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Fatsia polycarpa

Fatsia polycarpa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403c022e94f189344033
Scientific name Fatsia polycarpa
Authority Hayata
First published in J. Coll. Sci. Imp. Univ. Tokyo 25(19): 105 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Diplofatsia polycarpa (Hayata) Nakai J. Arnold Arbor. 5: 18 (1924)

Common names Top

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Language Common/alternative name
Japanese タイワンヤツデ
Russian Фатсия многоплодная
Chinese 八角金盤
Chinese 多室八角金盘
Chinese 多果八角金盤
Chinese 臺灣八角金盤
Chinese 多果八角金盘
Chinese 多室八角金盤

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000966913
Tropicos 2201385
KEW urn:lsid:ipni.org:names:90500-1
The Plant List kew-84273
Open Tree Of Life 738090
NCBI Taxonomy 230586
IUCN Red List 32404
IPNI 90500-1
iNaturalist 192378
GBIF 3039044
Freebase /m/02x94g9
EOL 1143542
USDA GRIN 468003
Wikipedia Fatsia_polycarpa

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
Anti-viral triterpenes: a review Darshani P, Sen Sarma S, Srivastava AK, Baishya R, Kumar D Phytochem Rev 05-Mar-2022
PMCID:PMC8896976
doi:10.1007/s11101-022-09808-1
PMID:35283698
Autophagy and Digestive Disorders: Advances in Understanding and Therapeutic Approaches Thein W, Po WW, Choi WS, Sohn UD Biomol Ther (Seoul) 15-Jun-2021
PMCID:PMC8255139
doi:10.4062/biomolther.2021.086
PMID:34127572
Eudesmin attenuates Helicobacter pylori-induced epithelial autophagy and apoptosis and leads to eradication of H. pylori infection Yang JS, Wang CM, Su CH, Ho HC, Chang CH, Chou CH, Hsu YM Exp Ther Med 04-Jan-2018
PMCID:PMC5795382
doi:10.3892/etm.2018.5701
PMID:29456644
Antimicrobial Activity of Oleanolic and Ursolic Acids: An Update Jesus JA, Lago JH, Laurenti MD, Yamamoto ES, Passero LF Evid Based Complement Alternat Med 22-Feb-2015
PMCID:PMC4352472
doi:10.1155/2015/620472
PMID:25793002
Triterpenes as Potentially Cytotoxic Compounds Chudzik M, Korzonek-Szlacheta I, Król W Molecules 19-Jan-2015
PMCID:PMC6272502
doi:10.3390/molecules20011610
PMID:25608043
Anti-Inflammatory Effects and Mechanisms of Fatsia polycarpa Hayata and Its Constituents Cheng HL, Nurkholis, Cheng SY, Huang SD, Lu YT, Wang XW, Liu YL, Chou CH Evid Based Complement Alternat Med 10-Dec-2013
PMCID:PMC3899712
doi:10.1155/2013/857213
PMID:24489593
Biological Activity of Oleanane Triterpene Derivatives Obtained by Chemical Derivatization Cheng SY, Wang CM, Cheng HL, Chen HJ, Hsu YM, Lin YC, Chou CH Molecules 18-Oct-2013
PMCID:PMC6269735
doi:10.3390/molecules181013003
PMID:24145793
Oleanane-type triterpenoids from the leaves and twigs of Fatsia polycarpa. Cheng SY, Wang CM, Hsu YM, Huang TJ, Chou SC, Lin EH, Chou CH J Nat Prod 26-Aug-2011
doi:10.1021/NP2002435
PMID:21766884

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
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP2002435
10-Hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 14589211 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1)OC3=O)C)O)(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP2002435
3alpha-Hydroxyolean-11-en-28,13beta-olide 10766158 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1)OC3=O)C)O)(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP2002435
3alpha-Hydroxyolean-11,13(18)-dien-28-oic acid 10766159 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP2002435
fatsicarpain A 53493446 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP2002435
fatsicarpain B 53493447 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)OS(=O)(=O)O)C)C)C)C(=O)O)C 534.70 unknown https://doi.org/10.1021/NP2002435
fatsicarpain C 53493448 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)C)C(=O)O)C 468.70 unknown https://doi.org/10.1021/NP2002435
fatsicarpain D 53493582 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP2002435
fatsicarpain E 53493583 Click to see CC1(CCC2(CCC3(C(C2=C1)CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP2002435
Fatsicarpain F 53493584 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1)C)C(=O)O)C 486.70 unknown https://doi.org/10.1021/NP2002435
Fatsicarpain G 53493585 Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3=O)(CCC(C6(C)CO)O)C)C)C)C 470.70 unknown https://doi.org/10.1021/NP2002435

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Collections Top

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