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Angiopteris helferiana

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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 UUID643fd48288e95631613451
Scientific name Angiopteris helferiana
Authority C.Presl
First published in Suppl. Tent. Pterid. 22 (1845)

Description Top

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Synonyms Top

Scientific name Authority First published in
Angiopteris boninensis Hieron. Hedwigia 61. 266. 1919. (1919)
Angiopteris campsophlebia de Vriese Monogr. Marattiac. 31. 1853
Angiopteris gaudichaudiana de Vriese Monogr. Marattiac. 30, t.3, f.13; t.4, f.13. 1853
Angiopteris griffithiana de Vriese Monogr. Marattiac. : 29 (1853)
Angiopteris leschenaultiana de Vriese Monogr. Marattiac. 31, t.3, f.14; t.4, f.14. 1853
Angiopteris macrocephala C.Presl Suppl. Tent. Pterid. 26. 1845; de Vriese, Mon. 32 (1845)
Angiopteris macrophylla de Vriese Monogr. Marattiac. 34 (1853)
Angiopteris magnifica Miq. in Verh. Nederl. Inst. III(4): 54, t.7, f.B. 1851 ; & de Vriese, Mon. 32
Angiopteris marginata de Vriese Monogr. Marattiac. 29 (1853)
Angiopteris polysporangia de Vriese Monogr. Marattiac. 23 (1853)
Angiopteris salicifolia (Pr.) de Vriese Monogr. Marattiac. 34. 1853
Angiopteris sylhetensis de Vriese Monogr. Marattiac. 27 (1853)
Angiopteris wallichiana C.Presl Suppl. Tent. Pterid. 22. 1845; de Vriese, Mon. 27 (1845)
Angiopteris wightiana de Vriese Monogr. Marattiac. 28 (1853)
Marattia pinnata Roxb. Calcutta J. Nat. Hist. 4: 519 (1844)
Psilodochea salicifolia C.Presl Suppl. Tent. Pterid. 28. 1845. (1845)
Angiopteris lygodiifolia Rosenst. Meded. Rijks-Herb. 31: 2 (1917)
Angiopteris caudatiformis Hieron. Hedwigia 61. 278 (1919)
Angiopteris crassiuscula Ching Acta Phytotax. Sin. 8: 279. 1963., nom. nov. (1963)
Angiopteris late-marginata Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 336. 1959. (1959)
Angiopteris majuscula Ching Acta Phytotax. Sin. 8: 279. 1963., nom. nov. (1963)
Angiopteris multijuga Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 335. 1959. (1959)
Angiopteris hainanensis Ching Acta Phytotax. Sin. 8: 158 (1959)
Angiopteris magna Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 341. 1959 {non Ching ex C. (1959)
Angiopteris megaphylla Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 335. 1959. (1959)
Angiopteris nuda Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 331. 1959. (1959)
Angiopteris subcuneata Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 336. 1959. (1959)
Angiopteris vasta Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 337. 1959. (1959)
Angiopteris henryi Hieron. Hedwigia 61. 260. 1919. (1919)
Angiopteris sakuraii Hieron. Hedw. 61: 280. 1919
Angiopteris rahaoensis Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 333. 1959. (1959)
Angiopteris taiwanensis Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 334. 1959. (1959)
Angiopteris lobulata Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 334. 1959. (1959)
Angiopteris formosa Ching in Chien & Chun Fl. Reipubl. Popularis Sin. 2: 335. 1959. (1959)
Angiopteris oldhamii Hieron. Hedwigia 61. 265 (1919)
Angiopteris repandula de Vriese Monogr. Marattiac. 30 (1853)
Angiopteris suboppositifolia de Vriese Monogr. Marattiac. 23 (1853)

Common names Top

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Language Common/alternative name
Chinese 广西莲座蕨
Chinese 楔形观音座莲
Chinese 楔基观音座莲
Chinese 楔基莲座蕨

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Thailand
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000147217
Tropicos 100388830
KEW urn:lsid:ipni.org:names:17021930-1
Open Tree Of Life 336832
NCBI Taxonomy 397668
IPNI 17021930-1
iNaturalist 1002019
GBIF 5615588
CMAUP NPO24883

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
Angiopteris cochinchinensis de Vriese Ameliorates LPS-Induced Acute Lung Injury via Src Inhibition Jang WY, Lee HP, Kim SA, Huang L, Yoon JH, Shin CY, Mitra A, Kim HG, Cho JY Plants (Basel) 13-May-2022
PMCID:PMC9143704
doi:10.3390/plants11101306
PMID:35631731
Anti-Adipogenic and Anti-Inflammatory Activities of (−)-epi-Osmundalactone and Angiopteroside from Angiopteris helferiana C.Presl Lamichhane R, Pandeya PR, Lee KH, Kim SG, Devkota HP, Jung HJ Molecules 15-Mar-2020
PMCID:PMC7144557
doi:10.3390/molecules25061337
PMID:32183470

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
3alpha-Hydroxyfriedelane-2-one 14465808 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(23S,25R)-23-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]spirosta-5-ene-3beta-ol 100982641 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 754.90 unknown via CMAUP database
(23S)-1beta-[[2-O-[3-O-(beta-D-Glucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyl]oxy]-23-(beta-D-glucopyranosyloxy)spirosta-5,25(27)-diene-3beta-ol 10581939 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19C(CC(=C)CO9)OC1C(C(C(C(O1)CO)O)O)O 1047.10 unknown via CMAUP database
(25R)-1beta-(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyloxy)spirosta-5-ene-3beta-ol 44575746 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 708.90 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
1beta-[2-O-(3-O-beta-D-Glucopyranosyl-alpha-L-rhamnopyranosyl)-4-O-acetyl-alpha-L-arabinopyranosyloxy]spirosta-5,25(27)-dien-3beta-ol 101937241 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 911.00 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside [WHO-DD] 91936850 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC1(CCC(=C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C 254.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database

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