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Populus yunnanensis

Populus yunnanensis - 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 UUID64404da29ad32435507457
Scientific name Populus yunnanensis
Authority Dode
First published in Bull. Soc. Hist. Nat. Autun 18: 221. 1905

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
English yunnan poplar
Arabic حور يوناني
Russian Тополь юнаньский
Turkish yunnan kavağı
udm Юньнаньысь тополь
Chinese 滇杨
Chinese 云南白杨
Chinese 滇楊

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Populus yunnanensis var. microphylla Z.Wang & S.L.Tung Bull. Bot. Res., Harbin 2(2): 115. 1982
Populus yunnanensis var. pedicellata Z.Wang & S.L.Tung Bull. Bot. Res., Harbin 2(2): 115. 1982

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001133818
Tropicos 28300982
INPN 115182
KEW urn:lsid:ipni.org:names:776932-1
The Plant List tro-28300982
Open Tree Of Life 247373
NCBI Taxonomy 242124
NBN Atlas NBNSYS0000042172
IPNI 776932-1
iNaturalist 405191
GBIF 7266406
EPPO POPYU
EOL 2872015
USDA GRIN 29432
Wikipedia Populus_yunnanensis
CMAUP NPO13743

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_044906095.1 ASM4490609v1 Chromosome Southwest Forestry University 2024-11-19 150.2x 419.73 Mb

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
Genome-wide identification and expression analysis of ARF gene family in embryonic development of Korean pine (Pinus koraiensis) Zhang Y, Wu W, Shen H, Yang L BMC Plant Biol 10-Apr-2024
PMCID:PMC11005186
doi:10.1186/s12870-024-04827-w
PMID:38600459
Characterization of the complete chloroplast genome of ‘Quanhong poplar’ (Populus deltoides W. Bartram ex Humphry Marshall, 2011) Zhuang W, Li Y, Shu X, Wang Z, Wang Y, Wang T Mitochondrial DNA B Resour 23-Feb-2024
PMCID:PMC10896124
doi:10.1080/23802359.2024.2318391
PMID:38410200
Synergistic interactions of assorted ameliorating agents to enhance the potential of heavy metal phytoremediation Sanjana S, Jazeel K, Janeeshma E, Nair SG, Shackira AM Stress Biol 16-Feb-2024
PMCID:PMC10873264
doi:10.1007/s44154-024-00153-1
PMID:38363436
Genome-Wide Identification, Expression Analysis, and Subcellular Localization of DET2 Gene Family in Populus yunnanensis Qiao Z, Li J, Zhang X, Guo H, He C, Zong D Genes (Basel) 23-Jan-2024
PMCID:PMC10888042
doi:10.3390/genes15020148
PMID:38397138
Advances in the Involvement of Metals and Metalloids in Plant Defense Response to External Stress Zhang L, Liu Z, Song Y, Sui J, Hua X Plants (Basel) 20-Jan-2024
PMCID:PMC10820295
doi:10.3390/plants13020313
PMID:38276769
Genome-Wide Analysis of the Universal Stress Protein Gene Family in Blueberry and Their Transcriptional Responses to UV-B Irradiation and Abscisic Acid Song Y, Ma B, Feng X, Guo Q, Zhou L, Zhang X, Zhang C Int J Mol Sci 27-Nov-2023
PMCID:PMC10706445
doi:10.3390/ijms242316819
PMID:38069138
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Increased Tolerance of Massion’s pine to Multiple-Toxic-Metal Stress Mediated by Ectomycorrhizal Fungi Zhang T, Zhang P, Pang W, Zhang Y, Alwathnani HA, Rensing C, Yang W Plants (Basel) 05-Sep-2023
PMCID:PMC10535352
doi:10.3390/plants12183179
PMID:37765343
Function and Characteristic Analysis of Candidate PEAR Proteins in Populus yunnanensis Li P, Wang J, Jiang D, Yu A, Sun R, Liu A Int J Mol Sci 23-Aug-2023
PMCID:PMC10488302
doi:10.3390/ijms241713101
PMID:37685908
The Role of Lignin in the Compartmentalization of Cadmium in Maize Roots Is Enhanced by Mycorrhiza Lao R, Guo Y, Hao W, Fang W, Li H, Zhao Z, Li T J Fungi (Basel) 15-Aug-2023
PMCID:PMC10455880
doi:10.3390/jof9080852
PMID:37623623
Plant sex influences on riparian communities and ecosystems Scheuerell RP, LeRoy CJ Ecol Evol 12-Jul-2023
PMCID:PMC10337289
doi:10.1002/ece3.10308
PMID:37449021
Fungal Selectivity and Biodegradation Effects by White and Brown Rot Fungi for Wood Biomass Pretreatment Qi J, Li F, Jia L, Zhang X, Deng S, Luo B, Zhou Y, Fan M, Xia Y Polymers (Basel) 20-Apr-2023
PMCID:PMC10144154
doi:10.3390/polym15081957
PMID:37112109
Advances in the Research on Plant WRKY Transcription Factors Responsive to External Stresses Wang H, Cheng X, Yin D, Chen D, Luo C, Liu H, Huang C Curr Issues Mol Biol 01-Apr-2023
PMCID:PMC10136515
doi:10.3390/cimb45040187
PMID:37185711
Effects of vegetation restoration on distribution characteristics of heavy metals in soil in Karst plateau area of Guizhou Wu Y, Tian X, Wang R, Zhang M, Wang S PeerJ 17-Mar-2023
PMCID:PMC10026723
doi:10.7717/peerj.15044
PMID:36949760
Molecular responses to salinity stress in Salix matsudana (Koidz) females and males Liu G, Wang Y, Lian B, Ma Z, Xiang X, Wu J, Luo C, Ma D, Chen Y, Yu C, Zhong F, Wei H, Zhang J Front Plant Sci 27-Jan-2023
PMCID:PMC9911873
doi:10.3389/fpls.2023.1122197
PMID:36778681

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 7163172 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(b1-2b)Fruf 44420456 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown via CMAUP database
Stachyose 439531 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O 666.60 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-[(E)-3-(beta-D-glucopyranosyloxy)-1-propenyl]-7-methoxy-2,3-dihydrobenzofuran-3beta-methanol 11027727 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O 520.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5320625 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 478.40 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 110062419 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown via CMAUP database
Calceolarioside B 5273567 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown via CMAUP database
Hellicoside 5281778 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(OC(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)OCC(C4=CC(=C(C=C4)O)O)O)CO)O)O 656.60 unknown via CMAUP database
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Isomartynoside 91895373 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown via CMAUP database
Leucosceptoside A 10394343 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown via CMAUP database
Martynoside 5319292 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown via CMAUP database
Plantainoside B 9847922 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 478.40 unknown via CMAUP database
Plantamajoside 5281788 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 640.60 unknown via CMAUP database
Plantasioside 44423103 Click to see C1C(OC2C(C(C(OC2O1)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)C4=CC(=C(C=C4)O)O 476.40 unknown via CMAUP database
Sanangoside 6915840 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 478.40 unknown via CMAUP database
Scroside B 9831187 Click to see COC1=C(C=C(C=C1)CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 668.60 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNC-1992-0624
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1515/ZNC-1992-0624
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1515/ZNC-1992-0624
Prenylcaffeic acid 129723082 Click to see CC(=CCC(=CC1=CC(=C(C=C1)O)O)C(=O)O)C 248.27 unknown https://doi.org/10.1515/ZNC-1992-0624
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1515/ZNC-1992-0624
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3-O-Acetylpinobanksin 148556 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 314.29 unknown https://doi.org/10.1515/ZNC-1992-0624
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown https://doi.org/10.1515/ZNC-1992-0624
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1515/ZNC-1992-0624
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1515/ZNC-1992-0624
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Plantagoside 174157 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)chromen-4-one 101756416 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(00)85159-6
5,7-Dihydroxy-3-[5-hydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)chromen-4-one 74978014 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(00)85159-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown via CMAUP database
Plantaginin 5320623 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Pinocembrin chalcone 6474295 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown https://doi.org/10.1515/ZNC-1992-0624

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