Language	Common/alternative name
English	alpine wormwood
English	alps wormwood
English	white genepi
Bulgarian	алпийски пелин
Catalan	artemisia de muntanya
German	silber-edelraute
German	silberraute
German	echte edelraute
French	genepi blanc
French	génépi blanc
Russian	Полынь альпийская

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Artemisia umbelliformis subsp. eriantha	(Ten.) Vallès-Xirau & Oliva Brañas	Monogr. Inst. Piren. Ecol. 5: 328 (1990)
Artemisia umbelliformis subsp. umbelliformis	Lam.

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

Suggest a correction or add new data!

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
  - Austria
  - Czechoslovakia
  - Germany
  - Poland
  - Switzerland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000007413
UNII	BI6LY4V6G3
USDA Plants	ARUM
Tropicos	2740281
INPN	84053
Flora of Italy	5718
KEW	urn:lsid:ipni.org:names:180243-1
The Plant List	gcc-107163
Open Tree Of Life	324916
Observations.org	149047
NCBI Taxonomy	72355
IUCN Red List	202935
IPNI	180243-1
iNaturalist	340554
GBIF	3120864
Freebase	/m/0p8tbbk
EPPO	ARTUM
EOL	596476
USDA GRIN	407703
Wikipedia	Artemisia_umbelliformis
CMAUP	NPO26573

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

Comparative Evaluation of Anticancer Activity of Natural Methoxylated Flavones Xanthomicrol and Eupatilin in A375 Skin Melanoma Cells

Rosa A, Piras F, Pollastro F, Sogos V, Appendino G, Nieddu M

Life (Basel)

26-Feb-2024

PMCID:	PMC10971382
doi:	10.3390/life14030304
PMID:	38541630

Wild and Micropropagated Artemisia eriantha Infusions: In Vitro Digestion Effects on Phenolic Pattern and Antioxidant Activity

Rocchi R, Pellegrini M, Pittia P, Pace L

Plants (Basel)

27-Dec-2023

PMCID:	PMC10780599
doi:	10.3390/plants13010085
PMID:	38202393

Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy

Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780445
doi:	10.3390/plants13010043
PMID:	38202351

Antiseizure Effects of Scoparone, Borneol and Their Impact on the Anticonvulsant Potency of Four Classic Antiseizure Medications in the Mouse MES Model—An Isobolographic Transformation

Łuszczki JJ, Bojar H, Góralczyk A, Skalicka-Woźniak K

Int J Mol Sci

11-Jan-2023

PMCID:	PMC9867083
doi:	10.3390/ijms24021395
PMID:	36674911

Xanthomicrol Activity in Cancer HeLa Cells: Comparison with Other Natural Methoxylated Flavones

Nieddu M, Pollastro F, Caria P, Salamone S, Rosa A

Molecules

05-Jan-2023

PMCID:	PMC9864045
doi:	10.3390/molecules28020558
PMID:	36677614

Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview

Motti R, Paura B, Cozzolino A, de Falco B

Plants (Basel)

28-Nov-2022

PMCID:	PMC9736219
doi:	10.3390/plants11233272
PMID:	36501312

Ethnobotanical Review and Dataset Compiling on Wild and Cultivated Plants Traditionally Used as Medicinal Remedies in Italy

Monari S, Ferri M, Salinitro M, Tassoni A

Plants (Basel)

04-Aug-2022

PMCID:	PMC9370752
doi:	10.3390/plants11152041
PMID:	35956518

Arbuscular mycorrhizal fungi and production of secondary metabolites in medicinal plants

Zhao Y, Cartabia A, Lalaymia I, Declerck S

Mycorrhiza

13-May-2022

PMCID:	PMC9184413
doi:	10.1007/s00572-022-01079-0
PMID:	35556179

Halophyte Artemisia caerulescens L.: Metabolites from In Vitro Shoots and Wild Plants

Pieracci Y, Vento M, Pistelli L, Lombardi T, Pistelli L

Plants (Basel)

15-Apr-2022

PMCID:	PMC9027092
doi:	10.3390/plants11081081
PMID:	35448809

Neuropsychopharmacological profiling of scoparone in mice

Kowalczyk J, Budzyńska B, Kurach Ł, Pellegata D, El Sayed NS, Gertsch J, Skalicka-Woźniak K

Sci Rep

17-Jan-2022

PMCID:	PMC8764054
doi:	10.1038/s41598-021-04741-3
PMID:	35039558

Ethnomedicinal and Ethnobotanical Survey in the Aosta Valley Side of the Gran Paradiso National Park (Western Alps, Italy)

Danna C, Poggio L, Smeriglio A, Mariotti M, Cornara L

Plants (Basel)

09-Jan-2022

PMCID:	PMC8778718
doi:	10.3390/plants11020170
PMID:	35050058

Effect of Polyploidy Induction on Natural Metabolite Production in Medicinal Plants

Madani H, Escrich A, Hosseini B, Sanchez-Muñoz R, Khojasteh A, Palazon J

Biomolecules

17-Jun-2021

PMCID:	PMC8234191
doi:	10.3390/biom11060899
PMID:	34204200

Occurrence and biosynthesis of plant sesterterpenes (C25), a new addition to terpene diversity

Chen Q, Li J, Ma Y, Yuan W, Zhang P, Wang G

Plant Commun

30-Mar-2021

PMCID:	PMC8553974
doi:	10.1016/j.xplc.2021.100184
PMID:	34746758

Research Advances on Health Effects of Edible Artemisia Species and Some Sesquiterpene Lactones Constituents

Trendafilova A, Moujir LM, Sousa PM, Seca AM

Foods

30-Dec-2020

PMCID:	PMC7823681
doi:	10.3390/foods10010065
PMID:	33396790

Topical Effects of Artemisia Absinthium Ointment and Liniment in Comparison with Piroxicam Gel in Patients with Knee Joint Osteoarthritis: A Randomized Double-Blind Controlled Trial

Basiri Z, Zeraati F, Esna-Ashari F, Mohammadi F, Razzaghi K, Araghchian M, Moradkhani S

Iran J Med Sci

01-Nov-2017

PMCID:	PMC5684373
PMID:	29184260

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Cyathinin A	139590317	Click to see CC(C)C1=C2C3C(C=C4C5C(C3(CCC2(CC1)C)C)OC6C5(C7C(CO6)(OC4O7)O)O)O	446.50	unknown	https://doi.org/10.1021/NP800468M
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aS,1bS,3R,4R,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol	57394792	Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C	238.37	unknown	via CMAUP database
(1aS,1bS,3R,4S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol	57396552	Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C	238.37	unknown	via CMAUP database
(1aS,1bS,3S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1b,2,3,5,6,6a-hexahydro-1H-cyclopropa[a]inden-4-one	57398335	Click to see CC12CC3CC3(C1CC(C(=O)C2)C(C)(C)O)C	236.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,8aR)-8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	57391287	Click to see CC12CCC=C(C1CC(CC2)C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)CO	400.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	57396551	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	via CMAUP database
1-oxo-3beta,23-dihydroxyolean-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52952751	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	648.80	unknown	via CMAUP database
3beta,22alpha-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52950912	Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)O	634.80	unknown	via CMAUP database
3beta,23-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside	52950911	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	634.80	unknown	via CMAUP database
Arjunglucoside II	52951052	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	via CMAUP database
hederagenin 28-O-beta-D-glucopyranosyl ester	21120798	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	634.80	unknown	via CMAUP database
quadranoside IV	10372074	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-hydroperoxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	99961	Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1021/NP800468M
7-hydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	99962	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1021/NP800468M
Artemorin	5281428	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1021/NP800468M
Verlotorin	13895607	Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1021/NP800468M
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aS,8aR,9aR)-4a-hydroperoxy-8a-methyl-3,5-dimethylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one	13889985	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)OO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1
(8a-methyl-3,5-dimethylidene-2-oxo-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-4a-yl) N-(2,2,2-trichloroacetyl)carbamate	163055197	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)OC(=O)NC(=O)C(Cl)(Cl)Cl	436.70	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1
[(3aR,4aR,8aR,9aR)-8a-methyl-3,5-dimethylidene-2-oxo-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-4a-yl] N-(2,2,2-trichloroacetyl)carbamate	163055198	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)OC(=O)NC(=O)C(Cl)(Cl)Cl	436.70	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1
4a-hydroperoxy-8a-methyl-3,5-dimethylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one	13889983	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)OO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1
5-Deoxy-5-hydroperoxytelekin	13889984	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)OO	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1 https://doi.org/10.1016/0305-1978(86)90059-1
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one	98958	Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C	248.32	unknown	https://doi.org/10.1021/NP800468M
Reynosin	482788	Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C	248.32	unknown	https://doi.org/10.1021/NP800468M
Santamarine	188297	Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O	248.32	unknown	https://doi.org/10.1021/NP800468M
Telekin	12443309	Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)O	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)97692-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	133640194	Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C	232.32	unknown	https://doi.org/10.1021/NP800468M
6,10-Dimethyl-1'-(4-methylpent-3-enyl)spiro[3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-3,4'-cyclohexene]-2-one	162968492	Click to see CC1=CCCC(=CC2C(CC1)C3(CCC(=CC3)CCC=C(C)C)C(=O)O2)C	368.60	unknown	https://doi.org/10.1021/NP800468M
Costunolide	5281437	Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C	232.32	unknown	https://doi.org/10.1021/NP800468M
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3S,4aS,6aS,6aR,6bR,8aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene-1,3-diol	57391286	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C)C)C	442.70	unknown	via CMAUP database
1-Oxo-3beta-hydroxyolean-18-ene	52950910	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C)C)C	440.70	unknown	via CMAUP database
1-Oxo-3beta,23-dihydroxyolean-12-en-28-oic acid	11134679	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C	486.70	unknown	via CMAUP database
23-Hydroxyursolic Acid	14136881	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
3-Oxo-23-hydroxyurs-12-en-28-oic acid	14396856	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1C)C)C(=O)O	470.70	unknown	via CMAUP database
3beta-Acetoxyolean-18-en-28-oic acid	21594125	Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C(=O)O)(C)C)C	498.70	unknown	via CMAUP database
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Esculentic acid	9898760	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
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	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
Virgatic acid	14489125	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(3aS,6S,7aS)-6-methyl-3-methylidene-6-(4-oxopentyl)-3a,4,7,7a-tetrahydro-1-benzofuran-2,5-dione	133568303	Click to see CC(=O)CCCC1(CC2C(CC1=O)C(=C)C(=O)O2)C	264.32	unknown	https://doi.org/10.1039/P19830002705
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
Juglanin A	70697839	Click to see COC1=C2C=C(CCC(=O)CCCCC3=C(C(=C(O2)C=C3)OC)O)C=C1	356.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5R)-1-(4-Hydroxyphenyl)-5-hydroxy-7-(3-methoxy-4-hydroxyphenyl)heptane-3-one	637003	Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O	344.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin	5273755	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	https://doi.org/10.1021/NP800468M

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Artemisia umbelliformis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top