Halocnemum strobilaceum - Unknown
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Internal ID UUID64401fa743502818014142
Scientific name Halocnemum strobilaceum
Authority (Pall.) M.Bieb.
First published in Fl. Taur.-Caucas. 3: 3 (1819)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salicornia cruciata Forssk. Fl. Aegypt.-Arab. : 2 (1775)
Salicornia strobilacea Pall. Reise Russ. Reich. 1: 481 (1771)
Halopeplis strobilacea (Pall.) Ces. Comp. Fl. Ital. [Cesati] 2(12): 271. 1874

Common names Top

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Language Common/alternative name
Spanish garbancillo
Spanish salado
Arabic ثليث مخروطي
Azerbaijani ziyilli hallimon
Persian شور باتلاقی
Armenian Աղապատուկ
Armenian աղապատուկ
Russian Сарсаза́н шишкова́тый
Russian Сарсазан шишковатый
sc sossoìni
Turkish Çuvan
Chinese 盐节木

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Tuva
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Eastern Europe
      • East European Russia
    • Southeastern Europe
      • Albania
      • Greece
      • Turkey-in-Europe

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000714941
USDA Plants HAST9
Tropicos 7200054
Flora of Italy 506
KEW urn:lsid:ipni.org:names:165766-1
The Plant List kew-2838537
Open Tree Of Life 713258
Observations.org 146120
NCBI Taxonomy 239185
IPNI 165766-1
iNaturalist 514995
GBIF 3760350
EPPO HCNST
EOL 2872968
Elurikkus 409301
USDA GRIN 18223
Wikipedia Halocnemum_strobilaceum

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
Impact of meteorological variability on diurnal and seasonal net ecosystem productivity in a desert riparian forest ecosystem Teng D, Gong X, He X, Wang J, Lv G, Wang J, Yang X Front Plant Sci 18-Apr-2024
PMCID:PMC11063279
doi:10.3389/fpls.2024.1332192
PMID:38699537
Endophytes: a uniquely tailored source of potential antibiotic adjuvants Moussa AY Arch Microbiol 06-Apr-2024
PMCID:PMC10998792
doi:10.1007/s00203-024-03891-y
PMID:38581477
Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
High-throughput sequencing reveals the structure and metabolic resilience of desert microbiome confronting climate change Mousa WK, Abu-Izneid T, Salah-Tantawy A Front Plant Sci 05-Mar-2024
PMCID:PMC10953687
doi:10.3389/fpls.2024.1294173
PMID:38510442
Naturalization and invasion potential of Sesuvium portulacastrum L. recorded as alien species in Egypt Heneidy SZ, Bidak LM, Halmy MW, Fakhry AM, Toto SM, El Kenany ET Sci Rep 07-Feb-2024
PMCID:PMC10850471
doi:10.1038/s41598-024-53627-7
PMID:38326540
Valorization of Salicornia patula Duval-Jouve Young Shoots in Healthy and Sustainable Diets Sánchez Gavilán I, Velázquez Ybarzabal D, de la Fuente V, Cámara RM, Sánchez-Mata MC, Cámara M Nutrients 25-Jan-2024
PMCID:PMC10857085
doi:10.3390/nu16030358
PMID:38337643
Relict Plants Are Better Able to Adapt to Climate Change: Evidence from Desert Shrub Communities Lu Y, Zhang B, Zhang M, Jie M, Guo S, Wang Y Plants (Basel) 04-Dec-2023
PMCID:PMC10707734
doi:10.3390/plants12234065
PMID:38068700
Halophilic Plant-Associated Bacteria with Plant-Growth-Promoting Potential Meinzer M, Ahmad N, Nielsen BL Microorganisms 02-Dec-2023
PMCID:PMC10745547
doi:10.3390/microorganisms11122910
PMID:38138054
Economic Uses of Salt-Tolerant Plants Garcia-Caparros P, Al-Azzawi MJ, Flowers TJ Plants (Basel) 17-Jul-2023
PMCID:PMC10385539
doi:10.3390/plants12142669
PMID:37514283
Phylogeny and Flow Cytometry of the Genus Kalidium Moq. (Amaranthaceae s.l.) in Kazakhstan Osmonali BB, Vesselova PV, Kudabayeva GM, Skaptsov MV, Shmakov AI, Friesen N Plants (Basel) 11-Jul-2023
PMCID:PMC10383796
doi:10.3390/plants12142619
PMID:37514234
Coastal Halophytes: Potent Source of Bioactive Molecules from Saline Environment Stanković M, Stojanović-Radić Z, Jakovljević D, Zlatić N, Luković M, Dajić-Stevanović Z Plants (Basel) 30-Apr-2023
PMCID:PMC10181147
doi:10.3390/plants12091857
PMID:37176915
Response to Hypersalinity of Four Halophytes Growing in Hydroponic Floating Systems: Prospects in the Phytomanagement of High Saline Wastewaters and Extreme Environments Barbafieri M, Bretzel F, Scartazza A, Di Baccio D, Rosellini I, Grifoni M, Pini R, Clementi A, Franchi E Plants (Basel) 22-Apr-2023
PMCID:PMC10181242
doi:10.3390/plants12091737
PMID:37176795
Biochemical Profile and In Vitro Therapeutic Properties of Two Euhalophytes, Halocnemum strobilaceum Pall. and Suaeda fruticosa (L.) Forske., Grown in the Sabkha Ecosystem in the Algerian Sahara Gheraissa N, Chemsa AE, Cherrada N, Erol E, Elsharkawy ER, Ghemam-Amara D, Zeghoud S, Rebiai A, Messaoudi M, Sawicka B, Atanassova M, Abdel-Kader MS Molecules 19-Apr-2023
PMCID:PMC10141351
doi:10.3390/molecules28083580
PMID:37110814
An insight into endophytic antimicrobial compounds: an updated analysis Digra S, Nonzom S Plant Biotechnol Rep 14-Mar-2023
PMCID:PMC10013304
doi:10.1007/s11816-023-00824-x
PMID:37359493
Research Progress on Nutritional Value, Preservation and Processing of Fish—A Review Ali A, Wei S, Ali A, Khan I, Sun Q, Xia Q, Wang Z, Han Z, Liu Y, Liu S Foods 16-Nov-2022
PMCID:PMC9689683
doi:10.3390/foods11223669
PMID:36429260

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 / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Docosyl 3,4-dihydroxy-trans-cinnamate 20980926 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(99)00007-2
Docosyl caffeate 5316952 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(99)00007-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(2R)-2-propan-2-ylfuro[3,2-g]chromene-3,7-dione 677579 Click to see CC(C)C1C(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3 244.24 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
Oreoselone 2841563 Click to see CC(C)C1C(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3 244.24 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
Oxyimperatorin 182251 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-3-methoxycoumarin 12466112 Click to see COC1=CC2=C(C=C(C=C2)O)OC1=O 192.17 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
7-hydroxy-3-methyl-2H-chromen-2-one 13235410 Click to see CC1=CC2=C(C=C(C=C2)O)OC1=O 176.17 unknown https://doi.org/10.1016/S0367-326X(00)00301-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1007/BF02238224
Rhamnazin 5320945 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1007/BF02238224
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/BF02238224
Isoquercetin 5280804 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/BF02238224
Isorhamnetin 3-galactoside 13245586 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1007/BF02238224
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1007/BF02238224
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2R,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 15378351 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)N)O)O)O 477.40 unknown https://doi.org/10.1007/BF02238224
7-[3-Amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 74978277 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)N)O)O)O 477.40 unknown https://doi.org/10.1007/BF02238224

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