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Cryptocarya concinna

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 UUID64401437cd6ed250090931
Scientific name Cryptocarya concinna
Authority Hance
First published in J. Bot. 20: 79 (1882)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Cryptocarya konishii Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 237 (1911)
Cryptocarya lenticellata Lecomte Notul. Syst. (Paris) 2: 333 (1913)
Cryptocarya microcarpa F.N.Wei Guihaia 15: 210 (1995)

Common names Top

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Language Common/alternative name
Chinese 海南厚壳桂
Chinese 黄果
Chinese 土楠
Chinese 黄果厚壳桂
Chinese 生虫树
Chinese 长果厚壳桂
Chinese 香港厚壳桂
Chinese 黄果桂

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 South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000627846
Tropicos 17800700
KEW urn:lsid:ipni.org:names:463851-1
The Plant List kew-2745905
Open Tree Of Life 490063
NCBI Taxonomy 666371
IUCN Red List 147647419
IPNI 463851-1
iNaturalist 736726
GBIF 4177718
EOL 5398001

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
Dynamics of soil microbial communities involved in carbon cycling along three successional forests in southern China Hu M, Zhou S, Xiong X, Wang X, Sun Y, Meng Z, Hui D, Li J, Zhang D, Deng Q Front Microbiol 15-Jan-2024
PMCID:PMC10822976
doi:10.3389/fmicb.2023.1326057
PMID:38287955
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
Transcriptomic and Metabolomic Analyses Reveal the Key Genes Related to Shade Tolerance in Soybean Jiang A, Liu J, Gao W, Ma R, Zhang J, Zhang X, Du C, Yi Z, Fang X, Zhang J Int J Mol Sci 18-Sep-2023
PMCID:PMC10531609
doi:10.3390/ijms241814230
PMID:37762532
Community structure and species diversity dynamics of a subtropical evergreen broad-leaved forest in China: 2005 to 2020 Wei SG, Li L, Bai KD, Wen ZF, Zhou JG, Lin Q Plant Divers 20-Jul-2023
PMCID:PMC10851295
doi:10.1016/j.pld.2023.07.005
PMID:38343594
Cryptocarya chinensis from the Upper Pleistocene of South China and its biogeographic and paleoecological implications Huang LL, Li SF, Huang WY, Jin JH, Oskolski AA iScience 10-Jul-2023
PMCID:PMC10405060
doi:10.1016/j.isci.2023.107313
PMID:37554461
Dynamic changes of the contents of photoprotective substances and photosynthetic maturation during leaf development of evergreen tree species in subtropical forests Yu ZC, Lin W, He W, Yan GZ, Zheng XT, Luo YN, Zhu H, Peng CL Tree Physiol 02-Mar-2023
PMCID:PMC10785039
doi:10.1093/treephys/tpad026
PMID:36864631
Distinct Responses of Abundant and Rare Soil Bacteria to Nitrogen Addition in Tropical Forest Soils He J, Tan X, Nie Y, Ma L, Liu J, Lu X, Mo J, Leloup J, Nunan N, Ye Q, Shen W Microbiol Spectr 09-Jan-2023
PMCID:PMC9927163
doi:10.1128/spectrum.03003-22
PMID:36622236
Molecular Docking of Cryptoconcatones to α-Tubulin and Related Pironetin Analogues Vergoten G, Bailly C Plants (Basel) 08-Jan-2023
PMCID:PMC9860703
doi:10.3390/plants12020296
PMID:36679009
Comprehensive Review of Recent Advances in Chiral A-Ring Flavonoid Containing Compounds: Structure, Bioactivities, and Synthesis Zhang C, Liu Y, Liu X, Chen X, Chen R Molecules 02-Jan-2023
PMCID:PMC9822200
doi:10.3390/molecules28010365
PMID:36615559
Photosynthetic product allocations of Pinus massoniana seedlings inoculated with ectomycorrhizal fungi along a nitrogen addition gradient Pengfei S, Yafei S, Lijun W, Tian C, Meng Z, Wenfa X, Ruimei C Front Plant Sci 12-Aug-2022
PMCID:PMC9412729
doi:10.3389/fpls.2022.948676
PMID:36035728
Combined Treatment with Cryptocaryone and Ultraviolet C Promotes Antiproliferation and Apoptosis of Oral Cancer Cells Wang SC, Chang HS, Tang JY, Farooqi AA, Kuo YT, Hsuuw YD, Lee JW, Chang HW Int J Mol Sci 10-Mar-2022
PMCID:PMC8950770
doi:10.3390/ijms23062981
PMID:35328402
Influence of Plant Origins and Seasonal Variations on Nutritive Values, Phenolics and Antioxidant Activities of Adenia viridiflora Craib., an Endangered Species from Thailand Wannasaksri W, Temviriyanukul P, Aursalung A, Sahasakul Y, Thangsiri S, Inthachat W, On-Nom N, Chupeerach C, Pruesapan K, Charoenkiatkul S, Suttisansanee U Foods 14-Nov-2021
PMCID:PMC8623237
doi:10.3390/foods10112799
PMID:34829080
An Interannual Comparative Study on Ecosystem Carbon Exchange Characteristics in the Dinghushan Biosphere Reserve, a Dominant Subtropical Evergreen Forest Ecosystem Njoroge B, Li Y, Wei S, Meng Z, Liu S, Zhang Q, Tang X, Zhang D, Liu J, Chu G Front Plant Sci 18-Oct-2021
PMCID:PMC8558562
doi:10.3389/fpls.2021.715340
PMID:34733299
Adaptation of Soil Fungal Community Structure and Assembly to Long- Versus Short-Term Nitrogen Addition in a Tropical Forest He J, Jiao S, Tan X, Wei H, Ma X, Nie Y, Liu J, Lu X, Mo J, Shen W Front Microbiol 25-Aug-2021
PMCID:PMC8424203
doi:10.3389/fmicb.2021.689674
PMID:34512567
Influences of temperature and moisture on abiotic and biotic soil CO2 emission from a subtropical forest Chen X, Liu M, Xu Z, Wei H Carbon Balance Manag 25-May-2021
PMCID:PMC8152076
doi:10.1186/s13021-021-00181-8
PMID:34032935

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 / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-[(1R,6E)-5-oxo-6-[(E)-4-phenylbut-3-en-2-ylidene]cyclohex-3-en-1-yl]acetic acid 163188463 Click to see CC(=C1C(CC=CC1=O)CC(=O)O)C=CC2=CC=CC=C2 282.30 unknown https://doi.org/10.1007/S11418-009-0368-Y
2-[5-Oxo-6-(4-phenylbut-3-en-2-ylidene)cyclohex-3-en-1-yl]acetic acid 163016309 Click to see 282.30 unknown https://doi.org/10.1007/S11418-009-0368-Y
methyl 2-[(1R,6E)-5-oxo-6-[(E)-4-phenylbut-3-en-2-ylidene]cyclohex-3-en-1-yl]acetate 163192859 Click to see 296.40 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Ganefromycin alpha 44584259 Click to see 1226.40 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Organoheterocyclic compounds / Benzofurans
(3aR,4Z,7aR)-4-[(E)-1-hydroxy-3-phenylprop-2-enylidene]-3a,7a-dihydro-3H-1-benzofuran-2,5-dione 162921191 Click to see 282.29 unknown https://doi.org/10.1007/S11418-009-0368-Y
(3aR,7aR)-4-(1-hydroxy-3-phenylprop-2-enylidene)-3a,7a-dihydro-3H-1-benzofuran-2,5-dione 162921193 Click to see 282.29 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Coclaurine 160487 Click to see 285.34 unknown https://doi.org/10.1248/YAKUSHI1947.86.4_296
dl-N-Norarmepavine 317405 Click to see 299.40 unknown https://doi.org/10.1248/YAKUSHI1947.86.4_296
L-(-)-N-norarmepavine 6999736 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)OC 299.40 unknown https://doi.org/10.1248/YAKUSHI1947.86.4_296
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1248/YAKUSHI1947.86.4_296
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1007/S11418-009-0368-Y
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1007/S11418-009-0368-Y
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(1R,13S,15S)-5,15-dihydroxy-15-[(E)-2-phenylethenyl]-4-[(E)-3-phenylprop-2-enoyl]-8,14-dioxatricyclo[11.3.1.02,7]heptadeca-2,4,6-trien-9-one 163188215 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=CC(=C(C=C4OC(=O)C1)O)C(=O)C=CC5=CC=CC=C5 510.60 unknown https://doi.org/10.1007/S11418-009-0368-Y
2-Propen-1-one, 1-(2-hydroxyphenyl)-3-phenyl- 14611 Click to see C1=CC=C(C=C1)C=CC(=O)C2=CC=CC=C2O 224.25 unknown https://doi.org/10.1007/S11418-009-0368-Y
2'-Hydroxychalcone 638276 Click to see C1=CC=C(C=C1)C=CC(=O)C2=CC=CC=C2O 224.25 unknown https://doi.org/10.1007/S11418-009-0368-Y
5,15-Dihydroxy-15-(2-phenylethenyl)-4-(3-phenylprop-2-enoyl)-8,14-dioxatricyclo[11.3.1.02,7]heptadeca-2,4,6-trien-9-one 162873209 Click to see C1CC2CC(CC(O2)(C=CC3=CC=CC=C3)O)C4=CC(=C(C=C4OC(=O)C1)O)C(=O)C=CC5=CC=CC=C5 510.60 unknown https://doi.org/10.1007/S11418-009-0368-Y

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