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Fraxinus uhdei

Fraxinus uhdei - 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 UUID64402cd704a8e334469853
Scientific name Fraxinus uhdei
Authority Lingelsh.
First published in Bot. Jahrb. Syst. 40: 22 (1907)

Description Top

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Synonyms Top

Scientific name Authority First published in
Fraxinus americana f. ovalifolia Wenz. Bot. Jahrb. Syst. 4: 182 1883
Fraxinus americana var. uhdei Wenz. Bot. Jahrb. Syst. 4: 182 (1883)
Fraxinus cavekiana Standl. & Steyerm. Publ. Field Columb. Mus., Bot. Ser. 23: 74 (1944)
Fraxinus chiapensis Lundell Contr. Univ. Michigan Herb. 7: 45 (1942)
Fraxinus hondurensis Standl. Publ. Field Columb. Mus., Bot. Ser. 17: 386 (1938)
Fraxinus ovalifolia Lingelsh. Bot. Jahrb. Syst. 40: 221 (1907)
Fraxinus uhdei var. pseudoperiptera Lingelsh. Pflanzenr. , IV, 243(1): 44 (1920)
Fraxinus uhdei var. typica Lingelsh. Pflanzenr. , IV, 243(1): 45 (1920)

Common names Top

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Language Common/alternative name
English shamel ash
English ash
English tropical ash
Arabic مران شامل
Hebrew מילה ירוקת עד
Chinese 墨西哥梣

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Puerto Rico
    • Central America
      • Costa Rica
      • Guatemala
      • Honduras
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000833009
UNII 74L99T921J
USDA Plants FRUH
Tropicos 23000317
KEW urn:lsid:ipni.org:names:105922-2
The Plant List kew-370187
Open Tree Of Life 358560
NCBI Taxonomy 490853
Nature Serve 2.152937
IUCN Red List 96444707
IPNI 105922-2
iNaturalist 134212
GBIF 3172371
EPPO FRXUH
EOL 487569
Calflora (Californian flora) 8655
USDA GRIN 318
Wikipedia Fraxinus_uhdei

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
Phytochemical Analysis and Biological Activities of Ripe Fruits of Mistletoe (Psittacanthus calyculatus) Ochoa-Cruz Z, Molina-Torres J, Angoa-Pérez MV, Cárdenas-Valdovinos JG, García-Ruiz I, Ceja-Díaz JA, Bernal-Gallardo JO, Mena-Violante HG Plants (Basel) 12-Jun-2023
PMCID:PMC10305055
doi:10.3390/plants12122292
PMID:37375917
Irrigated urban trees exhibit greater functional trait plasticity compared to natural stands Ibsen PC, Santiago LS, Shiflett SA, Chandler M, Jenerette GD Biol Lett 04-Jan-2023
PMCID:PMC9810417
doi:10.1098/rsbl.2022.0448
PMID:36596464
An exotic plant successfully invaded as a passenger driven by light availability Liu Y, Li W, Sui X, Li A, Li K, Gong Y Front Plant Sci 07-Dec-2022
PMCID:PMC9767969
doi:10.3389/fpls.2022.1047670
PMID:36570959
Global Trends of Acidity in Rainfall and Its Impact on Plants and Soil Prakash J, Agrawal SB, Agrawal M J Soil Sci Plant Nutr 17-Nov-2022
PMCID:PMC9672585
doi:10.1007/s42729-022-01051-z
PMID:36415481
Five Visual and Olfactory Target Genes for RNAi in Agrilus Planipennis Fan Z, Zhang Z, Zhang X, Kong X, Liu F, Zhang S Front Genet 04-Feb-2022
PMCID:PMC8855093
doi:10.3389/fgene.2022.835324
PMID:35186047
Spectral Characteristics Related to Chemical Substructures and Structures Indicative of Organic Precursors from Fulvic Acids in Sediments by NMR and HPLC-ESI-MS López-Martínez VG, Guerrero-Álvarez JA, Ronderos-Lara JG, Murillo-Tovar MA, Solá-Pérez JE, León-Rivera I, Saldarriaga-Noreña H Molecules 02-Jul-2021
PMCID:PMC8272027
doi:10.3390/molecules26134051
PMID:34279390
Antiproliferative and antibacterial activity of extracts of Ganoderma strains grown in vitro Serrano-Márquez L, Trigos Á, Couttolenc A, Padrón JM, Shnyreva AV, Mendoza G Food Sci Biotechnol 05-May-2021
PMCID:PMC8144262
doi:10.1007/s10068-021-00903-1
PMID:34123467
Identification of Phytoplasmas Representing Multiple New Genetic Lineages from Phloem-Feeding Leafhoppers Highlights the Diversity of Phytoplasmas and Their Potential Vectors Wei W, Trivellone V, Dietrich CH, Zhao Y, Bottner-Parker KD, Ivanauskas A Pathogens 16-Mar-2021
PMCID:PMC8002289
doi:10.3390/pathogens10030352
PMID:33809759
Comparing the success of active and passive restoration in a tropical cloud forest landscape: A multi-taxa fauna approach Díaz-García JM, López-Barrera F, Pineda E, Toledo-Aceves T, Andresen E PLoS One 10-Nov-2020
PMCID:PMC7654786
doi:10.1371/journal.pone.0242020
PMID:33170890
Does Acid Rain Alter the Leaf Anatomy and Photosynthetic Pigments in Urban Trees? Rodríguez-Sánchez VM, Rosas U, Calva-Vásquez G, Sandoval-Zapotitla E Plants (Basel) 08-Jul-2020
PMCID:PMC7411892
doi:10.3390/plants9070862
PMID:32650420
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Morphological and Molecular Characterization of Three Endolichenic Isolates of Xylaria (Xylariaceae), from Cladonia curta Ahti & Marcelli (Cladoniaceae) Cañón ER, de Albuquerque MP, Alves RP, Pereira AB, Victoria FD Plants (Basel) 08-Oct-2019
PMCID:PMC6843379
doi:10.3390/plants8100399
PMID:31597306
This town ain't big enough for both of us…or is it? Spatial co-occurrence between exotic and native species in an urban reserve Ramírez-Cruz GA, Solano-Zavaleta I, Mendoza-Hernández PE, Méndez-Janovitz M, Suárez-Rodríguez M, Zúñiga-Vega JJ PLoS One 18-Jan-2019
PMCID:PMC6338412
doi:10.1371/journal.pone.0211050
PMID:30657793
Effect of seed removal by ants on the host-epiphyte associations in a tropical dry forest of central Mexico Vergara-Torres CA, Corona-López AM, Díaz-Castelazo C, Toledo-Hernández VH, Flores-Palacios A AoB Plants 25-Sep-2018
PMCID:PMC6185717
doi:10.1093/aobpla/ply056
PMID:30338050
Climate variation alters the synchrony of host–parasitoid interactions Wetherington MT, Jennings DE, Shrewsbury PM, Duan JJ Ecol Evol 14-Sep-2017
PMCID:PMC5648684
doi:10.1002/ece3.3384
PMID:29075473

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(4S,5E,6S)-5-(2-hydroxyethylidene)-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-carboxylic acid 101922701 Click to see C1=CC(=CC=C1CCOC(=O)CC2C(=COC(C2=CCO)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)O 526.50 unknown https://doi.org/10.1055/S-2006-958076
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/10.1016/0031-9422(93)85128-E
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/10.1055/S-2006-958076
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/10.1055/S-2006-958076
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-carboxylic acid 75111140 Click to see C1=CC(=CC=C1CCOC(=O)CC2C(=COC(C2=CCO)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)O 526.50 unknown https://doi.org/10.1055/S-2006-958076
Ligstroside 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/10.1055/S-2006-958076
methyl (4S,5E,6R)-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 75492723 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/10.1055/S-2006-958076
methyl (4S,5E,6S)-5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163187815 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(93)85128-E
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-(2-hydroxyethylidene)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 78410094 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/10.1055/S-2006-958076
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(93)85128-E
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(13S,14E,15S)-14-ethylidene-4,15-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,10,16,20-tetraoxatetracyclo[21.2.2.13,7.013,18]octacosa-1(25),3,5,7(28),17,23,26-heptaene-11,19-dione 163189001 Click to see CC=C1C2CC(=O)OCCC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC=C(CCOC(=O)C2=COC1OC6C(C(C(C(O6)CO)O)O)O)C=C5 790.80 unknown https://doi.org/10.1016/0031-9422(93)85128-E
14-Ethylidene-4,15-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,10,16,20-tetraoxatetracyclo[21.2.2.13,7.013,18]octacosa-1(25),3,5,7(28),17,23,26-heptaene-11,19-dione 163076167 Click to see CC=C1C2CC(=O)OCCC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC=C(CCOC(=O)C2=COC1OC6C(C(C(C(O6)CO)O)O)O)C=C5 790.80 unknown https://doi.org/10.1016/0031-9422(93)85128-E
> Organoheterocyclic compounds / Benzofurans
methyl 4a,7-dimethyl-4,6-dioxo-7,8-dihydro-5H-cyclopenta[f][1]benzofuran-7a-carboxylate 162918740 Click to see CC1C(=O)CC2(C1(CC3=C(C2=O)C=CO3)C(=O)OC)C 276.28 unknown https://doi.org/10.1016/0031-9422(93)85128-E
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
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/10.1021/NP50101A006
https://doi.org/10.1016/0031-9422(93)85128-E
Acteoside;Kusaginin;TJC160 354009 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/10.1016/0031-9422(93)85128-E
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/10.1021/NP50101A006
https://doi.org/10.1016/0031-9422(93)85128-E
> Phenylpropanoids and polyketides / Macrolides and analogues
(13S,14E,15S)-14-ethylidene-4-hydroxy-15-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,10,16,20-tetraoxatetracyclo[21.2.2.13,7.013,18]octacosa-1(25),3,5,7(28),17,23,26-heptaene-11,19-dione 21575882 Click to see CC=C1C2CC(=O)OCCC3=CC(=C(C=C3)O)OC4=CC=C(CCOC(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C=C4 628.60 unknown https://doi.org/10.1016/0031-9422(93)85128-E
(15R,16Z,17R)-16-ethylidene-4-hydroxy-15-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,10,14,20-tetraoxatetracyclo[21.2.2.13,7.012,17]octacosa-1(25),3,5,7(28),12,23,26-heptaene-11,19-dione 133556426 Click to see CC=C1C2CC(=O)OCCC3=CC=C(C=C3)OC4=C(C=CC(=C4)CCOC(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O 628.60 unknown https://doi.org/10.1021/NP50101A006

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