Populus balsamifera is a fast-growing, hardy tree species native to North America. It is known for its strong, sweet fragrance, which emanates from its sticky, resinous buds. The light, soft wood of the tree is used for pulp and construction, and its resinous sap is used as a hive disinfectant by bees. The tree is also a source of food for various animals, and its buds are used in traditional medicines.

Synonyms Top

Scientific name	Authority	First published in
Populus tacamahacca	Mill.	Gard. Dict. ed. 8 : 6 (1768)
Populus latifolia	Moench	Methodus : 338 (1794)
Aigiros balsamifera	Lunell	Amer. Midl. Naturalist 4: 298 (1916)

Common names Top

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Filter by language:

Language	Common/alternative name
English	ontario balsam poplar
English	balsam poplar
Arabic	حور بلسمي
Azerbaijani	balzam qovağı
azb	بالزام قوْواغی
Belarusian	Таполя бальзамічная
Bulgarian	балсамова топола
Czech	topol balzámový
Welsh	poplysen falmaidd y dwyrain
German	balsam-pappel
Estonian	palsamipappel
Finnish	palsamipoppeli
Hebrew	צפצפה בלסמית
Upper Sorbian	wonjaty topoł
Armenian	բարդի խոշորոտերև
Armenian	Բարդի բալասանաբեր
Icelandic	balsamösp
Lithuanian	balzaminė tuopa
Latvian	balzāma papele
Norwegian Bokmål	balsampoppel
Dutch	ontariopopulier
Polish	topola balsamiczna
Russian	Тополь бальзамический
Swedish	balsampoppel
Turkish	balsam kavağı
udm	Бальзамической тополь
Ukrainian	Тополя бальзамічна
Chinese	欧洲大叶杨
Chinese	香脂杨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Middle Asia
  - Kazakhstan
- Russian Far East
  - Magadan

Europe click to expand
- Eastern Europe
  - East European Russia
- Middle Europe
  - Belgium
  - Poland
- Southwestern Europe
  - France

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New York
  - Ohio
  - Pennsylvania
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Montana
  - Wyoming
- Southeastern U.S.A.
  - Delaware
  - Kentucky
  - Maryland
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Nunavut
  - Yukon
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Southern America click to expand
- Western South America
  - Ecuador

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000928157
UNII	D667V81N7U
Canadensys	9044
USDA Plants	POBA2
Tropicos	28300003
INPN	115113
Flora of Italy	8584
KEW	urn:lsid:ipni.org:names:776600-1
The Plant List	kew-5000130
Open Tree Of Life	374288
Observations.org	7231
NCBI Taxonomy	73824
NBN Atlas	NBNSYS0000033571
Nature Serve	2.139406
IUCN Red List	61959749
IPNI	776600-1
iNaturalist	54838
GBIF	3040184
Freebase	/m/02rb7lf
WisFlora	13230
EPPO	POPBA
EOL	584254
Elurikkus	6484
USDA GRIN	29365
Wikipedia	Populus_balsamifera
CMAUP	NPO21410

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

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

Positive selection and relaxed purifying selection contribute to rapid evolution of male-biased genes in a dioecious flowering plant

Zhao L, Zhou W, He J, Li DZ, Li HT

eLife

14-Feb-2024

PMCID:	PMC10942601
doi:	10.7554/eLife.89941
PMID:	38353667

Invasive earthworms shift soil microbial community structure in northern North American forest ecosystems

Ferlian O, Goldmann K, Bonkowski M, Dumack K, Wubet T, Eisenhauer N

iScience

12-Jan-2024

PMCID:	PMC10844042
doi:	10.1016/j.isci.2024.108889
PMID:	38322986

Lake Superior's summer cooling of shorelines and adjacent inland forests: Implications for refugia of boreal forests and disjunct arctic–alpine plants

Hillman A, Nielsen SE

Ecol Evol

28-Dec-2023

PMCID:	PMC10753639
doi:	10.1002/ece3.10833
PMID:	38155816

Domains of scale in cumulative effects of energy sector development on boreal birds

Crosby AD, Leston L, Bayne EM, Sólymos P, Mahon CL, Toms JD, Docherty TD, Song SJ

Landsc Ecol

25-Oct-2023

PMCID:	PMC10754738
doi:	10.1007/s10980-023-01779-8
PMID:	38161780

Admixture mapping and selection scans identify genomic regions associated with stomatal patterning and disease resistance in hybrid poplars

Fetter KC, Keller SR

Ecol Evol

24-Oct-2023

PMCID:	PMC10597741
doi:	10.1002/ece3.10579
PMID:	37881228

Effects of maize resistance and leaf chemical substances on the structure of phyllosphere fungal communities

Luo K, Zhao G, Chen M, Tian X

Front Plant Sci

14-Aug-2023

PMCID:	PMC10461017
doi:	10.3389/fpls.2023.1241055
PMID:	37645458

Composition and Biological Activity of the Essential Oils from Wild Horsemint, Yarrow, and Yampah from Subalpine Meadows in Southwestern Montana: Immunomodulatory Activity of Dillapiole

Schepetkin IA, Özek G, Özek T, Kirpotina LN, Klein RA, Khlebnikov AI, Quinn MT

Plants (Basel)

14-Jul-2023

PMCID:	PMC10383985
doi:	10.3390/plants12142643
PMID:	37514257

GWAS identifies candidate genes controlling adventitious rooting in Populus trichocarpa

Nagle MF, Yuan J, Kaur D, Ma C, Peremyslova E, Jiang Y, Zahl B, Niño de Rivera A, Muchero W, Fuxin L, Strauss SH

Hortic Res

14-Jun-2023

PMCID:	PMC10407606
doi:	10.1093/hr/uhad125
PMID:	37560019

Habitat and climatic associations of climate‐sensitive species along a southern range boundary

Wilson EC, Cousins S, Etter DR, Humphreys JM, Roloff GJ, Carter NH

Ecol Evol

17-May-2023

PMCID:	PMC10191803
doi:	10.1002/ece3.10083
PMID:	37214615

Metabolome analysis reveals flavonoid changes during the leaf color transition in Populus × euramericana ‘Zhonghuahongye’

Chen M, Chang C, Li H, Huang L, Zhou Z, Zhu J, Liu D

Front Plant Sci

08-May-2023

PMCID:	PMC10200940
doi:	10.3389/fpls.2023.1162893
PMID:	37223816

Salt Stress—Regulation of Root Water Uptake in a Whole-Plant and Diurnal Context

Lu Y, Fricke W

Int J Mol Sci

29-Apr-2023

PMCID:	PMC10179082
doi:	10.3390/ijms24098070
PMID:	37175779

Drought stress triggers alterations of adaxial and abaxial stomatal development in basil leaves increasing water-use efficiency

Driesen E, De Proft M, Saeys W

Hortic Res

19-Apr-2023

PMCID:	PMC10251137
doi:	10.1093/hr/uhad075
PMID:	37303614

Does coat colour influence survival? A test in a cyclic population of snowshoe hares

Oli MK, Kenney AJ, Boonstra R, Boutin S, Murray DL, Peers MJ, Gilbert BS, Jung TS, Chaudhary V, Hines JE, Krebs CJ

Proc Biol Sci

05-Apr-2023

PMCID:	PMC10072933
doi:	10.1098/rspb.2022.1421
PMID:	37015272

Applying molecular and genetic methods to trees and their fungal communities

Müller M, Kües U, Budde KB, Gailing O

Appl Microbiol Biotechnol

29-Mar-2023

PMCID:	PMC10106355
doi:	10.1007/s00253-023-12480-w
PMID:	36988668

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
> Alkaloids and derivatives / Aporphines
(-)-Phanostenine	12305138	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)O)OC)OCO3	325.40	unknown	via CMAUP database
(-)-Roemeroline	15559920	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)O)OCO3	295.30	unknown	via CMAUP database
(6aS)-1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol	793837	Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)OC	297.30	unknown	via CMAUP database
(7aS)-6,7,7aalpha,8-Tetrahydro-7-methyl-9,10-dimethoxy-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline	10042806	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)OC)OCO3	339.40	unknown	via CMAUP database
8H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one, 9,10-dimethoxy-	3084713	Click to see COC1=C(C2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC	335.30	unknown	via CMAUP database
Cepharadione A	94577	Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O	305.30	unknown	via CMAUP database
Dehydroaporheine	161899	Click to see CN1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3	277.30	unknown	via CMAUP database
Dehydrocrebanine	149600	Click to see CN1CCC2=CC3=C(C4=C5C=CC(=C(C5=CC1=C24)OC)OC)OCO3	337.40	unknown	via CMAUP database
Dehydrophanostenine	179675	Click to see CN1CCC2=CC3=C(C4=C5C=C(C(=CC5=CC1=C24)OC)O)OCO3	323.30	unknown	via CMAUP database
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	via CMAUP database
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
Steporphine	155631	Click to see CN1CC(C2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3)O	295.30	unknown	via CMAUP database
Stesakine	157110	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)O)OCO3	325.40	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydrocrebanine	149599	Click to see CN1C2=C3C(=CC4=C(C3=C5C=CC(=C(C5=C2)OC)OC)OCO4)C(=O)C1=O	365.30	unknown	via CMAUP database
> Alkaloids and derivatives / Hasubanan alkaloids
Aknadilactam	15764659	Click to see CN1C(=O)CC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC	373.40	unknown	via CMAUP database
Aknadinine	159966	Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC	359.40	unknown	via CMAUP database
Cepharamine	12302744	Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C=C(C(=O)C3)OC	329.40	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-Pronuciferine	200480	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC	311.40	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
2-Isoprenylemodin	442750	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)O)CC=C(C)C)O	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / m-Hydroxybenzoic acid esters
Benzyl 2,5-dihydroxybenzoate	11322503	Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC(=C2)O)O	244.24	unknown	https://doi.org/10.1016/S0031-9422(00)84838-4
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Gentisyl alcohol	188287	Click to see C1=CC(=C(C=C1O)CO)O	140.14	unknown	https://doi.org/10.1016/S0031-9422(00)84838-4
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	https://doi.org/10.1515/ZNC-1992-0602
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1515/ZNC-1992-0602
> Lignans, neolignans and related compounds
(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-14-methyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2 inverted exclamation marka,3 inverted exclamation marka:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline	14488278	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(O3)C8=C(C=C7CCN6)OCO8)C=C5)OC	592.70	unknown	via CMAUP database
Berbamine	275182	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC	608.70	unknown	via CMAUP database
Cepharanthine	10206	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3	606.70	unknown	via CMAUP database
Obaberine	100231	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC	622.70	unknown	via CMAUP database
Thalrugosine	100257	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
8-iso Prostaglandin E1	214	Click to see CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00580060
8-iso PROSTAGLANDIN E2	158	Click to see CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O	352.50	unknown	https://doi.org/10.1007/BF00580060
Alprostadil	5280723	Click to see CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00580060
Dinoprostone	5280360	Click to see CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O	352.50	unknown	https://doi.org/10.1007/BF00580060
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
5,8,11,14-Icosatetraenoic Acid	231	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O	304.50	unknown	https://doi.org/10.1016/0031-9422(90)83062-6
Arachidonic Acid	444899	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O	304.50	unknown	https://doi.org/10.1007/BF00597798 https://doi.org/10.1016/0031-9422(90)83062-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
Gibberellin 1	3509874	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	348.40	unknown	https://doi.org/10.1016/0031-9422(88)80585-5
Gibberellin A1	5280379	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	348.40	unknown	https://doi.org/10.1016/0031-9422(88)80585-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6097621	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1515/ZNC-1992-0602
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1515/ZNC-1992-0602
alpha-Bisabolol, (-)-epi-	1616126	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid	311	Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O	192.12	unknown	https://doi.org/10.1007/BF00576226
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/BF00576226
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(6-Oxocyclohex-2-ene-1-carbonyl) 2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162929414	Click to see C1CC(=O)C(C=C1)C(=O)OC(=O)C2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O	422.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
[(1R)-6-oxocyclohex-2-ene-1-carbonyl] 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162929415	Click to see C1CC(=O)C(C=C1)C(=O)OC(=O)C2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O	422.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl 2-hydroxybenzoate	162896795	Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC=CC=C3O)O)O)O	406.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate	133554354	Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O	424.40	unknown	https://doi.org/10.1139/B96-012
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl (1R)-1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate	38348839	Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O	424.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl 2-hydroxybenzoate	162896794	Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)COC(=O)C3=CC=CC=C3O)O)O)O	406.40	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
Salicin	439503	Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1139/B96-012
Salicortin	115158	Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O	424.40	unknown	https://doi.org/10.1139/B96-012 https://doi.org/10.1016/S0031-9422(00)97369-2
Tremulacin	442544	Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O	528.50	unknown	https://doi.org/10.1139/B96-012
Trichocarpin	442989	Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O	406.40	unknown	https://doi.org/10.1139/B96-012
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	via CMAUP database
Acetophenone-2',3',4',5',6'-d5	11457690	Click to see CC(=O)C1=CC=CC=C1	125.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-methoxy-3-[4-[[(5S)-11-methoxy-6,19-dimethyl-20-oxo-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3,9,11,15,21-hexaen-5-yl]methyl]phenoxy]benzaldehyde	389057	Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(O3)C=C7CCN(C(=O)C7=C6)C)OC	606.70	unknown	via CMAUP database
Secocepharanthine	102157843	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(C=C7CCN(C(=O)C7=C6)C)OC)OCO3	636.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-Dimethoxy-2-methylisoquinolin-1(2H)-one	11367984	Click to see CN1C=CC2=CC(=C(C=C2C1=O)OC)OC	219.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Cinnamyl cinnamate	1550890	Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2	264.30	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(E)-Benzyl 3-(4-hydroxyphenyl)acrylate	10083644	Click to see C1=CC=C(C=C1)COC(=O)C=CC2=CC=C(C=C2)O	254.28	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
2-Propenoic acid, 3-(4-hydroxyphenyl)-, 2-phenylethyl ester, (2E)-	14389411	Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC=C(C=C2)O	268.31	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
3-(4-Hydroxyphenyl)propenoic acid 3-phenyl-2-propenyl ester	11288990	Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=C(C=C2)O	280.30	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate	72727649	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	326.30	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
1-O-(4-Coumaroyl)-beta-D-glucose	14158117	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	326.30	unknown	https://doi.org/10.1016/S0031-9422(00)97307-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1515/ZNC-1992-0602
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1007/BF00607554
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6 https://doi.org/10.1007/BF00607554
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1007/BF00607554
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/10.1007/BF00607554 https://doi.org/10.1016/S0021-9673(00)94139-6
> 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/10.1007/BF00607554 https://doi.org/10.1016/S0021-9673(00)94139-6 https://doi.org/10.1515/ZNC-1992-0602
Rhamnetin	5281691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1007/BF00607554
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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	https://doi.org/10.1016/S0031-9422(00)97307-2
Isoquercetin	5280804	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	https://doi.org/10.1016/S0031-9422(00)97307-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1007/BF00607554
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1007/BF00607554
Pinostrobin	6950539	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1007/BF00607554
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Phloretin	4788	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O	274.27	unknown	https://doi.org/10.1016/S0021-9673(00)94139-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
(E)-3-(2,6-dihydroxy-4-methoxyphenyl)-1-phenylprop-2-en-1-one	10468341	Click to see COC1=CC(=C(C(=C1)O)C=CC(=O)C2=CC=CC=C2)O	270.28	unknown	https://doi.org/10.1007/BF00607554
3-(2,6-Dihydroxy-4-methoxyphenyl)-1-phenylprop-2-en-1-one	85151698	Click to see COC1=CC(=C(C(=C1)O)C=CC(=O)C2=CC=CC=C2)O	270.28	unknown	https://doi.org/10.1007/BF00607554

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Populus balsamifera

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