Ulmus thomasii - Unknown
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Internal ID UUID643ffa321f98c109440454
Scientific name Ulmus thomasii
Authority Sarg.
First published in Silva (Sargent) 14: 102. 1902

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Synonyms Top

Scientific name Authority First published in
Ulmus racemosa D.Thomas Amer. J. Sci. Arts 19: 170. 1831

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Language Common/alternative name
English cork elm
English rock elm
Arabic دردار توماسي
German felsenulme
German ulmus racemosa
German felsen-ulme
Persian اولموس توماسی (نارون چوبپنبه)
Russian Вяз Томаса
Turkish mantar karaağacı
Ukrainian В'яз скельний

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000416829
Canadensys 9431
USDA Plants ULTH
Tropicos 33300073
KEW urn:lsid:ipni.org:names:300247-2
The Plant List kew-2448843
PFAF Ulmus thomasii
Open Tree Of Life 136509
NCBI Taxonomy 180953
NBN Atlas NBNSYS0000042217
Nature Serve 2.141424
IUCN Red List 61967392
IPNI 294727-2
iNaturalist 54861
GBIF 5361875
Freebase /m/0681nz
WisFlora 5301
EPPO ULMTH
EOL 594776
USDA GRIN 101705
Wikipedia Ulmus_thomasii

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Recent Strategies and Tactics for the Enantioselective Total Syntheses of Cyclolignan Natural Products Reynolds RG, Nguyen HQ, Reddel JC, Thomson RJ Nat Prod Rep 23-Mar-2022
PMCID:PMC8957534
doi:10.1039/d1np00057h
PMID:34664594
Fusarium: more than a node or a foot-shaped basal cell Crous PW, Lombard L, Sandoval-Denis M, Seifert KA, Schroers HJ, Chaverri P, Gené J, Guarro J, Hirooka Y, Bensch K, Kema GH, Lamprecht SC, Cai L, Rossman AY, Stadler M, Summerbell RC, Taylor JW, Ploch S, Visagie CM, Yilmaz N, Frisvad JC, Abdel-Azeem AM, Abdollahzadeh J, Abdolrasouli A, Akulov A, Alberts JF, Araújo JP, Ariyawansa HA, Bakhshi M, Bendiksby M, Ben Hadj Amor A, Bezerra JD, Boekhout T, Câmara MP, Carbia M, Cardinali G, Castañeda-Ruiz RF, Celis A, Chaturvedi V, Collemare J, Croll D, Damm U, Decock CA, de Vries RP, Ezekiel CN, Fan XL, Fernández NB, Gaya E, González CD, Gramaje D, Groenewald JZ, Grube M, Guevara-Suarez M, Gupta VK, Guarnaccia V, Haddaji A, Hagen F, Haelewaters D, Hansen K, Hashimoto A, Hernández-Restrepo M, Houbraken J, Hubka V, Hyde KD, Iturriaga T, Jeewon R, Johnston PR, Jurjević Ž, Karalti İ, Korsten L, Kuramae EE, Kušan I, Labuda R, Lawrence DP, Lee HB, Lechat C, Li HY, Litovka YA, Maharachchikumbura SS, Marin-Felix Y, Matio Kemkuignou B, Matočec N, McTaggart AR, Mlčoch P, Mugnai L, Nakashima C, Nilsson RH, Noumeur SR, Pavlov IN, Peralta MP, Phillips AJ, Pitt JI, Polizzi G, Quaedvlieg W, Rajeshkumar KC, Restrepo S, Rhaiem A, Robert J, Robert V, Rodrigues AM, Salgado-Salazar C, Samson RA, Santos AC, Shivas RG, Souza-Motta CM, Sun GY, Swart WJ, Szoke S, Tan YP, Taylor JE, Taylor PW, Tiago PV, Váczy KZ, van de Wiele N, van der Merwe NA, Verkley GJ, Vieira WA, Vizzini A, Weir BS, Wijayawardene NN, Xia JW, Yáñez-Morales MJ, Yurkov A, Zamora JC, Zare R, Zhang CL, Thines M Stud Mycol 17-Aug-2021
PMCID:PMC8379525
doi:10.1016/j.simyco.2021.100116
PMID:34466168
Utilizing the density of inventory samples to define a hybrid lattice for species distribution models: DISTRIB‐II for 135 eastern U.S. trees Peters MP, Iverson LR, Prasad AM, Matthews SN Ecol Evol 17-Jul-2019
PMCID:PMC6686326
doi:10.1002/ece3.5445
PMID:31410287
Learning from history, predicting the future: the UK Dutch elm disease outbreak in relation to contemporary tree disease threats Potter C, Harwood T, Knight J, Tomlinson I Philos Trans R Soc Lond B Biol Sci 12-Jul-2011
PMCID:PMC3130388
doi:10.1098/rstb.2010.0395
PMID:21624917
Asymmetric Biomimetic Oxidations of Phenols: The Mechanism of the Diastereo- and Enantioselective Synthesis of Thomasidioic Acid Zoia L, Bruschi M, Orlandi M, Tolppa EL, Rindone B Molecules 23-Jan-2008
PMCID:PMC6245400
doi:10.3390/molecules13010129
PMID:18259136
Lignans of Ulmus thomasii heartwood—I M.K. Seikel, F.D. Hostettler, D.B. Johnson Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(68)88100-1
Rapid determination of free tryptophan in plant samples by gas chromatography-selected ion monitoring mass spectrometry Lech Michalczuk, Krystyna Bialek, Jerry D. Cohen Elsevier BV 25-Jul-2002
doi:10.1016/0021-9673(92)85021-K
Lignans of Ulmus thomasii heartwood. II. Lignans related to thomasic acid. Hostettler FD, Seikel MK Tetrahedron 01-Jan-1970
doi:10.1016/S0040-4020(01)82782-4
PMID:5796577

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
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
2-Naphthalenecarboxylic acid, 6-hydroxy-5,7-dimethoxy- 10857810 Click to see COC1=C(C(=C2C=CC(=CC2=C1)C(=O)O)OC)O 248.23 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1S,2R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid 44384523 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)O)C(=O)O 446.40 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
(3R,4S)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid 92168875 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)O)CO 432.40 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
(3S,4S)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid 92168874 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)O)CO 432.40 unknown https://doi.org/10.1016/0040-4020(68)88100-1
6-Hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid 266966 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)O)CO 432.40 unknown https://doi.org/10.1016/0040-4020(68)88100-1
https://doi.org/10.1016/S0040-4020(01)82782-4
7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid 12444312 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)O)C(=O)O 446.40 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Lyoniresinol 9888378 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
[(2S,3S,4R)-3-(hydroxymethyl)-5,6,7-trimethoxy-4-(3,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydronaphthalen-2-yl]methanol 163190193 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC(=C(C(=C23)OC)OC)OC)CO)CO 448.50 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
[3-(Hydroxymethyl)-5,6,7-trimethoxy-4-(3,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydronaphthalen-2-yl]methanol 72773069 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC(=C(C(=C23)OC)OC)OC)CO)CO 448.50 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1016/S0040-4020(01)82782-4
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/0021-9673(92)85021-K

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