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Artemisia eriopoda

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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 UUID643fd2a28e572864309505
Scientific name Artemisia eriopoda
Authority Bunge
First published in Enum. Pl. China Bor. : 37 (1833)

Description Top

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Synonyms Top

Scientific name Authority First published in
Artemisia desertorum var. fontanesiana Besser Bull. Soc. Imp. Naturalistes Moscou 8: 66 (1835)
Artemisia eriopoda subsp. jiagedaqiensis G.Y.Zhang & X.Jun Liu Bull. Bot. Res., Harbin 13(1): 50 (1993)

Common names Top

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Language Common/alternative name
Chinese 米蒿
Chinese 黄蒿
Chinese 牡蒿
Chinese 一支蒿
Chinese 南牡蒿
Chinese 乌苏力格-沙里尔日
Chinese 拔拉蒿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Artemisia eriopoda var. gansuensis Ling & Y.R.Ling Bull. Bot. Res., Harbin 8(3): 7 (1988)
Artemisia eriopoda var. maritima Ling & Y.R.Ling Bull. Bot. Res., Harbin 8(3): 6 (1988)
Artemisia eriopoda var. rotundifolia (Debeaux) Y.R.Ling Bull. Bot. Res., Harbin 8(4): 56 (1988)
Artemisia eriopoda var. shanxiensis Y.R.Ling Bull. Bot. Res., Harbin 8(3): 7 (1988)

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
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
    • Mongolia
      • Mongolia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000125369
Tropicos 50054764
KEW urn:lsid:ipni.org:names:179457-1
The Plant List gcc-86448
Open Tree Of Life 291390
NCBI Taxonomy 1027781
IPNI 179457-1
GBIF 3121189
EOL 6179978

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
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Phytochemistry, Pharmacology and Molecular Mechanisms of Herbal Bioactive Compounds for Sickness Behaviour Alotaibi GH, Shivanandappa TB, Chinnadhurai M, Reddy Dachani S, Dabeer Ahmad M, Abdullah Aldaajanii K Metabolites 02-Dec-2022
PMCID:PMC9782141
doi:10.3390/metabo12121215
PMID:36557252
Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP Plants (Basel) 13-Nov-2022
PMCID:PMC9696113
doi:10.3390/plants11223070
PMID:36432799
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
High nutrient uptake efficiency and high water use efficiency facilitate the spread of Stellera chamaejasme L. in degraded grasslands Guo L, Li J, He W, Liu L, Huang D, Wang K BMC Ecol 04-Dec-2019
PMCID:PMC6894284
doi:10.1186/s12898-019-0267-3
PMID:31801501
Effects of species-dominated patches on soil organic carbon and total nitrogen storage in a degraded grassland in China Zhang Y, Tang S, Xie S, Liu K, Li J, Chen Q, Huang D, Wang K PeerJ 03-May-2019
PMCID:PMC6501767
doi:10.7717/peerj.6897
PMID:31110928
Effects of precipitation and clipping intensity on net primary productivity and composition of a Leymus chinensis temperate grassland steppe He F, Wang K, Hannaway DB, Li X PLoS One 29-Dec-2017
PMCID:PMC5747479
doi:10.1371/journal.pone.0190450
PMID:29287115
Agricultural Activities of a Meadow Eliminated Plant Litter from the Periphery of a Farmland in Inner Mongolia, China Kawada K, Borjigin W, Nakamura T PLoS One 04-Aug-2015
PMCID:PMC4524670
doi:10.1371/journal.pone.0135077
PMID:26241943
Eudesmane sesquiterpenes from Artemisia eriopoda Jin-Feng Hu, Su-Ping Bai, Zhong-Jian Jia Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00325-1
Two new polyacetylenes from Artemisia eriopoda. Hu J, Jia H, Bai S Planta Med 01-May-1998
doi:10.1055/S-2006-957457
PMID:17253253

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 / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3S,8E,11R,12E,14Z)-heptadeca-1,8,12,14-tetraen-4,6-diyne-3,11-diol 162849256 Click to see CCC=CC=CC(CC=CC#CC#CC(C=C)O)O 256.34 unknown https://doi.org/10.1055/S-2006-957457
(3S,8E,11R,12S,13Z)-heptadeca-1,8,13,16-tetraen-4,6-diyne-3,11,12-triol 162937772 Click to see C=CCC=CC(C(CC=CC#CC#CC(C=C)O)O)O 272.34 unknown https://doi.org/10.1055/S-2006-957457
Heptadeca-1,8,13,16-tetraen-4,6-diyne-3,11,12-triol 162937771 Click to see C=CCC=CC(C(CC=CC#CC#CC(C=C)O)O)O 272.34 unknown https://doi.org/10.1055/S-2006-957457
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2S,4aR,5R,8aS)-4a-methyl-8-methylidene-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,5-diol 44559564 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(96)00325-1
(4aS,6R,8aS)-4a-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 11601274 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(C)(C)O)O)C 252.35 unknown https://doi.org/10.1016/0031-9422(96)00325-1
(4R,4aR,6R,8aR)-4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-3,4a,5,6,7,8-hexahydro-2H-naphthalen-1-one 102247107 Click to see CC12CCC(CC1C(CCC2=O)(C)O)C(C)(C)O 254.36 unknown https://doi.org/10.1016/0031-9422(96)00325-1
4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-3,4a,5,6,7,8-hexahydro-2H-naphthalen-1-one 163012247 Click to see CC12CCC(CC1C(CCC2=O)(C)O)C(C)(C)O 254.36 unknown https://doi.org/10.1016/0031-9422(96)00325-1
4a-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 73025726 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(C)(C)O)O)C 252.35 unknown https://doi.org/10.1016/0031-9422(96)00325-1
Platambin 613194 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(96)00325-1
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(96)00325-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(96)00325-1
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(96)00325-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(96)00325-1
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(96)00325-1
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(96)00325-1
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(96)00325-1
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(96)00325-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
8-(2,3-Dihydroxy-3-methylbutyl)-5,7-dimethoxy-2-methylchromen-4-one 15280395 Click to see CC1=CC(=O)C2=C(C=C(C(=C2O1)CC(C(C)(C)O)O)OC)OC 322.40 unknown https://doi.org/10.1055/S-2006-957457
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1016/0031-9422(96)00325-1
> 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/10.1016/0031-9422(96)00325-1

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