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Populus suaveolens

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440368731f4b635740159
Scientific name Populus suaveolens
Authority Fisch.
First published in Allg. Gartenzeitung (Otto & Dietrich) 9(no. 51): 404. 1841 [18 Dec 1841]

Ethnobotanical Use Top

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General Uses Top

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Scientific and model-organism use:
Populus suaveolens is employed as a research organism in China for genetic diversity assessment, population structure analysis, and ecological studies of riparian and boreal poplars. It is included in local genetic and phenological databases, supporting species delimitation, conservation planning, and responses to environmental gradients (e.g., in Heilongjiang and Inner Mongolia). These applications rely on nuclear and chloroplast molecular markers, including RAPD, ISSR, and SSR, which have been validated in peer‑reviewed studies.

Synonyms Top

Scientific name Authority First published in
Populus ussuriensis Kom. Bot. Zhurn. S.S.S.R. 19: 510 (1934)
Populus maximowiczii Henry Gard. Chron. , ser. 3, 53: 198 (1913)
Populus maximowiczii var. barbinervis Nakai Fl. Sylv. Kor. 18: 201 1930
Populus suaveolens var. latifolia Gombócz Math. Term. Közlem. 30: 112 1908
Populus koreana Rehder J. Arnold Arbor. 3: 226 (1922)
Populus vetla R.I.Schröd. Russk. Ogorod , ed. 2: 573 (1881)
Populus balsamifera var. suaveolens (Fisch. ex Camuzet) Kuntze Revis. Gen. Pl. 2: 642. 1891 [5 Nov 1891]

Common names Top

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Language Common/alternative name
Arabic حور عطري
Azerbaijani Ətirli qovaq
Belarusian таполя пахучая
Bengali উত্তরী তেরেক
Danish sibirisk balsampoppel
Estonian lõhnav pappel
Finnish tuoksupoppeli
Icelandic rússaösp
Russian тополь душистый
Russian Тополь байкальский
Chinese 甜杨
Chinese 西伯利亚白杨

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000928194
Tropicos 28300008
KEW urn:lsid:ipni.org:names:77155538-1
The Plant List kew-5000204
PaleoBotany 116675
Open Tree Of Life 951072
Observations.org 146165
NCBI Taxonomy 245546
IUCN Red List 147371325
IPNI 776871-1
iNaturalist 824442
GBIF 3805205
EPPO POPSU
EOL 2872002
Elurikkus 6501
USDA GRIN 29416
Wikipedia Populus_suaveolens
CMAUP NPO22941
Plantarium 29732

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
Advances in the Study of the Transcriptional Regulation Mechanism of Plant miRNAs Teng C, Zhang C, Guo F, Song L, Fang Y Life (Basel) 15-Sep-2023
PMCID:PMC10533097
doi:10.3390/life13091917
PMID:37763320
Characterization of a Novel Superoxide Dismutase from a Deep-sea Sea Cucumber (Psychoropotes verruciaudatus) Li Y, Chen Z, Zhang P, Gao F, Wang J, Lin L, Zhang H Antioxidants (Basel) 07-Jun-2023
PMCID:PMC10295708
doi:10.3390/antiox12061227
PMID:37371957
Botanical Origins and Antioxidant Activities of Two Types of Flavonoid-Rich Poplar-Type Propolis Qiao J, Wang Y, Zhang Y, Kong L, Zhang H Foods 07-Jun-2023
PMCID:PMC10297319
doi:10.3390/foods12122304
PMID:37372514
Response of wild rodents to red fox feces: implication for the echinococcus infection SASAKI R, OKUMA I, ASARI Y J Vet Med Sci 29-Mar-2023
PMCID:PMC10209468
doi:10.1292/jvms.22-0395
PMID:36990791
ZmG6PDH1 in glucose-6-phosphate dehydrogenase family enhances cold stress tolerance in maize Li X, Cai Q, Yu T, Li S, Li S, Li Y, Sun Y, Ren H, Zhang J, Zhao Y, Zhang J, Zuo Y Front Plant Sci 09-Mar-2023
PMCID:PMC10034328
doi:10.3389/fpls.2023.1116237
PMID:36968417
Ecological and Geographical Structure of the Plant Cover of the East Asian Boreal–Nemoral Ecotone (the Lower Amur Region, Far East Russia) Kryukova MV Plants (Basel) 30-Jan-2023
PMCID:PMC9919551
doi:10.3390/plants12030615
PMID:36771699
Effects of Wood-Derived Biochar on Germination, Physiology, and Growth of European Beech (Fagus sylvatica L.) and Turkey Oak (Quercus cerris L.) Vannini A, Carbognani M, Chiari G, Forte TG, Lumiero F, Malcevschi A, Rodolfi M, Ganino T, Petraglia A Plants (Basel) 26-Nov-2022
PMCID:PMC9741182
doi:10.3390/plants11233254
PMID:36501294
Steering restoration of coal mining degraded ecosystem to achieve sustainable development goal-13 (climate action): United Nations decade of ecosystem restoration (2021–2030) Bandyopadhyay S, Maiti SK Environ Sci Pollut Res Int 03-Nov-2022
PMCID:PMC9630816
doi:10.1007/s11356-022-23699-x
PMID:36327066
Cold adaptation strategies in plants—An emerging role of epigenetics and antifreeze proteins to engineer cold resilient plants Satyakam, Zinta G, Singh RK, Kumar R Front Genet 25-Aug-2022
PMCID:PMC9459425
doi:10.3389/fgene.2022.909007
PMID:36092945
Genera of phytopathogenic fungi: GOPHY 4 Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW Stud Mycol 02-Jun-2022
PMCID:PMC9365048
doi:10.3114/sim.2022.101.06
PMID:36059898
Allocation Strategies of Carbon, Nitrogen, and Phosphorus at Species and Community Levels With Recovery After Wildfire Song Z, Wang X, Liu Y, Luo Y, Li Z Front Plant Sci 11-Apr-2022
PMCID:PMC9037545
doi:10.3389/fpls.2022.850353
PMID:35481138
Phylogenomics and Biogeography of Populus Based on Comprehensive Sampling Reveal Deep-Level Relationships and Multiple Intercontinental Dispersals Wang Y, Huang J, Li E, Xu S, Zhan Z, Zhang X, Yang Z, Guo F, Liu K, Liu D, Shen X, Shang C, Zhang Z Front Plant Sci 04-Feb-2022
PMCID:PMC8855119
doi:10.3389/fpls.2022.813177
PMID:35185985
Frequent ploidy changes in Salicaceae indicates widespread sharing of the salicoid whole genome duplication by the relatives of Populus L. and Salix L. Zhang ZS, Zeng QY, Liu YJ BMC Plant Biol 13-Nov-2021
PMCID:PMC8590345
doi:10.1186/s12870-021-03313-x
PMID:34773988
Saussurea involucrata (Snow Lotus) ICE1 and ICE2 Orthologues Involved in Regulating Cold Stress Tolerance in Transgenic Arabidopsis Wu CL, Lin LF, Hsu HC, Huang LF, Hsiao CD, Chou ML Int J Mol Sci 07-Oct-2021
PMCID:PMC8509503
doi:10.3390/ijms221910850
PMID:34639192
MicroRNAs in Woody Plants Fang L, Wang Y Front Plant Sci 31-Aug-2021
PMCID:PMC8438446
doi:10.3389/fpls.2021.686831
PMID:34531880

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
(2S,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 6931410 Click to see 286.28 unknown via CMAUP database
Salireposide 117440 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1515/ZNC-1992-3-424
> 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-1992-3-424
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see 272.25 unknown https://doi.org/10.1515/ZNC-1992-3-424
Pinobanksin 3-acetate 148556 Click to see 314.29 unknown https://doi.org/10.1515/ZNC-1992-3-424
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1515/ZNC-1992-3-424
> 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-1992-3-424
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1515/ZNC-1992-3-424
Rhamnocitrin 5320946 Click to see 300.26 unknown https://doi.org/10.1515/ZNC-1992-3-424
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=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 / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Isosakuranetin 160481 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O 286.28 unknown https://doi.org/10.1515/ZNC-1992-3-424
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1515/ZNC-1992-3-424
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',4,4',6'-Tetrahydroxychalcone 5280960 Click to see 272.25 unknown https://doi.org/10.1515/ZNC-1992-3-424
2',6'-Dihydroxy-4'-methoxychalcone 5316793 Click to see 270.28 unknown https://doi.org/10.1515/ZNC-1992-3-424
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-1992-3-424

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