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Schizolaena hystrix

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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 UUID6440143493a04616559473
Scientific name Schizolaena hystrix
Authority Capuron
First published in Adansonia , n.s., 3: 393 (1963)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000627787
Tropicos 28800065
KEW urn:lsid:ipni.org:names:790101-1
The Plant List kew-274585
Open Tree Of Life 6119164
NCBI Taxonomy 1915033
IUCN Red List 64563494
IPNI 790101-1
GBIF 3783170
EOL 6860581
Wikipedia Schizolaena_hystrix
CMAUP NPO16269

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
In Vitro and In Silico Anti-Acetylcholinesterase Activity from Macaranga tanarius and Syzygium jambos Amir Rawa MS, Nurul Azman NA, Mohamad S, Nogawa T, Wahab HA Molecules 20-Apr-2022
PMCID:PMC9102781
doi:10.3390/molecules27092648
PMID:35565998
3-Acetoxy-fatty acid isoprenyl esters from androconia of the ithomiine butterfly Ithomia salapia Mann F, Szczerbowski D, de Silva L, McClure M, Elias M, Schulz S Beilstein J Org Chem 16-Nov-2020
PMCID:PMC7684689
doi:10.3762/bjoc.16.228
PMID:33281981
Cytotoxic geranylflavonoids from Bonannia graeca Rosselli S, Bruno M, Maggio A, Raccuglia RA, Safder M, Lai CY, Bastow KF, Lee KH Phytochemistry 01-Apr-2011
PMCID:PMC3151324
doi:10.1016/j.phytochem.2011.03.005
PMID:21459391
Cytotoxic flavanones of Schizolaena hystrix from the Madagascar rainforest. Murphy BT, Cao S, Norris A, Miller JS, Ratovoson F, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 01-Mar-2005
doi:10.1021/NP049639X
PMID:15787448

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
[(1R,2E,4S,6Z,9E,11R)-11-hydroxy-7-(hydroxymethyl)-4-[(3R)-3-hydroxy-4-methylpent-4-enyl]-4,11-dimethyl-8-oxocycloundeca-2,6,9-trien-1-yl] 3-methylbut-2-enoate 163032735 Click to see CC(=CC(=O)OC1C=CC(CC=C(C(=O)C=CC1(C)O)CO)(C)CCC(C(=C)C)O)C 432.50 unknown https://doi.org/10.1021/NP049639X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,3S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 132988975 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C)C 424.50 unknown https://doi.org/10.1021/NP049639X
2-(3,4-Dihydroxyphenyl)-6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 66839793 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O)C)C 424.50 unknown https://doi.org/10.1021/NP049639X
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 72954473 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C)C 476.60 unknown https://doi.org/10.1021/NP049639X
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4,5-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 72972306 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)O)C)C 492.60 unknown https://doi.org/10.1021/NP049639X
4'-O-methylbonannione A 11750568 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)OC)O)C)C 422.50 unknown https://doi.org/10.1021/NP049639X
5,7-Dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)chroman-4-one 480769 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1021/NP049639X
6-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 54494857 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1021/NP049639X
6-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 73085040 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)OC)O)C)C 422.50 unknown https://doi.org/10.1021/NP049639X
Bonannione A 5716903 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1021/NP049639X
Bonnaniol 21721861 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C)C 424.50 unknown https://doi.org/10.1021/NP049639X
Macarangaflavanone B 14309760 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1021/NP049639X
Nymphaeol A 639465 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O)C)C 424.50 unknown https://doi.org/10.1021/NP049639X
schizolaenone A 11420157 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C)C 476.60 unknown https://doi.org/10.1021/NP049639X
schizolaenone B 11466031 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)O)C)C 492.60 unknown https://doi.org/10.1021/NP049639X

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