Ammodendron bifolium
Table of Contents
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 |
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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) |
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
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Asia-temperate click to expand
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China
- Xinjiang
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Middle Asia
- Kazakhstan
- Turkmenistan
- Uzbekistan
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China
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.
If you wish to see all the related articles click here.
Title | Authors | Publication | Released | IDs | ||||||
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 | R. Melville, J. J. Willaman, Hui-Lin Li | JSTOR | 27-Nov-2007 |
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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 |
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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 |
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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 |
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Structure of a new chalcone ammothamnidin fromAmmothamnus lehmanni | A. Sattikulov, Sh. V. Abdullaev, É. Kh. Batirov, Yu. V. Kurbatov, V. M. Malikov, A. D. Vdovin, M. R. Yagudaev | Springer Science and Business Media LLC | 20-Nov-2004 |
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Organic acids ofAmmothamnus lehmannii | A. Sattikulov, Sh. V. Abdullaev, É. Kh. Batirov, Yu. V. Kurbatov | Springer Science and Business Media LLC | 20-Nov-2004 |
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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 |
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> 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 | |||||
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 |
Oxymatrine | 114850 | Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] | 264.36 | unknown | https://doi.org/10.1007/BF00571215 |
Oxysophocarpine | 161544 | Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-] | 262.35 | 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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