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Fraxinus angustifolia

Fraxinus angustifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Fraxinus angustifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Fraxinus angustifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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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

Common names Top

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Language Common/alternative name
English fraxinus oxycarpa
English narrow-leafed ash
Afrikaans smalblaaresseboom
Arabic مران رفيع الأوراق
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 du midi
French frêne à feuilles étroites
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
Norwegian Bokmål smalbladask
Dutch smalbladige es
Polish jesion wąskolistny
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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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
    • 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

Suggest others/fix!
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!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_903798275.1 FRAX16-0.1 Scaffold QMUL 2020-06-16 37.0x 558.81 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
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
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
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
Diaporthe Species on Palms: Molecular Re-Assessment and Species Boundaries Delimitation in the D. arecae Species Complex Pereira DS, Hilário S, Gonçalves MF, Phillips AJ Microorganisms 06-Nov-2023
PMCID:PMC10673533
doi:10.3390/microorganisms11112717
PMID:38004729
Wide Range of Brachyceran Fly Taxa Attracted to Synthetic and Semi-Synthetic Generic Noctuid Lures and the Description of New Attractants for Sciomyzidae and Heleomyzidae Families Nagy A, Katona P, Molnár A, Rádai Z, Tóth M, Szanyi K, Szanyi S Insects 14-Aug-2023
PMCID:PMC10456120
doi:10.3390/insects14080705
PMID:37623415
Commodity risk assessment of Fagus sylvatica 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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Anthracological study of a Chalcolithic funerary deposit from Perdigões (Alentejo, Portugal): A new analytical methodology to establish the wood burning temperature Coradeschi G, Jiménez Morillo NT, Dias CB, Beltrame M, Belo AD, Granged AJ, Sadori L, Valera A PLoS One 07-Jul-2023
PMCID:PMC10328357
doi:10.1371/journal.pone.0287531
PMID:37418445
Commodity risk assessment of Acer campestre 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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018

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
> 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 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 3-formyl-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-2-methyl-3,4-dihydro-2H-pyran-5-carboxylate 75214713 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
> 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OCCC3=CC(=C(C=C3)O)O)CC(=O)OCCC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OCCC3=CC(=C(C=C3)O)O)CC(=O)OCCC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OCCC3=CC(=C(C=C3)O)O)CC(=O)OCCC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 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
Ligustroside 14136859 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 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 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
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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 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 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 (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 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
methyl (4S,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 3789874 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
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 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 (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 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)OC(=O)C 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 524.50 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 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
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
(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
Chlorogenin 12303065 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 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
Hecogenin 91453 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown via CMAUP database
Manogenin 10253011 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 446.60 unknown via CMAUP database
Rockogenin 167555 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(CCC(C6)O)C)O)C)C)OC1 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 CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Yuccagenin 3083608 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CC(C(C6)O)O)C)C)C)OC1 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 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 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
Camassioside 101620741 Click to see CC(C)CC(=O)CC(C)C1C(CC2C1(CCC3C2C(C=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)OC6C(C(C(C(O6)CO)O)O)O 756.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[2-O-(3-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)-3-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl]-beta-D-galactopyranosyloxy]-5alpha-spirostane 21625854 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(CO2)O)O)O)O)O)O)C)C)C)OC1 1167.30 unknown via CMAUP database
(25R)-3beta-[4-O-[2-O-beta-D-Glucopyranosyl-3-O-(4-O-alpha-L-rhamnopyranosyl-beta-D-xylopyranosyl)-beta-D-glucopyranosyl]-beta-D-galactopyranosyloxy]-5alpha-spirostan-2alpha-ol 71716476 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)OC2C(C(C(C(O2)C)O)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1 1197.30 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,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15S,16R,18R)-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-6-(hydroxymethyl)oxane-3,4,5-triol 10605143 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)OC1 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
[(25R)-12-Oxo-5beta-spirostane-3beta-yl]2-O-beta-D-glucopyranosyl-beta-D-galactopyranoside 101243911 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 754.90 unknown via CMAUP database
[(25R)-12beta-Hydroxy-5beta-spirostane-3beta-yl]2-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside 101784690 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)O)C)C)OC1 756.90 unknown via CMAUP database
[(25R)-26-(beta-D-Glucopyranosyloxy)-5beta-furosta-20(22)-ene-3beta-yl]2-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside 101784691 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 903.10 unknown via CMAUP database
12-Oxo-5beta-spirosta-25(27)-ene-3beta-yl 2-O,3-O-bis(beta-D-glucopyranosyl)-beta-D-glucopyranoside 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
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-galactopyranoside 21603424 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
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 10628815 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
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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OC4C(=CC)C(C(=CO4)C(=O)OC)CC(=O)OCC5C(C(C(C(O5)OCCC6=CC=C(C=C6)O)O)O)O)O)OC(=O)CC7C(=COC(C7=CC)OC8C(C(C(C(O8)CO)O)O)O)C(=O)OC)O 1459.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332458/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2'R,3R)-4-[2-[(2'R,3R)-2'-(4-Hydroxyphenyl)-4',6,6'-trihydroxy-2-oxo-7-methoxyspiro[benzofuran-3(2H),3'(2'H)-benzofuran]-4-yl]ethenyl]-2'-(4-hydroxyphenyl)-4',6,6'-trihydroxy-2-oxospiro[benzofuran-3(2H),3'(2'H)-benzofuran] 17757603 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
(2'R,3S)-4-[2-[(2'R,3S)-2'-(4-Hydroxyphenyl)-4',6,6'-trihydroxy-2-oxo-7-methoxyspiro[benzofuran-3(2H),3'(2'H)-benzofuran]-4-yl]ethenyl]-2'-(4-hydroxyphenyl)-4',6,6'-trihydroxy-2-oxospiro[benzofuran-3(2H),3'(2'H)-benzofuran] 17755939 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
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 CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332458/

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