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Polypodium fauriei

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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 UUID644079dce5113066439602
Scientific name Polypodium fauriei
Authority (Copel.) Makino & Nemoto
First published in Fl. Japan. (Makino & Nemoto) 2: 87. 1931

Description Top

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Synonyms Top

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Common names Top

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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
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001260770
Tropicos 50196642
KEW urn:lsid:ipni.org:names:17188660-1
The Plant List tro-50196642
Open Tree Of Life 488762
Observations.org 124985
NCBI Taxonomy 38391
IPNI 17188660-1
iNaturalist 501204
GBIF 5648547
EOL 6113384
Elurikkus 629006

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
DNA barcoding ferns in an unexplored tropical montane cloud forest area of southeast Oaxaca, Mexico Trujillo-Argueta S, del Castillo RF, Tejero-Diez D, Matias-Cervantes CA, Velasco-Murguía A Sci Rep 24-Nov-2021
PMCID:PMC8613246
doi:10.1038/s41598-021-02237-8
PMID:34819549
A review of the use of pteridophytes for treating human ailments Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB J Zhejiang Univ Sci B 01-Feb-2018
PMCID:PMC5833325
doi:10.1631/jzus.B1600344
PMID:29405039
Fern constituents: Eupha-7,24-diene and (20R)-dammara-13(17),24-diene, tetracyclic triterpenoid hydrocarbons isolated from Polypodium species. YOKO ARAI, KAZUO MASUDA, HIROYUKI AGETA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.30.4219
Fern constituents: Polypodatetraenes, novel bicyclic triterpenoids, isolated from polypodiaceous and aspidiaceous plants Kenji Shiojima, Yôko Arai, Kazuo Masuda, Toshifumi Kamada, Hiroyuki Ageta Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)94187-X
Fern constituents: Triterpenoids isolated from Polypodium vulgare, P. fauriei and P. virginianum Yōko Arai, Motoko Yamaide, Sachiko Yamazaki, Hiroyuki Ageta Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83212-4

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 / Prenol lipids / Triterpenoids
(3R,3aR,5aR,5bR,7aR,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene 12085176 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
(3S,6S,11S,12S,15R,16S,21R)-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 162985011 Click to see CC1(CCCC2(C1CCC3(C2CCC4C(=CCC5C4(CCCC5(C)C)C)C3)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
(4aS,8S,8aS)-4,4,8a-trimethyl-7-methylidene-8-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-2,3,4a,5,6,8-hexahydro-1H-naphthalene 11304437 Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCCC2(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4039(00)94187-X
(5R,8R,9R,10S,13R,14R,17E)-4,4,8,10,14-pentamethyl-17-(6-methylhept-5-en-2-ylidene)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene 15838272 Click to see CC(=CCCC(=C1CCC2(C1CCC3C2(CCC4C3(CCCC4(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
(5S,9R,10S,13S,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene 162900167 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCCC4(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
1,3,7,7,11,16,20,20-Octamethyl-2-oxapentacyclo[13.8.0.03,12.06,11.016,21]tricosane 73821074 Click to see CC1(CCCC2(C1CCC3(C2CCC4C5(CCCC(C5CCC4(O3)C)(C)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysene 12311004 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857699 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
4,4,8,10,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,9,11,12,15,16-decahydro-1H-cyclopenta[a]phenanthrene 14465967 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCCC(C4CCC3(C2(CC1)C)C)(C)C)C 410.70 unknown https://doi.org/10.1248/CPB.30.4219
https://doi.org/10.1016/0031-9422(91)83212-4
4,4,8,10,14-Pentamethyl-17-(6-methylhept-5-en-2-ylidene)-1,2,3,5,6,7,9,11,12,13,15,16-dodecahydrocyclopenta[a]phenanthrene 162998012 Click to see CC(=CCCC(=C1CCC2(C1CCC3C2(CCC4C3(CCCC4(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
8-Fernene 12311007 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Dammara-13(17),24-diene 14465969 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCCC(C4CCC3(C2(CC1)C)C)(C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
https://doi.org/10.1248/CPB.30.4219
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,8S,11R,12S,15R,16R)-15-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 163061141 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C)C(=C)C 496.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[(1S,3R,6S,8S,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 163094183 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 470.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[(1S,3R,6S,8S,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162935454 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[15-(5-Ethyl-6-methylhept-6-en-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312800 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C)C(=C)C 496.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[15-(5,6-Dimethylhept-6-en-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312788 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4

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