Scientific name	Authority	First published in
Onychium carvifolium	Fée	Mém. Foug., 5. Gen. Filic. : 132 (1852)
Asplenium swartzianum	Kunze	Linnaea 19: 404 (1846)
Trichomanes japonicum	Thunb.	Syst. Veg. ed. 14 : 941 (1784)
Caenopteris japonica	(Thunb.) Thunb.	Nova Acta Petr. 9: 161, t.G, f.2. 1795
Darea japonica	(Thunb.) Willd.	Sp. Pl., ed. 4 [Willdenow] 5: 302. 1810
Pteris japonica	Mett.	Fil. Hort. Bot. Lips. : 54 (1856)
Cryptogramma japonica	Prantl	Bot. Jahrb. Syst. 3(5): 413 (1882)
Onychium chinense	Fée	Mém. Foug., 5. Gen. Filic. : 132 (1852)
Onychium japonicum f. echizenense	Yo.Saito & Y.Yoshim.	J. Phytogeogr. Taxon. 60(2): 69. 2013 [1 Mar 2013]

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	タチシノブ
Chinese	小野鸡尾
Chinese	日本金粉蕨
Chinese	野雉尾金粉蕨
Chinese	野雉尾金粉蕨、野鸡尾）
Chinese	金粉蕨
Chinese	小尾草
Chinese	小野雉尾草
Chinese	日本鸟蕨
Chinese	柏香莲
Chinese	毛黄莲
Chinese	草黄莲
Chinese	野鸡尾

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Onychium japonicum var. lucidum	(D.Don) Christ	Bull. Soc. Bot. France: Mem. 1: 60 1905

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
- Indo-China
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001107373
Tropicos	26600247
Flora of Italy	10249
KEW	urn:lsid:ipni.org:names:17167030-1
The Plant List	tro-26600247
Open Tree Of Life	562403
Observations.org	129712
NCBI Taxonomy	32172
IPNI	17167030-1
iNaturalist	362547
GBIF	7335697
USDA GRIN	461903
Wikipedia	Onychium_japonicum
CMAUP	NPO10606

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

The size diversity of the Pteridaceae family chloroplast genome is caused by overlong intergenic spacers

Gu X, Li L, Zhong X, Su Y, Wang T

BMC Genomics

22-Apr-2024

PMCID:	PMC11036588
doi:	10.1186/s12864-024-10296-0
PMID:	38649816

Companion Plants of Tea: From Ancient to Terrace to Forest

Wu H, Long X, Geng Y

Plants (Basel)

25-Aug-2023

PMCID:	PMC10490072
doi:	10.3390/plants12173061
PMID:	37687308

“Diminishing returns” and leaf area-biomass scaling of ferns in subtropical ecosystems

Chen S, Li J, Sun J, Zhong Q, Hu D, Cheng D

Front Plant Sci

27-Jun-2023

PMCID:	PMC10333482
doi:	10.3389/fpls.2023.1187704
PMID:	37441171

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Plastome phylogenomic analysis reveals evolutionary divergences of Polypodiales suborder Dennstaedtiineae

Lu JM, Du XY, Kuo LY, Ebihara A, Perrie LR, Zuo ZY, Shang H, Chang YH, Li DZ

BMC Plant Biol

02-Nov-2022

PMCID:	PMC9628275
doi:	10.1186/s12870-022-03886-1
PMID:	36319964

Chicoric Acid: Natural Occurrence, Chemical Synthesis, Biosynthesis, and Their Bioactive Effects

Yang M, Wu C, Zhang T, Shi L, Li J, Liang H, Lv X, Jing F, Qin L, Zhao T, Wang C, Liu G, Feng S, Li F

Front Chem

23-Jun-2022

PMCID:	PMC9262330
doi:	10.3389/fchem.2022.888673
PMID:	35815211

When it only takes one to tango: assessing the impact of apomixis in the fern genus Pteris

Picard KT, Ranft H, Grusz AL, Windham MD, Schuettpelz E

Am J Bot

03-Nov-2021

PMCID:	PMC9298017
doi:	10.1002/ajb2.1761
PMID:	34618360

Inventorization of traditional ethnobotanical uses of wild plants of Dawarian and Ratti Gali areas of District Neelum, Azad Jammu and Kashmir Pakistan

Ajaib M, Ishtiaq M, Bhatti KH, Hussain I, Maqbool M, Hussain T, Mushtaq W, Ghani A, Azeem M, Khan SM, Thind S, Bashir R

PLoS One

29-Jul-2021

PMCID:	PMC8321310
doi:	10.1371/journal.pone.0255010
PMID:	34324561

Ethnobotanical survey of the medicinal flora of Harighal, Azad Jammu & Kashmir, Pakistan

Amjad MS, Zahoor U, Bussmann RW, Altaf M, Gardazi SM, Abbasi AM

J Ethnobiol Ethnomed

27-Oct-2020

PMCID:	PMC7590686
doi:	10.1186/s13002-020-00417-w
PMID:	33109243

Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China

Hu R, Lin C, Xu W, Liu Y, Long C

J Ethnobiol Ethnomed

02-Jul-2020

PMCID:	PMC7333293
doi:	10.1186/s13002-020-00387-z
PMID:	32616044

Ethnomedicinal knowledge of the rural communities of Dhirkot, Azad Jammu and Kashmir, Pakistan

Farooq A, Amjad MS, Ahmad K, Altaf M, Umair M, Abbasi AM

J Ethnobiol Ethnomed

30-Aug-2019

PMCID:	PMC6716831
doi:	10.1186/s13002-019-0323-2
PMID:	31470868

Mobile Elements Shape Plastome Evolution in Ferns

Robison TA, Grusz AL, Wolf PG, Mower JP, Fauskee BD, Sosa K, Schuettpelz E

Genome Biol Evol

25-Aug-2018

PMCID:	PMC6166771
doi:	10.1093/gbe/evy189
PMID:	30165616

Phytochemicals from fern species: potential for medicine applications

Cao H, Chai TT, Wang X, Morais-Braga MF, Yang JH, Wong FC, Wang R, Yao H, Cao J, Cornara L, Burlando B, Wang Y, Xiao J, Coutinho HD

Phytochem Rev

28-Jan-2017

PMCID:	PMC7089528
doi:	10.1007/s11101-016-9488-7
PMID:	32214919

Convergent Evolution of Fern-Specific Mitochondrial Group II Intron atp1i361g2 and Its Ancient Source Paralogue rps3i249g2 and Independent Losses of Intron and RNA Editing among Pteridaceae

Zumkeller SM, Knoop V, Knie N

Genome Biol Evol

04-Aug-2016

PMCID:	PMC5010907
doi:	10.1093/gbe/evw173
PMID:	27492234

Ethnobotany of wild plants used for starting fermented beverages in Shui communities of southwest China

Hong L, Zhuo J, Lei Q, Zhou J, Ahmed S, Wang C, Long Y, Li F, Long C

J Ethnobiol Ethnomed

28-May-2015

PMCID:	PMC4458060
doi:	10.1186/s13002-015-0028-0
PMID:	26017691

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(3R)-3-(3,4-dihydroxyphenyl)-5,6-dihydroxy-3,4-dihydroisochromen-1-one	163081853	Click to see C1C(OC(=O)C2=C1C(=C(C=C2)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1002/CBDV.201000224
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Indanes / Indanones
(2R)-4-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one	92468652	Click to see CC1CC2=C(C1=O)C(=C(C(=C2O)C)CCO)C	234.29	unknown	https://doi.org/10.1016/S0031-9422(00)91246-9
(2S)-4-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one	46849085	Click to see CC1CC2=C(C1=O)C(=C(C(=C2O)C)CCO)C	234.29	unknown	https://doi.org/10.1016/S0031-9422(00)91246-9
4-Hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one	14104894	Click to see CC1CC2=C(C1=O)C(=C(C(=C2O)C)CCO)C	234.29	unknown	https://doi.org/10.1016/S0031-9422(00)91246-9
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,5S,8R,9S,10S,11R,15S,16S,18S)-9,10,15,16,18-pentahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	162904216	Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3O)O)O)O)C	380.40	unknown	https://doi.org/10.1002/CBDV.201000224
> 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/10.1016/0031-9422(93)85552-3
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/10.1016/0031-9422(93)85552-3
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/10.1016/0031-9422(93)85552-3
Chondrillasterol	5283663	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
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/10.1016/0031-9422(93)85552-3
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-4-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one	102090488	Click to see CC1CC2=C(C1=O)C(=C(C(=C2O)C)CCOC3C(C(C(C(O3)CO)O)O)O)C	396.40	unknown	https://doi.org/10.1016/S0031-9422(00)91246-9
4-Hydroxy-2,5,7-trimethyl-6-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one	75220709	Click to see CC1CC2=C(C1=O)C(=C(C(=C2O)C)CCOC3C(C(C(C(O3)CO)O)O)O)C	396.40	unknown	https://doi.org/10.1016/S0031-9422(00)91246-9
6-(2-Hydroxyethyl)-2,5,7-trimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroinden-1-one	322489	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O	396.40	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
Wallichoside	23260007	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O	396.40	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
4-Methylindeno[1,2-b]pyridin-5-one	72584	Click to see CC1=C2C(=NC=C1)C3=CC=CC=C3C2=O	195.22	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
(3S)-3-Ethyl-5,6-dimethoxy-7-hydroxyisobenzofuran-1(3H)-one	25135573	Click to see CCC1C2=CC(=C(C(=C2C(=O)O1)O)OC)OC	238.24	unknown	via CMAUP database
(R)-3-Ethyl-7-hydroxy-6-methoxyphthalide	25135575	Click to see CCC1C2=C(C(=C(C=C2)OC)O)C(=O)O1	208.21	unknown	via CMAUP database
(S)-3-Ethyl-5,6,7-trimethoxyphthalide	25135574	Click to see CCC1C2=CC(=C(C(=C2C(=O)O1)OC)OC)OC	252.26	unknown	via CMAUP database
(S)-3-Ethyl-7-hydroxy-6-methoxyphthalide	25137302	Click to see CCC1C2=C(C(=C(C=C2)OC)O)C(=O)O1	208.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones
(3Z)-3-Ethylidene-6,7-dimethoxyisobenzofuran-1(3H)-one	25135577	Click to see CC=C1C2=C(C(=C(C=C2)OC)OC)C(=O)O1	220.22	unknown	via CMAUP database
(Z)-3-Ethylidene-7-hydroxy-6-methoxyphthalide	25135576	Click to see CC=C1C2=C(C(=C(C=C2)OC)O)C(=O)O1	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dimethylfraxetin	3083928	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC	236.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
3-[(3,4-Dihydroxyphenyl)methyl]-6,7-dihydroxychromen-2-one	123684269	Click to see C1=CC(=C(C=C1CC2=CC3=CC(=C(C=C3OC2=O)O)O)O)O	300.26	unknown	https://doi.org/10.1002/CBDV.201000224
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(E)-1-(3,4-dihydroxyphenyl)-3-[3-[(3,4-dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl]prop-2-en-1-one	53361355	Click to see COC1=C(C(=C(C(=C1)O)C=CC(=O)C2=CC(=C(C=C2)O)O)OC)CC3=CC(=C(C=C3)O)O	438.40	unknown	https://doi.org/10.1002/CBDV.201000224
(E)-3-[3-[(3,4-dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl]-1-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one	53361356	Click to see COC1=C(C=C(C=C1)C(=O)C=CC2=C(C(=C(C=C2O)OC)CC3=CC(=C(C=C3)O)O)OC)O	452.50	unknown	https://doi.org/10.1002/CBDV.201000224
1-(3,4-Dihydroxyphenyl)-3-[3-[(3,4-dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl]prop-2-en-1-one	76023584	Click to see COC1=C(C(=C(C(=C1)O)C=CC(=O)C2=CC(=C(C=C2)O)O)OC)CC3=CC(=C(C=C3)O)O	438.40	unknown	https://doi.org/10.1002/CBDV.201000224
3-[3-[(3,4-Dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl]-1-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one	76023585	Click to see COC1=C(C=C(C=C1)C(=O)C=CC2=C(C(=C(C=C2O)OC)CC3=CC(=C(C=C3)O)O)OC)O	452.50	unknown	https://doi.org/10.1002/CBDV.201000224
3-[3-[(3,4-Dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl]-1-(5-hydroxy-2-methoxyphenyl)propan-1-one	162867641	Click to see COC1=C(C=C(C=C1)O)C(=O)CCC2=C(C(=C(C=C2O)OC)CC3=CC(=C(C=C3)O)O)OC	454.50	unknown	https://doi.org/10.1002/CBDV.201000224
6-[(3,4-Dihydroxyphenyl)methyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	162867642	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)CC4=CC(=C(C=C4)O)O)O)O	392.40	unknown	https://doi.org/10.1002/CBDV.201000224
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one	3519898	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=CC=C5)O)CO)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
Pinocembrin 7-rhamnosylglucoside	442454	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=CC=C5)O)CO)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/0031-9422(93)85552-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-2,3-dihydrochromen-4-one	162937038	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1002/CBDV.201000224
2-(3,4-Dihydroxyphenyl)-7-hydroxy-5-methoxy-2,3-dihydrochromen-4-one	17841897	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1002/CBDV.201000224
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
1-(3,4-Dihydroxyphenyl)-3-(4-hydroxy-2,6-dimethoxyphenyl)prop-2-en-1-one	123186082	Click to see COC1=CC(=CC(=C1C=CC(=O)C2=CC(=C(C=C2)O)O)OC)O	316.30	unknown	https://doi.org/10.1002/CBDV.201000224

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Onychium japonicum

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