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Ammodendron bifolium

Ammodendron bifolium - 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 UUID643fd9754ac10005718120
Scientific name Ammodendron bifolium
Authority (Pall.) Yakovlev
First published in Bot. Zhurn. (Moscow & Leningrad)57: 592 (1972)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ammodendron argenteum (Siev.) Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada10: 180 (1887)
Sophora bifolia Pall. Sp. Astragal.: 124 (1800)
Ammodendron floribundum V.J.Zinger
Ammodendron lehmannii Bunge ex Boiss. Fl. Orient.2: 626 (1872)
Podalyria argentea (Siev.) Willd. Sp. Pl., ed. 4, 2: 502 (1799)
Robinia argentea Siev. Neueste Nord. Beytr. Phys. Geogr. Erd- Völkerbeschreib.7: 326 (1796)
Virgilia argentea Poir. J.B.A.M.de Lamarck, Encycl.8: 679 (1808)
Hallia argentea Spreng. Syst. Veg. ed. 16, 3: 195 (1826)
Ammodendron bifolium var. lehmannianum (Bunge) Yakovlev Bot. Zhurn. (Moscow & Leningrad)67: 60 (1982)

Common names Top

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Language Common/alternative name
Chinese 银砂槐

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
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Turkmenistan
      • Uzbekistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185596
Tropicos 13056476
KEW urn:lsid:ipni.org:names:473728-1
The Plant List ild-31873
Open Tree Of Life 288754
Observations.org 114393
NCBI Taxonomy 247904
IPNI 473728-1
GBIF 2971159
EOL 643533
Elurikkus 2740
USDA GRIN 102024

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
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
Combining Multiple Plant Attributes to Reveal Differences in Community Structure in Two Distant Deserts in Central Asia Tao Y, Zhou XB, Yin BF, Dimeyeva L, Zhang J, Zang YX, Zhang YM Plants (Basel) 17-Sep-2023
PMCID:PMC10537988
doi:10.3390/plants12183286
PMID:37765450
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Deciphering the genetic and functional diversity of cultivable bacteria from chasmophytic pigweed (Chenopodium album) from Tsomoriri, Ladakh, India Das S, Verma S, Choudhary P, Singh R, Saxena AK 3 Biotech 23-Aug-2022
PMCID:PMC9399335
doi:10.1007/s13205-022-03278-0
PMID:36032512
The Multifunctions and Future Prospects of Endophytes and Their Metabolites in Plant Disease Management Xia Y, Liu J, Chen C, Mo X, Tan Q, He Y, Wang Z, Yin J, Zhou G Microorganisms 23-May-2022
PMCID:PMC9146654
doi:10.3390/microorganisms10051072
PMID:35630514
Is Plant Life-History of Biseasonal Germination Consistent in Response to Extreme Precipitation? Chen Y, Zhang H, Zhang L, Zhang L, Cao Q, Liu H, Zhang D Plants (Basel) 10-Aug-2021
PMCID:PMC8402233
doi:10.3390/plants10081642
PMID:34451688
Harnessing Bacterial Endophytes for Promotion of Plant Growth and Biotechnological Applications: An Overview Eid AM, Fouda A, Abdel-Rahman MA, Salem SS, Elsaied A, Oelmüller R, Hijri M, Bhowmik A, Elkelish A, Hassan SE Plants (Basel) 07-May-2021
PMCID:PMC8151188
doi:10.3390/plants10050935
PMID:34067154
Arbuscular Mycorrhizal Fungal Communities in the Soils of Desert Habitats Vasar M, Davison J, Sepp SK, Öpik M, Moora M, Koorem K, Meng Y, Oja J, Akhmetzhanova AA, Al-Quraishy S, Onipchenko VG, Cantero JJ, Glassman SI, Hozzein WN, Zobel M Microorganisms 22-Jan-2021
PMCID:PMC7912695
doi:10.3390/microorganisms9020229
PMID:33499315
Dataset of pollen morphological traits of 56 dominant species among desert vegetation in the eastern arid central Asia Lu KQ, Xie G, Li M, Li JF, Trivedi A, Ferguson DK, Yao YF, Wang YF Data Brief 31-Mar-2018
PMCID:PMC5996618
doi:10.1016/j.dib.2018.03.122
PMID:29900271
Evolutionary response to the Qinghai-Tibetan Plateau uplift: phylogeny and biogeography of Ammopiptanthus and tribe Thermopsideae (Fabaceae) Shi W, Liu PL, Duan L, Pan BR, Su ZH PeerJ 31-Jul-2017
PMCID:PMC5541923
doi:10.7717/peerj.3607
PMID:28785518
Effects of Salt-Drought Stress on Growth and Physiobiochemical Characteristics of Tamarix chinensis Seedlings Liu J, Xia J, Fang Y, Li T, Liu J ScientificWorldJournal 22-Jul-2014
PMCID:PMC4130323
doi:10.1155/2014/765840
PMID:25140348
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899
Chemical study of the epigeal parts of the plantsAmmothamnus lehmannii andCicer mogoltavicum A. Zh. Gafurov, A. Sattikulov, �. Kh. Batirov, V. M. Malikov Springer Science and Business Media LLC 15-Feb-2005
doi:10.1007/BF01170227
Flavonoids of Ammothamnus lehmannii. Structure of lehmannin and of ammothamnidin É. Kh. Bakirov, S. S. Yusupova, A. Sattikulov, A. D. Vdovin, V. M. Malikov, M. R. Yagudaev Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00597799
Flavonoids fromAmmothamnus lehmannii Sh. V. Abdullaev, A. Sattikulov, �. Kh. Batirov, Yu. V. Kurbatov, V. M. Malikov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579979

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00571215
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(1R,2R,9S,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 161544 Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] 262.35 unknown https://doi.org/10.1007/BF00571215
Ammothamnine 114850 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown https://doi.org/10.1007/BF00571215
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1007/BF00571215
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1007/BF00571215
Sophocarpidine 24721085 Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] 262.35 unknown https://doi.org/10.1007/BF00571215
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1007/BF00571215
https://doi.org/10.2307/4117899
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/BF00575055
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00575055
> 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/10.1007/BF00575055
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Malonic acid 867 Click to see C(C(=O)O)C(=O)O 104.06 unknown https://doi.org/10.1007/BF00575055
Oxalic Acid 971 Click to see C(=O)(C(=O)O)O 90.03 unknown https://doi.org/10.1007/BF00575055
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.1007/BF00575055
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid 311 Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O 192.12 unknown https://doi.org/10.1007/BF00575055
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
Lactic Acid 612 Click to see CC(C(=O)O)O 90.08 unknown https://doi.org/10.1007/BF00575055
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid 525 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.1007/BF00575055
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
DL-Tartaric acid 875 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown https://doi.org/10.1007/BF00575055
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00575055
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00575055
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Lehmannin 4359200 Click to see CC(=CCC(CC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 408.50 unknown https://doi.org/10.1016/0305-1978(95)00056-9
https://doi.org/10.1007/BF01170227
https://doi.org/10.1007/BF00597799
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00579979
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/BF00579979
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00579979
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 https://doi.org/10.1007/BF00579979
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00579979
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[2,4-dihydroxy-3-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-3-(2-hydroxyphenyl)prop-2-en-1-one 163185433 Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2O)O)C(=C)C)C 392.50 unknown https://doi.org/10.1007/BF00579979
1-[2,4-Dihydroxy-3-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)phenyl]-3-(2-hydroxyphenyl)prop-2-en-1-one 73814661 Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2O)O)C(=C)C)C 392.50 unknown https://doi.org/10.1007/BF00579979
Ammothamnidin 6247097 Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C 408.50 unknown https://doi.org/10.1016/0305-1978(95)00056-9
https://doi.org/10.1007/BF00575695
https://doi.org/10.1007/BF01170227
https://doi.org/10.1007/BF00597799

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