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Diospyros morrisiana

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440176889ea8316506078
Scientific name Diospyros morrisiana
Authority Hance
First published in Ann. Bot. Syst. 3: 14 (1852)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Diospyros nipponica Nakai Bot. Mag. (Tokyo) 35: 137 (1921)
Diospyros sasakii Hayata Icon. Pl. Formosan. 7: 33 (1918)

Common names Top

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Language Common/alternative name
Japanese トキワガキ
Chinese 野柿花
Chinese 乌蛇木
Chinese 山椑树
Chinese 山红柿
Chinese 牛古柿
Chinese 罗浮柿
Chinese 油柿
Chinese 山柿
Chinese 山紅柿
Chinese 罗浮柿果
Chinese 罗浮柿根

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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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
    • China
      • China Southeast
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000649374
KEW urn:lsid:ipni.org:names:322737-1
The Plant List kew-2770182
Open Tree Of Life 514561
NCBI Taxonomy 1008904
IUCN Red List 173408
IPNI 322737-1
iNaturalist 425419
GBIF 4070710
EPPO DOSMO
EOL 2892224
USDA GRIN 14307

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
Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196 He Y, Xu Y, Chen X Insects 31-Jan-2024
PMCID:PMC10889426
doi:10.3390/insects15020093
PMID:38392559
Plant species identity and mycorrhizal type explain the root-associated fungal pathogen community assembly of seedlings based on functional traits in a subtropical forest Li Y, Xie Y, Liu Z, Shi L, Liu X, Liang M, Yu S Front Plant Sci 27-Oct-2023
PMCID:PMC10641815
doi:10.3389/fpls.2023.1251934
PMID:37965023
Comparative analysis of Diospyros (Ebenaceae) plastomes: Insights into genomic features, mutational hotspots, and adaptive evolution Huang Y, Ma Q, Sun J, Zhou L, Lai C, Li P, Jin X, Zhang Y Ecol Evol 12-Jul-2023
PMCID:PMC10338900
doi:10.1002/ece3.10301
PMID:37456073
Responses of carbon, nitrogen, and phosphorus contents and stoichiometry in soil and fine roots to natural vegetation restoration in a tropical mountainous area, Southern China Hu G, Zhang Z, Li L Front Plant Sci 09-May-2023
PMCID:PMC10203608
doi:10.3389/fpls.2023.1181365
PMID:37229113
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review He Y, Xu Y, Chen X Insects 16-Feb-2023
PMCID:PMC9967332
doi:10.3390/insects14020196
PMID:36835765
Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y Ecol Evol 03-Dec-2022
PMCID:PMC9719084
doi:10.1002/ece3.9587
PMID:36479033
Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Sep-2022
PMCID:PMC9500622
doi:10.3390/insects13090826
PMID:36135527
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Seed rain and soil seed bank in Chinese fir plantations and an adjacent natural forest in southern China: Implications for the regeneration of native species Liu B, Liu Q, Zhu C, Liu Z, Huang Z, Tigabu M, He Z, Liu Y, Wang Z Ecol Evol 26-Jan-2022
PMCID:PMC8796942
doi:10.1002/ece3.8539
PMID:35127042
Plant Functional Groups Dominate Responses of Plant Adaptive Strategies to Urbanization Xiao Y, Liu S, Zhang M, Tong F, Xu Z, Ford R, Zhang T, Shi X, Wu Z, Luo T Front Plant Sci 30-Nov-2021
PMCID:PMC8669269
doi:10.3389/fpls.2021.773676
PMID:34917107
Sexual competition and kin recognition co-shape the traits of neighboring dioecious Diospyros morrisiana seedlings He Y, Xu H, Liu H, Luo M, Chu C, Fang S Hortic Res 01-Jul-2021
PMCID:PMC8245536
doi:10.1038/s41438-021-00598-9
PMID:34193863
Co-ordination between leaf biomechanical resistance and hydraulic safety across 30 sub-tropical woody species Wang YQ, Ni MY, Zeng WH, Huang DL, Xiang W, He PC, Ye Q, Cao KF, Zhu SD Ann Bot 30-Apr-2021
PMCID:PMC8324032
doi:10.1093/aob/mcab055
PMID:33930116
Compatible Mycorrhizal Types Contribute to a Better Design for Mixed Eucalyptus Plantations Qin F, Yu S Front Plant Sci 12-Feb-2021
PMCID:PMC7907608
doi:10.3389/fpls.2021.616726
PMID:33643349
Taxonomy and phylogeny of cercosporoid ascomycetes on Diospyros spp. with special emphasis on Pseudocercospora spp. Braun U, Nakashima C, Bakhshi M, Zare R, Shin HD, Alves RF, Sposito MB Fungal Syst Evol 03-Apr-2020
PMCID:PMC7453130
doi:10.3114/fuse.2020.06.06
PMID:32904397

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 / Naphthalenes / Naphthoquinones
1',4-Dihydroxy-7'-methoxy-2,3'-dimethyl-,(-)-[1,2'-binaphthalene]-5,5',8,8'-tetrone 14237022 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
5-Hydroxy-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-7-methylnaphthalene-1,4-dione 14237024 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
8-Hydroxy-2-methoxynaphthalene-1,4-dione 609303 Click to see COC1=CC(=O)C2=C(C1=O)C(=CC=C2)O 204.18 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
8-Hydroxy-7-(4-hydroxy-6-methoxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-6-methylnaphthalene-1,4-dione 162821343 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
8-Hydroxy-7-(4-hydroxy-7-methoxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-methoxy-6-methylnaphthalene-1,4-dione 14237026 Click to see CC1=CC2=C(C(=C1C3=C4C(=C(C=C3C)O)C(=O)C=C(C4=O)OC)O)C(=O)C(=CC2=O)OC 434.40 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
Bisisodiospyrin 169144 Click to see CC1=CC2=C(C(=C1C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O)O)C(=O)C(=CC2=O)C5=CC(=O)C6=C(C5=O)C(=C(C(=C6)C)C7=C8C(=O)C=CC(=O)C8=C(C=C7C)O)O 746.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
Isodiospyrin 99298 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
https://doi.org/10.1002/(SICI)1099-1573(199805)12:3<155::AID-PTR214>3.0.CO;2-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aS,6aR,6bR,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 40557056 Click to see 428.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
(4aR,6aS,6aR,6bR,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 162861352 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 162861351 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
4,4,6a,6b,8a,11,11,14b-Octamethyl-docosahydropicen-3-ol 605867 Click to see 428.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
Olean-12-en-3-one 6454747 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97787-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3R,3aR,4S,9aS,9bR)-9a-acetyloxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 12967183 Click to see CC=C(C)C(=O)OC1CC(=C2C(=O)C=C(C2(C3C1C(C(=O)O3)C)OC(=O)C)C)C 402.40 unknown https://doi.org/10.1016/S0031-9422(97)01020-0

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