Phlebodium aureum - Unknown
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Internal ID UUID6440773dc16c1579970736
Scientific name Phlebodium aureum
Authority J.Sm.
First published in J. Bot. (Hooker) 4: 59 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chrysopteris martinicensis Fée 1867
Chrysopteris pulvinata Link Fil. Spec. 121. 1841 (1841)
Phlebodium grande T.Moore Index Fil. : 258 (1861)
Phlebodium microdictyum T.Moore Index Fil. : 258 (1861)
Phlebodium pulvinatum J.Sm. Bot. Mag. 72(Companion): 13 (1846)
Polypodium aureum L. Sp. Pl. : 1087 (1753)
Pleopeltis aurea C.Presl Tent. Pterid. 193. 1836. (1836)
Chrysopteris aurea Link Fil. Spec. : 121 (1841)
Polypodium pulvinatum Link Hort. Berol. 2: 99 (1833)
Chrysopteris grandis Fée Mém. Soc. Sci. Nat. Strasbourg 5: 96 1857
Chrysopteris microdictya Fée Mém. Soc. Sci. Nat. Strasbourg 5: 97 1857
Polypodium auratum Vell. Fl. Flumin. 11: t. 74 (1831)
Polypodium aureum var. pulvinatum (Link) Baker Syn. Fil. : 347 (1867)

Common names Top

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Language Common/alternative name
English polypodium leucotomos
English golden polypody
Bulgarian златист флебодиум
German goldtüpfelfarn
Finnish kultaimarre
Hungarian polypodium leucotomos
Japanese ダイオウウラボシ
Japanese フレボジウム・アウリウム
Japanese ポリポジウム・ロイコトモス
Macedonian златна дамчеста папрат
Dutch blauwvaren
Dutch zinkvaren
Polish flebodium złociste
Russian Флебодиум золотистый
Ukrainian Флебодіум золотий
Chinese 金水龙骨

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
      • Madeira
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Central American Pacific
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001109224
UNII 5CG94E4721
Florida Plant Atlas 3613
Flora of Alabama 159
USDA Plants PHAU6
Tropicos 26602380
INPN 706636
KEW urn:lsid:ipni.org:names:17175390-1
The Plant List tro-26602380
Open Tree Of Life 898321
NCBI Taxonomy 218620
Nature Serve 2.136270
IPNI 17175390-1
iNaturalist 127908
GBIF 2650479
Freebase /m/025v9d0
EPPO PBDAU
EOL 597266
USDA GRIN 27742
Wikipedia Phlebodium_aureum
CMAUP NPO23822

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
Bioactive Compounds for Combating Oxidative Stress in Dermatology Turcov D, Zbranca-Toporas A, Suteu D Int J Mol Sci 15-Dec-2023
PMCID:PMC10744063
doi:10.3390/ijms242417517
PMID:38139345
Investigating the biochemical signatures and physiological roles of the FMO family using molecular phylogeny Nicoll CR, Mascotti ML BBA Adv 04-Nov-2023
PMCID:PMC10682829
doi:10.1016/j.bbadva.2023.100108
PMID:38034983
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Metabolic link between auxin production and specialized metabolites in Sorghum bicolor Perez VC, Dai R, Tomiczek B, Mendoza J, Wolf ES, Grenning A, Vermerris W, Block AK, Kim J J Exp Bot 27-Oct-2022
PMCID:PMC9786853
doi:10.1093/jxb/erac421
PMID:36300527
Hydathodes in ferns: their phylogenetic distribution, structure and function Mehltreter K, Wachter H, Trabi C, Testo W, Sundue M, Jansen S Ann Bot 13-Jun-2022
PMCID:PMC9486916
doi:10.1093/aob/mcac076
PMID:35696156
Role of Phytochemicals in Skin Photoprotection via Regulation of Nrf2 Chaiprasongsuk A, Panich U Front Pharmacol 12-May-2022
PMCID:PMC9133606
doi:10.3389/fphar.2022.823881
PMID:35645796
Medicinal Plant Extracts and Natural Compounds for the Treatment of Cutaneous Lupus Erythematosus: A Systematic Review Lubov JE, Jamison AS, Baltich Nelson B, Amudzi AA, Haas KN, Richmond JM Front Pharmacol 31-Mar-2022
PMCID:PMC9008762
doi:10.3389/fphar.2022.802624
PMID:35431950
scGR-seq: Integrated analysis of glycan and RNA in single cells Odaka H, Ozaki H, Tateno H STAR Protoc 18-Feb-2022
PMCID:PMC8861808
doi:10.1016/j.xpro.2022.101179
PMID:35243371
Caliata: An Indigenous Community in Ecuador Offers Lessons on Food Sovereignty and Sustainable Diets Gallegos-Riofrío CA, Waters WF, Carrasco A, Riofrío LA, Pintag M, Caranqui M, Caranqui J, BlackDeer AA, Iannotti LL Curr Dev Nutr 13-May-2021
PMCID:PMC8242225
doi:10.1093/cdn/nzab009
PMID:34222768
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Discovery and Structural Analysis to Improve the Enantioselectivity of Hydroxynitrile Lyase from Parafontaria laminata Millipedes for (R)-2-Chloromandelonitrile Synthesis Nuylert A, Nakabayashi M, Yamaguchi T, Asano Y ACS Omega 15-Oct-2020
PMCID:PMC7643134
doi:10.1021/acsomega.0c03070
PMID:33163773
Synthesis of (R)-mandelic acid and (R)-mandelic acid amide by recombinant E. coli strains expressing a (R)-specific oxynitrilase and an arylacetonitrilase Müller E, Sosedov O, Gröning JA, Stolz A Biotechnol Lett 16-Sep-2020
PMCID:PMC7796878
doi:10.1007/s10529-020-02998-8
PMID:32936375
A flavin-dependent monooxygenase catalyzes the initial step in cyanogenic glycoside synthesis in ferns Thodberg S, Sørensen M, Bellucci M, Crocoll C, Bendtsen AK, Nelson DR, Motawia MS, Møller BL, Neilson EH Commun Biol 11-Sep-2020
PMCID:PMC7486406
doi:10.1038/s42003-020-01224-5
PMID:32917937
Effects of Exogenous Putrescine on Delaying Senescence of Cut Foliage of Nephrolepis cordifolia Qu Y, Jiang L, Wuyun T, Mu S, Xie F, Chen Y, Zhang L Front Plant Sci 10-Sep-2020
PMCID:PMC7511530
doi:10.3389/fpls.2020.566824
PMID:33013988
Insights into the evolutionary history and widespread occurrence of antheridiogen systems in ferns Hornych O, Testo WL, Sessa EB, Watkins JE Jr, Campany CE, Pittermann J, Ekrt L New Phytol 25-Aug-2020
PMCID:PMC7754499
doi:10.1111/nph.16836
PMID:32740926

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
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
N-[2-(4-Hydroxyphenyl)ethyl]benzamide 577614 Click to see C1=CC=C(C=C1)C(=O)NCCC2=CC=C(C=C2)O 241.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 304.50 unknown https://doi.org/10.1016/S0944-7113(98)80026-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Hexadecanamide 69421 Click to see CCCCCCCCCCCCCCCC(=O)N 255.44 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0944-7113(98)80026-3
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0944-7113(98)80026-3
Octadeca-9,12,15-trienoic acid 5282822 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0944-7113(98)80026-3
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Diploptene 92155 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1002/PCA.2800060106
Diplopterol 164874 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1002/PCA.2800060106
Hop-21-ene 121232688 Click to see CC(=C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1002/PCA.2800060106
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Fernene 441679 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1002/PCA.2800060106
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 38349717 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Obacunone 119041 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Zapoterin 441812 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
Hopene II 12310619 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1002/PCA.2800060106
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Monomethyl proline 6951137 Click to see C[NH+]1CCCC1C(=O)[O-] 129.16 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
N,N-Dimethylhistamine 12656 Click to see CN(C)CCC1=CN=CN1 139.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
Casimiroedine 5281818 Click to see CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3 417.50 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidinethiones
Zapotidine 12445018 Click to see CN1CCC2=CN=CN2C1=S 167.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown via CMAUP database
2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one 24766568 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O 369.40 unknown via CMAUP database
5-Hydroxy-1-methyl-2-phenylquinolin-4(1H)-one 71307707 Click to see CN1C2=C(C(=CC=C2)O)C(=O)C=C1C3=CC=CC=C3 251.28 unknown via CMAUP database
5,6-Dimethoxy-2-(2',5',6'-trimethoxyphenyl)-1h-quinolin-4-one 11132423 Click to see COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC 371.40 unknown via CMAUP database
5,6-dimethoxy-2-(3-methoxyphenyl)-1H-quinolin-4-one 11109704 Click to see COC1=C(C2=C(C=C1)NC(=CC2=O)C3=CC(=CC=C3)OC)OC 311.30 unknown via CMAUP database
5,6-Dimethoxy-2-(3,4-dimethoxyphenyl)-1h-quinolin-4-one 11131642 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC)OC 341.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3'-methoxyphenyl)-3-propyl-1h-quinolin-4-one 24766570 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=CC=C3)OC 353.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3',4'-dimethoxyphenyl)-3-propyl-1h-quinolin-4-one 24766569 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=C(C=C3)OC)OC 383.40 unknown via CMAUP database
Eduleine 253834 Click to see CN1C(=CC(=O)C2=C1C=C(C=C2)OC)C3=CC=CC=C3 265.31 unknown via CMAUP database
Eduline 622180 Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3 265.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
Casimiroin 124075 Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC 233.22 unknown via CMAUP database
Edulitine 826073 Click to see COC1=CC=CC2=C1NC(=O)C=C2OC 205.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-one 92475864 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)CCC(C(C)(C)O)O 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O 232.19 unknown via CMAUP database
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6R,7S,13R,21S)-5,13-bis(4-hydroxyphenyl)-7-[(2R,3S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 102094440 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC=C(C=C8)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC=C(C=C1)O)O 816.80 unknown https://doi.org/10.1016/S0944-7113(98)80026-3
> 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/10.1016/0305-1978(86)90025-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0305-1978(86)90025-6
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1016/0305-1978(86)90025-6
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/10.1016/0305-1978(86)90025-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
3',5,6-Trimethoxyflavone 44257599 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=CC=C3)OC)OC 312.30 unknown via CMAUP database
5,6-Dimethoxyflavone 14349486 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3)OC 282.29 unknown via CMAUP database
5,6,2'-Trimethoxyflavone 14484690 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3OC)OC 312.30 unknown via CMAUP database
Zapotin 629965 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC 342.30 unknown via CMAUP database
Zapotinin 44257595 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3O)OC 328.30 unknown via CMAUP database

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