Euryale ferox - Unknown
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Internal ID UUID64401bf2e157f607224430
Scientific name Euryale ferox
Authority Salisb.
First published in Ann. Bot. (König & Sims) 2: 74 (1805)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anneslea spinosa Andrews Bot. Repos. x. t. 618.
Euryale indica Planch. Ann. Sci. Nat., Bot. , sér. 3, 19: 29 (1853)

Common names Top

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Language Common/alternative name
English prickly water lily
English gorgon
English fox nut
English gorgon plant
English prickly waterlily
Spanish aneslea
Azerbaijani qorxunc evrial
Azerbaijani evrial
Bengali মাখনা
Persian نیلوفر آبی روباه
Hindi मखाना
Croatian eurijale
Japanese オニバス
Japanese オニバス属
Korean 가시연꽃
Korean 가시연
lzh
mai मखान
Burmese ဆင်ကြာ
Punjabi ਮਖਾਣਾ
Polish rozłożnia kolczasta
Polish eurjala
Polish eurjala kolczasta
Polish rozłożnia
Russian Эвриала устрашающая
Russian Эвриала
Swedish rävnäckros
Swedish rävnäckrossläktet
Thai เคียมซิก
Vietnamese khiếm thực
Chinese 芡实根
Chinese 芡实茎
Chinese 假莲藕
Chinese 刺莲藕
Chinese 湖南根
Chinese 芡实叶
Chinese 芡实(芡)
Chinese 芡实
Chinese
Chinese 芡屬
Chinese 芡实属
Chinese 肇實
Chinese 水鸡头
Chinese 鸡头莲
Chinese 鸡头荷
Chinese 鸡头米

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
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Primorye
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000683330
UNII A1528YW4L9
USDA Plants EUFE6
Tropicos 22600010
KEW urn:lsid:ipni.org:names:605350-1
The Plant List kew-2805127
Open Tree Of Life 583533
Observations.org 125130
NCBI Taxonomy 4414
IUCN Red List 168756
IPNI 605350-1
iNaturalist 183481
GBIF 5333335
Freebase /m/0bs5jz
EPPO EYUFE
EOL 485242
USDA GRIN 16447
Wikipedia Euryale_ferox
CMAUP NPO2438
PaleoBotany 116405

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
Jian-Pi-Gu-Shen-Hua-Yu Decoction Alleviated Diabetic Nephropathy in Mice through Reducing Ferroptosis Lv S, Fan L, Chen X, Su X, Dong L, Wang Q, Wang Y, Zhang H, Cui H, Zhang S, Wang L J Diabetes Res 16-Mar-2024
PMCID:PMC10960652
doi:10.1155/2024/9990304
PMID:38523631
SKP alleviates the ferroptosis in diabetic kidney disease through suppression of HIF-1α/HO-1 pathway based on network pharmacology analysis and experimental validation Yan Y, Yuan N, Chen Y, Ma Y, Chen A, Wang F, Yan S, He Z, He J, Zhang C, Wang H, Wang M, Diao J, Xiao W Chin Med 25-Feb-2024
PMCID:PMC10894492
doi:10.1186/s13020-024-00901-5
PMID:38403669
Research Progress in Modifications, Bioactivities, and Applications of Medicine and Food Homologous Plant Starch Chen K, Wei P, Jia M, Wang L, Li Z, Zhang Z, Liu Y, Shi L Foods 12-Feb-2024
PMCID:PMC10888398
doi:10.3390/foods13040558
PMID:38397535
An exploration of the effect of Chinese herbal compound on the occurrence and development of large intestine cancer and intestinal flora Liu P, Ying J, Guo X, Tang X, Zou W, Wang T, Xu X, Zhao B, Song N, Cheng J Heliyon 10-Dec-2023
PMCID:PMC10761579
doi:10.1016/j.heliyon.2023.e23533
PMID:38173486
Diverse O-methyltransferases catalyze the biosynthesis of floral benzenoids that repel aphids from the flowers of waterlily Nymphaea prolifera Liu G, Fu J, Wang L, Fang M, Zhang W, Yang M, Yang X, Xu Y, Shi L, Ma X, Wang Q, Chen H, Yu C, Yu D, Chen F, Jiang Y Hortic Res 06-Nov-2023
PMCID:PMC10753166
doi:10.1093/hr/uhad237
PMID:38156285
Non-Traditional Starches, Their Properties, and Applications Šárka E, Sinica A, Smrčková P, Sluková M Foods 16-Oct-2023
PMCID:PMC10606120
doi:10.3390/foods12203794
PMID:37893687
Bioinformatics Analysis of MSH1 Genes of Green Plants: Multiple Parallel Length Expansions, Intron Gains and Losses, Partial Gene Duplications, and Alternative Splicing Bai MZ, Guo YY Int J Mol Sci 03-Sep-2023
PMCID:PMC10487979
doi:10.3390/ijms241713620
PMID:37686425
Effect of heat-clearing and dampness-eliminating Chinese medicine for high-risk cervical cancer papillomavirus infection: a systematic review and meta-analysis of randomized controlled trials Huang S, Qi Y, Chen S, He B, Chen X, Xu J Front Med (Lausanne) 24-Aug-2023
PMCID:PMC10484520
doi:10.3389/fmed.2023.1022030
PMID:37692777
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
DNA from herbs can be obtained from air and authenticated by polymerase chain reaction Ngai HL, Lee HK, Shaw PC Heliyon 06-Aug-2023
PMCID:PMC10447936
doi:10.1016/j.heliyon.2023.e18946
PMID:37636375
Study on the function of Huazhuo Jiedu Decoction in promoting the homing of bone marrow mesenchymal stem cells and contributing to the treatment of ulcerative colitis Ma Y, Li Y, Zhang S, Liu Z, Du L, Zhang X, Jia X, Yang Q Heliyon 28-Jul-2023
PMCID:PMC10415889
doi:10.1016/j.heliyon.2023.e18802
PMID:37576246
Editorial: Advances in plant hormone research in the face of a changing environment Müller M, Wang R, Kudoyarova G Front Plant Sci 25-Jul-2023
PMCID:PMC10408289
doi:10.3389/fpls.2023.1239758
PMID:37560027
Chromosome-level genome assembly of watershield (Brasenia schreberi) Lu B, Shi T, Chen J Sci Data 19-Jul-2023
PMCID:PMC10356934
doi:10.1038/s41597-023-02380-z
PMID:37468511
Field assessment of yield and its contributing traits in cowpea treated with lower, intermediate, and higher doses of gamma rays and sodium azide Raina A, Khan S Front Plant Sci 14-Jul-2023
PMCID:PMC10382141
doi:10.3389/fpls.2023.1188077
PMID:37521916
Polysaccharides from natural resource: ameliorate type 2 diabetes mellitus via regulation of oxidative stress network He LY, Li Y, Niu SQ, Bai J, Liu SJ, Guo JL Front Pharmacol 11-Jul-2023
PMCID:PMC10367013
doi:10.3389/fphar.2023.1184572
PMID:37497112

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R)-2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-4,8-dien-2-yl]docosanamide 16757499 Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCC)O)O 770.10 unknown https://doi.org/10.1021/NP070095J
(2R)-2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-4,8-dien-2-yl]tetracosanamide 16757500 Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCC)O)O 798.20 unknown https://doi.org/10.1021/NP070095J
2-hydroxy-N-[3-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-4,8-dien-2-yl]docosanamide 73324218 Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCC)O)O 770.10 unknown https://doi.org/10.1021/NP070095J
2-hydroxy-N-[3-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-4,8-dien-2-yl]tetracosanamide 73324219 Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCC)O)O 798.20 unknown https://doi.org/10.1021/NP070095J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,7R,7'R,14S,16R,19S)-4',5',7,7',10,11,16,21,22-nonamethyl-7,7',16-tris[(4R,8R)-4,8,12-trimethyltridecyl]spiro[8,13,15-trioxapentacyclo[12.4.4.01,14.03,12.04,9]docosa-3(12),4(9),10,21-tetraene-19,2'-8,9-dihydro-1H-furo[3,2-f]chromene]-20-one 163100590 Click to see CC1=C(C2=C(CC34CCC(OC3(O2)C(=C(C(=O)C45CC6=C(O5)C(=C(C7=C6CCC(O7)(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C)C)(C)CCCC(C)CCCC(C)CCCC(C)C)C8=C1OC(CC8)(C)CCCC(C)CCCC(C)CCCC(C)C)C 1272.00 unknown https://doi.org/10.1021/NP070095J
(1S,7R,7'R,14R,16R,19R)-4',5',7,7',10,11,16,21,22-nonamethyl-7,7',16-tris[(4R,8R)-4,8,12-trimethyltridecyl]spiro[8,13,15-trioxapentacyclo[12.4.4.01,14.03,12.04,9]docosa-3(12),4(9),10,21-tetraene-19,2'-8,9-dihydro-1H-furo[3,2-f]chromene]-20-one 163100589 Click to see CC1=C(C2=C(CC34CCC(OC3(O2)C(=C(C(=O)C45CC6=C(O5)C(=C(C7=C6CCC(O7)(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C)C)(C)CCCC(C)CCCC(C)CCCC(C)C)C8=C1OC(CC8)(C)CCCC(C)CCCC(C)CCCC(C)C)C 1272.00 unknown https://doi.org/10.1021/NP070095J
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3abeta,4R,6abeta,9abeta,9balpha)-3,6,9-Trismethylene-4alpha-(4-hydroxyphenylacetyloxy)-8alpha-(beta-D-glucopyranosyloxy)dodecahydroazuleno[4,5-b]furan-2-one 10076444 Click to see C=C1CC(C2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C)OC(=O)CC5=CC=C(C=C5)O 558.60 unknown via CMAUP database
8-Epicrepiside E 21636138 Click to see C=C1CC(C2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C)O 424.40 unknown via CMAUP database
Ftidkiazunxncj-wbyqcalvsa- 21636136 Click to see CC1(CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C)O 426.50 unknown via CMAUP database
Macrocliniside A 10455028 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown via CMAUP database
Vernoflexuoside 442320 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6021 Click to see C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)CO)O)O 268.23 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides / Purine 2-deoxyribonucleosides
2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 187790 Click to see C1C(C(OC1N2C=NC3=C2NC(=NC3=O)N)CO)O 267.24 unknown via CMAUP database
2-Deoxyadenosine 636 Click to see C1C(C(OC1N2C=NC3=C(N=CN=C32)N)CO)O 251.24 unknown via CMAUP database
2'-Deoxyadenosine 13730 Click to see C1C(C(OC1N2C=NC3=C(N=CN=C32)N)CO)O 251.24 unknown via CMAUP database
9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-ol 5280798 Click to see C1C(C(OC1N2C=NC3=C2N=CN=C3O)CO)O 252.23 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Cytidine 6175 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O 243.22 unknown via CMAUP database
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
2'-dC B-D-threo 451823 Click to see C1C(C(OC1N2C=CC(=NC2=O)N)CO)O 227.22 unknown via CMAUP database
2'-Deoxycytidine 13711 Click to see C1C(C(OC1N2C=CC(=NC2=O)N)CO)O 227.22 unknown via CMAUP database
2'-Deoxyuridine 13712 Click to see C1C(C(OC1N2C=CC(=O)NC2=O)CO)O 228.20 unknown via CMAUP database
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol 5274265 Click to see CC1=CN=C(N=C1O)O 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Cytosine 597 Click to see C1=C(NC(=O)N=C1)N 111.10 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
D-ascorbic acid 54690394 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790 790 Click to see C1=NC2=C(N1)C(=O)N=CN2 136.11 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Xanthine 1188 Click to see C1=NC2=C(N1)C(=O)NC(=O)N2 152.11 unknown via CMAUP database

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