Language	Common/alternative name
English	iron walnut
Arabic	جوز مختوم
Hungarian	jünnani dió
Chinese	泡核桃
Chinese	青胡桃果
Chinese	漾濞核桃
Chinese	茶核桃
Chinese	铁核桃
Chinese	三台核桃

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

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

Area

Hover over an area

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001067481
Tropicos	16700111
KEW	urn:lsid:ipni.org:names:442436-1
The Plant List	tro-16700111
PaleoBotany	91007
Open Tree Of Life	492312
NCBI Taxonomy	224355
IPNI	442436-1
iNaturalist	544425
GBIF	4205692
Freebase	/m/03wfl1y
EOL	2872274
USDA GRIN	20778
Wikipedia	Juglans_sigillata

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_003123805.1	ASM312380v1	Scaffold	University of California Davis	2018-05-14	300.0x	618.09 Mb

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

Screening and Characterization of Antioxidant Film Applicable to Walnut Kernels from Juglans sigillata

Li P, Zhang Y, Cao C, Luo Y, Kan H, Liu Y

Foods

25-Apr-2024

PMCID:	PMC11083998
doi:	10.3390/foods13091313
PMID:	38731685

Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry

Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC

Front Pharmacol

08-Mar-2024

PMCID:	PMC10957545
doi:	10.3389/fphar.2024.1349725
PMID:	38523640

Chromosome-level genome assembly of Platycarya strobilacea

Zhou H, Zhang X, Liu H, Ma J, Hao F, Ye H, Wang Y, Zhang S, Yue M, Zhao P

Sci Data

05-Mar-2024

PMCID:	PMC10914804
doi:	10.1038/s41597-024-03107-4
PMID:	38443357

Genome-Wide Identification of the CBF Gene Family and ICE Transcription Factors in Walnuts and Expression Profiles under Cold Conditions

Zhou H, Ma J, Liu H, Zhao P

Int J Mol Sci

19-Dec-2023

PMCID:	PMC10778614
doi:	10.3390/ijms25010025
PMID:	38203199

Effects of different oleogelators on the structural properties and composition of iron walnut-oil oleogels

Gao P, Liu Y, Wang S, Huang C, Zhong W, Yin J, Hu C, He D, Wang X

Ultrason Sonochem

14-Dec-2023

PMCID:	PMC10764282
doi:	10.1016/j.ultsonch.2023.106729
PMID:	38103368

A Multiplex PCR System of Novel Microsatellite Loci for Population Genetic Application in Walnuts

Xiahou ZY, Wambulwa MC, Xu ZC, Ye LJ, Fan PZ, Magige EA, Luo YH, Liu J

Plants (Basel)

07-Dec-2023

PMCID:	PMC10747719
doi:	10.3390/plants12244101
PMID:	38140428

Integrative Analysis of Metabolome and Transcriptome Provides Insights into the Mechanism of Flower Induction in Pineapple (Ananas comosus (L.) Merr.) by Ethephon

Lin W, Liu S, Xiao X, Sun W, Lu X, Gao Y, He J, Zhu Z, Wu Q, Zhang X

Int J Mol Sci

05-Dec-2023

PMCID:	PMC10742410
doi:	10.3390/ijms242417133
PMID:	38138962

Draft genome sequence of endophytic fungus Talaromyces purpureogenus strain YAFEF302, isolated from Juglans sigillata

Wang Y, Yang Y, Yuan X, Ma S, Wang D, Qiao L

Microbiol Resour Announc

05-Dec-2023

PMCID:	PMC10793358
doi:	10.1128/mra.00829-23
PMID:	38051076

Rapid and accurate detection of multi-target walnut appearance quality based on the lightweight improved YOLOv5s_AMM model

Zhan Z, Li L, Lin Y, Lv Z, Zhang H, Li X, Zhang F, Zeng Y

Front Plant Sci

08-Nov-2023

PMCID:	PMC10663328
doi:	10.3389/fpls.2023.1247156
PMID:	38023833

Genome-wide identification and molecular expression profile analysis of FHY3/FAR1 gene family in walnut (Juglans sigillata L.) development

Chen S, Chen Y, Liang M, Qu S, Shen L, Zeng Y, Hou N

BMC Genomics

08-Nov-2023

PMCID:	PMC10634098
doi:	10.1186/s12864-023-09629-2
PMID:	37940838

Conserved structured domains in plant non-coding RNA enod40, their evolution and recruitment of sequences from transposable elements

Gultyaev AP, Koster C, van Batenburg DC, Sistermans T, van Belle N, Vijfvinkel D, Roussis A

NAR Genom Bioinform

16-Oct-2023

PMCID:	PMC10578108
doi:	10.1093/nargab/lqad091
PMID:	37850034

Advanced Insights into Walnut Protein: Structure, Physiochemical Properties and Applications

Zhao Y, He W, Zhao S, Jiao T, Hu H, Li J, Zhang L, Zang J

Foods

28-Sep-2023

PMCID:	PMC10572233
doi:	10.3390/foods12193603
PMID:	37835256

Genetic imprints of grafting in wild iron walnut populations in southwestern China

Liu J, Magige EA, Fan PZ, Wambulwa MC, Luo YH, Qi HL, Gao LM, Milne RI

BMC Plant Biol

13-Sep-2023

PMCID:	PMC10498525
doi:	10.1186/s12870-023-04428-z
PMID:	37700228

Comprehensive agrobiological assessment and analysis of genetic relationships of promising walnut varieties of the Nikitsky Botanical Gardens

Plugatar YV, Suprun II, Khokhlov SY, Stepanov IV, Al-Nakib EA

Vavilovskii Zhurnal Genet Selektsii

01-Sep-2023

PMCID:	PMC10587009
doi:	10.18699/VJGB-23-55
PMID:	37867608

Current Studies on Bakanae Disease in Rice: Host Range, Molecular Identification, and Disease Management

An YN, Murugesan C, Choi H, Kim KD, Chun SC

Mycobiology

21-Aug-2023

PMCID:	PMC10498795
doi:	10.1080/12298093.2023.2241247
PMID:	37711983

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1007/S10600-011-9956-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1S)-4-oxo-2,3-dihydro-1H-naphthalen-1-yl]oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	163190099	Click to see C1CC(=O)C2=CC=CC=C2C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	476.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1S)-7-hydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl]oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	163040151	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C=C(C=C2)O	492.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1S)-8-hydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl]oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	45258236	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C(=CC=C2)O	492.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[(2R,3S,4S,5R,6R)-6-[[(1R)-7,8-dihydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162944937	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C(=C(C=C2)O)O	508.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[3,4,5-trihydroxy-6-[(4-oxo-2,3-dihydro-1H-naphthalen-1-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	163028277	Click to see C1CC(=O)C2=CC=CC=C2C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	476.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[3,4,5-trihydroxy-6-[(7-hydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	163040150	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C=C(C=C2)O	492.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[3,4,5-trihydroxy-6-[(8-hydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	75104336	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C(=CC=C2)O	492.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
[6-[(7,8-dihydroxy-4-oxo-2,3-dihydro-1H-naphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162944936	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)C(=C(C=C2)O)O	508.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
> Benzenoids / Tetralins
(4S)-4,5,8-trihydroxytetralone	46239261	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)O)O	194.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
1(2H)-Naphthalenone, 3,4-dihydro-3,4-dihydroxy-, (3S,4S)-	86330907	Click to see C1C(C(C2=CC=CC=C2C1=O)O)O	178.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-, (4S)-	11240662	Click to see C1CC(=O)C2=CC=CC=C2C1O	162.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
1(2H)-Naphthalenone, 3,4-dihydro-4,5-dihydroxy-, (S)-	22217226	Click to see C1CC(=O)C2=C(C1O)C(=CC=C2)O	178.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
3,4-Dihydroxy-3,4-dihydronaphthalen-1(2H)-one	53439501	Click to see C1C(C(C2=CC=CC=C2C1=O)O)O	178.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
4-hydroxy-3,4-dihydronaphthalen-1(2H)-one	152325	Click to see C1CC(=O)C2=CC=CC=C2C1O	162.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
4,5,8-Trihydroxytetralone	10921397	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)O)O	194.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
> Organic nitrogen compounds / Organonitrogen compounds / N-arylamides / N-acetylarylamines
Thiolutin	6870	Click to see CC(=O)NC1=C2C(=CSS2)N(C1=O)C	228.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S)-5-hydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	21577028	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C(=CC=C2)O	340.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802865	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C(=CC=C2)O	340.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819225/
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	130556	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1007/S10600-011-9956-7
Procyanidin B3	146798	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1007/S10600-011-9956-7
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose	374874	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1007/S10600-011-9956-7
1,2,4,6-Tetragalloyl-beta-D-glucopyranose	14464350	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1007/S10600-011-9956-7
1,2,4,6-Tetragalloylglucose	11297287	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1007/S10600-011-9956-7
Pentagalloylglucose	65238	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1007/S10600-011-9956-7
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1007/S10600-011-9956-7

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Juglans sigillata

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

Area

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top