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Limonium aureum

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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 UUID64404afe33b0f960604257
Scientific name Limonium aureum
Authority (L.) Hill ex Kuntze
First published in Suppl. Dict. Jard. 2: 35 (1790)

Description Top

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Synonyms Top

Scientific name Authority First published in
Statice aurea L. Sp. Pl. : 276 (1753)
Limonium erythrorrhizum Ikonn.-Gal. ex Lincz. Novosti Sist. Vyssh. Rast. 8: 211 (1971)

Common names Top

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Language Common/alternative name
Chinese 石花子
Chinese 金佛花
Chinese 金匙叶草
Chinese 黄花补血草
Chinese 全匙叶草
Chinese 干活草
Chinese 金色补血草
Chinese 黄花矶松
Chinese 黄花苍蝇架
Chinese 黄里子白

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
      • China North-central
      • Inner Mongolia
      • Qinghai
    • Mongolia
      • Mongolia
    • Siberia
      • Buryatiya
      • Chita
      • Tuva

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001095225
Tropicos 25400330
KEW urn:lsid:ipni.org:names:686651-1
The Plant List tro-25400330
Open Tree Of Life 1079247
Observations.org 119412
NCBI Taxonomy 1072387
IPNI 686651-1
iNaturalist 909803
GBIF 7298206
EOL 2892140
Elurikkus 610533

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
A dataset for fine-grained seed recognition Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y Sci Data 06-Apr-2024
PMCID:PMC10998916
doi:10.1038/s41597-024-03176-5
PMID:38582756
Chemical Characterization and Leishmanicidal Activity In Vitro and In Silico of Natural Products Obtained from Leaves of Vernonanthura brasiliana (L.) H. Rob (Asteraceae) Fróes YN, Araújo JG, Gonçalves JR, de Oliveira MD, Everton GO, Filho VE, Silva MR, Silva LD, Silva LA, Neto LG, de Oliveira RM, Torres MA, da Silva LC, Lopes AJ, Aliança AS, da Rocha CQ, Sousa JC Metabolites 16-Feb-2023
PMCID:PMC9967733
doi:10.3390/metabo13020285
PMID:36837904
Application of In Vitro Plant Tissue Culture Techniques to Halophyte Species: A Review Custódio L, Charles G, Magné C, Barba-Espín G, Piqueras A, Hernández JA, Ben Hamed K, Castañeda-Loaiza V, Fernandes E, Rodrigues MJ Plants (Basel) 27-Dec-2022
PMCID:PMC9824063
doi:10.3390/plants12010126
PMID:36616255
Proteomics of Salt Gland–Secreted Sap Indicates a Pivotal Role for Vesicle Transport and Energy Metabolism in Plant Salt Secretion Lu C, Zhang Y, Mi P, Guo X, Wen Y, Han G, Wang B Int J Mol Sci 11-Nov-2022
PMCID:PMC9693062
doi:10.3390/ijms232213885
PMID:36430364
Effects of Strong Earthquake on Plant Species Composition, Diversity, and Productivity of Alpine Grassland on Qinghai-Tibetan Plateau Zuo H, Shen H, Dong S, Wu S, He F, Zhang R, Wang Z, Shi H, Hao X, Tan Y, Ma C, Li S, Liu Y, Zhang F Front Plant Sci 12-Apr-2022
PMCID:PMC9039666
doi:10.3389/fpls.2022.870613
PMID:35498647
Antioxidant Effects and Potential Molecular Mechanism of Action of Limonium aureum Extract Based on Systematic Network Pharmacology Yang Z, Mo Y, Cheng F, Zhang H, Shang R, Wang X, Liang J, Liu Y, Hao B Front Vet Sci 05-Jan-2022
PMCID:PMC8767100
doi:10.3389/fvets.2021.775490
PMID:35071383
The complete chloroplast genome of the medicinal plant Polygonum cuspidatum (Polygonaceae) and its phylogenetic implications within the subfamily Polygonoideae Ye X, Lin J, Zhou M, He X, Yan M, Cheng R Mitochondrial DNA B Resour 26-Apr-2021
PMCID:PMC8078928
doi:10.1080/23802359.2021.1917313
PMID:33969219
Plastome and phylogenetic relationship of the woody buckwheat Fagopyrum tibeticum in the Qinghai-Tibet Plateau Yang B, Li L, Liu J, Zhang L Plant Divers 24-Oct-2020
PMCID:PMC8233517
doi:10.1016/j.pld.2020.10.001
PMID:34195504
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Convergent Variations in the Leaf Traits of Desert Plants Akram MA, Wang X, Hu W, Xiong J, Zhang Y, Deng Y, Ran J, Deng J Plants (Basel) 04-Aug-2020
PMCID:PMC7463800
doi:10.3390/plants9080990
PMID:32759791
Complete plastome sequence of Limonium aureum, a medicinal and ornamental species in China Zhang X, Xu Y, Liu X Mitochondrial DNA B Resour 18-Dec-2019
PMCID:PMC7748777
doi:10.1080/23802359.2019.1703608
PMID:33366544
Long-Term Effects of Xerophytic Shrub Haloxylon ammodendron Plantations on Soil Properties and Vegetation Dynamics in Northwest China Fan B, Zhang A, Yang Y, Ma Q, Li X, Zhao C PLoS One 16-Dec-2016
PMCID:PMC5161353
doi:10.1371/journal.pone.0168000
PMID:27992458
Indigenous knowledge for plant species diversity: a case study of wild plants' folk names used by the Mongolians in Ejina desert area, Inner Mongolia, P. R. China Khasbagan, Soyolt J Ethnobiol Ethnomed 16-Jan-2008
PMCID:PMC2268917
doi:10.1186/1746-4269-4-2
PMID:18199323
Flavonoids of Limonium aureum Guan Ye, Chenggang Huang Springer Science and Business Media LLC 14-Jun-2006
doi:10.1007/S10600-006-0089-3

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 / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
CID 85150831 85150831 Click to see CC1CC2(CC(C3(O2)CCC4(C3(CCC5=C4CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC2C(C(C(CO2)O)O)OC2C(C(C(O2)CO)O)O)OC2C(C(C(C(O2)C)O)O)O)O)O)O)C)C)C)C)OC1=O 1353.40 unknown https://doi.org/10.1007/S10600-006-0089-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1007/S10600-006-0089-3
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1007/S10600-006-0089-3
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1007/S10600-006-0089-3
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1007/S10600-006-0089-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/S10600-006-0089-3
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-006-0089-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-006-0089-3
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 3-arabinoside 21672568 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 3-galactoside 5491408 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 3-O-beta-D-galactoside 6''-O-gallate 5319985 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 632.50 unknown https://doi.org/10.1007/S10600-006-0089-3
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricetin-3-O-xyloside 21477996 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1007/S10600-006-0089-3
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-006-0089-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Homoeriodictyol 7-O-glucoside 21629877 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
Viscumiside A 14035424 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-006-0089-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1007/S10600-006-0089-3
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1007/S10600-006-0089-3

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