Litsea rotundifolia

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Internal ID UUID644047394f835041167676
Scientific name Litsea rotundifolia
Authority (Nees) Hemsl.
First published in J. Linn. Soc., Bot. 26: 385 (1891)

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Synonyms Top

Scientific name Authority First published in
Actinodaphne rotundifolia (Nees) Merr. Lingnan Sci. J. 15: 419 (1936)
Iozoste rotundifolia Nees Pl. Asiat. Rar. 2: 63 (1831)
Actinodaphne chinensis var. rotundifolia (Nees) Nees Syst. Laur. 600 1836
Iozoste chinensis var. rotundifolia (Nees) Blume Mus. Bot. 1: 364 1851

Common names Top

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Language Common/alternative name
Chinese 木姜子
Chinese 圆叶豺皮樟

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Litsea rotundifolia var. oblongifolia (Nees) C.K.Allen Ann. Missouri Bot. Gard. 25: 386. 1938 (1938 publ. 1937)
Litsea rotundifolia var. ovatifolia Yen C.Yang & P.H.Huang Acta Phytotax. Sin. 16(4): 49 (1978)
Litsea rotundifolia var. rotundifolia Unknown

Subvarieties (abbr. subvar.) 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 Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070312
Tropicos 17800398
KEW urn:lsid:ipni.org:names:465995-1
The Plant List tro-17800398
Open Tree Of Life 1052061
NCBI Taxonomy 1009485
IUCN Red List 146516904
IPNI 465995-1
iNaturalist 556173
GBIF 7304563
EOL 5397678
USDA GRIN 22426
CMAUP NPO25381

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
The Analgesic Potential of Litsea Species: A Systematic Review Goh MP, Samsul RN, Mohaimin AW, Goh HP, Zaini NH, Kifli N, Ahmad N Molecules 30-Apr-2024
PMCID:PMC11085224
doi:10.3390/molecules29092079
PMID:38731572
Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S BMC Ecol Evol 10-Apr-2024
PMCID:PMC11005248
doi:10.1186/s12862-024-02227-0
PMID:38600505
Damage by typhoon Hato compared among three different plant communities in Macau, China Yi Q, Ye W, Wang F, Xing F, Harris A, Duan L, Chen H Ecol Evol 05-Oct-2023
PMCID:PMC10555504
doi:10.1002/ece3.10574
PMID:37809357
Taxonomic Advances from Fungal Flora Associated with Ferns and Fern-like Hosts in Northern Thailand Seifollahi E, de Farias AR, Jayawardena RS, Hyde KD Plants (Basel) 03-Feb-2023
PMCID:PMC9922025
doi:10.3390/plants12030683
PMID:36771768
Pestalotioid Species Associated with Medicinal Plants in Southwest China and Thailand Sun YR, Jayawardena RS, Sun JE, Wang Y Microbiol Spectr 10-Jan-2023
PMCID:PMC9927317
doi:10.1128/spectrum.03987-22
PMID:36625649
Pest categorisation of Icerya aegyptiaca Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A EFSA J 09-Jan-2023
PMCID:PMC9827230
doi:10.2903/j.efsa.2023.7739
PMID:36628331
Estimating above-ground biomass of subtropical forest using airborne LiDAR in Hong Kong Chan EP, Fung T, Wong FK Sci Rep 18-Jan-2021
PMCID:PMC7814143
doi:10.1038/s41598-021-81267-8
PMID:33462354
Disentangling the Contributions of Plant Taxonomic and Functional Diversities in Shaping Aboveground Biomass of a Restored Forest Landscape in Southern China Hanif MA, Yu Q, Rao X, Shen W Plants (Basel) 16-Dec-2019
PMCID:PMC6963651
doi:10.3390/plants8120612
PMID:31888237
Plant Taxonomic Diversity Better Explains Soil Fungal and Bacterial Diversity than Functional Diversity in Restored Forest Ecosystems Hanif MA, Guo Z, Moniruzzaman M, He D, Yu Q, Rao X, Liu S, Tan X, Shen W Plants (Basel) 06-Nov-2019
PMCID:PMC6918236
doi:10.3390/plants8110479
PMID:31698841
Constructing a DNA barcode reference library for southern herbs in China: A resource for authentication of southern Chinese medicine Gong L, Qiu XH, Huang J, Xu W, Bai JQ, Zhang J, Su H, Xu CM, Huang ZH PLoS One 25-Jul-2018
PMCID:PMC6059470
doi:10.1371/journal.pone.0201240
PMID:30044868
Tree functional types simplify forest carbon stock estimates induced by carbon concentration variations among species in a subtropical area Wu H, Xiang W, Fang X, Lei P, Ouyang S, Deng X Sci Rep 10-Jul-2017
PMCID:PMC5504068
doi:10.1038/s41598-017-05306-z
PMID:28694496
Tree growth traits and social status affect the wood density of pioneer species in secondary subtropical forest Chen L, Xiang W, Wu H, Lei P, Zhang S, Ouyang S, Deng X, Fang X Ecol Evol 14-Jun-2017
PMCID:PMC5528239
doi:10.1002/ece3.3110
PMID:28770074
DNA barcoding evaluation and implications for phylogenetic relationships in Lauraceae from China Liu ZF, Ci XQ, Li L, Li HW, Conran JG, Li J PLoS One 17-Apr-2017
PMCID:PMC5393608
doi:10.1371/journal.pone.0175788
PMID:28414813
Influence of Tree Species Composition and Community Structure on Carbon Density in a Subtropical Forest Hu Y, Su Z, Li W, Li J, Ke X PLoS One 28-Aug-2015
PMCID:PMC4552639
doi:10.1371/journal.pone.0136984
PMID:26317523
Circumscription and Taxonomic Arrangement of Nigroboletus roseonigrescens Gen. Et Sp. Nov., a New Member of Boletaceae from Tropical South–Eastern China Gelardi M, Vizzini A, Ercole E, Horak E, Ming Z, Li T PLoS One 11-Aug-2015
PMCID:PMC4532479
doi:10.1371/journal.pone.0134295
PMID:26263180

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2S)-4-dodec-11-enyl-3-hydroxy-2-methyl-2H-furan-5-one 54680603 Click to see 280.40 unknown https://doi.org/10.1002/HLCA.200590019
(2S)-4-dodec-11-ynyl-3-hydroxy-2-methyl-2H-furan-5-one 54685892 Click to see 278.40 unknown https://doi.org/10.1002/HLCA.200590019
4-dodec-11-enyl-3-hydroxy-2-methyl-2H-furan-5-one 76169500 Click to see 280.40 unknown https://doi.org/10.1002/HLCA.200590019
4-dodec-11-ynyl-3-hydroxy-2-methyl-2H-furan-5-one 76170759 Click to see 278.40 unknown https://doi.org/10.1002/HLCA.200590019
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Haperforin F 11114000 Click to see CC1(C23CC(=O)OC2(C4CCC(C(C(=O)C4(C3CC(=O)O1)C)(C(=O)OC)O)(C)C(=O)C5=COC=C5)C)C 516.50 unknown https://doi.org/10.1002/HLCA.200590019
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Tetradec-13-yn-2-one 86057622 Click to see 208.34 unknown https://doi.org/10.1080/10286020310001596006
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3Z,4S,5R)-3-dodec-11-enylidene-4-hydroxy-5-methyloxolan-2-one 11219742 Click to see 280.40 unknown https://doi.org/10.1002/HLCA.200590019
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallic Acid 341 Click to see 322.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1080/1028602031000111969
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Quercetin 3-arabinoside 10252339 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
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database

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