Ostryopsis davidiana - Unknown
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Internal ID UUID643fe5b4ca5e1541244319
Scientific name Ostryopsis davidiana
Authority Decne.
First published in Bull. Soc. Bot. France 20: 155 (1873)

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Synonyms Top

Scientific name Authority First published in
Corylus davidiana (Decne.) Baill. Hist. Pl. 6: 224 (1876)

Common names Top

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Language Common/alternative name
Bulgarian остриопсис на Давид
Bulgarian Давидов остриопсис
Russian Остриопсис Давида
Vietnamese dầu nóng
Chinese 牡蛎肉
Chinese 虎榛子
Chinese 棱榆
Chinese 胡榛
Chinese 虎榛

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000261481
Tropicos 3600820
KEW urn:lsid:ipni.org:names:295677-1
The Plant List kew-144649
Open Tree Of Life 274190
NCBI Taxonomy 78607
IUCN Red List 194451
IPNI 295677-1
GBIF 2876094
EPPO OSRDA
EOL 1153521
USDA GRIN 26166
CMAUP NPO40

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
Seasonal Diet Composition of Goitered Gazelle (Gazella subgutturosa) in an Arid and Semi-Arid Region of Western China Zhang N, Zhang Z, Liu C, Xiong Z, Wei Y, Meng D, Zhan M, Li Z, Zhao Y, Teng L, Liu Z Animals (Basel) 20-Feb-2024
PMCID:PMC10931280
doi:10.3390/ani14050663
PMID:38473048
The mechanism effects of root exudate on microbial community of rhizosphere soil of tree, shrub, and grass in forest ecosystem under N deposition Jing H, Wang H, Wang G, Liu G, Cheng Y ISME Commun 20-Nov-2023
PMCID:PMC10662252
doi:10.1038/s43705-023-00322-9
PMID:37985715
Comparison of plant diversity-carbon storage relationships along altitudinal gradients in temperate forests and shrublands Lu S, Zhang D, Wang L, Dong L, Liu C, Hou D, Chen G, Qiao X, Wang Y, Guo K Front Plant Sci 11-Aug-2023
PMCID:PMC10453807
doi:10.3389/fpls.2023.1120050
PMID:37636113
Genomic Analysis of Plastid–Nuclear Interactions and Differential Evolution Rates in Coevolved Genes across Juglandaceae Species Yang Y, Forsythe ES, Ding YM, Zhang DY, Bai WN Genome Biol Evol 29-Jul-2023
PMCID:PMC10410296
doi:10.1093/gbe/evad145
PMID:37515592
The Effect of Landscape Environmental Factors on Gene Flow of Red Deer (Cervus canadensis xanthopygus) in the Southern of the Greater Khingan Mountains, China Li Z, Guo J, Hong Y, Zhang N, Zhang M Biology (Basel) 10-Apr-2023
PMCID:PMC10135690
doi:10.3390/biology12040576
PMID:37106776
Genome structure-based Juglandaceae phylogenies contradict alignment-based phylogenies and substitution rates vary with DNA repair genes Ding YM, Pang XX, Cao Y, Zhang WP, Renner SS, Zhang DY, Bai WN Nat Commun 04-Feb-2023
PMCID:PMC9899254
doi:10.1038/s41467-023-36247-z
PMID:36739280
Plastome phylogenomics provide new perspective into the phylogeny and evolution of Betulaceae (Fagales) Yang Z, Ma W, Yang X, Wang L, Zhao T, Liang L, Wang G, Ma Q BMC Plant Biol 24-Dec-2022
PMCID:PMC9789603
doi:10.1186/s12870-022-03991-1
PMID:36566190
Altitudinal Variation Influences Soil Fungal Community Composition and Diversity in Alpine–Gorge Region on the Eastern Qinghai–Tibetan Plateau Chen J, Shi Z, Liu S, Zhang M, Cao X, Chen M, Xu G, Xing H, Li F, Feng Q J Fungi (Basel) 30-Jul-2022
PMCID:PMC9410234
doi:10.3390/jof8080807
PMID:36012795
Genetic diversity and population dynamic of Ziziphus jujuba var. spinosa (Bunge) Hu ex H. F. Chow in Central China Du S, Hu X, Yang X, Yu W, Wang Z Ecol Evol 24-Jul-2022
PMCID:PMC9309028
doi:10.1002/ece3.9101
PMID:35898427
Molecular signatures of parallel adaptive divergence causing reproductive isolation and speciation across two genera Wang Z, Jiang Y, Yang X, Bi H, Li J, Mao X, Ma Y, Ru D, Zhang C, Hao G, Wang J, Abbott RJ, Liu J Innovation (Camb) 20-Apr-2022
PMCID:PMC9065898
doi:10.1016/j.xinn.2022.100247
PMID:35519515
Genomic evidence for homoploid hybrid speciation between ancestors of two different genera Wang Z, Kang M, Li J, Zhang Z, Wang Y, Chen C, Yang Y, Liu J Nat Commun 13-Apr-2022
PMCID:PMC9008057
doi:10.1038/s41467-022-29643-4
PMID:35418567
Chromosome-Level Genome Assembly and HazelOmics Database Construction Provides Insights Into Unsaturated Fatty Acid Synthesis and Cold Resistance in Hazelnut (Corylus heterophylla) Liu J, Wei H, Zhang X, He H, Cheng Y, Wang D Front Plant Sci 09-Dec-2021
PMCID:PMC8695561
doi:10.3389/fpls.2021.766548
PMID:34956265
Near-natural transformation of Pinus tabuliformis better improve soil nutrients and soil microbial community Yin Y, Li Q, Du H PeerJ 23-Sep-2021
PMCID:PMC8465996
doi:10.7717/peerj.12098
PMID:34631311
Stoichiometry of Carbon, Nitrogen and Phosphorus in Shrub Organs Linked Closely With Mycorrhizal Strategy in Northern China Yang S, Shi Z, Zhang M, Li Y, Gao J, Wang X, Liu D Front Plant Sci 07-Sep-2021
PMCID:PMC8453024
doi:10.3389/fpls.2021.687347
PMID:34557207
Demographic history and local adaptation of Myripnois dioica (Asteraceae) provide insight on plant evolution in northern China flora Lin N, Landis JB, Sun Y, Huang X, Zhang X, Liu Q, Zhang H, Sun H, Wang H, Deng T Ecol Evol 17-May-2021
PMCID:PMC8216978
doi:10.1002/ece3.7628
PMID:34188867

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1R)-1-Ethenyl-1,5-dimethyl-4-hexen-1-yl I(2)-D-glucopyranoside 38358979 Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C 316.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,3S,5R,7S,9S)-3-acetyl-4,4,7-trimethyl-9-(3-methylbut-2-enyl)-9-(2-methylpropanoyl)tricyclo[5.3.1.01,5]undecane-8,10,11-trione 101846599 Click to see CC(C)C(=O)C1(C(=O)C2(CC3C(C(CC3(C2=O)C1=O)C(=O)C)(C)C)C)CC=C(C)C 414.50 unknown via CMAUP database
Takaneone B 101846600 Click to see CC(C)C(=O)C1(C(=O)C2(CC3C(C(CC3(C2=O)C1=O)C(=O)C)(C)C)C)CC=C(C)C 414.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
butyl (1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylate 6481825 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown via CMAUP database
methyl (1S,3R,4R,5R)-3-[(Z)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylate 71720841 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3S)-3-ethyl-5,7-dihydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 25243492 Click to see CCC1C(OC2=CC(=CC(=C2C1=O)O)O)OC3C(C(C(C(O3)CO)O)O)O 386.30 unknown via CMAUP database
(2S,3S)-5,7-dihydroxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 25243497 Click to see CC1C(OC2=CC(=CC(=C2C1=O)O)O)OC3C(C(C(C(O3)CO)O)O)O 372.32 unknown via CMAUP database
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-ethyl-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 25243427 Click to see CCC1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 368.30 unknown via CMAUP database
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
7-(beta-d-Glucopyranosyloxy)-5-hydroxy-3-methyl-4h-1-benzopyran-4-one 25243496 Click to see CC1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
8-Glucosyl-5,7-dihydroxy-2-isopropylchromone 5317688 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)O 382.40 unknown via CMAUP database
Urachromone A 25243498 Click to see CC(C)C1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 382.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
Benzoyl-beta-D-glucoside 12314096 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(C(O2)CO)O)O)O 284.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-3-methylchromone 22978769 Click to see CC1=COC2=CC(=CC(=C2C1=O)O)O 192.17 unknown via CMAUP database
Lathodoratin 5281344 Click to see CCC1=COC2=CC(=CC(=C2C1=O)O)O 206.19 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5-Trihydroxyxanthone 5281663 Click to see C1=CC2=C(C(=C1)O)OC3=CC(=CC(=C3C2=O)O)O 244.20 unknown via CMAUP database
Isomangiferin 5318597 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Hyperxanthone 14757909 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C=C(C=C4)O)O)C 310.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 101851760 Click to see CC(=O)OC1C(C(C(OC1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)CO)O)O 506.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 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 via CMAUP database
Isoquercetin 5280804 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 via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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