Ammopiptanthus mongolicus
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
Suggest a correction!
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
Suggest a correction!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
Add a new one! Suggest a correction!| 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 |
Germination/Propagation Top
Suggest a correction or add new data!
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 click to expand
-
China
- China North-central
- Inner Mongolia
- Xinjiang
-
Mongolia
- Mongolia
-
China
Links to other databases Top
Suggest others/fix!| 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.
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.
If you wish to see all the related articles click here.
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
You can also contribute to this by clicking here.
| 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |