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Ulmus wallichiana

Ulmus wallichiana - 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 UUID64405a4e3a2fd417935614
Scientific name Ulmus wallichiana
Authority Planch.
First published in Ann. Sci. Nat., Bot. sér. 3, 10: 277. 1848 [Nov 1848]

Description Top

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Synonyms Top

Scientific name Authority First published in
Ulmus laevigata Royle Ill. Bot. Himal. Mts. : 341 (1839)
Ulmus villosa Brandis ex Gamble Man. Ind. Timb. , ed. 2: 628 (1902)
Ulmus wallichiana var. tomentosa Melville & Heybroek Kew Bull. 26: 10 (1971)

Common names Top

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Language Common/alternative name
English himalayan elm
Arabic دردار واليشياني
Russian Вяз Валлиха

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Ulmus wallichiana subsp. xanthoderma Melville & Heybroek Kew Bull. 26: 10 (1971)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001284765
Tropicos 50325030
KEW urn:lsid:ipni.org:names:856961-1
The Plant List tro-50325030
PFAF Ulmus wallichiana
Open Tree Of Life 5749177
NCBI Taxonomy 647291
IUCN Red List 30410
IPNI 837183-1
iNaturalist 444538
GBIF 7303567
Freebase /m/0chr6x
EPPO ULMWA
USDA GRIN 40862
Wikipedia Ulmus_wallichiana

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
Potential use of barks of woody vascular plants in bone mending: A review Joshi DD, Deb L, Somkuwar BG, Rana VS Saudi Pharm J 27-Jul-2023
PMCID:PMC10406872
doi:10.1016/j.jsps.2023.101714
PMID:37559869
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
Promising Therapeutic Treatments for Cardiac Fibrosis: Herbal Plants and Their Extracts Yu X Cardiol Ther 29-May-2023
PMCID:PMC10423196
doi:10.1007/s40119-023-00319-4
PMID:37247171
Exploring soil bacterial diversity in different micro-vegetational habitats of Dachigam National Park in North-western Himalaya Mushtaq H, Ganai BA, Jehangir A Sci Rep 22-Feb-2023
PMCID:PMC9947166
doi:10.1038/s41598-023-30187-w
PMID:36813837
Editorial: Ethnoveterinary practices in livestock: Animal production, healthcare, and livelihood development Rahman IU, Ijaz F, Bussmann RW Front Vet Sci 04-Jan-2023
PMCID:PMC9846765
doi:10.3389/fvets.2022.1086311
PMID:36686157
Bioactive Natural Products against Systemic Arterial Hypertension: A Past 20-Year Systematic and Prospective Review da Silva MG, Barbosa SL, Silva DS, Bezerra IB, Alves Bezerra É, Coelho AG, Pinheiro da Silva Morais IC, Rezende-Júnior LM, do Carmo IS, Lima-Neto JD, Comerma-Steffensen SG, Citó AM, Arcanjo DD Evid Based Complement Alternat Med 20-Jun-2022
PMCID:PMC9236778
doi:10.1155/2022/8499625
PMID:35769156
A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N Biology (Basel) 23-Mar-2022
PMCID:PMC9032642
doi:10.3390/biology11040491
PMID:35453691
Jeopardy of COVID-19: Rechecking the Perks of Phytotherapeutic Interventions Saha P, Bose S, Srivastava AK, Chaudhary AA, Lall R, Prasad S Molecules 10-Nov-2021
PMCID:PMC8621307
doi:10.3390/molecules26226783
PMID:34833873
Molecular Basis of Prostate Cancer and Natural Products as Potential Chemotherapeutic and Chemopreventive Agents Bai B, Chen Q, Jing R, He X, Wang H, Ban Y, Ye Q, Xu W, Zheng C Front Pharmacol 23-Sep-2021
PMCID:PMC8495205
doi:10.3389/fphar.2021.738235
PMID:34630112
De novo transcriptome assembly and EST-SSR markers development for Zelkova schneideriana Hand.-Mazz. (Ulmaceae) Wang L, Zhang R, Geng M, Qin Y, Liu H, Li L, Li M 3 Biotech 30-Aug-2021
PMCID:PMC8405759
doi:10.1007/s13205-021-02968-5
PMID:34603920
UHPLC-HRMS Analysis of Fagus sylvatica (Fagaceae) Leaves: A Renewable Source of Antioxidant Polyphenols Formato M, Piccolella S, Zidorn C, Pacifico S Antioxidants (Basel) 19-Jul-2021
PMCID:PMC8301150
doi:10.3390/antiox10071140
PMID:34356373
Biogeographic Overview of Ulmaceae: Diversity, Distribution, Ecological Preferences, and Conservation Status Fragnière Y, Song YG, Fazan L, Manchester SR, Garfì G, Kozlowski G Plants (Basel) 31-May-2021
PMCID:PMC8227750
doi:10.3390/plants10061111
PMID:34072896
An ethnopharmacological survey and comparative analysis of plants from the Sudhnoti District, Azad Jammu and Kashmir, Pakistan Khan MF, Mashwani ZU, Mehmood A, Qureshi R, Sarwar R, Ahmad KS, Quave CL J Ethnobiol Ethnomed 20-Mar-2021
PMCID:PMC7980561
doi:10.1186/s13002-021-00435-2
PMID:33743778
A comprehensive guide to the pharmacologic regulation of angiotensin converting enzyme 2 (ACE2), the SARS-CoV-2 entry receptor Oz M, Lorke DE, Kabbani N Pharmacol Ther 01-Dec-2020
PMCID:PMC7854082
doi:10.1016/j.pharmthera.2020.107750
PMID:33275999
Should ACE2 be given a chance in COVID-19 therapeutics: A semi-systematic review of strategies enhancing ACE2 Kaur U, Acharya K, Mondal R, Singh A, Saso L, Chakrabarti S, Chakrabarti SS Eur J Pharmacol 11-Sep-2020
PMCID:PMC7485553
doi:10.1016/j.ejphar.2020.173545
PMID:32926917

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
methyl 2,4,6-trihydroxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]benzoate 45269381 Click to see COC(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)CO)O)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
Methyl 2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]benzoate 56661005 Click to see COC(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)CO)O)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2S,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)chroman-4-one 44199474 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
(2S,3S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 44517759 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 21676320 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 14376479 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 56670810 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 44715644 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 6426860 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 24721625 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 56680918 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 56674291 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 23502664 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2009.06.074

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