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Halocharis hispida

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405b54cdbb7569788286
Scientific name Halocharis hispida
Authority (Schrenk) Bunge
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(11): 62 (1862)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Halimocnemis hispida Schrenk Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 1: 360 (1843)

Common names Top

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Language Common/alternative name
German halimocnemis hispida

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
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001294924
Tropicos 7201200
KEW urn:lsid:ipni.org:names:165737-1
The Plant List tro-7201200
Open Tree Of Life 778176
NCBI Taxonomy 454494
IPNI 165737-1
iNaturalist 906158
GBIF 6035919
EOL 2904168

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 Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Nutrient availability affects the polar lipidome of Halimione portulacoides leaves cultured in hydroponics Custódio M, Maciel E, Domingues MR, Lillebø AI, Calado R Sci Rep 20-Apr-2020
PMCID:PMC7171145
doi:10.1038/s41598-020-63551-1
PMID:32313165
Heptatriacontanol and Phenolic Compounds from Halochris hispida Ahmed A. Gohar . Science Alert 19-Mar-2009
doi:10.3923/JBS.2001.843.845

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.3923/JBS.2001.843.845
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.3923/JBS.2001.843.845
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptatriacontanol 537071 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 537.00 unknown https://doi.org/10.3923/JBS.2001.843.845
> 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/10.3923/JBS.2001.843.845
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/10.3923/JBS.2001.843.845
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/10.3923/JBS.2001.843.845
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.3923/JBS.2001.843.845
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.3923/JBS.2001.843.845
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.3923/JBS.2001.843.845
Isoferulic Acid 736186 Click to see 194.18 unknown https://doi.org/10.3923/JBS.2001.843.845
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.3923/JBS.2001.843.845
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.3923/JBS.2001.843.845
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.3923/JBS.2001.843.845

Gallery Top

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Contributors Top

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Collections Top

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