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Oleandra wallichii

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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 UUID64404c5168ad2401151584
Scientific name Oleandra wallichii
Authority (Hook.) C.Presl
First published in Tent. Pterid. 78. 1836 ; & HB. 303

Description Top

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Synonyms Top

Scientific name Authority First published in
Neuronia asplenioides D.Don Prodr. Fl. Nepal. : 7 (1825)
Aspidium wallichii Hook. Exot. Fl. 1(1): t. 5 (1822)
Oleandra wallichii var. lepidota Christ Bull. Acad. Int. Géogr. Bot. 16(199–200–201): 140 1906

Common names Top

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Language Common/alternative name
Chinese 蓧蕨
Chinese 高山条蕨
Chinese 高山蓧蕨

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 South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001107372
Tropicos 26600244
KEW urn:lsid:ipni.org:names:17165820-1
The Plant List tro-26600244
Open Tree Of Life 1092272
NCBI Taxonomy 328223
IPNI 17165820-1
iNaturalist 707177
GBIF 4196795
EOL 6102884
Elurikkus 487334

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
Plastome phylogenomic analysis reveals evolutionary divergences of Polypodiales suborder Dennstaedtiineae Lu JM, Du XY, Kuo LY, Ebihara A, Perrie LR, Zuo ZY, Shang H, Chang YH, Li DZ BMC Plant Biol 02-Nov-2022
PMCID:PMC9628275
doi:10.1186/s12870-022-03886-1
PMID:36319964
Structural Variation of Plastomes Provides Key Insight Into the Deep Phylogeny of Ferns Du XY, Kuo LY, Zuo ZY, Li DZ, Lu JM Front Plant Sci 02-May-2022
PMCID:PMC9134734
doi:10.3389/fpls.2022.862772
PMID:35645990
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Squalene-Tetrahymanol Cyclase Expression Enables Sterol-Independent Growth of Saccharomyces cerevisiae Wiersma SJ, Mooiman C, Giera M, Pronk JT Appl Environ Microbiol 18-Aug-2020
PMCID:PMC7440791
doi:10.1128/AEM.00672-20
PMID:32561581
Ecological stoichiometry of the epiphyte community in a subtropical forest canopy Huang J, Liu W, Li S, Song L, Lu H, Shi X, Chen X, Hu T, Liu S, Liu T Ecol Evol 28-Nov-2019
PMCID:PMC6953686
doi:10.1002/ece3.5875
PMID:31938527
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 : Triterpenoids from Oleandra wallichii Rumiko KAMAYA, Toshimine MORI, Kie SHOJI, Hiroyuki AGETA, HsienChang CHANG, HongYen HSU Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.111.2_120
A revision of the fern genus Oleandra (Oleandraceae) in Asia Hovenkamp PH, Ho BC PhytoKeys 06-Apr-2012
PMCID:PMC3332033
doi:10.3897/phytokeys.11.2955
PMID:22577332
Lateral transfer of tetrahymanol-synthesizing genes has allowed multiple diverse eukaryote lineages to independently adapt to environments without oxygen Takishita K, Chikaraishi Y, Leger MM, Kim E, Yabuki A, Ohkouchi N, Roger AJ Biol Direct 01-Feb-2012
PMCID:PMC3317845
doi:10.1186/1745-6150-7-5
PMID:22296756
Constituents of Oleandra wallichii G.N. Pandey, C.R. Mitra Elsevier BV 12-Feb-2003
doi:10.1016/S0031-9422(00)85836-7
The presence of tetrahymanol in Oleandra wallichii J.M. Zander, E. Caspi, G.N. Pandey, C.R. Mitra Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88195-9
Triterpene hydrocarbons from Oleandra wallichii G.N. Pandey, C.R. Mitra Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)89580-0

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 acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> 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/10.1248/YAKUSHI1947.111.2_120
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Octadeca-9,12,15-trienoic acid 5282822 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(2R)-2-[(3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-1-ol 12313308 Click to see CC(CO)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Diploptene 92155 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
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/10.1248/YAKUSHI1947.111.2_120
Dryocrassol 11453141 Click to see CC(CO)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aS,7aS,11aS,11bR,13aS,13bR)-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 13857703 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
(3S,4aR,6aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,9,9,12a,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicen-3-ol 162936077 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
(4aR,6aS,6aR,6bR,8aS,12aS,14aR,14bR)-4,4,6a,6b,9,9,12a,14b-octamethyl-2,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydro-1H-picen-3-one 162897372 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
[(3S,4aR,6aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,9,9,12a,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicen-3-yl] acetate 162937996 Click to see CC(=O)OC1CCC2(C3CCC4C5(CCCC(C5CCC4(C3(CCC2C1(C)C)C)C)(C)C)C)C 470.80 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
4,4,6a,6b,9,9,12a,14b-Octamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicen-3-ol 5253703 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
https://doi.org/10.1016/S0031-9422(00)85836-7
CID 14447666 14447666 Click to see CC(=O)OC1CCC2(C3CCC4C5(CCCC(C5CCC4(C3(CCC2C1(C)C)C)C)(C)C)C)C 470.80 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Fern-8-ene 12311006 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
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/10.1248/YAKUSHI1947.111.2_120
Tetrahymanol 168951 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
https://doi.org/10.1016/S0031-9422(00)85836-7
Tetrahymanol acetate 14447664 Click to see CC(=O)OC1CCC2(C3CCC4C5(CCCC(C5CCC4(C3(CCC2C1(C)C)C)C)(C)C)C)C 470.80 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
Tetrahymanone 137796415 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)88195-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives
3a,5a,5b,8,8,11a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13-tetradecahydrocyclopenta[a]chrysene 12310615 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4039(01)89580-0
Adian-5-ene 15558361 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
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/10.1248/YAKUSHI1947.111.2_120
https://doi.org/10.1016/S0040-4039(01)89580-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 101658822 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(=C)C 454.80 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
Cyclolaudenol 101729 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120
> Organoheterocyclic compounds / Oxepanes
(1S,6S,7R,10S,11R,14R,15R,18R,19S)-2,2,7,10,15,18-hexamethyl-14-propan-2-yl-22,23,24-trioxahexacyclo[19.2.1.01,6.07,19.010,18.011,15]tetracosane 14544123 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC5OC6(C4CCCC6(C)C)OO5)C)C)C)C 458.70 unknown https://doi.org/10.1248/YAKUSHI1947.111.2_120

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