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Ammopiptanthus mongolicus

Ammopiptanthus mongolicus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd9959c5f5212214600
Scientific name Ammopiptanthus mongolicus
Authority (Maxim. ex Kom.) S.H.Cheng
First published in Bot. Zhurn. (Moscow & Leningrad)44: 1382 (1959)

Description Top

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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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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
      • 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!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_037576485.1 ASM3757648v1 Chromosome Minzu University of China 2024-03-27 167.2x 778.83 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
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
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
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
Quantitative Phosphoproteomic Analysis Provides Insights into the Sodium Bicarbonate Responsiveness of Glycine max Li Q, Li M, Ma H, Xue M, Chen T, Ding X, Zhang S, Xiao J Biomolecules 13-Oct-2023
PMCID:PMC10605096
doi:10.3390/biom13101520
PMID:37892202
Leaf–Root–Soil Stoichiometric Characteristics in Different Shrub Ages of Ammopiptanthus mongolicus  Dong X, Xu D, Wang D, Han C, Huang Y, Zhang J Plants (Basel) 29-Aug-2023
PMCID:PMC10490301
doi:10.3390/plants12173103
PMID:37687349
Comparative analysis of the complete mitogenome of Geoffroea decorticans: a native tree surviving in the Atacama Desert Contreras-Díaz R, Carevic FS, van den Brink L Front Genet 10-Aug-2023
PMCID:PMC10448962
doi:10.3389/fgene.2023.1226052
PMID:37636265
Differences in the Suitable Distribution Area between Northern and Southern China Landscape Plants Wang C, Sheng Q, Zhao R, Zhu Z Plants (Basel) 20-Jul-2023
PMCID:PMC10385631
doi:10.3390/plants12142710
PMID:37514324
Identification of the Efficacy of Ex Situ Conservation of Ammopiptanthus nanus Based on Its ETS-SSR Markers Liu J, Wang X, Lu T, Wang J, Shi W Plants (Basel) 17-Jul-2023
PMCID:PMC10386304
doi:10.3390/plants12142670
PMID:37514284
Plant dehydrins and dehydrin-like proteins: characterization and participation in abiotic stress response Szlachtowska Z, Rurek M Front Plant Sci 06-Jul-2023
PMCID:PMC10358736
doi:10.3389/fpls.2023.1213188
PMID:37484455

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 C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.4268/CJCMM20110821
https://doi.org/10.1135/CCCC19901257
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
(-)-Sparteine 3966 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1007/BF00564846
3alpha-Hydroxylupanine 44559669 Click to see C1CCN2CC3CC(C2C1)CN4C3CCC(C4=O)O 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 C1CCN2CC3CC(C2C1)CN4C3CCC(C4=O)O 264.36 unknown https://doi.org/10.1135/CCCC19901257
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.4268/CJCMM20110821
Lupanine 91471 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.4268/CJCMM20110821
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 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 C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1135/CCCC19901257
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol dimethyl ether 14237703 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 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 CC12CCC(=O)C(C1CCC34C2CCC(C3)C(=C)C4)(CO)CO 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Demethoxycacalohastine 638210 Click to see CC1CC=CC2=CC3=C(C(=CO3)C)C(=C12)C 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 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)O)O)O)O)O)O)O 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-Hydroxy-3',4',7-trimethoxyflavone 5272653 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 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
Isothymonin 4'-methyl ether 72714814 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)O)OC)OC)O)OC 374.30 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 COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
5-o-Desmethylnobiletin 358832 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 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 C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1002/HLCA.200890108
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1002/HLCA.200890108
Glycitein 5317750 Click to see COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)O 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 CC=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 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 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
[3,4,5-Trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl but-2-enoate 162867737 Click to see CC=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 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 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1135/CCCC19901257
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3733033 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1135/CCCC19901257
https://doi.org/10.1002/HLCA.200890108
5-Hydroxy-3-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 137796468 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 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 COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O 460.40 unknown https://doi.org/10.1002/HLCA.200890108
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1002/HLCA.200890108
Pratensein 7-O-glucopyranoside 16202157 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1002/HLCA.200890108
Wistin 10095770 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O 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
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1002/HLCA.200890108
https://doi.org/10.1135/CCCC19901257
Pratensein 5281803 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown 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 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1135/CCCC19901257
https://doi.org/10.1002/HLCA.200890108
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1002/CHIN.199036288
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1002/CHIN.199036288

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