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Fraxinus angustifolia subsp. oxycarpa

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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 UUID64402ccb39ec7377733023
Scientific name Fraxinus angustifolia subsp. oxycarpa
Authority (Willd.) Franco & Rocha Afonso
First published in Bot. J. Linn. Soc. 64: 377 (1971)

Description Top

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Common names Top

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Language Common/alternative name
English fraxinus angustifolia oxycarpa
Spanish fraxinus angustifolia oxycarpa
Bulgarian fraxinus angustifolia oxycarpa
French fraxinus angustifolia oxycarpa
Russian fraxinus angustifolia oxycarpa
Chinese 尖果梣

Varieties (abbr. var.) 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
  • Europe
    • Eastern Europe
      • Krym
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Hungary
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000832310
Tropicos 23000361
INPN 134709
Flora of Italy 3978
KEW urn:lsid:ipni.org:names:887126-1
The Plant List kew-369531
Open Tree Of Life 272101
Observations.org 117991
NCBI Taxonomy 56026
NBN Atlas NBNSYS0000042112
IPNI 887126-1
iNaturalist 82884
GBIF 6432925
EPPO FRXAX
USDA GRIN 315869

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
Bio-Guided Isolation of Compounds from Fraxinus excelsior Leaves with Anti-Inflammatory Activity Kołtun-Jasion M, Sawulska P, Patyra A, Woźniak M, Dudek MK, Filipek A, Kiss AK Int J Mol Sci 13-Feb-2023
PMCID:PMC9964138
doi:10.3390/ijms24043750
PMID:36835169
A Decrease in Mesophyll Conductance by Cell-Wall Thickening Contributes to Photosynthetic Downregulation Sugiura D, Terashima I, Evans JR Plant Physiol 09-Jun-2020
PMCID:PMC7401118
doi:10.1104/pp.20.00328
PMID:32518201
Ground beetles in Mediterranean olive agroecosystems: Their significance and functional role as bioindicators (Coleoptera, Carabidae) Pizzolotto R, Mazzei A, Bonacci T, Scalercio S, Iannotta N, Brandmayr P PLoS One 20-Mar-2018
PMCID:PMC5860759
doi:10.1371/journal.pone.0194551
PMID:29558493
Multistep food plant processing at Grotta Paglicci (Southern Italy) around 32,600 cal B.P. Mariotti Lippi M, Foggi B, Aranguren B, Ronchitelli A, Revedin A Proc Natl Acad Sci U S A 08-Sep-2015
PMCID:PMC4593080
doi:10.1073/pnas.1505213112
PMID:26351674
Plant Architecture: A Dynamic, Multilevel and Comprehensive Approach to Plant Form, Structure and Ontogeny Barthélémy D, Caraglio Y Ann Bot 11-Jan-2007
PMCID:PMC2802949
doi:10.1093/aob/mcl260
PMID:17218346
Phylogenetic Variation in the Silicon Composition of Plants HODSON MJ, WHITE PJ, MEAD A, BROADLEY MR Ann Bot 21-Sep-2005
PMCID:PMC4247092
doi:10.1093/aob/mci255
PMID:16176944
Epoxyconiferyl alcohol from Fraxinus oxycarpa bark Ivanka Kostova, Dragomir Dinchev, Bozhana Mikhova, Tanya Iossifova Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00656-E
Secoiridoid glucosides from Fraxinus oxycarba Mohammed Hosny Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00790-5

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3R,3aS,6S,6aR)-3a-hydroxy-6-(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14756314 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 536.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
Fraxiresinol 1-O-glucoside 21632948 Click to see COC1=CC(=CC(=C1O)OC)C2C3(COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC5C(C(C(C(O5)CO)O)O)O 566.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
> 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/S0031-9422(97)00790-5
10-Hydroxyligstroside 14756316 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
10-Hydroxyoleuropein 6440747 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 556.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
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(94)00656-E
https://doi.org/10.1016/S0031-9422(97)00790-5
methyl (4S,5E,6S)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162947192 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/S0031-9422(97)00790-5
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/S0031-9422(97)00790-5
https://doi.org/10.1016/0031-9422(94)00656-E
methyl 5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74184139 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(94)00656-E
https://doi.org/10.1016/S0031-9422(97)00790-5
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/S0031-9422(97)00790-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496101 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
6-O-caffeoyl-beta-glucose 101419460 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-6-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 5281418 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 370.31 unknown https://doi.org/10.1016/0031-9422(94)00656-E
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1016/0031-9422(94)00656-E
Fraxin 5273568 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 370.31 unknown https://doi.org/10.1016/0031-9422(94)00656-E
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/0031-9422(94)00656-E
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1016/0031-9422(94)00656-E
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 208.17 unknown https://doi.org/10.1016/0031-9422(94)00656-E
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497089 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(97)00790-5
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(97)00790-5

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