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Nitraria tangutorum

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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 UUID6440559a5d9f7950358610
Scientific name Nitraria tangutorum
Authority Bobrov
First published in Sovetsk. Bot. 14: 26 (1946)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 白刺
Chinese 酸胖
Chinese 唐古特白刺

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
      • Tibet
      • Xinjiang

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001243823
Tropicos 50126119
KEW urn:lsid:ipni.org:names:873347-1
The Plant List tro-50126119
Open Tree Of Life 659276
NCBI Taxonomy 357929
IPNI 873347-1
iNaturalist 852386
GBIF 3986821
EOL 2907564
CMAUP NPO13459

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
The Multiple Promoting Effects of Suaeda glauca Root Exudates on the Growth of Alfalfa under NaCl Stress Dong L, Hua Y, Gao Z, Wu H, Hou Y, Chu Y, Zhang J, Cui G Plants (Basel) 07-Mar-2024
PMCID:PMC10974879
doi:10.3390/plants13060752
PMID:38592745
Chemical and Transcriptomic Analyses of Leaf Cuticular Wax Metabolism in Ammopiptanthus mongolicus under Osmotic Stress Sumbur B, Zhou M, Dorjee T, Bing J, Ha S, Xu X, Zhou Y, Gao F Biomolecules 16-Feb-2024
PMCID:PMC10886927
doi:10.3390/biom14020227
PMID:38397464
Genome-wide analysis of respiratory burst oxidase homolog (Rboh) genes in Aquilaria species and insight into ROS-mediated metabolites biosynthesis and resin deposition Begum K, Das A, Ahmed R, Akhtar S, Kulkarni R, Banu S Front Plant Sci 09-Feb-2024
PMCID:PMC10893762
doi:10.3389/fpls.2023.1326080
PMID:38405033
Proteomic and Metabolomic Analysis of the Quercus ilex–Phytophthora cinnamomi Pathosystem Reveals a Population-Specific Response, Independent of Co-Occurrence of Drought Hernández-Lao T, Tienda-Parrilla M, Labella-Ortega M, Guerrero-Sánchez VM, Rey MD, Jorrín-Novo JV, Castillejo-Sánchez MÁ Biomolecules 29-Jan-2024
PMCID:PMC10887186
doi:10.3390/biom14020160
PMID:38397397
Didymium arenosum, a myxomycete new to science from the confluence of deserts in northwestern China Wei S, Li S, Liu P, Qi B, Wang Q, Li Y PeerJ 08-Jan-2024
PMCID:PMC10782953
doi:10.7717/peerj.16725
PMID:38213774
Selection and Verification of Standardized Reference Genes of Angelica dahurica under Various Abiotic Stresses by Real-Time Quantitative PCR Zhang J, He X, Zhou J, Dong Z, Yu H, Tang Q, Yuan L, Peng S, Zhong X, He Y Genes (Basel) 07-Jan-2024
PMCID:PMC10815136
doi:10.3390/genes15010079
PMID:38254968
Enhanced wedelolactone content in in vitro-raised genetically uniform Wedelia chinensis under the influence of CuSO4 Swami RK, Nimker S, Narula A, Farooqi H Front Plant Sci 19-Dec-2023
PMCID:PMC10758438
doi:10.3389/fpls.2023.1281445
PMID:38169740
Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses Bejerman N, Dietzgen R, Debat H Viruses 10-Dec-2023
PMCID:PMC10747219
doi:10.3390/v15122402
PMID:38140643
GhIMP10D, an inositol monophosphates family gene, enhances ascorbic acid and antioxidant enzyme activities to confer alkaline tolerance in Gossypium hirsutum L. Fan Y, Peng F, Cui R, Wang S, Cui Y, Lu X, Huang H, Ni K, Liu X, Jiang T, Feng X, Liu M, Lei Y, Chen W, Meng Y, Han M, Wang D, Yin Z, Chen X, Wang J, Li Y, Guo L, Zhao L, Ye W BMC Plant Biol 22-Sep-2023
PMCID:PMC10515029
doi:10.1186/s12870-023-04462-x
PMID:37736713
The influence of precipitation timing and amount on soil microbial community in a temperate desert ecosystem Xiao Y, Bao F, Xu X, Yu K, Wu B, Gao Y, Zhang J Front Microbiol 07-Sep-2023
PMCID:PMC10512721
doi:10.3389/fmicb.2023.1249036
PMID:37744930
Identification, Formation, and Occurrence of Perlolyrine: A β-Carboline Alkaloid with a Furan Moiety in Foods Herraiz T, Peña A, Salgado A J Agric Food Chem 31-Aug-2023
PMCID:PMC10510388
doi:10.1021/acs.jafc.3c03612
PMID:37651628
The Application of Arbuscular Mycorrhizal Fungi as Microbial Biostimulant, Sustainable Approaches in Modern Agriculture Sun W, Shahrajabian MH Plants (Basel) 29-Aug-2023
PMCID:PMC10490045
doi:10.3390/plants12173101
PMID:37687348
Modelling the effects of topographic heterogeneity on distribution of Nitraria tangutorum Bobr. species in deserts using LiDAR-data Zhou H, Feng L, Fu L, Sharma RP, Zhou X, Zhao X Sci Rep 22-Aug-2023
PMCID:PMC10444836
doi:10.1038/s41598-023-40678-5
PMID:37608034
Water use strategies of Nitraria tangutorum in the lake-basin region of the Badain Jaran Desert Qin J, Si J, Jia B, Zhao C, Zhou D, He X, Wang C, Zhu X Front Plant Sci 15-Aug-2023
PMCID:PMC10465167
doi:10.3389/fpls.2023.1240656
PMID:37649998

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 / Biphenyls and derivatives
Amarogentin 115149 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 586.50 unknown via CMAUP database
Amaroswerin 45359883 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 602.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Vitamin K 5280483 Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)CCCC(C)CCCC(C)CCCC(C)C 450.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
24-Hydroxyursolic acid 44568920 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Scabraside 159134 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=C(C(=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 844.80 unknown via CMAUP database
Trifloroside 101688128 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C)OC(=O)C)OC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 782.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4aS)-5beta-Vinyl-6alpha-(6-O-acetyl-beta-D-glucopyranosyloxy)-4,4aalpha,5,6-tetrahydro-1H,3H-pyrano[3,4-c]pyran-1-one 102580780 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)O)O)O 400.40 unknown via CMAUP database
Swertiamarin 442435 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O 374.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(4aS)-5beta-Ethenyl-6alpha-[6-O-[2-hydroxy-3-(beta-D-glucopyranosyloxy)benzoyl]-beta-D-glucopyranosyloxy]-4,4aalpha,5,6-tetrahydro-1H,3H-pyrano[3,4-c]pyran-1-one 49802965 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)COC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 656.60 unknown via CMAUP database
(4aS)-5beta-Vinyl-6alpha-[3-O-[2-hydroxy-3-(beta-D-glucopyranosyloxy)benzoyl]-6-O-acetyl-beta-D-glucopyranosyloxy]-4,4aalpha,5,6-tetrahydro-1H,3H-pyrano[3,4-c]pyran-1-one 102580781 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)O)OC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O 698.60 unknown via CMAUP database
Gentistraminoside A 102280042 Click to see CC(=O)OC1C(OC(C(C1O)O)OC2C(C3CCOC(=O)C3=CO2)C=C)COC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 698.60 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
[(1R,14R,19R)-3,13-diazapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-2(10),4,6,8,17-pentaen-17-yl]methanol 11220563 Click to see C1CC2C3=C(CCN2C4C1C=C(CC4)CO)C5=CC=CC=C5N3 308.40 unknown https://doi.org/10.1016/S0040-4039(99)00306-8
3,13-Diazapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-2(10),4,6,8,17-pentaen-17-ylmethanol 72756660 Click to see C1CC2C3=C(CCN2C4C1C=C(CC4)CO)C5=CC=CC=C5N3 308.40 unknown https://doi.org/10.1016/S0040-4039(99)00306-8
Tangutorine 15406418 Click to see C1CC2C3=C(CCN2C4C1C=C(CC4)CO)C5=CC=CC=C5N3 308.40 unknown https://doi.org/10.1016/S0040-4039(99)00306-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Vincetoxicoside B 5748601 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O 448.40 unknown via CMAUP database

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