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Carya cathayensis

Carya cathayensis - 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 UUID64400f8205a21459652105
Scientific name Carya cathayensis
Authority Sarg.
First published in Pl. Wilson. 3: 187 (1916)

Description Top

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Carya cathayensis, also known as Chinese hickory, is a type of hickory tree found in China. Its peeled and roasted nuts, called 山核桃仁, are a popular delicacy in Hangzhou.

Synonyms Top

Scientific name Authority First published in
Carya dabieshanensis M.C.Liu & Z.J.Li J. Zhejiang Forest. Coll. 1(1): 41 (1984), with two types cited.
Hicorius cathayensis Chun Chin. Econ. Trees : 62 (1921)
Hicoria cathayensis (Sarg.) Chun Chin. Econom. Trees 62, pl. 20 1921

Common names Top

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Language Common/alternative name
Hungarian kínai hikoridió
Chinese 山核桃
Chinese 山蟹
Chinese 野漆树
Chinese 山核桃叶
Chinese 核桃
Chinese 山核桃仁
Chinese 山核桃皮
Chinese 小核桃
Chinese 山胡桃

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

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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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000588741
Tropicos 16700152
KEW urn:lsid:ipni.org:names:442154-1
The Plant List kew-2701763
PaleoBotany 55031
Open Tree Of Life 199047
NCBI Taxonomy 139927
IPNI 442154-1
GBIF 4205744
EPPO CYACA
EOL 2872261
USDA GRIN 9251
Wikipedia Carya_cathayensis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_011037825.1 ASM1103782v1 Scaffold Zhejiang A&F University 2020-02-27 248.0x 673.67 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
Identification and functional analysis of the LEAFY gene in longan flower induction Jue D, Li Z, Zhang W, Tang J, Xie T, Sang X, Guo Q BMC Genomics 25-Mar-2024
PMCID:PMC10962150
doi:10.1186/s12864-024-10229-x
PMID:38528464
Comparative Analysis of Chloroplast Pan-Genomes and Transcriptomics Reveals Cold Adaptation in Medicago sativa Zhang T, Chen X, Yan W, Li M, Huang W, Liu Q, Li Y, Guo C, Shu Y Int J Mol Sci 01-Feb-2024
PMCID:PMC10855486
doi:10.3390/ijms25031776
PMID:38339052
A Sustainable Extraction Approach of Phytochemicals from Date (Phoenix dactylifera L.) Fruit Cultivars Using Ultrasound-Assisted Deep Eutectic Solvent: A Comprehensive Study on Bioactivity and Phenolic Variability Djaoudene O, Bachir-Bey M, Schisano C, Djebari S, Tenore GC, Romano A Antioxidants (Basel) 31-Jan-2024
PMCID:PMC10886234
doi:10.3390/antiox13020181
PMID:38397779
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
Screening and Characterization of an α-Amylase Inhibitor from Carya cathayensis Sarg. Peel Zhang X, Huang G, Liu H, Chen W, Zhao J, Jia Z, Tao F Foods 10-Dec-2023
PMCID:PMC10742785
doi:10.3390/foods12244425
PMID:38137229
The Roles of GRETCHEN HAGEN3 (GH3)-Dependent Auxin Conjugation in the Regulation of Plant Development and Stress Adaptation Luo P, Li TT, Shi WM, Ma Q, Di DW Plants (Basel) 08-Dec-2023
PMCID:PMC10747189
doi:10.3390/plants12244111
PMID:38140438
Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA Molecules 05-Dec-2023
PMCID:PMC10745828
doi:10.3390/molecules28247937
PMID:38138427
PacBio Full-Length Transcriptome Sequencing Reveals the Mechanism of Salt Stress Response in Sonneratia apetala Chen B, Liu T, Yang Z, Yang S, Chen J Plants (Basel) 14-Nov-2023
PMCID:PMC10675792
doi:10.3390/plants12223849
PMID:38005746
Promoter cloning and activities analysis of JmLFY, a key gene for flowering in Juglans mandshurica Zhang L, Fu J, Dong T, Zhang M, Wu J, Liu C Front Plant Sci 12-Oct-2023
PMCID:PMC10602732
doi:10.3389/fpls.2023.1243030
PMID:37900747
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
Green extraction of phenolics and flavonoids from black mulberry fruit using natural deep eutectic solvents: optimization and surface morphology Vo TP, Pham TV, Weina K, Tran TN, Vo LT, Nguyen PT, Bui TL, Phan TH, Nguyen DQ BMC Chem 21-Sep-2023
PMCID:PMC10512608
doi:10.1186/s13065-023-01041-x
PMID:37735704
Analysis of Delta(9) fatty acid desaturase gene family and their role in oleic acid accumulation in Carya cathayensis kernel Si X, Lyu S, Hussain Q, Ye H, Huang C, Li Y, Huang J, Chen J, Wang K Front Plant Sci 12-Sep-2023
PMCID:PMC10523321
doi:10.3389/fpls.2023.1193063
PMID:37771493
Melatonin interaction with abscisic acid in the regulation of abiotic stress in Solanaceae family plants Ali M, Pan Y, Liu H, Cheng Z Front Plant Sci 11-Sep-2023
PMCID:PMC10520282
doi:10.3389/fpls.2023.1271137
PMID:37767290
Transcriptome Analysis Reveals the Response Mechanism of Digitaria sanguinalis, Arabidopsis thaliana and Poa annua under 4,8-Dihydroxy-1-tetralone Treatment Sun Q, Wang T, Huang J, Gu X, Dong Y, Yang Y, Da X, Mo X, Xie X, Jiang H, Yan D, Zheng B, He Y Plants (Basel) 22-Jul-2023
PMCID:PMC10385526
doi:10.3390/plants12142728
PMID:37514341
Genome-Wide Identification, Characterization, and Expression Analysis of Long-Chain Acyl-CoA Synthetases in Carya illinoinensis under Different Treatments Ma W, Zhu K, Zhao J, Chen M, Wei L, Qiao Z, Tan P, Peng F Int J Mol Sci 17-Jul-2023
PMCID:PMC10380667
doi:10.3390/ijms241411558
PMID:37511313

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
3-Hydroxy-5-methoxybenzaldehyde 5314561 Click to see COC1=CC(=CC(=C1)O)C=O 152.15 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Ligballinol 9796282 Click to see C1C2C(COC2C3=CC=C(C=C3)O)C(O1)C4=CC=C(C=C4)O 298.30 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
4-[(3R,3aS,6R,6aS)-3-(4-hydroxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]phenol 21722914 Click to see C1C2C(COC2C3=CC=C(C=C3)O)C(O1)C4=CC=C(C=C4)O 298.30 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
4-[[(3R,4S,5R)-4-(hydroxymethyl)-5-(4-hydroxyphenyl)oxolan-3-yl]methyl]phenol 57328685 Click to see C1C(C(C(O1)C2=CC=C(C=C2)O)CO)CC3=CC=C(C=C3)O 300.30 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
2-Hydroxy-6-(3-hydroxypropyl)benzaldehyde 163006819 Click to see C1=CC(=C(C(=C1)O)C=O)CCCO 180.20 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paroxypropione 6271 Click to see CCC(=O)C1=CC=C(C=C1)O 150.17 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Balanophonin 23252258 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
(+/-)-Balanophonin 72729357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
Balanophonin 21582569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(4-Hydroxyphenyl)prop-2-enal 440733 Click to see C1=CC(=CC=C1C=CC=O)O 148.16 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
p-Coumaraldehyde 641301 Click to see C1=CC(=CC=C1C=CC=O)O 148.16 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
5-[(1R,2S)-1-hydroxy-3-(2-hydroxyethoxy)-1-(4-hydroxyphenyl)propan-2-yl]-2-methoxyphenol 162947287 Click to see COC1=C(C=C(C=C1)C(COCCO)C(C2=CC=C(C=C2)O)O)O 334.40 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
5-[(1R,2S)-3-hydroxy-1-(4-hydroxyphenyl)-1-methoxypropan-2-yl]-2-methoxyphenol 162866825 Click to see COC1=C(C=C(C=C1)C(CO)C(C2=CC=C(C=C2)O)OC)O 304.34 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
5-[(1S,2R)-3-hydroxy-1-(4-hydroxyphenyl)-1-methoxypropan-2-yl]-2-methoxyphenol 162866824 Click to see COC1=C(C=C(C=C1)C(CO)C(C2=CC=C(C=C2)O)OC)O 304.34 unknown https://doi.org/10.1016/J.BMCL.2012.01.062
Evofolin B 5317306 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown https://doi.org/10.1016/J.BMCL.2012.01.062

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Collections Top

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