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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!
If you wish to browse all genomes for this plant click here.
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
The Comparative Genomics of Botryosphaeriaceae Suggests Gene Families of Botryosphaeria dothidea Related to Pathogenicity on Chinese Hickory Tree Liang D, Jiang Y, Zhang Y, Mao C, Ma T, Zhang C J Fungi (Basel) 22-Apr-2024
PMCID:PMC11051394
doi:10.3390/jof10040299
PMID:38667970
Thaumatin-like Proteins in Legumes: Functions and Potential Applications—A Review Feng L, Wei S, Li Y Plants (Basel) 17-Apr-2024
PMCID:PMC11055134
doi:10.3390/plants13081124
PMID:38674533
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
Melatonin Mitigates Water Deficit Stress in Cenchrus alopecuroides (L.) Thunb through Up-Regulating Gene Expression Related to the Photosynthetic Rate, Flavonoid Synthesis, and the Assimilatory Sulfate Reduction Pathway Jiang L, Yun M, Ma Y, Qu T Plants (Basel) 03-Mar-2024
PMCID:PMC10934972
doi:10.3390/plants13050716
PMID:38475560
Gut microbiota facilitate adaptation of invasive moths to new host plants Zhang S, Song F, Wang J, Li X, Zhang Y, Zhou W, Xu L ISME J 29-Feb-2024
PMCID:PMC10980833
doi:10.1093/ismejo/wrae031
PMID:38423525
High-quality genome assembly and genetic transformation system of Lasiodiplodia theobromae strain LTTK16-3, a fungal pathogen of Chinese hickory Ma T, Yan C, Zhang S, Liang D, Mao C, Zhang C Microbiol Spectr 13-Feb-2024
PMCID:PMC10913528
doi:10.1128/spectrum.03311-23
PMID:38349153
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
Coordinated Lipid Mobilization during Seed Development and Germination in Peanut (Arachis hypogaea L.) Cao D, Ma Y, Cao Z, Hu S, Li Z, Li Y, Wang K, Wang X, Wang J, Zhao K, Zhao K, Qiu D, Li Z, Ren R, Ma X, Zhang X, Gong F, Jung MY, Yin D J Agric Food Chem 29-Dec-2023
PMCID:PMC10870768
doi:10.1021/acs.jafc.3c06697
PMID:38157443
Pest categorisation of Pestalotiopsis microspora Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 21-Dec-2023
PMCID:PMC10733803
doi:10.2903/j.efsa.2023.8493
PMID:38130321
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
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
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

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 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
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
> 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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