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Artemisia tripartita

Artemisia tripartita - 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 UUID643fc8ae23eba146185336
Scientific name Artemisia tripartita
Authority Rydb.
First published in Mem. New York Bot. Gard. 1: 432. 1900

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English threetip sagebrush
Spanish seriphidium tripartitum

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Artemisia tripartita subsp. rupicola Beetle Rhodora 61: 82 (1959)
Artemisia tripartita subsp. tripartita Rydb.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000024384
Canadensys 2917
USDA Plants ARTR4
Tropicos 2701816
KEW urn:lsid:ipni.org:names:20802-2
The Plant List gcc-123562
Open Tree Of Life 202523
NCBI Taxonomy 86319
Nature Serve 2.158323
IPNI 291415-2
iNaturalist 158726
GBIF 3121425
Freebase /m/0hzqpjz
FEIS plants/shrub/arttrp
EOL 850404
Calflora (Californian flora) 10503
USDA GRIN 456362
Wikipedia Artemisia_tripartita
PFAF Artemisia tripartita

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
Isolation of Secondary Metabolites from Achillea grandifolia Friv. (Asteraceae) and Main Compounds’ Effects on a Glioblastoma Cellular Model Tsiftsoglou OS, Krigas N, Gounaris C, Papitsa C, Nanouli M, Vartholomatos E, Markopoulos GS, Isyhou R, Alexiou G, Lazari D Pharmaceutics 30-Apr-2023
PMCID:PMC10224520
doi:10.3390/pharmaceutics15051383
PMID:37242625
Statistical considerations of nonrandom treatment applications reveal region-wide benefits of widespread post-fire restoration action Simler-Williamson AB, Germino MJ Nat Commun 16-Jun-2022
PMCID:PMC9203498
doi:10.1038/s41467-022-31102-z
PMID:35710763
Livestock Use on Public Lands in the Western USA Exacerbates Climate Change: Implications for Climate Change Mitigation and Adaptation Kauffman JB, Beschta RL, Lacy PM, Liverman M Environ Manage 02-Apr-2022
PMCID:PMC9079022
doi:10.1007/s00267-022-01633-8
PMID:35366068
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
Grazing behavior and production for cattle on differing late-season rangeland grazing systems with or without protein supplementation Sprinkle JE, Sagers JK, Hall JB, Ellison MJ, Yelich JV, Brennan JR, Taylor JB, Lamb JB Transl Anim Sci 16-Dec-2019
PMCID:PMC6999180
doi:10.1093/tas/txz100
PMID:32704954
Neutral Polysaccharide from the Leaves of Pseuderanthemum carruthersii: Presence of 3-O-Methyl Galactose and Anti-Inflammatory Activity in LPS-Stimulated RAW 264.7 Cells Bac VH, Paulsen BS, Truong LV, Koschella A, Trinh TC, Wold CW, Yogarajah S, Heinze T Polymers (Basel) 22-Jul-2019
PMCID:PMC6680566
doi:10.3390/polym11071219
PMID:31336597
Ecosystem functional response across precipitation extremes in a sagebrush steppe Tredennick AT, Kleinhesselink AR, Taylor JB, Adler PB PeerJ 13-Mar-2018
PMCID:PMC5855887
doi:10.7717/peerj.4485
PMID:29576958
Environmental responses, not species interactions, determine synchrony of dominant species in semiarid grasslands Tredennick AT, de Mazancourt C, Loreau M, Adler PB Ecology 01-Apr-2017
PMCID:PMC5386145
doi:10.1002/ecy.1757
PMID:28144939
Recent Advances in Nanoparticle-Mediated Delivery of Anti-Inflammatory Phytocompounds Conte R, Marturano V, Peluso G, Calarco A, Cerruti P Int J Mol Sci 28-Mar-2017
PMCID:PMC5412295
doi:10.3390/ijms18040709
PMID:28350317
Direct effects dominate responses to climate perturbations in grassland plant communities Chu C, Kleinhesselink AR, Havstad KM, McClaran MP, Peters DP, Vermeire LT, Wei H, Adler PB Nat Commun 08-Jun-2016
PMCID:PMC4899860
doi:10.1038/ncomms11766
PMID:27273085
Soil Respiration and Bacterial Structure and Function after 17 Years of a Reciprocal Soil Transplant Experiment Bond-Lamberty B, Bolton H, Fansler S, Heredia-Langner A, Liu C, McCue LA, Smith J, Bailey V PLoS One 02-Mar-2016
PMCID:PMC4775055
doi:10.1371/journal.pone.0150599
PMID:26934712
Immunomodulatory and Hemagglutinating Activities of Acidic Polysaccharides Isolated from Combretum racemosum Schepetkin IA, Kouakou K, Yapi A, Kirpotina LN, Jutila MA, Quinn MT Int Immunopharmacol 01-Feb-2013
PMCID:PMC3647372
doi:10.1016/j.intimp.2013.01.015
PMID:23380150
Systematic review of herbals as potential anti-inflammatory agents: Recent advances, current clinical status and future perspectives Beg S, Swain S, Hasan H, Barkat MA, Hussain MS Pharmacogn Rev 01-Jul-2011
PMCID:PMC3263046
doi:10.4103/0973-7847.91102
PMID:22279370
Polysaccharides derived from Yamoa™ (Funtumia elastica) prime γδ T cells in vitro and enhance innate immune responses in vivo Graff JC, Kimmel EM, Freedman B, Schepetkin IA, Holderness J, Quinn MT, Jutila MA, Hedges JF Int Immunopharmacol 09-Aug-2009
PMCID:PMC2749908
doi:10.1016/j.intimp.2009.07.015
PMID:19671448
Inhibition of the Human Neutrophil NADPH Oxidase by Coxiella burnetii Siemsen DW, Kirpotina LN, Jutila MA, Quinn MT Microbes Infect 18-Apr-2009
PMCID:PMC2704257
doi:10.1016/j.micinf.2009.04.005
PMID:19379824

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (5E,6S)-4-[2-[2-[3-acetyloxy-4-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-5-ethylidene-6-[(3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163010818 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1081.00 unknown https://doi.org/10.1016/0031-9422(73)80693-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aS,7R,9R,10E,11aR)-7,9-dihydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 162908739 Click to see CC1=CC2C(CCC(=C)C(CC1O)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
2H-1-Benzopyran-2-one, 6,8-dimethoxy-7-(((2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl)oxy)- 6440748 Click to see CC(=CCCC(=CCCC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)C)C)C 426.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
6,8-Dimethoxy-7-(3,7,11-trimethyldodeca-2,6,10-trienoxy)chromen-2-one 158685 Click to see CC(=CCCC(=CCCC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)C)C)C 426.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
7-[(2E,6E)-9-[(2R)-3,3-dimethyloxiran-2-yl]-3,7-dimethylnona-2,6-dienoxy]-6,8-dimethoxychromen-2-one 162930565 Click to see CC(=CCCC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)C)CCC3C(O3)(C)C 442.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
7-[9-(3,3-Dimethyloxiran-2-yl)-3,7-dimethylnona-2,6-dienoxy]-6,8-dimethoxychromen-2-one 159135 Click to see CC(=CCCC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)C)CCC3C(O3)(C)C 442.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
7,9-dihydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 3488095 Click to see CC1=CC2C(CCC(=C)C(CC1O)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3S,3aS,5aR,9R,9aS,9bS)-9-hydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 159971 Click to see CC1C2CCC3(CCCC(C3C2OC1=O)(C)O)C 252.35 unknown https://doi.org/10.1016/S0031-9422(00)88163-7
Ridentin B 14779601 Click to see CC12CCC3C(C1C(=C)C(CC2O)O)OC(=O)C3=C 264.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,6E,9R,10E,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 162948080 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C 290.40 unknown https://doi.org/10.1016/0031-9422(73)80694-6
[(3aS,6E,9S,10E,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 13895556 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C 290.40 unknown https://doi.org/10.1016/0031-9422(73)80694-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1S,2R,4S,5R,9S,10S,11R,13S,14R)-2,4-dihydroxy-2,11-dimethyl-6-methylidene-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-7-one 101316845 Click to see CC1(CC(C2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O)O 294.30 unknown https://doi.org/10.1016/0031-9422(73)80692-2
(1S,2S,6R,7S,9R,10R,12R,14S)-7,9-dihydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 163011621 Click to see CC1(CC(C2C(C3C1CC4C3(O4)C)OC(=O)C2=C)O)O 280.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
(3aR,4S,6R,6aS,9aR,9bR)-4,6-dihydroxy-6,9-dimethyl-3-methylidene-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one 162989862 Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/S0031-9422(00)85829-X
(3aS,4R,6aS,9aR,9bS)-4,6a-dihydroxy-6,9-dimethyl-3-methylidene-4,7,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2-one 162912238 Click to see CC1=CCC2(C1C3C(C(C=C2C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1016/0031-9422(73)80692-2
[(1R,2S,4R,5S,9R,10R,11R,13S,14S)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-4-yl] acetate 162849940 Click to see CC(=O)OC1CC(C23C(C4C1C(=C)C(=O)O4)C5(C(C2O3)O5)C)(C)O 336.30 unknown https://doi.org/10.1016/0031-9422(73)80692-2
4,6-Dihydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,9a,9b-octahydroazuleno[4,5-b]furan-2(3h)-one 99115 Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/S0031-9422(00)85829-X
4,6a-Dihydroxy-9-methyl-3,6-dimethylidene-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 13895589 Click to see CC1=CCC2(C1C3C(C(CC2=C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1016/0031-9422(73)80693-4
7,9-Dihydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 163011620 Click to see CC1(CC(C2C(C3C1CC4C3(O4)C)OC(=O)C2=C)O)O 280.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
Rupicolin A 3082541 Click to see CC1=CCC2(C1C3C(C(C=C2C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1016/0031-9422(73)80692-2
https://doi.org/10.1016/0031-9422(73)80693-4
Rupicolin B 3082542 Click to see CC1=CCC2(C1C3C(C(CC2=C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1016/0031-9422(73)80693-4
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(6-Hydroxy-1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methoxy]-6,8-dimethoxychromen-2-one 162848420 Click to see CC1CC=C2C(C1(C)COC3=C(C=C4C=CC(=O)OC4=C3OC)OC)CCC(C2(C)C)O 442.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
7-[[(1R,2S,6S,8aR)-6-hydroxy-1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl]methoxy]-6,8-dimethoxychromen-2-one 162848421 Click to see CC1CC=C2C(C1(C)COC3=C(C=C4C=CC(=O)OC4=C3OC)OC)CCC(C2(C)C)O 442.50 unknown https://doi.org/10.1016/0031-9422(83)80032-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown https://doi.org/10.1016/0031-9422(83)80032-6
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(83)80032-6

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