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Prunus ssiori

Prunus ssiori - 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 UUID64403eeb10b6e576322351
Scientific name Prunus ssiori
Authority F.Schmidt
First published in Reis. Amur-Land., Bot. : 124 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Padus ssiori C.K.Schneid. Ill. Handb. Laubholzk. 1: 641 (1906)

Common names Top

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Language Common/alternative name
Finnish sahalinintuomi
Japanese シウリザクラ
Chinese 库页稠李
Chinese 日本稠李

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
  • Asia-temperate
    • Eastern Asia
      • Japan
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000988088
Tropicos 27803678
KEW urn:lsid:ipni.org:names:730304-1
The Plant List rjp-15933
Open Tree Of Life 3902756
NCBI Taxonomy 1926489
IUCN Red List 64127860
IPNI 730304-1
iNaturalist 922442
GBIF 3023738
EPPO PRNSJ
EOL 632464
USDA GRIN 30120
Wikipedia Prunus_ssiori

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
Response of an Indicator Species, Dryopteris crassirhizoma, to Temporal and Spatial Variations in Sika Deer Density Inatomi Y, Uno H, Ueno M, Takafumi H, Osa Y Biology (Basel) 12-Feb-2022
PMCID:PMC8868673
doi:10.3390/biology11020302
PMID:35205168
Dining from the coast to the summit: Salmon and pine nuts determine the summer body condition of female brown bears on the Shiretoko Peninsula Shirane Y, Jimbo M, Yamanaka M, Nakanishi M, Mori F, Ishinazaka T, Sashika M, Tsubota T, Shimozuru M Ecol Evol 18-Mar-2021
PMCID:PMC8131783
doi:10.1002/ece3.7410
PMID:34026001
Naturally Occurring Cinnamic Acid Sugar Ester Derivatives Tian Y, Liu W, Lu Y, Wang Y, Chen X, Bai S, Zhao Y, He T, Lao F, Shang Y, Guo Y, She G Molecules 24-Oct-2016
PMCID:PMC6273327
doi:10.3390/molecules21101402
PMID:27783048
Paternity analysis reveals significant isolation and near neighbor pollen dispersal in small Cariniana legalis Mart. Kuntze populations in the Brazilian Atlantic Forest Tambarussi EV, Boshier D, Vencovsky R, Freitas ML, Sebbenn AM Ecol Evol 13-Nov-2015
PMCID:PMC4813111
doi:10.1002/ece3.1816
PMID:27069608
Female and male fitness consequences of clonal growth in a dwarf bamboo population with a high degree of clonal intermingling Matsuo A, Tomimatsu H, Suzuki JI, Saitoh T, Shibata S, Makita A, Suyama Y Ann Bot 15-Sep-2014
PMCID:PMC4171080
doi:10.1093/aob/mcu176
PMID:25228034
Two new lignan xylosides from the barks of Prunus ssiori and Prunus padus. Kiyoshi YOSHINARI, Yutaka SASHIDA, Hiroko SHIMOMURA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.3301
Common allometric response of open-grown leader shoots to tree height in co-occurring deciduous broadleaved trees Miyata R, Kubo T, Nabeshima E, Kohyama TS Ann Bot 13-Sep-2011
PMCID:PMC3197456
doi:10.1093/aob/mcr228
PMID:21914698
Phenylpropanoid glycosides ofPrunus ssiori O.M. Abdallah, M.S. Kamel, M.H. Mohamed Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89593-X

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(3-hydroxy-4-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 163193509 Click to see COC1=C(C=C(C=C1)C2C(C(CC3=CC(=C(C=C23)O)OC)CO)COC4C(C(C(CO4)O)O)O)O 492.50 unknown https://doi.org/10.1248/CPB.37.3301
2-[[7-Hydroxy-1-(3-hydroxy-4-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 162937453 Click to see COC1=C(C=C(C=C1)C2C(C(CC3=CC(=C(C=C23)O)OC)CO)COC4C(C(C(CO4)O)O)O)O 492.50 unknown https://doi.org/10.1248/CPB.37.3301
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R,5R)-4-hydroxy-2,5-bis(hydroxymethyl)-2-[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxolan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 101678893 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OC(=O)C)OC(=O)C)OC(=O)C 672.60 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
[4-Hydroxy-2,5-bis(hydroxymethyl)-2-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxolan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 162980019 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OC(=O)C)OC(=O)C)OC(=O)C 672.60 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Syringin 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.37.3301
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.37.3301
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.37.3301
Leonuriside 14237626 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)O 332.30 unknown https://doi.org/10.1248/CPB.37.3301
Leonuriside A 14237625 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)O 332.30 unknown https://doi.org/10.1248/CPB.37.3301
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2,3,4-trihydroxybenzoate 5317726 Click to see C1=CC(=C(C(=C1C(=O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O 332.26 unknown https://doi.org/10.1248/CPB.37.3301
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85140196 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
[(2R,3S,4S,5R,6R)-6-[2-(1,3-benzodioxol-5-yl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 101678892 Click to see C1OC2=C(O1)C=C(C=C2)CCOC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 490.50 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
[6-[2-(1,3-Benzodioxol-5-yl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 162909817 Click to see C1OC2=C(O1)C=C(C=C2)CCOC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 490.50 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 78380900 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
6-O-caffeoyl-beta-glucose 101419460 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
Calceolarioside B 5273567 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)89593-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Glucosyringic acid 10383888 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1248/CPB.37.3301
Syringic acid-4-beta-D-glucopyranoside 14132338 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1248/CPB.37.3301

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