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Dystaenia takesimana

Dystaenia takesimana - 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 UUID644018bcb1c08024759232
Scientific name Dystaenia takesimana
Authority (Nakai) Kitag.
First published in Bot. Mag. (Tokyo) 51: 807 (1937)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ligusticum takeshimanum (Nakai) M.Hiroe Acta Phytotax. Geobot. 18: 19 (1959)
Angelica takeshimana Nakai Bot. Mag. (Tokyo) 32: 219 (1918)

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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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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-0000658896
Tropicos 50267019
KEW urn:lsid:ipni.org:names:841498-1
The Plant List kew-2780257
Open Tree Of Life 6054464
Open Tree Of Life 213820
NCBI Taxonomy 57122
IUCN Red List 97498950
IPNI 841498-1
GBIF 8424688
GBIF 3635469
EOL 5048997

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
Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy Van Doan H, Soltani M, Leitão A, Shafiei S, Asadi S, Lymbery AJ, Ringø E Animals (Basel) 16-Sep-2022
PMCID:PMC9495100
doi:10.3390/ani12182443
PMID:36139303
Genome-Wide Single Nucleotide Polymorphism Analysis Elucidates the Evolution of Prunus takesimensis in Ulleung Island: The Genetic Consequences of Anagenetic Speciation Cho MS, Takayama K, Yang J, Maki M, Kim SC Front Plant Sci 02-Sep-2021
PMCID:PMC8445234
doi:10.3389/fpls.2021.706195
PMID:34539700
Chloroplast DNA insights into the phylogenetic position and anagenetic speciation of Phedimus takesimensis (Crassulaceae) on Ulleung and Dokdo Islands, Korea Seo HS, Kim SH, Kim SC PLoS One 28-Sep-2020
PMCID:PMC7521733
doi:10.1371/journal.pone.0239734
PMID:32986762
Multiple origins and the population genetic structure of Rubus takesimensis (Rosaceae) on Ulleung Island: Implications for the genetic consequences of anagenetic speciation Yang J, Pak JH, Maki M, Kim SC PLoS One 19-Sep-2019
PMCID:PMC6752786
doi:10.1371/journal.pone.0222707
PMID:31536553
Genetic consequences of cladogenetic vs. anagenetic speciation in endemic plants of oceanic islands Takayama K, López-Sepúlveda P, Greimler J, Crawford DJ, Peñailillo P, Baeza M, Ruiz E, Kohl G, Tremetsberger K, Gatica A, Letelier L, Novoa P, Novak J, Stuessy TF AoB Plants 26-Aug-2015
PMCID:PMC4605995
doi:10.1093/aobpla/plv102
PMID:26311732
Anagenetic speciation in Ullung Island, Korea: genetic diversity and structure in the island endemic species, Acer takesimense (Sapindaceae) Takayama K, Sun BY, Stuessy TF J Plant Res 23-Oct-2012
PMCID:PMC3633782
doi:10.1007/s10265-012-0529-z
PMID:23090156
Genetic consequences of anagenetic speciation in Acer okamotoanum (Sapindaceae) on Ullung Island, Korea Takayama K, Sun BY, Stuessy TF Ann Bot 04-Nov-2011
PMCID:PMC3268531
doi:10.1093/aob/mcr280
PMID:22056411
Chemical constituents of the root of Dystaenia takeshimana and their anti-inflammatory activity. Kim JS, Kim JC, Shim SH, Lee EJ, Jin W, Bae K, Son KH, Kim HP, Kang SS, Chang HW Arch Pharm Res 01-Aug-2006
doi:10.1007/BF02968244
PMID:16964755

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
> Benzenoids / Benzene and substituted derivatives / Benzylethers
2-Methoxy-2-(4-methoxyphenyl)ethanol 88713017 Click to see COC1=CC=C(C=C1)C(CO)OC 182.22 unknown https://doi.org/10.1007/BF02968244
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
1-(4-Hydroxyphenyl)ethane-1,2-diol 3081980 Click to see C1=CC(=CC=C1C(CO)O)O 154.16 unknown https://doi.org/10.1007/BF02968244
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF02968244
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF02968244
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1007/BF02968244
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 https://doi.org/10.1007/BF02968244
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1007/BF02968244
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1007/BF02968244
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1007/BF02968244
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1007/BF02968244
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/BF02968244
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF02968244
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/BF02968244
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF02968244
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF02968244

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