PlantaeDB Logo
Login Sign-up

Ulmus davidiana

Ulmus davidiana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

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

Add a new one! Suggest a correction!

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

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Ulmus davidiana var. japonica (Rehder) Nakai Fl. Sylv. Kor. 19: 26 (1932)

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
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
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
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
Discovery and optimized extraction of the anti-osteoclastic agent epicatechin-7-O-β-D-apiofuranoside from Ulmus macrocarpa Hance bark Jeong C, Cho YJ, Lee Y, Wang W, Park KH, Roh E, Lee CH, Son YJ, Park JH, Kang H, Lee KW Sci Rep 09-Jul-2023
PMCID:PMC10330169
doi:10.1038/s41598-023-38208-4
PMID:37423923
Commodity risk assessment of Acer palmatum 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:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Commodity risk assessment of Acer platanoides 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:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
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
Commodity risk assessment of Acer pseudoplatanus 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:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
A glimpse into the foraging and movement behaviour of Nyctalus aviator; a complementary study by acoustic recording and GPS tracking Niga Y, Fujioka E, Heim O, Nomi A, Fukui D, Hiryu S R Soc Open Sci 28-Jun-2023
PMCID:PMC10300664
doi:10.1098/rsos.230035
PMID:37388314

Phytochemical Profile Top

Add a new one!
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
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
Friedelinol 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
> 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
Acernikol 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

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.