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Salsola laricifolia

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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 UUID64405b57e4c17959594360
Scientific name Salsola laricifolia
Authority Litv. ex Drobow
First published in Byull. Sredne-Aziatsk. Gosud. Univ. 16: 210 (1927)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 松叶猪毛菜

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
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001294972
Tropicos 7201312
KEW urn:lsid:ipni.org:names:166904-1
The Plant List tro-7201312
Open Tree Of Life 623572
Observations.org 131402
NCBI Taxonomy 151252
IPNI 166904-1
iNaturalist 985676
GBIF 3757712
EOL 2873029
Elurikkus 408956

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
The old world salsola as a source of valuable secondary metabolites endowed with diverse pharmacological activities: a review ElNaggar MH, Eldehna WM, Abourehab MA, Abdel Bar FM J Enzyme Inhib Med Chem 25-Jul-2022
PMCID:PMC9327781
doi:10.1080/14756366.2022.2102005
PMID:35875938
Selection of the Reference Gene for Expression Normalization in Salsola ferganica under Abiotic Stress Wang S, Zhang S Genes (Basel) 24-Mar-2022
PMCID:PMC9029158
doi:10.3390/genes13040571
PMID:35456377
Genus Salsola: Chemistry, Biological Activities and Future Prospective—A Review Murshid SS, Atoum D, Abou-Hussein DR, Abdallah HM, Hareeri RH, Almukadi H, Edrada-Ebel R Plants (Basel) 08-Mar-2022
PMCID:PMC8953912
doi:10.3390/plants11060714
PMID:35336596
Function of Chloroplasts in Plant Stress Responses Song Y, Feng L, Alyafei MA, Jaleel A, Ren M Int J Mol Sci 15-Dec-2021
PMCID:PMC8705820
doi:10.3390/ijms222413464
PMID:34948261
Chloroplastic SaNADP-ME4 of C3–C4 Woody Desert Species Salsola laricifolia Confers Drought and Salt Stress Resistance to Arabidopsis Wen Z, Wang Y, Xia C, Zhang Y, Zhang H Plants (Basel) 03-Sep-2021
PMCID:PMC8471237
doi:10.3390/plants10091827
PMID:34579361
Diversity of beetles (Coleoptera) in natural and planted saxaul forests (Haloxylon ammodendron) in the South Gobi Desert, Mongolia Batchuluun B, Wunderlich J, Schmitt M Zookeys 03-Dec-2020
PMCID:PMC7728731
doi:10.3897/zookeys.1000.56856
PMID:33354135
The Developmental Enhancement of a C4 System With Non-Typical C4 Physiological Characteristics in Salsola ferganica (Kranz Anatomy), an Annual Desert Halophyte Liu Y, Maimaitijiang T, Zhang J, Ma Y, Lan H Front Plant Sci 06-Mar-2020
PMCID:PMC7069449
doi:10.3389/fpls.2020.00152
PMID:32210984
Phylogenetic structure and formation mechanism of shrub communities in arid and semiarid areas of the Mongolian Plateau Zheng Y, Dong L, Li Z, Zhang J, Li Z, Miao B, Jia C, Liang C, Wang L, Li FY Ecol Evol 16-Nov-2019
PMCID:PMC6912910
doi:10.1002/ece3.5787
PMID:31871647
Molecular phylogeny and forms of photosynthesis in tribe Salsoleae (Chenopodiaceae) Schüssler C, Freitag H, Koteyeva N, Schmidt D, Edwards G, Voznesenskaya E, Kadereit G J Exp Bot 21-Dec-2016
PMCID:PMC5853613
doi:10.1093/jxb/erw432
PMID:28003310
Structural and physiological analyses in Salsoleae (Chenopodiaceae) indicate multiple transitions among C3, intermediate, and C4 photosynthesis Voznesenskaya EV, Koteyeva NK, Akhani H, Roalson EH, Edwards GE J Exp Bot 23-Jul-2013
PMCID:PMC3745723
doi:10.1093/jxb/ert191
PMID:23881394
A chemical study of plants of the Mongolian flora lariside ? A new scopoletin glycoside fromSalsola laricifolia S. Narantuyaa, D. Batsur�n, �. Kh. Batirov, V. M. Malikov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00598293

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1007/BF00598293
6,7-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 21633144 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)OC 384.30 unknown https://doi.org/10.1007/BF00598293
6,7-Dimethoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 73816163 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)OC 384.30 unknown https://doi.org/10.1007/BF00598293
6,8-Dimethoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 12302276 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O 384.30 unknown https://doi.org/10.1007/BF00598293
7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-methoxychromen-2-one 162933054 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(CO)O)O 486.40 unknown https://doi.org/10.1007/BF00598293
7-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-methoxychromen-2-one 162933053 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(CO)O)O 486.40 unknown https://doi.org/10.1007/BF00598293
Calycanthoside 5318566 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O 384.30 unknown https://doi.org/10.1007/BF00598293
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1007/BF00598293
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown https://doi.org/10.1007/BF00598293
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 208.17 unknown https://doi.org/10.1007/BF00598293
> 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/10.1007/BF00598293

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