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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
Patterns and driving factors of functional traits of desert species with different elevational distributions in the Tibetan Plateau and adjacent areas Hu Y, Li X, Wang S, Lv P, Yue P, Chen M, Zuo X BMC Plant Biol 09-May-2024
PMCID:PMC11080261
doi:10.1186/s12870-024-05080-x
PMID:38724940
Integrated transcriptome and metabolome analysis reveals the regulation of phlorizin synthesis in Lithocarpus polystachyus under nitrogen fertilization Zeng S, Yu L, He P, Feng H, Wang J, Zhang H, Song Y, Liu R, Li Y BMC Plant Biol 06-May-2024
PMCID:PMC11071233
doi:10.1186/s12870-024-05090-9
PMID:38711037
Adaptive strategies based on shrub leaf-stem anatomy and their environmental interpretations in the eastern Qaidam Basin Liu S, Zheng J BMC Plant Biol 24-Apr-2024
PMCID:PMC11040798
doi:10.1186/s12870-024-05026-3
PMID:38658848
Enhancing Rumen Fermentation and Bacteria Community in Sika Deer (Cervus nippon) through Varying Levels of Dragon Fruit Peel Polyphenolic Extract: An In Vitro Study Ban C, Tian X, Lu Q, Lounglawan P, Wen G Animals (Basel) 09-Apr-2024
PMCID:PMC11047680
doi:10.3390/ani14081139
PMID:38672287
Effects of Salt Stress on Salt-Repellent and Salt-Secreting Characteristics of Two Apple Rootstocks Zhang D, Zhang Z, Wang Y Plants (Basel) 08-Apr-2024
PMCID:PMC11013418
doi:10.3390/plants13071046
PMID:38611575
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
Separation Methods of Phenolic Compounds from Plant Extract as Antioxidant Agents Candidate Susanti I, Pratiwi R, Rosandi Y, Hasanah AN Plants (Basel) 27-Mar-2024
PMCID:PMC11013868
doi:10.3390/plants13070965
PMID:38611494
Physiological responses to drought stress of three pine species and comparative transcriptome analysis of Pinus yunnanensis var. pygmaea Xiao F, Zhao Y, Wang X, Jian X, Yang Y BMC Genomics 16-Mar-2024
PMCID:PMC10944613
doi:10.1186/s12864-024-10205-5
PMID:38493093
Formation, Identification, and Occurrence of the Furan-Containing β-Carboline Flazin Derived from l-Tryptophan and Carbohydrates Herraiz T, Salgado A J Agric Food Chem 12-Mar-2024
PMCID:PMC10979450
doi:10.1021/acs.jafc.3c07773
PMID:38470992
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
Shrub Growth Improves Morphological Features of Nebkhas: A Case Study of Nitraria tangutorum in the Tengger Desert Cheng L, Wu B, Pang Y, Jia X Plants (Basel) 24-Feb-2024
PMCID:PMC10934661
doi:10.3390/plants13050624
PMID:38475471
An Experimental Investigation of the Precipitation Utilization of Plants in Arid Regions Feng W, Ma X, Yuan Z, Li W, Yan Y, Yang W Plants (Basel) 22-Feb-2024
PMCID:PMC10934922
doi:10.3390/plants13050594
PMID:38475440
Research Progress in Traditional Applications, Phytochemistry, Pharmacology, and Safety Evaluation of Cynomorium songaricum Zhang J, Chen X, Han L, Ma B, Tian M, Bai C, Zhang Y Molecules 21-Feb-2024
PMCID:PMC10935076
doi:10.3390/molecules29050941
PMID:38474452
Demographic patterns of two related desert shrubs with overlapping distributions in response to past climate changes Yu Q, Hu J, Hu X, Zhou Y, Wang F, Jiang S, Wang Y Front Plant Sci 21-Feb-2024
PMCID:PMC10915042
doi:10.3389/fpls.2024.1345624
PMID:38450397
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

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
[(2R,3S,4S,5R,6S)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 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
[(2R,3R,4S,5R,6S)-2-(acetyloxymethyl)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-3,5-dihydroxyoxan-4-yl] 2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 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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