Fraxinus sieboldiana, also known as the Chinese or Japanese flowering ash, is a flowering plant in the Oleaceae family. It is found in southeastern China, the Korean peninsula, and Japan, typically growing on slopes and near streams. This plant is able to thrive in USDA zone 6 and a variegated variety called 'Rising Sun' is also available.

Synonyms Top

Scientific name	Authority	First published in
Fraxinus angustata	(Blume) Hatsusima	Bot. Surv. S. Chosen, Rep. : V (1934)
Fraxinus longicuspis f. lancea	Nakai	Fl. Sylv. Korean. 40 1921
Fraxinus longicuspis var. sieboldiana	(Blume) Lingelsh.	Pflanzenr. IV, 243(1): 23. 1920
Fraxinus longicuspis var. subintegra	Koidz.	Bot. Mag. (Tokyo) 28: 286. 1914
Fraxinus mariesii	Hook.f.	Bot. Mag. 109: t. 6678 (1883)
Fraxinus quadrijuga	Nakai	Bot. Mag. (Tokyo) 49: 419 (1935)
Fraxinus sieboldiana var. angustata	Blume	Mus. Bot. 1: 311. 1851
Fraxinus sieboldiana var. barbinervis	Nakai	Tennenkinenbutu-Tyosa-Hokoku, Syokubutu 19: 43. 1942
Fraxinus sieboldiana f. tobana	(Honda) Koidz.	Acta Phytotax. Geobot. 3: 41 1934
Fraxinus sieboldiana var. trijuga	Nakai	Bot. Mag. (Tokyo) 49: 421. 1935
Fraxinus tobana	Honda	Bot. Mag. (Tokyo) 46: 677 (1932)

Common names Top

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Filter by language:

Language	Common/alternative name
German	siebolds blumen-esche
Japanese	マルバアオダモ
Korean	쇠물푸레
Norwegian Bokmål	kinaask
Chinese	庐山梣
Chinese	小萼白蜡树
Chinese	小蜡树

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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No forms added yet.

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 click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000832949
Tropicos	23000379
KEW	urn:lsid:ipni.org:names:609216-1
The Plant List	kew-370130
PFAF	Fraxinus sieboldiana
Open Tree Of Life	358547
NCBI Taxonomy	490850
IUCN Red List	96444571
IPNI	609216-1
iNaturalist	452338
GBIF	3684169
EPPO	FRXSI
EOL	483933
USDA GRIN	315
Wikipedia	Fraxinus_sieboldiana

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

Role of phytocompounds as the potential anti-viral agent: an overview

Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN

Naunyn Schmiedebergs Arch Pharmacol

09-May-2023

PMCID:	PMC10169142
doi:	10.1007/s00210-023-02517-2
PMID:	37160482

Tocilizumab-coated solid lipid nanoparticles loaded with cannabidiol as a novel drug delivery strategy for treating COVID-19: A review

Zielińska A, Eder P, Karczewski J, Szalata M, Hryhorowicz S, Wielgus K, Szalata M, Dobrowolska A, Atanasov AG, Słomski R, Souto EB

Front Immunol

22-Mar-2023

PMCID:	PMC10073701
doi:	10.3389/fimmu.2023.1147991
PMID:	37033914

Identification of Natural Lead Compounds against Hemagglutinin-Esterase Surface Glycoprotein in Human Coronaviruses Investigated via MD Simulation, Principal Component Analysis, Cross-Correlation, H-Bond Plot and MMGBSA

Ali I, Rasheed MA, Cavalu S, Rahim K, Ijaz S, Yahya G, Goh LP, Popoviciu MS

Biomedicines

06-Mar-2023

PMCID:	PMC10044901
doi:	10.3390/biomedicines11030793
PMID:	36979773

Natural products as a therapy to combat against SARS-CoV-2 virus infection

Malviya S, Parihar A, Parihar DS, Khan R

Computational Approaches for Novel Therapeutic and Diagnostic Designing to Mitigate SARS-CoV-2 Infection

15-Jul-2022

PMCID:	PMC9300459
doi:	10.1016/B978-0-323-91172-6.00017-0

Natural compounds may contribute in preventing SARS-CoV-2 infection: a narrative review

Bizzoca ME, Leuci S, Mignogna MD, Muzio EL, Caponio VC, Muzio LL

02-Jun-2022

PMCID:	PMC9160299
doi:	10.1016/j.fshw.2022.04.005

A New Lichenized Fungus, Psoroglaena humidosilvae, from a Forested Wetland of Korea, with a Taxonomic Key to the Species of Psoroglaena

Lee BG, Hur JS

J Fungi (Basel)

12-Apr-2022

PMCID:	PMC9028879
doi:	10.3390/jof8040392
PMID:	35448623

Is the High Proportion of Males in a Population of the Self-Incompatible Fraxinus platypoda (Oleaceae) Indicative of True Androdioecy or Cryptic-Dioecy?

Sakio H, Nirei T

Plants (Basel)

11-Mar-2022

PMCID:	PMC8951091
doi:	10.3390/plants11060753
PMID:	35336635

Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer

Sakata Y, Shirahama N, Uechi A, Okano K

PeerJ

17-Sep-2021

PMCID:	PMC8451445
doi:	10.7717/peerj.12165
PMID:	34616621

Complete chloroplast genome sequence of an endangered plant Oreocharis cotinifolia (Gesneriaceae) from Guangxi, China

Tang J, Zhao B, Li C, Hong X

Mitochondrial DNA B Resour

15-Sep-2021

PMCID:	PMC8451614
doi:	10.1080/23802359.2021.1973918
PMID:	34553048

Bioactive molecules from plants: a prospective approach to combat SARS-CoV-2

Panigrahi GK, Sahoo SK, Sahoo A, Behera S, Sahu S, Dash A, Satapathy KB

20-Jul-2021

PMCID:	PMC8290388
doi:	10.1007/s13596-021-00599-y

Phylogeny and taxonomy of Phyllactinia species (powdery mildew: Erysiphaceae) occurring on the ash trees (Fraxinus spp.)

Maeda M, Meeboon J, Heluta VP, Liu SY, Tang S, Takamatsu S

Mycoscience

20-Jul-2021

PMCID:	PMC9721523
doi:	10.47371/mycosci.2021.04.001
PMID:	37092168

Therapeutic Potentials of Antiviral Plants Used in Traditional African Medicine With COVID-19 in Focus: A Nigerian Perspective

Attah AF, Fagbemi AA, Olubiyi O, Dada-Adegbola H, Oluwadotun A, Elujoba A, Babalola CP

Front Pharmacol

26-Apr-2021

PMCID:	PMC8108136
doi:	10.3389/fphar.2021.596855
PMID:	33981214

Role of phytoconstituents in the management of COVID-19

Das A, Pandita D, Jain GK, Agarwal P, Grewal AS, Khar RK, Lather V

Chem Biol Interact

30-Mar-2021

PMCID:	PMC8008820
doi:	10.1016/j.cbi.2021.109449
PMID:	33798507

Phylogeny and taxonomy of Erysiphe species (powdery mildew: Erysiphaceae) occurring on the ash trees (Fraxinus spp.)

Yamaguchi Y, Meeboon J, P. Heluta V, Liu SY, Feng J, Takamatsu S

Mycoscience

20-Mar-2021

PMCID:	PMC9157754
doi:	10.47371/mycosci.2020.11.009
PMID:	37089256

Medicinal plants: Treasure for antiviral drug discovery

Ali SI, Sheikh WM, Rather MA, Venkatesalu V, Muzamil Bashir S, Nabi SU

Phytother Res

16-Feb-2021

PMCID:	PMC8013762
doi:	10.1002/ptr.7039
PMID:	33590931

Phytochemical Profile Top

Add a new one!

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-(4S,5S,10R,20R)-12,18-dihydroxy-7-oxo-abieta-8,11,13-trien-20-aldehyde 18,20-ethyl acetal	50900596	Click to see CCOC1C23CCCC(C2CC(=O)C4=CC(=C(C=C34)O)C(C)C)(CO1)C	358.50	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde 18,20-ethyl acetal	50900595	Click to see CCOC1C23CCCC(C2CCC4=CC(=C(C=C34)O)C(C)C)(CO1)C	344.50	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde18,20-methyl acetal	50900510	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C24CCCC3(COC4OC)C)O	330.50	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,10R,20S)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde 18,20-methyl acetal	50900511	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C24CCCC3(COC4OC)C)O	330.50	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,10R)-10,12,18-trihydroxy-7-oxo-20-norabieta-8,11,13-triene	50900599	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)CO)O)O	318.40	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,7S,10R,20S)-7,12,18-trihydroxyabieta-8,11,13-trien-20-aldehyde 7,18,20-acetal	53326127	Click to see CC(C)C1=C(C=C2C(=C1)C3CC4C25CCCC4(COC5O3)C)O	314.40	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,8R,10R,20S)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-aldehyde 8,18,20-acetal	50900414	Click to see CC(C)C1=CC23CCC4C5(CCCC4(C2=CC1=O)C(O3)OC5)C	314.40	unknown	https://doi.org/10.1021/NP100583U
(-)-(5R,10S)-12-hydroxy-7-oxo-20-norabieta-8,11,13-triene	50900598	Click to see CC(C)C1=C(C=C2C3CCCC(C3CC(=O)C2=C1)(C)C)O	286.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(1R)-1,12-dihydroxy-20-norabieta-5(10),8,11,13-tetraene	50900600	Click to see CC(C)C1=C(C=C2C(=C1)CCC3=C2C(CCC3(C)C)O)O	286.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S,10R)-10,12-dihydroxy-7-oxo-20-norabieta-8,11,13-triene	50900597	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)O)O	302.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S,7R)-7-ethoxy-12-hydroxy-2-oxo-20-norabieta-1(10),8,11,13-tetraene	50900673	Click to see CCOC1CC2C(=CC(=O)CC2(C)C)C3=CC(=C(C=C13)C(C)C)O	328.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S)-12-hydroxy-2-oxo-20-norabieta-1(10),8,11,13-tetraene	50900602	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2=CC(=O)CC3(C)C)O	284.40	unknown	https://doi.org/10.1021/NP100583U
(+)-Pisiferal	13785026	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1021/NP100583U
(4aR,10aS)-6-hydroxy-1,1-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-4a-carbaldehyde	53320910	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C=O)O	314.40	unknown	https://doi.org/10.1021/NP100583U
(4S,5S,10R,20R)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde 18,20-hemiacetal	53326128	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C24CCCC3(COC4O)C)O	316.40	unknown	https://doi.org/10.1021/NP100583U
(4S,5S,10R,20S)-12,18-dihydroxyabieta-8,11,13-trien-20-aldehyde 18,20-hemiacetal	50900509	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C24CCCC3(COC4O)C)O	316.40	unknown	https://doi.org/10.1021/NP100583U
12-Hydroxy-1-oxo-20-norabieta-5(10),6,8,11,13-pentaene	50900601	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3=C2C(=O)CCC3(C)C)O	282.40	unknown	https://doi.org/10.1021/NP100583U
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	https://doi.org/10.1021/NP100583U
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Fraxinuacidoside	16681233	Click to see CC1=C(C(C(CC1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C3C=C(COC3C=C(C)C(=O)O)C	482.60	unknown	https://doi.org/10.1021/NP0700467
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(-)-(4S,5S,10R)-12,18-dihydroxyabieta-8,11,13-trien-20-oic acid-18,20-lactone	50900416	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C24CCCC3(COC4=O)C)O	314.40	unknown	https://doi.org/10.1021/NP100583U
(-)-(4S,5S,8R,10R)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-oic acid 18,20-lactone	50900413	Click to see CC(C)C1=CC2(CCC3C4(CCCC3(C2=CC1=O)C(=O)OC4)C)O	330.40	unknown	https://doi.org/10.1021/NP100583U
(-)-(5S,6S,7S,10R)-6,7,12-trihydroxyabieta-8,11,13-trien-20-oic acid 6,20-lactone	50900506	Click to see CC(C)C1=C(C=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S,6S,10R)-12-hydroxy-7-oxo-abieta-8,11,13-trien-20-oic acid6,20-lactone	50900507	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C3C4C2(CCCC4(C)C)C(=O)O3)O	328.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S,6S,7R,10R)-6,7,12-trihydroxyabieta-8,11,13-trien-20-oic acid 6,20-lactone	50900505	Click to see CC(C)C1=C(C=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1021/NP100583U
(+)-(5S,6S,7S,8R,10R)-6-hydroxy-7,8-epoxy-12-oxo-abieta-9(11),13-dien-20-oic acid 6,20-lactone	50900415	Click to see CC(C)C1=CC23C(O2)C4C5C(CCCC5(C3=CC1=O)C(=O)O4)(C)C	328.40	unknown	https://doi.org/10.1021/NP100583U
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]oxane-3,4,5-triol	16681196	Click to see COC1=C(C=CC(=C1)CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP0700467
Cuneataside C	11503277	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)O)O)O)(CO)O	448.40	unknown	https://doi.org/10.1021/NP0700467
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol	16681195	Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O	464.40	unknown	https://doi.org/10.1021/NP0700467
(2S,3R,4S,5S,6R)-2-[2,6-dimethoxy-4-[(1R,2R)-1,2,3-trihydroxypropyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	16681198	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(C(CO)O)O	406.40	unknown	https://doi.org/10.1021/NP0700467
(2S,3R,4S,5S,6R)-2-[2,6-dimethoxy-4-[(1R,2S)-1,2,3-trihydroxypropyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	16681197	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(C(CO)O)O	406.40	unknown	https://doi.org/10.1021/NP0700467
(2S,3R,4S,5S,6R)-2-[2,6-dimethoxy-4-[(1S,2S)-1,2,3-trihydroxypropyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	16681231	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(C(CO)O)O	406.40	unknown	https://doi.org/10.1021/NP0700467
(2S,3R,4S,5S,6R)-2-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	16681194	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)OC3C(C(C(C(O3)CO)O)O)O	494.40	unknown	https://doi.org/10.1021/NP0700467
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Plantasioside	44423103	Click to see C1C(OC2C(C(C(OC2O1)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)C4=CC(=C(C=C4)O)O	476.40	unknown	https://doi.org/10.1021/NP0700467
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	163030794	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)OC(CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1021/NP0700467
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(7-hydroxy-2-oxochromen-6-yl)oxyoxan-2-yl]methyl 3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	16681193	Click to see COC1=C(C=CC(=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(C=C4C(=C3)C=CC(=O)O4)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O	652.60	unknown	https://doi.org/10.1021/NP0700467

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Fraxinus sieboldiana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top