Scientific name	Authority	First published in
Artemisia australis	Ehrh. ex DC.	Prodr. 6: 120 (1838)
Artemisia tournefortiana	Rchb.	Iconogr. Bot. Exot. 1: 6, t. 5 (1824)
Artemisia armeniaca	Willd. ex Ledeb.	Fl. Ross. 2(2,6): 592 (1845)
Artemisia pinnatifida	Jacquem. ex DC.	Prodr. 6: 120 (1838)
Artemisia inconspicua	Spreng.	Nachr. 1(Bot. Gart. Halle): 12.
Artemisia jacquinii	Raeusch.	Nomencl. Bot. ed. 3, 237 (1797)
Artemisia biennis var. diffusa	Dorn	Vasc. Pl. Wyoming : 295 (1988)
Artemisia biennis var. biennis	Willd.	1988
Artemisia hispanica	Jacq.	Collectanea [Jacquin] 1: 98. 1787 [Jan-Sep 1787]

Common names Top

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Filter by language:

Language	Common/alternative name
English	biennial wormwood
Czech	pelyněk dvouletý
Welsh	y feidiog fain
German	zweijähriger beifuss
German	zweijähriger beifuß
Persian	برنجاسف دوساله
Finnish	sahamaruna
Hawaiian	ahinahina
Dutch	rechte alsem
Chinese	二年生蒿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Middle Europe
  - Belgium
  - Czechoslovakia
  - Germany
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
- Southeastern Europe
  - Italy
- Southwestern Europe
  - France

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Delaware
  - Kentucky
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Yukon
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000134690
UNII	GMU44V0605
Canadensys	2881
USDA Plants	ARBI2
Tropicos	2700129
INPN	83949
Flora of Italy	5732
KEW	urn:lsid:ipni.org:names:305619-2
The Plant List	gcc-95467
Open Tree Of Life	733647
Observations.org	6373
NCBI Taxonomy	206550
NBN Atlas	NBNSYS0000004471
Nature Serve	2.136867
IPNI	305619-2
iNaturalist	58798
GBIF	3121226
Freebase	/m/04q71kc
WisFlora	2626
EPPO	ARTBI
EOL	469725
Elurikkus	210648
Calflora (Californian flora)	703
USDA GRIN	4278
Wikipedia	Artemisia_biennis
CMAUP	NPO24416
PFAF	Artemisia biennis

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

Secondary Metabolites Isolated from Artemisia afra and Artemisia annua and Their Anti-Malarial, Anti-Inflammatory and Immunomodulating Properties—Pharmacokinetics and Pharmacodynamics: A Review

Shinyuy LM, Loe GE, Jansen O, Mamede L, Ledoux A, Noukimi SF, Abenwie SN, Ghogomu SM, Souopgui J, Robert A, Demeyer K, Frederich M

Metabolites

29-Apr-2023

PMCID:	PMC10222324
doi:	10.3390/metabo13050613
PMID:	37233654

Plant-derived natural products targeting ion channels for pain

Goyal S, Goyal S, Goins AE, Alles SR

Neurobiol Pain

17-Apr-2023

PMCID:	PMC10160805
doi:	10.1016/j.ynpai.2023.100128
PMID:	37151956

Chemical Composition and Antioxidant and Antibacterial Potencies of the Artemisia ordosica Aerial Parts Essential Oil during the Vegetative Period

Zhang J, Pan Q, Zhang X, Tana

Molecules

14-Dec-2022

PMCID:	PMC9781940
doi:	10.3390/molecules27248898
PMID:	36558030

Wild Egyptian medicinal plants show in vitro and in vivo cytotoxicity and antimalarial activities

Abdou AM, Seddek AL, Abdelmageed N, Badry MO, Nishikawa Y

BMC Complement Med Ther

12-May-2022

PMCID:	PMC9101831
doi:	10.1186/s12906-022-03566-5
PMID:	35550108

Extraction, Isolation and Characterization of Bioactive Compounds from Artemisia and Their Biological Significance: A Review

Anibogwu R, Jesus KD, Pradhan S, Pashikanti S, Mateen S, Sharma K

Molecules

19-Nov-2021

PMCID:	PMC8618776
doi:	10.3390/molecules26226995
PMID:	34834086

Chemical Analysis and Antioxidant and Antimicrobial Activity of Essential oils from Artemisia negrei L. against Drug-Resistant Microbes

Chebbac K, Moussaoui AE, Bourhia M, Salamatullah AM, Alzahrani A, Guemmouh R

Evid Based Complement Alternat Med

07-Sep-2021

PMCID:	PMC8443344
doi:	10.1155/2021/5902851
PMID:	34539801

Ethnoveterinary botanical survey of medicinal plants used in Pashto, Punjabi and Saraiki communities of Southwest Pakistan

Abidin SZ, Munem A, Khan R, Batiha GE, Amhad M, Zafar M, Khalil AA, Hetta HF, Mahmoud MH, Sami A, Bhatti MZ

Vet Med Sci

22-Jul-2021

PMCID:	PMC8464251
doi:	10.1002/vms3.582
PMID:	34291882

Host Range and Impact of Dichrorampha aeratana, the First Potential Biological Control Agent for Leucanthemum vulgare in North America and Australia

Stutz S, De Clerck-Floate R, Hinz HL, McClay A, McConnachie AJ, Schaffner U

Insects

12-May-2021

PMCID:	PMC8150849
doi:	10.3390/insects12050438
PMID:	34066124

Antioxidant Activity-guided Phytochemical Investigation of Artemisia aucheri Boiss.: Isolation of Ethyl Caffeate and a Spinacetin Glycoside

Jahanbani P, Nasseri S, Mojarrab M

Iran J Pharm Res

01-Jan-2021

PMCID:	PMC8170746
doi:	10.22037/ijpr.2019.15496.13140
PMID:	34400943

Isolation of Two Isochlorogenic Acid Isomers from Phenolic Rich Fraction of Artemisia turanica Krasch.

Moradi-Afrapoli F, Saremi G, Nasseri S, Emami SA, Mojarrab M

Iran J Pharm Res

01-Sep-2020

PMCID:	PMC8019880
doi:	10.22037/ijpr.2019.15182.12919
PMID:	33841521

Comparison of the cytotoxic effects of different fractions of Artemisia ciniformis and Artemisia biennis on B16/F10, PC3 and MCF7 Cells

Ramazani E, Tayarani-Najaran Z, Shokoohinia Y, Mojarrab M

Res Pharm Sci

03-Jul-2020

PMCID:	PMC7540818
doi:	10.4103/1735-5362.288434
PMID:	33088327

Sesquiterpene fractions of Artemisia plants as potent inhibitors of inducible nitric oxide synthase and cyclooxygenase-2 expression

Zamani S, Emami SA, Iranshahi M, Zamani Taghizadeh Rabe S, Mahmoudi M

Iran J Basic Med Sci

01-Jul-2019

PMCID:	PMC7196345
doi:	10.22038/ijbms.2019.34792.8249
PMID:	32373299

Plant diversity of the Kangchenjunga Landscape, Eastern Himalayas

Kandel P, Chettri N, Chaudhary RP, Badola HK, Gaira KS, Wangchuk S, Bidha N, Uprety Y, Sharma E

Plant Divers

26-Apr-2019

PMCID:	PMC6702437
doi:	10.1016/j.pld.2019.04.006
PMID:	31453415

Effects of Using Artemisia annua Leaves, Probiotic Blend, and Organic Acids on Performance, Egg Quality, Blood Biochemistry, and Antioxidant Status of Laying Hens

Baghban-Kanani P, Hosseintabar-Ghasemabad B, Azimi-Youvalari S, Seidavi A, Ragni M, Laudadio V, Tufarelli V

J Poult Sci

25-Apr-2019

PMCID:	PMC7005408
doi:	10.2141/jpsa.0180050
PMID:	32055206

Eleutherococcus Species Cultivated in Europe: A New Source of Compounds with Antiacetylcholinesterase, Antihyaluronidase, Anti-DPPH, and Cytotoxic Activities

Adamczyk K, Olech M, Abramek J, Pietrzak W, Kuźniewski R, Bogucka-Kocka A, Nowak R, Ptaszyńska AA, Rapacka-Gackowska A, Skalski T, Strzemski M, Sowa I, Wójciak-Kosior M, Feldo M, Załuski D

Oxid Med Cell Longev

10-Mar-2019

PMCID:	PMC6431473
doi:	10.1155/2019/8673521
PMID:	30984341

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 / 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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose	102086065	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	452.40	unknown	via CMAUP database
2,6-di-O-galloyl-beta-glucose	14034262	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1,7-Dihydroxy-3,7-dimethyl-2,5-octadiene-4-one	13855812	Click to see CC(=CCO)C(=O)C=CC(C)(C)O	184.23	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
1,7-Dihydroxy-3,7-dimethylocta-2,5-dien-4-one	85533588	Click to see CC(=CCO)C(=O)C=CC(C)(C)O	184.23	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4-Acetyloxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid	162909455	Click to see CC(=O)OC1CC(CC2C1(CCCC2=C)C)C(=C)C(=O)O	292.40	unknown	https://doi.org/10.1002/JLAC.1990199001102
2-(4-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid	13855809	Click to see CC1=C2CC(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O	292.40	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
2-(4-acetyloxy-8a-hydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid	162854247	Click to see CC(=O)OC1CC(CC2(C1(CCCC2=C)C)O)C(=C)C(=O)O	308.40	unknown	https://doi.org/10.1002/JLAC.1990199001102
2-(4a,8-Dimethyl-4-oxo-1,2,3,5,6,7-hexahydronaphthalen-2-yl)prop-2-enoic acid	13855806	Click to see CC1=C2CC(CC(=O)C2(CCC1)C)C(=C)C(=O)O	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid	496073	Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
2-[(2R,4S,4aR,8aR)-4-acetyloxy-8a-hydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	162854248	Click to see CC(=O)OC1CC(CC2(C1(CCCC2=C)C)O)C(=C)C(=O)O	308.40	unknown	https://doi.org/10.1002/JLAC.1990199001102
2-[(2R,4S,4aS)-4-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	163025528	Click to see CC1=C2CC(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O	292.40	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
2-[(2S,4aS)-4a,8-dimethyl-4-oxo-1,2,3,5,6,7-hexahydronaphthalen-2-yl]prop-2-enoic acid	13855808	Click to see CC1=C2CC(CC(=O)C2(CCC1)C)C(=C)C(=O)O	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
2-[(2S,4S,4aS,8aS)-4-acetyloxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid	162909456	Click to see CC(=O)OC1CC(CC2C1(CCCC2=C)C)C(=C)C(=O)O	292.40	unknown	https://doi.org/10.1002/JLAC.1990199001102
2-[(2S,4S,4aS)-4-hydroxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	14527143	Click to see CC1=C2CC(CC(C2(CCC1)C)O)C(=C)C(=O)O	250.33	unknown	https://doi.org/10.1002/JLAC.1990199001102
2-[(4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid	137795140	Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,5aS,9bR)-5a,9-dimethyl-3-methylidene-3a,4,6,7,8,9b-hexahydrobenzo[g][1]benzofuran-2,5-dione	13855800	Click to see CC1=C2C3C(CC(=O)C2(CCC1)C)C(=C)C(=O)O3	246.30	unknown	https://doi.org/10.1007/S10600-007-0190-2 https://doi.org/10.1016/S0031-9422(00)84708-1
(3aS,5S,5aS,9bR)-5-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	13855802	Click to see CC1=C2C3C(CC(C2(CCC1)C)O)C(=C)C(=O)O3	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
(3S,3aS,5aS,9bR)-3,5a,9-trimethyl-3a,4,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2,5-dione	10911889	Click to see CC1C2CC(=O)C3(CCCC(=C3C2OC1=O)C)C	248.32	unknown	https://doi.org/10.1002/JLAC.1990199001102
(5a,9-dimethyl-3-methylidene-2-oxo-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-5-yl) acetate	13855804	Click to see CC1=C2C3C(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O3	290.40	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
[(3aS,5S,5aS,9bR)-5a,9-dimethyl-3-methylidene-2-oxo-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-5-yl] acetate	13855805	Click to see CC1=C2C3C(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O3	290.40	unknown	https://doi.org/10.1016/S0031-9422(00)84708-1
3,5a,9-trimethyl-3a,4,6,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2,5-dione	78200909	Click to see CC1C2CC(=O)C3(CCCC(=C3C2OC1=O)C)C	248.32	unknown	https://doi.org/10.1002/JLAC.1990199001102
5a,9-Dimethyl-3-methylidene-3a,4,6,7,8,9b-hexahydrobenzo[g][1]benzouran-2,5-dione	13855799	Click to see CC1=C2C3C(CC(=O)C2(CCC1)C)C(=C)C(=O)O3	246.30	unknown	https://doi.org/10.1007/S10600-007-0190-2 https://doi.org/10.1016/S0031-9422(00)84708-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
17alpha-Hydroperoxy-28-norlupa-20(29)-ene-3beta-ol	25136231	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
17beta-Hydroperoxy-28-norlupa-20(29)-ene-3beta-ol	25136233	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
28-Nor-20(29)-lupene-diol	15838686	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	via CMAUP database
Asiatic Acid	119034	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulinaldehyde	99615	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)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
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Platanic acid	64980	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pimentol	9917512	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one	12304323	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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	51402820	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
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-[(1S)-1-hydroxy-2-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyethyl]oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	163185343	Click to see CC1C(C(C(C(O1)OCC(C2C(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/10.1002/JLAC.1990199001102
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	51402816	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)O	464.40	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
Leucoside	44566720	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	580.50	unknown	via CMAUP database
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside)	101138141	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside	16720461	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O	462.40	unknown	via CMAUP database
3,3'-Di-O-methylellagic acid	5488919	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O	330.24	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database

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Artemisia biennis

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