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Artemisia umbelliformis

Artemisia umbelliformis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fc6a96ed48746848835
Scientific name Artemisia umbelliformis
Authority Lam.
First published in Encycl. 1: 262 (1783)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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

Subspecies (abbr. subsp./ssp.) Top

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

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
PFAF Artemisia umbelliformis

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
Temporal Changes in the Use of Wild Medicinal Plants in Trentino–South Tyrol, Northern Italy Mattalia G, Graetz F, Harms M, Segor A, Tomarelli A, Kieser V, Zerbe S, Pieroni A Plants (Basel) 19-Jun-2023
PMCID:PMC10301116
doi:10.3390/plants12122372
PMID:37375997
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

Phytochemical Profile Top

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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
2Alpha,3Alpha,23-Trihydroxyurs-12-En-28-Oic 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
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
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)-5-Hydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone 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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