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Adiantum malesianum

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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 UUID6440784346bb3114777372
Scientific name Adiantum malesianum
Authority Ghatak
First published in Bull. Bot. Surv. India 5: 73, f.1, 4, 6, 7. 1963

Description Top

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Synonyms Top

Scientific name Authority First published in
Adiantum caudatum var. latilobatum Bonap. Notes Pteridol. 7: 174 1918

Common names Top

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Language Common/alternative name
Chinese 假鞭叶铁线蕨
Chinese 岩风子
Chinese 馬來鐵線蕨

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001124078
Tropicos 26620034
KEW urn:lsid:ipni.org:names:325045-2
The Plant List tro-26620034
Open Tree Of Life 835896
NCBI Taxonomy 451080
IPNI 17425960-1
iNaturalist 502021
GBIF 3747984
EOL 6122270
CMAUP NPO18670

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
A Large Intergenic Spacer Leads to the Increase in Genome Size and Sequential Gene Movement around IR/SC Boundaries in the Chloroplast Genome of Adiantum malesianum (Pteridaceae) Gu X, Zhu M, Su Y, Wang T Int J Mol Sci 09-Dec-2022
PMCID:PMC9778900
doi:10.3390/ijms232415616
PMID:36555263
How fern and fern allies respond to heterogeneous habitat — a case in Yuanjiang dry-hot valley Yang FC, Sarathchandra C, Liu JX, Huang HP, Gou JY, Li Y, Mao XY, Wen HT, Zhao J, Yang MF, Homya S, Prueksakorn K Commun Integr Biol 13-Dec-2021
PMCID:PMC8677019
doi:10.1080/19420889.2021.2007591
PMID:34925688
Growth performance and element concentrations reveal the calcicole-calcifuge behavior of three Adiantum species Liao JX, Liang DY, Jiang QW, Mo L, Pu GZ, Zhang D BMC Plant Biol 10-Jul-2020
PMCID:PMC7350575
doi:10.1186/s12870-020-02538-6
PMID:32650742
Chemical and Chemotaxonomical Studies of Filices. LXV. : A Few New Flavonoid Glycosides. (2)(Organic) TAKAO MURAKAMI, HIROSHI WADA, NOBUTOSHI TANAKA, TSUNEHIRO KIDO, HIDEKI IIDA, YASUHISA SAIKI, CHIU-MING CHEN Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.106.11_982
Chemical and Chemotaxonomical Studies on Filices. XLVI. A Few New Flavonoidglycosides (1) TAKAO MURAKAMI, TOSHIKO SATAKE, CHIAKI HIRASAWA, YOSHIKO IKENO, YASUHISA SAIKI, CHIUMING CHEN Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.104.2_142
Kaempferol – A dietary anticancer molecule with multiple mechanisms of action: Recent trends and advancements Kashyap D, Sharma A, Tuli HS, Sak K, Punia S, Mukherjee TK J Funct Foods 18-Jan-2017
PMCID:PMC7104980
doi:10.1016/j.jff.2017.01.022
PMID:32288791

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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8R,8aS,12aS,14aR,14bR)-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol 21594139 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)O)C)CO)C 474.70 unknown via CMAUP database
clethroidoside F 56601861 Click to see CC(=O)OC1C(C23COC4(C2CC1(C)C)CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(CO7)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)OC(=O)C 1163.30 unknown via CMAUP database
desglucoanagalloside B 21681168 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)CO)OC7C(C(C(CO7)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)C 1063.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1248/YAKUSHI1947.106.11_982
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/YAKUSHI1947.104.2_142
https://doi.org/10.1248/YAKUSHI1947.106.11_982
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 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/10.1248/YAKUSHI1947.104.2_142
https://doi.org/10.1248/YAKUSHI1947.106.11_982

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