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Ulmus davidiana

Ulmus davidiana - 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 UUID64404f61a7b78719936532
Scientific name Ulmus davidiana
Authority Planch.
First published in Prodr. 17: 158 (1873)

Description Top

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Ulmus davidiana, also known as the David elm, is a small deciduous tree found in China, Mongolia, Korea, Siberia, and Japan. It was first described in 1873 and has two recognized varieties. The tree is similar to the American elm in appearance, but smaller. It has a good resistance to Dutch elm disease and other pests and diseases. However, it is not commonly cultivated in the West due to its specific growing conditions. The tree has shown potential in American testing and has been named after Father Armand David, a French missionary and naturalist. It can be found in various botanical gardens and arboretums in North America and Europe.

Synonyms Top

Scientific name Authority First published in
Ulmus davidiana var. pubescens Skvortsov Manch. Monit. 52–58 1929
Ulmus davidiana var. mandshurica Skvortsov Manch. Monit. 52–58 1929

Common names Top

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Language Common/alternative name
English japanese elm
Arabic دردار دوادياني
Korean 당느릅나무
Chinese 翼枝榆
Chinese 黑榆
Chinese 东北黑榆
Chinese 山毛榆
Chinese 热河榆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Ulmus davidiana var. japonica (Rehder) Nakai Fl. Sylv. Kor. 19: 26 (1932)

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Buryatiya
      • Chita

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001143139
UNII 0962281PBS
USDA Plants ULDA
Tropicos 33300012
KEW urn:lsid:ipni.org:names:856844-1
The Plant List tro-33300012
PFAF Ulmus davidiana
Open Tree Of Life 4729838
Observations.org 514322
NCBI Taxonomy 1297873
IUCN Red List 135925802
IPNI 856844-1
iNaturalist 448047
GBIF 7141651
Freebase /m/0ff4d8
EPPO ULMDA
EOL 2864777
Elurikkus 8063
USDA GRIN 40827
Wikipedia Ulmus_davidiana

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
Taxonomy and Phylogeny of the Aphid Genus Nippolachnus Matsumura, 1917, with Synonymy of the Mysterious Neonippolachnus Shinji, 1924 (Hemiptera: Aphididae: Lachninae) Kanturski M, Lee M, Koszela K, Lee S Insects 08-Mar-2024
PMCID:PMC10971630
doi:10.3390/insects15030182
PMID:38535377
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Enhancing hamburger shelf life and quality using gallic acid encapsulated in gelatin/tragacanth gum complex coacervate Asghari-Varzaneh E, Sharifian-Mobarakeh S, Shekarchizadeh H Heliyon 18-Jan-2024
PMCID:PMC10830573
doi:10.1016/j.heliyon.2024.e24917
PMID:38304846
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
The role of symbiotic fungi in the life cycle of Gastrodia elata Blume (Orchidaceae): a comprehensive review Liu JJ, Yang XQ, Li ZY, Miao JY, Li SB, Zhang WP, Lin YC, Lin LB Front Plant Sci 08-Jan-2024
PMCID:PMC10804856
doi:10.3389/fpls.2023.1309038
PMID:38264031
Bakuchiol, a natural constituent and its pharmacological benefits Nizam NN, Mahmud S, Ark SM, Kamruzzaman M, Hasan MK F1000Res 07-Nov-2023
PMCID:PMC10683784
doi:10.12688/f1000research.129072.1
PMID:38021404
Natural Antimicrobials: A Reservoir to Contrast Listeria monocytogenes Ricci A, Lazzi C, Bernini V Microorganisms 15-Oct-2023
PMCID:PMC10609241
doi:10.3390/microorganisms11102568
PMID:37894226
Editorial: Advances in the research of diabetic retinopathy, volume II Nawaz MI Front Endocrinol (Lausanne) 08-Sep-2023
PMCID:PMC10516549
doi:10.3389/fendo.2023.1281490
PMID:37745717
Dyeing Performance and Anti-Superbacterial Activity of Cotton Fabrics Dyed with Chamaecyparis obtusa Choi NY, Park BI Molecules 07-Sep-2023
PMCID:PMC10537297
doi:10.3390/molecules28186497
PMID:37764272
Different responses of soil fungal and bacterial communities to nitrogen addition in a forest grassland ecotone Li D, Meng M, Ren B, Ma X, Bai L, Li J, Bai G, Yao F, Tan C Front Microbiol 06-Sep-2023
PMCID:PMC10510407
doi:10.3389/fmicb.2023.1211768
PMID:37736095
Effects of nitrogen addition on species composition and diversity of early spring herbs in a Korean pine plantation Yang G, Zhang M, Jin G Ecol Evol 05-Sep-2023
PMCID:PMC10480043
doi:10.1002/ece3.10498
PMID:37674646
Development of a new chromatographic method for the determination of bakuchiol in cosmetic products Kurpet K, Chwatko G Sci Rep 24-Aug-2023
PMCID:PMC10449805
doi:10.1038/s41598-023-41076-7
PMID:37620384
Evaluation of How Methacrylate Gelatin Hydrogel Loaded with Ximenia americana L. Extract (Steam Bark) Effects Bone Repair Activity Using Rats as Models Leal SS, Gusmão GO, Uchôa VT, Figueiredo-Silva J, Pinto LS, Tim CR, Assis L, Maia-Filho AL, de Oliveira RA, Lobo AO, Pavinatto A J Funct Biomater 23-Aug-2023
PMCID:PMC10531560
doi:10.3390/jfb14090438
PMID:37754851
Stoichiometry of carbon, nitrogen, and phosphorus released from the leaf litter of various temperate tree species Ho P, Nakajima S, Urabe J Ecol Evol 25-Jul-2023
PMCID:PMC10368945
doi:10.1002/ece3.10372
PMID:37502305
Anthropological significance of Tilia trees in Japan Janowski D Ecol Evol 12-Jul-2023
PMCID:PMC10338748
doi:10.1002/ece3.10303
PMID:37456068

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 / Naphthalenes / Naphthalenecarboxylic acids and derivatives
Methyl 4,12-dimethyl-10,11-dioxo-2-oxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,8-pentaene-8-carboxylate 10493278 Click to see CC1=COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C(=O)OC)C 284.26 unknown https://doi.org/10.1016/0031-9422(96)00279-8
> Benzenoids / Naphthalenes / Naphthoquinones
(4R)-4-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8-tetraene-10,11-dione 162945151 Click to see CC1=C2C3=C(C=C1)C(COC3=C(C(=O)C2=O)C)(C)O 258.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
(4R)-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8-tetraene-10,11-dione 139071911 Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C 242.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
(4S)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione 73353443 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C 258.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
4-(Hydroxymethyl)-8,12-dimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,8-pentaene-10,11-dione 10355035 Click to see CC1=C2C3=C(C=C1)C(=COC3=C(C(=O)C2=O)C)CO 256.25 unknown https://doi.org/10.1016/0031-9422(96)00279-8
4-Hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8-tetraene-10,11-dione 44393718 Click to see CC1=C2C3=C(C=C1)C(COC3=C(C(=O)C2=O)C)(C)O 258.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
8-(Dimethoxymethyl)-4,12-dimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,8-pentaene-10,11-dione 10266796 Click to see CC1=COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C(OC)OC)C 300.30 unknown https://doi.org/10.1016/0031-9422(96)00279-8
Mansonone E 94303 Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C 242.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
Mansonone F 94304 Click to see CC1=C2C3=C(C=C1)C(=COC3=C(C(=O)C2=O)C)C 240.25 unknown https://doi.org/10.1016/0031-9422(96)00279-8
Mansonone H 615515 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C 258.27 unknown https://doi.org/10.1016/0031-9422(96)00279-8
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1007/BF02978256
Nudiposide 14521040 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1007/BF02978256
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6bR,8aR,12aR,14aS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 5317077 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/S12272-010-0903-0
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1007/S12272-010-0903-0
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1007/S12272-010-0903-0
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/S12272-010-0903-0
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1088324
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S12272-010-0903-0
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S12272-010-0903-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
1-(4-hydroxy-3-methoxyphenyl)-2-[4-[(2R,3R)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenoxy]propane-1,3-diol 11146323 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)CCCO 586.60 unknown https://doi.org/10.1055/S-0028-1088324
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S12272-010-0903-0
(2R,3S)-5-[(2S,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,7-diol 163103721 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(CO3)(CO)O)O)C4=CC(=C(C=C4)O)O)O 422.40 unknown https://doi.org/10.1007/BF02855558
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S12272-010-0903-0
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF02855558
https://doi.org/10.1055/S-0028-1088324
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(+)-catechin 7-O-beta-D-xyloside 73533 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)O)O 422.40 unknown https://doi.org/10.1055/S-0028-1088324
Catechin-7-O-glucoside 44257085 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1055/S-0028-1088324

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