Adiantum monochlamys - Unknown
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Internal ID UUID64407715d8f56864223035
Scientific name Adiantum monochlamys
Authority D.C.Eaton
First published in Proc. Amer. Acad. Arts 4: 110 (1858)

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Synonyms Top

Scientific name Authority First published in
Adiantum veitchii Hance Ann. Sci. Nat., Bot. , sér. 4, 15: 229 (1861)

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Language Common/alternative name
Japanese ハコネシダ
lzh 石長生
Chinese 石長生
Chinese 單蓋鐵線蕨
Chinese 石长生
Chinese 单盖铁线蕨

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001107190
Tropicos 26600010
KEW urn:lsid:ipni.org:names:325049-2
The Plant List tro-26600010
Open Tree Of Life 1054507
NCBI Taxonomy 872338
IPNI 325049-2
iNaturalist 487750
GBIF 7335414

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)!
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Title Authors Publication Released IDs
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
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
Chicoric acid: chemistry, distribution, and production Lee J, Scagel CF Front Chem 31-Dec-2013
PMCID:PMC3982519
doi:10.3389/fchem.2013.00040
PMID:24790967
Fern Constituents: triterpenoids Isolated from the Leaves of Adiantum monochlamys. Filicenol A, Filicenol B, Isoadiantol B, Hakonanediol and Epihakonanediol. Kenji SHIOJIMA, Yoko ARAI, Toshio KASAMA, Hiroyuki AGETA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.41.262
4-Hydroxy-4,6a,6b,9,9,12a,14b-heptamethylperhydropicen-3-one hemihydrate isolated from Adiantum incisum Hussain A, Siddiqui HL, Zia-ur-Rehman M, Elsegood MR, M. Khan K Acta Crystallogr Sect E Struct Rep Online 12-Dec-2007
PMCID:PMC2915320
doi:10.1107/S1600536807064021
PMID:21200829

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 / Diterpenoids / Colensane and clerodane diterpenoids
(3a,5a,7a,8,13a-Pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-11b-yl)methyl acetate 85141982 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)COC(=O)C)C 468.80 unknown https://doi.org/10.1248/CPB.41.262
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3R,3aR,5aR,5bS,7aS,11aR,11bR,13aS,13bR)-3a,5a,7a,8,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-11b-yl]methyl acetate 163081700 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)COC(=O)C)C 468.80 unknown https://doi.org/10.1248/CPB.41.262
[(3R,3aR,5aR,5bS,7R,7aS,11aR,11bR,13aS,13bR)-3a,5a,7a,8,11b,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-7-yl] acetate 163062696 Click to see CC1=CCCC2C1(C(CC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1248/CPB.41.262
Filicenol B 101114249 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)CO)C 426.70 unknown https://doi.org/10.1248/CPB.41.262
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
(3a,5a,7a,8,11b,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-7-yl) acetate 85109873 Click to see CC1=CCCC2C1(C(CC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1248/CPB.41.262
[(1S)-1-[(3R,3aS,5aR,5bR,7aS,11aS,11bR,13aS,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]ethyl] acetate 162915056 Click to see CC(C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)OC(=O)C 456.70 unknown https://doi.org/10.1248/CPB.41.262
1-(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)ethyl acetate 14656418 Click to see CC(C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)OC(=O)C 456.70 unknown https://doi.org/10.1248/CPB.41.262
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,4S,4aS,6aR,6aR,6bR,8aS,12aS,14aR,14bR)-4,6a,6b,9,9,12a,14b-heptamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicene-3,4-diol 162936912 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)O)O)C)C)C)C)C 430.70 unknown https://doi.org/10.1248/CPB.41.262
(3S,4S,4aS,6aR,6aR,6bR,8aS,12aS,14aR,14bR)-4,6a,6b,9,9,12a,14b-heptamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicene-3,4-diol 162936911 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)O)O)C)C)C)C)C 430.70 unknown https://doi.org/10.1248/CPB.41.262
4,6a,6b,9,9,12a,14b-Heptamethyl-1,2,3,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-hexadecahydropicene-3,4-diol 73082459 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)O)O)C)C)C)C)C 430.70 unknown https://doi.org/10.1248/CPB.41.262
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(4S,4aR,6aR,6aR,6bR,8aR,12aS,14aR,14bR)-4-hydroxy-4,6a,6b,9,9,12a,14b-heptamethyl-2,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydro-1H-picen-3-one 163100029 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.262
Ketohakonanol 90720428 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.262

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