream Ecosystem Functioning Alonso A, Boyero L, Solla A, Ferreira V Microb Ecol 16-Jan-2024
PMCID:PMC10791780
doi:10.1007/s00248-024-02343-w
PMID:38228918
The Novel Invader Salpichroa origanifolia Modifies the Soil Seed Bank of a Mediterranean Mesophile Forest Arduini I, Alessandrini V Plants (Basel) 13-Jan-2024
PMCID:PMC10821032
doi:10.3390/plants13020226
PMID:38256778
Oleuropein-Rich Jasminum Grandiflorum Flower Extract Regulates the LKB1-PGC-1α Axis Related to the Attenuation of Hepatocellular Lipid Dysmetabolism Hou Y, Zhao X, Wang Y, Li Y, Chen C, Zhou X, Jin J, Ye J, Li D, Gan L, Wu R Nutrients 24-Dec-2023
PMCID:PMC10780778
doi:10.3390/nu16010058
PMID:38201888
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756
Botanical memory: five centuries of floristic changes revealed by a Renaissance herbarium (Ulisse Aldrovandi, 1551–1586) Buldrini F, Alessandrini A, Mossetti U, Muzzi E, Pezzi G, Soldano A, Nascimbene J R Soc Open Sci 08-Nov-2023
PMCID:PMC10645095
doi:10.1098/rsos.230866
PMID:38026021

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 / Tyrosols and derivatives
methyl (2S,3S,4S)-3-formyl-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-2-methyl-3,4-dihydro-2H-pyran-5-carboxylate 101393982 Click to see CC1C(C(C(=CO1)C(=O)OC)CC(=O)OCCC2=CC=C(C=C2)O)C=O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (2S,3S)-3-formyl-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-2-methyl-3,4-dihydro-2H-pyran-5-carboxylate 162845073 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl 3-formyl-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-2-methyl-3,4-dihydro-2H-pyran-5-carboxylate 75214713 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85109-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate 134688908 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
2-(3,4-dihydroxyphenyl)ethyl (4R,5Z,6S)-5-ethylidene-4-[2-[2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163190053 Click to see 824.80 unknown https://doi.org/10.1016/0031-9422(95)00815-2
2-(3,4-dihydroxyphenyl)ethyl (5Z,6S)-5-ethylidene-4-[2-[2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101695757 Click to see 824.80 unknown https://doi.org/10.1016/0031-9422(95)00815-2
2-(3,4-dihydroxyphenyl)ethyl 5-ethylidene-4-[2-[2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162890749 Click to see 824.80 unknown https://doi.org/10.1016/0031-9422(95)00815-2
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside 72727933 Click to see 524.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
Angustifolioside B 101637167 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O 686.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
Ligstroside 14136859 Click to see 524.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (4R,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 13232124 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (4R,5E,6S)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163194966 Click to see 524.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (4R,5E,6S)-5-ethylidene-4-[2-[2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163193522 Click to see 702.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (4R,5E,6S)-5-ethylidene-4-[2-oxo-2-[2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]ethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163194764 Click to see 686.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (4S,5E,6S)-5-ethylidene-4-[2-[2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101637166 Click to see 702.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (5E,6S)-4-[2-[2-[3-acetyloxy-4-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-5-ethylidene-6-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163010818 Click to see 1081.00 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (5E,6S)-5-ethylidene-4-[2-oxo-2-[2-[4-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]ethoxy]ethyl]-6-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163034140 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1022.90 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl (5Z)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 14136858 Click to see 524.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxo-ethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4H-pyran-3-carboxylate 3789874 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl 5-ethylidene-4-[2-[2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 78122785 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 702.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
methyl 5-ethylidene-4-[2-oxo-2-[2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163025549 Click to see 686.70 unknown https://doi.org/10.1016/0031-9422(93)85109-5
Oleuropein 5281544 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(93)85109-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Hecogenin 91453 Click to see 430.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 46865976 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 10253011 Click to see 446.60 unknown via CMAUP database
Chlorogenin 12303065 Click to see 432.60 unknown via CMAUP database
Gitogenin 441887 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Rockogenin 167555 Click to see 432.60 unknown via CMAUP database
Sarsasapogenin 92095 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Smilagenin 91439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
Yuccagenin 3083608 Click to see 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
methyl (4S,5Z,6S)-5-ethylidene-4-[2-oxo-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163194428 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1016/0031-9422(95)00815-2
methyl (5Z)-5-ethylidene-4-[2-oxo-2-[[3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 131801374 Click to see 686.70 unknown https://doi.org/10.1016/0031-9422(95)00815-2
methyl 5-ethylidene-4-[2-oxo-2-[[3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 72987608 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1016/0031-9422(95)00815-2
Nuezhenide 6440999 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1016/0031-9422(95)00815-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R)-2-[(3S,7R,8S,9S,10R,13S,14S,16S,17R)-7-hydroxy-10,13-dimethyl-3,16-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptan-4-one 101620741 Click to see 756.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101243911 Click to see 754.90 unknown via CMAUP database
(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101784689 Click to see CC1C2C(CC3C2(C(=O)CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9 915.00 unknown via CMAUP database
(25R)-2beta-OH-timosaponin A III 10605143 Click to see 756.90 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,8S,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101784691 Click to see 903.10 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(3R,4R,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 71716476 Click to see 1197.30 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol 21625854 Click to see 1167.30 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603422 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 903.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13S,16S,18R)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101784690 Click to see 756.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603426 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-galactopyranoside 21603424 Click to see 903.10 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 10628815 Click to see 740.90 unknown via CMAUP database
Timosaponin A-III 15953793 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 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
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
methyl (5Z)-5-ethylidene-4-[2-[[(2S,3S,4R,5S)-6-[[(3Z)-3-ethylidene-5-methoxycarbonyl-4-[2-oxo-2-[[(2R,3S,4S,5R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-4H-pyran-2-yl]oxy]-4-[2-[(3Z)-3-ethylidene-5-methoxycarbonyl-2-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,5-dihydroxyoxan-2-yl]methoxy]-2-oxoethyl]-6-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163189982 Click to see 1459.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332458/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17757603 Click to see 810.70 unknown via CMAUP database
(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17755939 Click to see 810.70 unknown via CMAUP database
Gloriosaol D 102380006 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 133612301 Click to see 454.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332458/

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