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Alhagi sparsifolia

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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
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Details Top

Internal ID UUID643fdc0081bee147393574
Scientific name Alhagi sparsifolia
Authority Shap.

Description Top

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Synonyms Top

Scientific name Authority First published in
Alhagi kirghizorum var. sparsifolia Shap.
Alhagi maurorum subsp. sparsifolium (Shap.) Yakovlev

Common names Top

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Language Common/alternative name
Chinese 骆驼刺
Chinese 刺蜜

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000198672
Tropicos 13072414
The Plant List ild-45184
Open Tree Of Life 708291
Observations.org 145279
NCBI Taxonomy 218100
iNaturalist 335473
GBIF 2945088
EOL 648859
Elurikkus 338898
USDA GRIN 435607

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
Unveiling the diversity, composition, and dynamics of phyllosphere microbial communities in Alhagi sparsifolia across desert basins and seasons in Xinjiang, China Zhang Y, Du Y, Zhang Z, Islam W, Zeng F Front Microbiol 25-Mar-2024
PMCID:PMC10999668
doi:10.3389/fmicb.2024.1361756
PMID:38591034
Effects of meteorological factors and groundwater depths on sap flow density of Populus euphratica in a desert oasis, Taklamakan Desert, China Wan Y, Peng L, Anwaier A, Shi H, Li D, Ma Y, Shi Q Front Plant Sci 09-Feb-2024
PMCID:PMC10884297
doi:10.3389/fpls.2024.1330426
PMID:38405581
Role of Microbes in Alleviating Crop Drought Stress: A Review Gu Z, Hu C, Gan Y, Zhou J, Tian G, Gao L Plants (Basel) 27-Jan-2024
PMCID:PMC10857462
doi:10.3390/plants13030384
PMID:38337917
Volatiles from cotton aphid (Aphis gossypii) infested plants attract the natural enemy Hippodamia variegata Yi C, Teng D, Xie J, Tang H, Zhao D, Liu X, Liu T, Ding W, Khashaveh A, Zhang Y Front Plant Sci 20-Dec-2023
PMCID:PMC10761428
doi:10.3389/fpls.2023.1326630
PMID:38173929
The Response of Oxytropis aciphylla Ledeb. Leaf Interface to Water and Light in Gravel Deserts Bei Z, Zhang X, Zhang F, Yan X Plants (Basel) 21-Nov-2023
PMCID:PMC10708387
doi:10.3390/plants12233922
PMID:38068558
Link between the aboveground and belowground biomass allocation with growing of Tamarix sp. seedlings in the hinterland of Taklimakan Desert, China Erkin F, Yue D, Abdureyim A, Huang W, Tayir M PLoS One 16-Aug-2023
PMCID:PMC10431640
doi:10.1371/journal.pone.0289670
PMID:37585434
Drought Tolerance of Legumes: Physiology and the Role of the Microbiome Petrushin IS, Vasilev IA, Markova YA Curr Issues Mol Biol 28-Jul-2023
PMCID:PMC10453936
doi:10.3390/cimb45080398
PMID:37623217
Validation of the shotgun metabarcoding approach for comprehensively identifying herbal products containing plant, fungal, and animal ingredients Zhang Z, Mu W, Kong W, Liu J, Zhao J, Zhao Q, Shi M, Zhao H, Liu J, Shi L PLoS One 03-Jul-2023
PMCID:PMC10317219
doi:10.1371/journal.pone.0286069
PMID:37399206
The complete chloroplast genome of Corethrodendron multijugum (Fabaceae: Corethrodendron) and phylogenetic analysis Zhang LJ, Liu Y, Shi JJ Mitochondrial DNA B Resour 01-Jun-2023
PMCID:PMC10236963
doi:10.1080/23802359.2023.2209387
PMID:37275398
Performance of a Pilot-Scale Continuous Flow Ozone-Based Hospital Wastewater Treatment System Azuma T, Katagiri M, Sasaki N, Kuroda M, Watanabe M Antibiotics (Basel) 19-May-2023
PMCID:PMC10215370
doi:10.3390/antibiotics12050932
PMID:37237835
Halophytes as new model plant species for salt tolerance strategies Mann A, Lata C, Kumar N, Kumar A, Kumar A, Sheoran P Front Plant Sci 11-May-2023
PMCID:PMC10211249
doi:10.3389/fpls.2023.1137211
PMID:37251767
Effects of AMF Compound Inoculants on Growth, Ion Homeostasis, and Salt Tolerance-Related Gene Expression in Oryza sativa L. Under Salt Treatments Zhang B, Shi F, Zheng X, Pan H, Wen Y, Song F Rice (N Y) 10-Apr-2023
PMCID:PMC10086084
doi:10.1186/s12284-023-00635-2
PMID:37036613
Root morphological and physiological traits are committed to the phosphorus acquisition of the desert plants in phosphorus-deficient soils Gao Y, Zhang Z, Zeng F, Ma X BMC Plant Biol 10-Apr-2023
PMCID:PMC10084647
doi:10.1186/s12870-023-04178-y
PMID:37032339
Physiological and Transcriptional Responses of Apocynum venetum to Salt Stress at the Seed Germination Stage Li X, Li J, Su H, Sun P, Zhang Z, Li M, Xing H Int J Mol Sci 11-Feb-2023
PMCID:PMC9966927
doi:10.3390/ijms24043623
PMID:36835035
Vein Network and Climatic Factors Predict the Leaf Economic Spectrum of Desert Plants in Xinjiang, China Du Y, Zhang Y, Guo Z, Zhang Z, Zeng F Plants (Basel) 28-Jan-2023
PMCID:PMC9920464
doi:10.3390/plants12030581
PMID:36771664

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 / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S10600-008-9064-5
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/10.1007/S10600-008-9064-5
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/10.1007/S10600-008-9064-5
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S10600-008-9064-5
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(-)-Epicatechin-(4beta->8)-(+)-gallocatechin 21769546 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF02291536
(-)-Epigallocatechin-(4beta->8)-(-)-epicatechin 13831064 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 594.50 unknown https://doi.org/10.1007/BF02291536
[(2R,3R,4R)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 13831074 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 746.60 unknown https://doi.org/10.1007/BF02291536
[4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 13831072 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 746.60 unknown https://doi.org/10.1007/BF02291536
Endotelon 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1007/BF02291536
Epicatechin-(4beta->8)-gallocatechin 14284599 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF02291536
Epigallocatechin-(4beta->8)-catechin 13831061 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 594.50 unknown https://doi.org/10.1007/BF02291536
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1007/BF02291536
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1007/BF02291536
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF02291536
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF02291536
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF02291536
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1007/BF02291536
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1007/BF02291536
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/BF02291536
Flavan-3,3',4',5,5',7-hexol 1249 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/BF02291536
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/BF02291536
> 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/S10600-008-9064-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13245589 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/S10600-008-9064-5
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 12313122 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-008-9064-5
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/S10600-008-9064-5
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-008-9064-5

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