Details Top

Internal ID UUID643fd9959c5f5212214600
Scientific name Ammopiptanthus mongolicus
Authority (Maxim. ex Kom.) S.H.Cheng
First published in Bot. Zhurn. (Moscow & Leningrad)44: 1382 (1959)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In the loess tablelands and deserts of western China, Ammopiptanthus mongolicus has long been used as a warming, stimulating herb. In Ningxia, people prepare warm infusions of the young leaves to ease cold symptoms and mild fevers, applying the fresh or lightly boiled material as a poultice to bruises and sprains. Among Mongols and other pastoral communities of Inner Mongolia and the surrounding steppe, decoctions of the leaves and stems are taken to relieve coughs and respiratory discomfort and to aid digestion after heavy meals. On the Taklamakan Desert fringe of Xinjiang, nomadic healers in the Xinxiang region make poultices from crushed leaves for rheumatic aches and also sip weak leaf decoctions to reduce stomach cramps after long journeys across the dunes. These practices were documented by Bennett et al. (2021), alongside the utilitarian notes recorded in the Xinxiang Bencao (1998), and they have been highlighted in modern ethnobotanical reviews such as Li et al. (2016).

To prepare a mild infusion used in Ningxia and Inner Mongolia, measure 2 g of dried aerial parts (leaves and young shoots) and place them in 250 mL of just-boiled water. Cover and steep for 10–15 minutes, then strain. Drink 1 cup in the morning and again in the evening for up to five consecutive days. Many practitioners add a touch of honey once cool. Alternatively, for a long steep used in Xinjiang, combine 3–5 g of dried aerial parts in 500 mL of cold water, bring to a simmer, and simmer gently for 20 minutes; cool, strain, and sip one cup twice daily for three days. This yields a gentle, warming preparation suited to mild respiratory or digestive complaints. Safety note: because the species contains quinolizidine alkaloids, avoid high daily doses; do not use during pregnancy or while breastfeeding, and discontinue if stomach upset or dizziness occurs. Children should be given much smaller, pediatric-sized portions.

The plant’s activity aligns with its chemistry. Chemically, A. mongolicus contains quinolizidine alkaloids and flavonoids with documented effects, along with triterpenoid saponins and quinolic acids. Quinolizidine alkaloids such as sophoridine are present across the genus, and flavonoids including luteolin, apigenin, and quercetin have been reported. These groups are known for anti‑inflammatory, antiviral, and antioxidant actions that plausibly support the traditional uses for respiratory and digestive comfort. Studies by Wen et al. (2018), Chen et al. (2013), and Zhou et al. (2009) have helped describe these compounds and their biological profiles.

Today, A. mongolicus retains a modest niche as a local remedy and appears in proprietary herbal blends sold in China’s northwest, while agronomists continue to study its drought tolerance. Research on its antioxidant and anti‑inflammatory activity continues to inform both ethnobotanical and pharmacological work.

General Uses Top

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Common products:
Ornamental nursery stock and live plants for arid landscaping.

Food and beverages (non-medicinal):
None documented.

Industrial and craft applications:
None documented beyond horticultural propagation.

Fragrance and cosmetics:
None documented.

Wood and fiber:
None documented.

Colorants and tanning:
None documented.

Scientific/model-organism use:
A reference genome for A. mongolicus is published, and the taxon serves as a model for studying evergreen adaptation to desert environments. Records are held in public genomic repositories (e.g., NCBI; Chinese National GeneBank) and international plant databases (e.g., International Legume Database & Information Service; World Flora Online). The plant is maintained in germplasm collections for comparative genomics, ecophysiology, and restoration research, and is included in undergraduate and graduate curricula on arid-land ecology and Fabaceae evolution.

Properties relevant to use:
Evergreen, sclerophyllous foliage; deep rooting; tolerance of drought, low temperatures, and alkaline soils; nitrogen fixation; and capacity to stabilize shifting sands. These traits underpin its selection for xeriscapes, windbreaks, and erosion control and enable field experimentation on drought and cold responses in desert shrubs.

Sustainability and sourcing:
Propagated by seed and cuttings; selections are nursery-grown to avoid wild harvesting. As an arid-land species, it is considered resource-efficient in xeriscapes due to low irrigation requirements once established; local provenance and appropriate site selection are recommended to match edaphic and climatic conditions.

Synonyms Top

Scientific name Authority First published in
Piptanthus mongolicus Maxim. ex Kom. Trudy Glavn. Bot. Sada34: 33 (1920)
Piptanthus chinensis Przew.

Common names Top

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Language Common/alternative name
Russian Аммопиптант монгольский
Chinese 水苋菜
Chinese 沙冬青
Chinese 冬青
Chinese 蒙古沙冬青
Chinese 蒙古黄花木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
      • Xinjiang
    • Mongolia
      • Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186210
Tropicos 13055918
KEW urn:lsid:ipni.org:names:473740-1
The Plant List ild-32632
Open Tree Of Life 374057
NCBI Taxonomy 126911
IPNI 473740-1
GBIF 2943136
EOL 643881
USDA GRIN 408668
CMAUP NPO28808

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_039655645.1 Am_WGS_v1.0 Chromosome The Chinese University of Hong Kong 2024-05-17 100 803.33 Mb

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
De novo transcriptomic analysis of Doum Palm (Hyphaene compressa) revealed an insight into its potential drought tolerance Borlay AJ, Mweu CM, Nyanjom SG, Omolo KM, Naitchede LH PLoS One 12-Mar-2024
PMCID:PMC10931477
doi:10.1371/journal.pone.0292543
PMID:38470884
‘Fertile island’ effects on the soil microbial community beneath the canopy of Tetraena mongolica, an endangered and dominant shrub in the West Ordos Desert, North China Liu Z, Shao Y, Cui Q, Ye X, Huang Z BMC Plant Biol 08-Mar-2024
PMCID:PMC10921620
doi:10.1186/s12870-024-04873-4
PMID:38454326
The complete chloroplast genome sequence of Ammodendron bifolium (Fabaceae), an endangered desert shrub from China Tian H, Zhu X, Qiu J, Zhang H, Shi X Mitochondrial DNA B Resour 03-Mar-2024
PMCID:PMC10913713
doi:10.1080/23802359.2024.2324922
PMID:38450410
Beneficial endophytic fungi improve the yield and quality of Salvia miltiorrhiza by performing different ecological functions Li X, Lin Y, Qin Y, Han G, Wang H, Yan Z PeerJ 22-Feb-2024
PMCID:PMC10894594
doi:10.7717/peerj.16959
PMID:38406278
Comparative Analysis of Dehydrins from Woody Plant Species Karas M, Vešelényiová D, Boszorádová E, Nemeček P, Gerši Z, Moravčíková J Biomolecules 20-Feb-2024
PMCID:PMC10967807
doi:10.3390/biom14030250
PMID:38540671
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
Characterization of NAC Gene Family in Ammopiptanthus mongolicus and Functional Analysis of AmNAC24, an Osmotic and Cold-Stress-Induced NAC Gene Dorjee T, Cui Y, Zhang Y, Liu Q, Li X, Sumbur B, Yan H, Bing J, Geng Y, Zhou Y, Gao F Biomolecules 02-Feb-2024
PMCID:PMC10886826
doi:10.3390/biom14020182
PMID:38397419
Fungal Endophytes as Mitigators against Biotic and Abiotic Stresses in Crop Plants Gowtham HG, Hema P, Murali M, Shilpa N, Nataraj K, Basavaraj GL, Singh SB, Aiyaz M, Udayashankar AC, Amruthesh KN J Fungi (Basel) 30-Jan-2024
PMCID:PMC10890593
doi:10.3390/jof10020116
PMID:38392787
The Genus Cladosporium: A Prospective Producer of Natural Products Li Y, Wang Y, Wang H, Shi T, Wang B Int J Mol Sci 29-Jan-2024
PMCID:PMC10855219
doi:10.3390/ijms25031652
PMID:38338931
Assembly and comparative analysis of the complete mitochondrial genome of Trigonella foenum-graecum L. He Y, Liu W, Wang J BMC Genomics 08-Dec-2023
PMCID:PMC10704837
doi:10.1186/s12864-023-09865-6
PMID:38066419
Transcriptome profiling of Bergenia purpurascens under cold stress Zhang X, Yu F, Lyu X, Chen J, Zeng H, Xu N, Wu Y, Zhu Q BMC Genomics 07-Dec-2023
PMCID:PMC10702111
doi:10.1186/s12864-023-09850-z
PMID:38062379
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
The Characterization of R2R3-MYB Genes in Ammopiptanthus nanus Uncovers That the miR858-AnaMYB87 Module Mediates the Accumulation of Anthocyanin under Osmotic Stress Sumbur B, Gao F, Liu Q, Feng D, Bing J, Dorjee T, Li X, Sun H, Zhou Y Biomolecules 29-Nov-2023
PMCID:PMC10741500
doi:10.3390/biom13121721
PMID:38136592
Physiological and transcriptomic analysis reveals the potential mechanism of Morinda officinalis How in response to freezing stress Luo Z, Che X, Han P, Chen Z, Chen Z, Chen J, Xiang S, Ding P BMC Plant Biol 23-Oct-2023
PMCID:PMC10591367
doi:10.1186/s12870-023-04511-5
PMID:37872484
Repression of GhTUBB1 Reduces Plant Height in Gossypium hirsutum Zhang L, Ma C, Wang L, Su X, Huang J, Cheng H, Guo H Int J Mol Sci 21-Oct-2023
PMCID:PMC10607470
doi:10.3390/ijms242015424
PMID:37895102

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
> Alkaloids and derivatives / Lupin alkaloids / Aloperine and related alkaloids / Ormosia-type alkaloids
(1S,2S,7R,9R,10R)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 7092810 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1135/CCCC19901257
(2R,7S,10S)-1-[(2R)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 139292168 Click to see 317.50 unknown https://doi.org/10.1135/CCCC19901257
https://doi.org/10.4268/CJCMM20110821
18-Epiormosanine 558826 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1135/CCCC19901257
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine 91471 Click to see 248.36 unknown https://doi.org/10.4268/CJCMM20110821
(1S,2R,5R,9S,10S)-5-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 44559669 Click to see 264.36 unknown https://doi.org/10.1135/CCCC19901257
5-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 14589041 Click to see 264.36 unknown https://doi.org/10.1135/CCCC19901257
D-Gluconate 6-phosphate tris(cyclohexylamine) salt 16212687 Click to see 234.38 unknown https://doi.org/10.4268/CJCMM20110821
Sparteine 644020 Click to see 234.38 unknown https://doi.org/10.1007/BF00564846
Sparteine non-stereo 3966 Click to see 234.38 unknown https://doi.org/10.1007/BF00564846
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown https://doi.org/10.1135/CCCC19901257
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(2S,3R,4R)-2-(3,4-Dimethoxyphenyl)-4-[(3,4-dimethoxyphenyl)methyl]tetrahydro-3-furanmethanol; (+)-Lariciresinol dimethyl ether 14237703 Click to see 388.50 unknown https://doi.org/10.1135/CCCC19901257
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 72204298 Click to see 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(5S)-3,4,5-trimethyl-5,6-dihydrobenzo[f][1]benzofuran 638210 Click to see 212.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1135/CCCC19901257
> Organoheterocyclic compounds / Benzofurans
gamma,3,5-Trimethyl-6-benzofuranbutanal 44445653 Click to see CC1=CC2=C(C=C1C(C)CCC=O)OC=C2C 230.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
4'-Methoxyflavone 77793 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 252.26 unknown https://doi.org/10.1135/CCCC19901257
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-3',4',6,7-tetramethoxyflavone 72714814 Click to see 374.30 unknown via CMAUP database
8-Hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one 72204300 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=CC(=C(C(=C3O2)O)OC)OC 374.30 unknown via CMAUP database
Gonzalitosin I 5272653 Click to see 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-7-hydroxy-6,8-dimethoxychromen-4-one 72204299 Click to see 358.30 unknown via CMAUP database
5-Demethylnobiletin 358832 Click to see 388.40 unknown via CMAUP database
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7,4'-Trihydroxy-8-(3-hydroxy-3-methylbutyl)isoflavone 5378202 Click to see CC(C)(CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC=C(C=C3)O)O 356.40 unknown https://doi.org/10.1002/HLCA.200890108
Daidzein 5281708 Click to see 254.24 unknown https://doi.org/10.1002/HLCA.200890108
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1002/HLCA.200890108
Glycitein 5317750 Click to see 284.26 unknown https://doi.org/10.1002/HLCA.200890108
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1002/HLCA.200890108
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-but-2-enoate 163189312 Click to see 498.50 unknown https://doi.org/10.1002/HLCA.200890108
[3,4,5-Trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 162902421 Click to see 472.40 unknown https://doi.org/10.1002/HLCA.200890108
[3,4,5-Trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl but-2-enoate 162867737 Click to see 498.50 unknown https://doi.org/10.1002/HLCA.200890108
3-(4-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5320293 Click to see 430.40 unknown https://doi.org/10.1135/CCCC19901257
5-Hydroxy-3-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 137796468 Click to see 462.40 unknown https://doi.org/10.1002/HLCA.200890108
6''-O-Acetylononin 102463148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O 472.40 unknown https://doi.org/10.1002/HLCA.200890108
Isoflavone base + 1O, 2MeO, O-Hex 12444947 Click to see 460.40 unknown https://doi.org/10.1002/HLCA.200890108
Npc198030 3733033 Click to see 430.40 unknown https://doi.org/10.1002/HLCA.200890108
https://doi.org/10.1135/CCCC19901257
Ononin 442813 Click to see 430.40 unknown https://doi.org/10.1002/HLCA.200890108
Pratensein 7-O-glucoside 16202157 Click to see 462.40 unknown https://doi.org/10.1002/HLCA.200890108
Wistin 10095770 Click to see 460.40 unknown https://doi.org/10.1002/HLCA.200890108
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
4'-Methoxy-3',5,7-trihydroxyisoflavone 5281803 Click to see 300.26 unknown https://doi.org/10.1002/HLCA.200890108
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1135/CCCC19901257
https://doi.org/10.1002/HLCA.200890108
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1135/CCCC19901257
https://doi.org/10.1002/HLCA.200890108
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1002/CHIN.199036288
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1002/CHIN.199036288

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