Scientific name	Authority	First published in
Asarum acuminatum	E.P.Bicknell	Ill. Fl. N. U.S. 3: 513 (1897)
Asarum ambiguum	Daniels	Univ. Missouri Stud., Sci. Ser. i. No. 2, 128 (1907).
Asarum canadense var. acuminatum	Ashe	Bot. Contr. My Herb. 1: 2 (1897)
Asarum canadense var. ambiguum	Farw.	Rep. (Annual) Michigan Acad. Sci. 20: 173 (1918)
Asarum canadense var. obtusum	Muhl.	Cat. Pl. Amer. Sept. : 46 (1813)
Asarum canadense f. phelpsiae	Fernald	Rhodora 40: 333, pl. 499. 1938
Asarum canadense f. prattii	Fassett	Torreya 42: 180 (1943)
Asarum canadense var. reflexum	B.L.Rob.	Rhodora 10: 32 (1908)
Asarum carolinianum	Walter	Fl. Carol. : 143 (1788)
Asarum furcatum	Raf.	New Fl. 2: 20 (1837)
Asarum latifolium	Salisb.	Prodr. Stirp. Chap. Allerton : 344 (1796)
Asarum medium	Raf.	New Fl. 2: 20 (1837)
Asarum parvifolium	Raf.	New Fl. 2: 20 (1837)
Asarum reflexum	E.P.Bicknell	Bull. Torrey Bot. Club 24: 533 (1897)
Asarum reflexum var. ambiguum	E.P.Bicknell	Bull. Torrey Bot. Club 24: 535 (1897)
Asarum rubrocinctum	Peattie	J. Elisha Mitchell Sci. Soc. 44: 192 (1929)
Asarum villosum	Muhl. ex Duch.	Prodr. 15(1): 424 (1864)
Asarum ypsilantense	Walpole	Fl. Washtenaw Co. : 33 (1924)
Asarum canadense var. acutifolium	Raf.	Med. Fl. 1: 264 (1828)

Common names Top

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Filter by language:

Language	Common/alternative name
English	canadian wildginger
English	broad-leaved asarabacca
English	canada wild ginger
English	canadian snakeroot
English	canadian wild ginger
Azerbaijani	kanada çobandüdüyü
French	asaret du canada
French	asaret gingembre
French	gingembre sauvage
Polish	kopytnik kanadyjski
Chinese	北美细辛
Chinese	蛇根草
Chinese	加拿大细辛
Chinese	加拿大細辛

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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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

hydrophilic

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Vermont
  - West Virginia
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Georgia
  - Kentucky
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Western Canada
  - Manitoba

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000550779
UNII	30ZWK18DKO
Flora of Alabama	443
Canadensys	2698
USDA Plants	ASCA
Tropicos	2500002
KEW	urn:lsid:ipni.org:names:93467-1
The Plant List	kew-2654269
Missouri Botanical Garden	276757
Open Tree Of Life	729868
NCBI Taxonomy	28498
Nature Serve	2.159592
IPNI	93467-1
iNaturalist	56325
GBIF	2873947
Freebase	/m/02qwynb
WisFlora	2634
EPPO	ASUCA
EOL	596511
USDA GRIN	402526
Wikipedia	Asarum_canadense

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

Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems

Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA

Nutrients

31-Oct-2023

PMCID:	PMC10647252
doi:	10.3390/nu15214630
PMID:	37960283

Overview of aristolochic acid nephropathy: an update

Zhou Q, Jiang L, Su T, Liu G, Yang L

Kidney Res Clin Pract

15-Jun-2023

PMCID:	PMC10565449
doi:	10.23876/j.krcp.22.211
PMID:	37448287

Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches

Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005506
doi:	10.3390/plants12051145
PMID:	36904005

A Large Intergenic Spacer Leads to the Increase in Genome Size and Sequential Gene Movement around IR/SC Boundaries in the Chloroplast Genome of Adiantum malesianum (Pteridaceae)

Gu X, Zhu M, Su Y, Wang T

Int J Mol Sci

09-Dec-2022

PMCID:	PMC9778900
doi:	10.3390/ijms232415616
PMID:	36555263

Defining plant ecological specialists and generalists: Building a framework for identification and classification

Kirsch A, Kaproth MA

Ecol Evol

24-Nov-2022

PMCID:	PMC9685674
doi:	10.1002/ece3.9527
PMID:	36440310

Current advances on the phytochemical composition, pharmacologic effects, toxicology, and product development of Phyllanthi Fructus

Yan X, Li Q, Jing L, Wu S, Duan W, Chen Y, Chen D, Pan X

Front Pharmacol

19-Oct-2022

PMCID:	PMC9626985
doi:	10.3389/fphar.2022.1017268
PMID:	36339628

The long‐term effects of invasive earthworms on plant community composition and diversity in a hardwood forest in northern Minnesota

Alexander G, Almendinger J, White P

Plant Environ Interact

21-Apr-2022

PMCID:	PMC10168095
doi:	10.1002/pei3.10075
PMID:	37284009

Complete Plastome of Three Korean Asarum (Aristolochiaceae): Confirmation Tripartite Structure within Korean Asarum and Comparative Analyses

Yoo MJ, Jin DP, Lee HO, Lim CE

Plants (Basel)

29-Sep-2021

PMCID:	PMC8540983
doi:	10.3390/plants10102056
PMID:	34685866

Evolution of the Subgroup 6 R2R3-MYB Genes and Their Contribution to Floral Color in the Perianth-Bearing Piperales

Muñoz-Gómez S, Suárez-Baron H, Alzate JF, González F, Pabón-Mora N

Front Plant Sci

09-Apr-2021

PMCID:	PMC8063865
doi:	10.3389/fpls.2021.633227
PMID:	33897722

The effects of a myrmecochore-produced chemical on entomopathogenic fungal growth and seed-dispersing ant survival rates and foraging patterns

Lash CL, Sturiale SL, Kisare SA, Kwit C

Insectes Soc

10-Nov-2020

PMCID:	PMC7993369
doi:	10.1007/s00040-020-00786-1
PMID:	33776132

Expression of gynoecium patterning transcription factors in Aristolochia fimbriata (Aristolochiaceae) and their contribution to gynostemium development

Peréz-Mesa P, Ortíz-Ramírez CI, González F, Ferrándiz C, Pabón-Mora N

EvoDevo

17-Feb-2020

PMCID:	PMC7027301
doi:	10.1186/s13227-020-00149-8
PMID:	32095226

Novel insights into how the mean and heterogeneity of abiotic conditions together shape forb species richness patterns in the Allegheny plateau ecoregion

Catella SA, Eysenbach SR, Abbott KC

Ecol Evol

30-Sep-2019

PMCID:	PMC6875668
doi:	10.1002/ece3.5508
PMID:	31788184

A Two-Stage Culture Method for Zygotic Embryos Effectively Overcomes Constraints Imposed by Hypocotyl and Epicotyl Seed Dormancy in Paeonia ostii ‘Fengdan’

Ren X, Liu Y, Jeong BR

Plants (Basel)

20-Sep-2019

PMCID:	PMC6843118
doi:	10.3390/plants8100356
PMID:	31547000

Advancing an interdisciplinary framework to study seed dispersal ecology

Beckman NG, Aslan CE, Rogers HS, Kogan O, Bronstein JL, Bullock JM, Hartig F, HilleRisLambers J, Zhou Y, Zurell D, Brodie JF, Bruna EM, Cantrell RS, Decker RR, Efiom E, Fricke EC, Gurski K, Hastings A, Johnson JS, Loiselle BA, Miriti MN, Neubert MG, Pejchar L, Poulsen JR, Pufal G, Razafindratsima OH, Sandor ME, Shea K, Schreiber S, Schupp EW, Snell RS, Strickland C, Zambrano J

AoB Plants

19-Aug-2019

PMCID:	PMC7179845
doi:	10.1093/aobpla/plz048
PMID:	32346468

Complete Chloroplast Genomes and Comparative Analysis of Sequences Evolution among Seven Aristolochia (Aristolochiaceae) Medicinal Species

Li X, Zuo Y, Zhu X, Liao S, Ma J

Int J Mol Sci

28-Feb-2019

PMCID:	PMC6429227
doi:	10.3390/ijms20051045
PMID:	30823362

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
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1021/JF00065A004
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1021/JF00065A004
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
Aristolochic acid	2236	Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O	341.27	unknown	https://doi.org/10.2307/4117899
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	https://doi.org/10.1021/JF00065A004
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	148.20	unknown	https://doi.org/10.1021/JF00065A004
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1021/JF00065A004
Neryl acetate	1549025	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF00065A004
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF00065A004
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1021/JF00065A004
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1021/JF00065A004
4-Isopropylbenzyl alcohol	325	Click to see CC(C)C1=CC=C(C=C1)CO	150.22	unknown	https://doi.org/10.1021/JF00065A004
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1039/CT9028100059
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one	6973628	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1021/JF00065A004
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF00065A004
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/JF00065A004 https://doi.org/10.1039/CT9028100059
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1021/JF00065A004
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1021/JF00065A004
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1021/JF00065A004
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF00065A004
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1021/JF00065A004
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/JF00065A004
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00065A004
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1039/CT9028100059
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF00065A004
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00065A004 https://doi.org/10.1039/CT9028100059
gamma-Terpineol	11467	Click to see CC(=C1CCC(CC1)(C)O)C	154.25	unknown	https://doi.org/10.1021/JF00065A004
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00065A004
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
Aristolone	165536	Click to see CC1CCCC2=CC(=O)C3C(C12C)C3(C)C	218.33	unknown	https://doi.org/10.1021/JF00065A004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Junenol	6452077	Click to see CC(C)C1CCC2(CCCC(=C)C2C1O)C	222.37	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol	6276	Click to see CCCCCO	88.15	unknown	https://doi.org/10.1021/JF00065A004
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Hotrienol	5366264	Click to see CC(=C)C=CCC(C)(C=C)O	152.23	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde	11552	Click to see CC(C)CC=O	86.13	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Methylfurfural	12097	Click to see CC1=CC=C(O1)C=O	110.11	unknown	https://doi.org/10.1021/JF00065A004
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
3-Methyl-2-butenal	61020	Click to see CC(=CC=O)C	84.12	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylfuran	14505	Click to see CC(=O)C1=CC=CO1	110.11	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
3-Methylcyclopentanone	15650	Click to see CC1CCC(=O)C1	98.14	unknown	https://doi.org/10.1021/JF00065A004
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Diacetone Alcohol	31256	Click to see CC(=O)CC(C)(C)O	116.16	unknown	https://doi.org/10.1021/JF00065A004
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Butylphthalide	61361	Click to see CCCCC1C2=CC=CC=C2C(=O)O1	190.24	unknown	https://doi.org/10.1021/JF00065A004
> Organoheterocyclic compounds / Isobenzofurans
Sedanolide	5018391	Click to see CCCCC1C2CCCC=C2C(=O)O1	194.27	unknown	https://doi.org/10.1021/JF00065A004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-1-[2-hydroxy-4,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	14854161	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
(E)-3-(4-hydroxyphenyl)-1-[2-hydroxy-4-[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	163191242	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
(E)-3-(4-hydroxyphenyl)-1-[2-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one	163076612	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
(E)-3-(4-hydroxyphenyl)-1-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one	163076613	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
(E)-3-(4-hydroxyphenyl)-1-[2-hydroxy-6-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one	163185808	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
1-[2-Hydroxy-4,6-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	72740138	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
3-(4-Hydroxyphenyl)-1-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one	74819244	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
> 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)00216-8
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	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	https://doi.org/10.1016/S0031-9422(00)00216-8
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	https://doi.org/10.1016/S0031-9422(00)00216-8
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	https://doi.org/10.1016/S0031-9422(00)00216-8
Quercetin 3-O-robinobioside	10371536	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
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	https://doi.org/10.1016/S0031-9422(00)00216-8
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162913283	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
Kaempferol-3-O-glucoside-7-O-rhamnoside	14035324	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
Quercetin 3-galactoside 7-rhamnoside	14130922	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8
Quercetin 3-O-galactoside-7-O-rhamnoside	5320843	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)00216-8

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Asarum canadense

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