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Artemisia adamsii

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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 UUID643fcd1175e46348220550
Scientific name Artemisia adamsii
Authority Besser
First published in Nouv. Mém. Soc. Imp. Naturalistes Moscou 3: 27 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Artemisia tenuifolia Adams ex DC. Prodr. 6: 107 (1838)
Artemisia depressa Turcz. ex DC. Prodr. 6: 107 (1838)

Common names Top

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Language Common/alternative name
Spanish adams yovşanı
Azerbaijani adams yovşanı
Chinese 阿氐蒿
Chinese 雅夫冈-沙里尔日
Chinese 雅夫冈一沙里尔日
Chinese 阿氏蒿
Chinese 东北丝裂蒿
Chinese 东北丝裂蒿（阿氏蒿）
Chinese 丝叶蒿
Chinese 乌姆希-沙里尔日
Chinese 乌姆希一沙里尔日
Chinese 呼尔干一沙里尔日
Chinese 東北絲裂蒿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
    • Mongolia
      • Mongolia
    • Siberia
      • Buryatiya
      • Chita

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000068926
Tropicos 2728764
KEW urn:lsid:ipni.org:names:179156-1
The Plant List gcc-25771
Open Tree Of Life 367874
Observations.org 114824
NCBI Taxonomy 401875
IPNI 179156-1
iNaturalist 1119318
GBIF 3121252

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
Fertilization reduces root architecture plasticity in Ulmus pumila used for afforesting Mongolian semi-arid steppe Montagnoli A, Lasserre B, Terzaghi M, Byambadorj SO, Nyam-Osor B, Scippa GS, Chiatante D Front Plant Sci 19-Jul-2022
PMCID:PMC9359110
doi:10.3389/fpls.2022.878299
PMID:35958214
Relationship between lactational performance and metabolic parameters of Mongolian native grazing mares SANDAGDORJ B, BAIGALMAA T, BURENJARGAL S, HORIUCHI M, ENKHDALAI M, BAYANBAT D, JANCHIV D, JAMYANDORJ O, ULZII-ORSHIKH P, NYAM-OSOR P J Equine Sci 06-Sep-2021
PMCID:PMC8437754
doi:10.1294/jes.32.91
PMID:34539210
Root Biomass Distribution of Populus sibirica and Ulmus pumila Afforestation Stands Is Affected by Watering Regimes and Fertilization in the Mongolian Semi-arid Steppe Nyam-Osor B, Byambadorj SO, Park BB, Terzaghi M, Scippa GS, Stanturf JA, Chiatante D, Montagnoli A Front Plant Sci 23-Apr-2021
PMCID:PMC8102691
doi:10.3389/fpls.2021.638828
PMID:33968099
Grazing effects on intraspecific trait variability vary with changing precipitation patterns in Mongolian rangelands Lang B, Ahlborn J, Oyunbileg M, Geiger A, von Wehrden H, Wesche K, Oyuntsetseg B, Römermann C Ecol Evol 26-Dec-2019
PMCID:PMC6988561
doi:10.1002/ece3.5895
PMID:32015835
Opportunities to integrate herders’ indicators into formal rangeland monitoring: an example from Mongolia Jamsranjav C, Fernández‐Giménez ME, Reid RS, Adya B Ecol Appl 17-May-2019
PMCID:PMC6851969
doi:10.1002/eap.1899
PMID:31020715
Effects of Nitrogen Addition on the Drought Susceptibility of the Leymus chinensis Meadow Ecosystem Vary with Drought Duration Shi B, Wang Y, Meng B, Zhong S, Sun W Front Plant Sci 27-Feb-2018
PMCID:PMC5835344
doi:10.3389/fpls.2018.00254
PMID:29535757
Phenolic compounds of Artemisia adamsii I. I. Chemesova, L. M. Belenovskaya, T. P. Nadezhina Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00579783
Guaianolides related to arborescin from Artemisia adamsii Ferdinand Bohlmann, Lievy Hartono, Jasmin Jakupovic, Siegfried Huneck Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83171-4

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
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Methylbenzyl alcohol 11505 Click to see CC1=CC=C(C=C1)CO 122.16 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphane 92108 Click to see CC1(C2CCC1(CC2)C)C 138.25 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6097621 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
alpha-Bisabolol, (-)-epi- 1616126 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S,3aS,6E,9S,10Z,11aS)-9-hydroxy-3,6,10-trimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one 162956731 Click to see CC1C2CCC(=CCC(C(=CC2OC1=O)C)O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
9-hydroxy-3,6,10-trimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one 4541177 Click to see CC1C2CCC(=CCC(C(=CC2OC1=O)C)O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,3R,6S,7S,10S,11R,14R)-14-hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 162900330 Click to see CC1C2CCC3(C4(O3)C(C=C(C4C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(1R,3R,6S,7S,10S,11R,14S)-14-hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 162900334 Click to see CC1C2CCC3(C4(O3)C(C=C(C4C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(1S,3R,5S,6R,7S,10S,11R)-5-hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 162937000 Click to see CC1C2C(CC3(C4(O3)CC=C(C4C2OC1=O)C)C)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(1S,3R,6S,7S,10S,11R)-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 10966851 Click to see CC1C2CCC3(C4(O3)CC=C(C4C2OC1=O)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6aR,9S,9aS,9bS)-6a,9-dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162889444 Click to see CC1C2CCC(=C)C3(C=CC(C3C2OC1=O)(C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6aS,9aR,9bS)-6a-hydroxy-3,6,9-trimethyl-3,3a,4,7,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162957469 Click to see CC1C2CC=C(C3(CC=C(C3C2OC1=O)C)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6aS,9aR,9bS)-6a-hydroxy-3,9-dimethyl-6-methylidene-3a,4,5,7,9a,9b-hexahydro-3H-azuleno[4,5-b]furan-2-one 11054006 Click to see CC1C2CCC(=C)C3(CC=C(C3C2OC1=O)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6aS,9R,9aR,9bS)-9-hydroperoxy-6a-hydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162951659 Click to see CC1C2CCC(=C)C3(C=CC(C3C2OC1=O)(C)OO)O 280.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6aS,9R,9aS,9bS)-6a,9-dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162889445 Click to see CC1C2CCC(=C)C3(C=CC(C3C2OC1=O)(C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6R,6aR,9R,9aS,9bS)-6,6a,9-trihydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 163041370 Click to see CC1C2CCC(C3(C=CC(C3C2OC1=O)(C)O)O)(C)O 282.33 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
(3S,3aS,6R,6aS,9R,9aS,9bS)-6,6a,9-trihydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 163041369 Click to see CC1C2CCC(C3(C=CC(C3C2OC1=O)(C)O)O)(C)O 282.33 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
1,4a,7-Trimethyl-5,6,6a,7,9a,9b-hexahydro-3H-oxireno[2',3':8,8a]azuleno[4,5-b]furan-8(4ah)-one 566062 Click to see CC1C2CCC3(C4(O3)CC=C(C4C2OC1=O)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
14-Hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 14589154 Click to see CC1C2CCC3(C4(O3)C(C=C(C4C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
5-Hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 73819174 Click to see CC1C2C(CC3(C4(O3)CC=C(C4C2OC1=O)C)C)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
5,14-Dimethyl-9-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 71405084 Click to see CC1C2CCC(=C)C3CC4C(C3C2OC1=O)(O4)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
6,6a,9-Trihydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 163041368 Click to see CC1C2CCC(C3(C=CC(C3C2OC1=O)(C)O)O)(C)O 282.33 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
6a-Hydroxy-3,6,9-trimethyl-3,3a,4,7,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162957468 Click to see CC1C2CC=C(C3(CC=C(C3C2OC1=O)C)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
6a-hydroxy-3,9-dimethyl-6-methylidene-3a,4,5,7,9a,9b-hexahydro-3H-azuleno[4,5-b]furan-2-one 85381911 Click to see CC1C2CCC(=C)C3(CC=C(C3C2OC1=O)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
6a,9-Dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 85100464 Click to see CC1C2CCC(=C)C3(C=CC(C3C2OC1=O)(C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
75956-97-7 637454 Click to see CC1C2CCC(=C)C3CC4C(C3C2OC1=O)(O4)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
9-Hydroperoxy-6a-hydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2-one 162951658 Click to see CC1C2CCC(=C)C3(C=CC(C3C2OC1=O)(C)OO)O 280.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
Arborescin 11807014 Click to see CC1C2CCC3(C4(O3)CC=C(C4C2OC1=O)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,3R,6S,7S,10S,13S)-13-hydroxy-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-11-en-8-one 163105566 Click to see CC1C2CCC3(C4(O3)CC(C(=C4C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
Achillin 291264 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
Desacetoxymatricarin 167683 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/S0031-9422(00)83171-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/BF00579783
https://doi.org/10.1016/S0031-9422(00)83171-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1007/BF00579783
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1007/BF00579783

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