Spiraea prunifolia - Unknown
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Internal ID UUID6440403ce07c2910459471
Scientific name Spiraea prunifolia
Authority Siebold & Zucc.
First published in Fl. Jap. 1: 131 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Spiraea prunifolia var. florepleno Siebold ; 1844 37 1844
Spiraea crenata var. folia-ovatis Thunb. Flora japonica ; 1784 211 1784
Spiraea crenata var. latioribus Thunb. Flora japonica ; 1784 211 1784
Spiraea prunifolia var. plena C.K.Schneid. Illustriertes Handbuch der Laubholzkunde ; 1904 450 1905
Spiraea pinnifolia Walp. Repert. Bot. Syst. (Walpers) ii. 50, sphalm.
Spiraea thunbergii var. prunifolia (Siebold & Zucc.) Wenz. Die Gattung Spiraea ; 1888 273 1888

Common names Top

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Language Common/alternative name
English bridalwreath spirea
Japanese シジミバナ
szy nipaluma-balubalu, balobalo
Chinese 李叶绣线菊
Chinese 笑靥花
Chinese 李叶笑靥花
Chinese 李葉繡線菊
Chinese 笑靨花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Spiraea prunifolia var. hupehensis (Rehder) Rehder J. Arnold Arbor. 1: 258. 1920 (1920)
Spiraea prunifolia var. pseudoprunifolia (Hayata ex Nakai) H.L.Li Lloydia 14: 236. 1952 (1952)
Spiraea prunifolia var. simpliciflora (Nakai) Nakai ; 1915 74 1915

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Missouri
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001015318
Flora of Alabama 3220
Cornell Woody Plants 410
Canadensys 8980
USDA Plants SPPR
UConn 467
Tropicos 27801445
INPN 611562
KEW urn:lsid:ipni.org:names:742467-1
The Plant List rjp-6219
Missouri Botanical Garden 262114
Open Tree Of Life 258077
Observations.org 139696
NCBI Taxonomy 409517
Nature Serve 2.132221
IPNI 742467-1
iNaturalist 169252
IFPNI A93788CD-9C71-42F6-8139-025A06583B63
GBIF 3026408
Freebase /m/0dvqsy
EPPO SPVPR
EOL 627324
Elurikkus 352296
USDA GRIN 311400
Wikipedia Spiraea_prunifolia
CMAUP NPO7344

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
Commodity risk assessment of plants of 12 selected Prunus species from Moldova Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Zappalà L, Di Serio F, Gómez P, Urek G, Lucchi A, Carluccio AV, Chiumenti M, Fanelli E, Bernardo U, Marzachì C, Bubici G, Dimitropoulou S, Correia CD, Mosbach‐Schulz O, Kaczmarek A, Yuen J EFSA J 12-Mar-2024
PMCID:PMC10928764
doi:10.2903/j.efsa.2024.8647
PMID:38476321
Re-identification of Colletotrichum acutatum Species Complex in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Hong SB Plant Pathol J 01-Aug-2023
PMCID:PMC10412970
doi:10.5423/PPJ.OA.05.2023.0078
PMID:37550984
High‐molecular‐weight DNA extraction for long‐read sequencing of plant genomes: An optimization of standard methods Kang M, Chanderbali A, Lee S, Soltis DE, Soltis PS, Kim S Appl Plant Sci 13-Jun-2023
PMCID:PMC10278927
doi:10.1002/aps3.11528
PMID:37342161
Effects of Herbs and Derived Natural Products on Lipopolysaccharide-Induced Toxicity: A Literature Review Kianmehr M, Behdadfard M, Hedayati-Moghadam M, Khazdair MR Oxid Med Cell Longev 17-Apr-2023
PMCID:PMC10125742
doi:10.1155/2023/7675183
PMID:37102170
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA Pharmaceuticals (Basel) 11-Nov-2022
PMCID:PMC9699253
doi:10.3390/ph15111392
PMID:36422521
Commodity risk assessment of Prunus domestica plants from Ukraine Bragard C, Chatzivassiliou E, Dehnen‐Schmutz K, Baptista P, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent A, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Gardi C, Mosbach‐Schulz O, de la Peña E, Yuen J EFSA J 22-Jun-2022
PMCID:PMC9214634
doi:10.2903/j.efsa.2022.7391
PMID:35774585
Commodity risk assessment of Malus domestica plants from Serbia Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Potting R, Zappalà L, Urek G, Gómez P, Lucchi A, Gardi C, de la Peña E, Yuen J EFSA J 13-May-2020
PMCID:PMC10464673
doi:10.2903/j.efsa.2020.6109
PMID:37649496
Spiraea prunifolia var. simpliciflora Attenuates Oxidative Stress and Inflammatory Responses in a Murine Model of Lipopolysaccharide-Induced Acute Lung Injury and TNF-α-Stimulated NCI-H292 Cells Lee BW, Ha JH, Shin HG, Jeong SH, Jeon DB, Kim JH, Park JY, Kwon HJ, Jung K, Lee WS, Kim HY, Kim SH, Jang HJ, Ryu YB, Lee IC Antioxidants (Basel) 26-Feb-2020
PMCID:PMC7139931
doi:10.3390/antiox9030198
PMID:32111036
Exploring the metabolomic diversity of plant species across spatial (leaf and stem) components and phylogenic groups Lee S, Oh DG, Singh D, Lee JS, Lee S, Lee CH BMC Plant Biol 28-Jan-2020
PMCID:PMC6986006
doi:10.1186/s12870-019-2231-y
PMID:31992195
Analysis of traditional knowledge of medicinal plants from residents in Gayasan National Park (Korea) Song MJ, Kim H, Lee BY, Brian H, Park CH, Hyun CW J Ethnobiol Ethnomed 21-Oct-2014
PMCID:PMC4216341
doi:10.1186/1746-4269-10-74
PMID:25336281
A Comparative Analysis of Ethnomedicinal Practices for Treating Gastrointestinal Disorders Used by Communities Living in Three National Parks (Korea) Kim H, Song MJ, Brian H, Choi K Evid Based Complement Alternat Med 17-Aug-2014
PMCID:PMC4150413
doi:10.1155/2014/108037
PMID:25202330
The absolute configuration of prunioside A from Spiraea prunifolia and biological activities of related compounds. Oh H, Shin H, Oh GS, Pae HO, Chai KY, Chung HT, Lee HS Phytochemistry 01-Nov-2003
doi:10.1016/S0031-9422(03)00499-0
PMID:14568077
Prunioside A: a new terpene glycoside from Spiraea prunifolia. Oh H, Oh GS, Seo WG, Pae HO, Chai KY, Kwon TO, Lee YH, Chung HT, Lee HS J Nat Prod 01-Jul-2001
doi:10.1021/NP0005513
PMID:11473429

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
N-[2-(4-Hydroxyphenyl)ethyl]benzamide 577614 Click to see C1=CC=C(C=C1)C(=O)NCCC2=CC=C(C=C2)O 241.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Hexadecanamide 69421 Click to see CCCCCCCCCCCCCCCC(=O)N 255.44 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 38349717 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Obacunone 119041 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Zapoterin 441812 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Monomethyl proline 6951137 Click to see C[NH+]1CCCC1C(=O)[O-] 129.16 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
N,N-Dimethylhistamine 12656 Click to see CN(C)CCC1=CN=CN1 139.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
Casimiroedine 5281818 Click to see CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3 417.50 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidinethiones
Zapotidine 12445018 Click to see CN1CCC2=CN=CN2C1=S 167.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown via CMAUP database
2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one 24766568 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O 369.40 unknown via CMAUP database
5-Hydroxy-1-methyl-2-phenylquinolin-4(1H)-one 71307707 Click to see CN1C2=C(C(=CC=C2)O)C(=O)C=C1C3=CC=CC=C3 251.28 unknown via CMAUP database
5,6-Dimethoxy-2-(2',5',6'-trimethoxyphenyl)-1h-quinolin-4-one 11132423 Click to see COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC 371.40 unknown via CMAUP database
5,6-dimethoxy-2-(3-methoxyphenyl)-1H-quinolin-4-one 11109704 Click to see COC1=C(C2=C(C=C1)NC(=CC2=O)C3=CC(=CC=C3)OC)OC 311.30 unknown via CMAUP database
5,6-Dimethoxy-2-(3,4-dimethoxyphenyl)-1h-quinolin-4-one 11131642 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC)OC 341.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3'-methoxyphenyl)-3-propyl-1h-quinolin-4-one 24766570 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=CC=C3)OC 353.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3',4'-dimethoxyphenyl)-3-propyl-1h-quinolin-4-one 24766569 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=C(C=C3)OC)OC 383.40 unknown via CMAUP database
Eduleine 253834 Click to see CN1C(=CC(=O)C2=C1C=C(C=C2)OC)C3=CC=CC=C3 265.31 unknown via CMAUP database
Eduline 622180 Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3 265.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
Casimiroin 124075 Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC 233.22 unknown via CMAUP database
Edulitine 826073 Click to see COC1=CC=CC2=C1NC(=O)C=C2OC 205.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1R)-2-methyl-1-[(2S,4Z)-5-oxo-4-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethylidene]oxolan-2-yl]prop-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11202939 Click to see CC(=C)C(C1CC(=CCOC2C(C(C(C(O2)CO)O)O)O)C(=O)O1)OC(=O)C=CC3=CC=C(C=C3)O 506.50 unknown https://doi.org/10.1016/S0031-9422(03)00499-0
[(1S)-2-methyl-1-[(2S,4Z)-5-oxo-4-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethylidene]oxolan-2-yl]prop-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101262400 Click to see CC(=C)C(C1CC(=CCOC2C(C(C(C(O2)CO)O)O)O)C(=O)O1)OC(=O)C=CC3=CC=C(C=C3)O 506.50 unknown https://doi.org/10.1016/S0031-9422(03)00499-0
https://doi.org/10.1021/NP0005513
[2-Methyl-1-[5-oxo-4-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethylidene]oxolan-2-yl]prop-2-enyl] 3-(4-hydroxyphenyl)prop-2-enoate 72748874 Click to see CC(=C)C(C1CC(=CCOC2C(C(C(C(O2)CO)O)O)O)C(=O)O1)OC(=O)C=CC3=CC=C(C=C3)O 506.50 unknown https://doi.org/10.1016/S0031-9422(03)00499-0
https://doi.org/10.1021/NP0005513
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-one 92475864 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)CCC(C(C)(C)O)O 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O 232.19 unknown via CMAUP database
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
3',5,6-Trimethoxyflavone 44257599 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=CC=C3)OC)OC 312.30 unknown via CMAUP database
5,6-Dimethoxyflavone 14349486 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3)OC 282.29 unknown via CMAUP database
5,6,2'-Trimethoxyflavone 14484690 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3OC)OC 312.30 unknown via CMAUP database
Zapotin 629965 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC 342.30 unknown via CMAUP database
Zapotinin 44257595 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3O)OC 328.30 unknown via CMAUP database

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