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Lindera megaphylla

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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 UUID6440473a0ec8d124914928
Scientific name Lindera megaphylla
Authority Hemsl.
First published in J. Linn. Soc., Bot. 26: 389 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Litsea amaroideocarpa Kosterm. Reinwardtia 7: 345 (1968)
Litsea touyunensis H.Lév. Repert. Spec. Nov. Regni Veg. 11: 63 (1912)
Benzoin oldhamii (Hemsl.) Rehder J. Arnold Arbor. 1: 145. 1919
Benzoin pricei (Hayata) Kamik. in Ann. Rep. Taihoku Bot. Gard. 1933, iii. 79.
Benzoin touyunense (H.Lév.) Rehder J. Arnold Arbor. 10: 194. 1929
Benzoin touyunense f. trichocladum Rehder J. Arnold Arbor. 11: 159 1930
Lindera megaphylla f. touyunensis (H.Lév.) Rehder J. Arnold Arbor. 18: 275 1937
Lindera megaphylla f. trichoclada (Rehder) W.C.Cheng Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. 9: 193 1934
Lindera oldhamii Hemsl. J. Linn. Soc., Bot. 26: 390 (1891)
Lindera pricei Hayata Icon. Pl. Formosan. 5: 178 (1915)
Benzoin touyunense f. megaphyllum (Hemsl.) Rehder J. Arnold Arbor. 11: 158 (1930)

Common names Top

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Language Common/alternative name
Chinese 大香葉樹
Chinese 毛黑壳楠
Chinese 黑壳楠

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 North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001070322
Tropicos 17800419
KEW urn:lsid:ipni.org:names:465396-1
The Plant List tro-17800419
Open Tree Of Life 356810
NCBI Taxonomy 155293
IUCN Red List 172738993
IPNI 465396-1
iNaturalist 556602
GBIF 5685614
EPPO LIEME
USDA GRIN 22298

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
Editorial: Highly contiguous plant genome assembly and transcriptional regulation Tian XC, Jia KH Front Plant Sci 13-Dec-2023
PMCID:PMC10751298
doi:10.3389/fpls.2023.1331498
PMID:38152147
Selection and Validation of Optimal RT-qPCR Reference Genes for the Normalization of Gene Expression under Different Experimental Conditions in Lindera megaphylla Liu H, Liu J, Chen P, Zhang X, Wang K, Lu J, Li Y Plants (Basel) 31-May-2023
PMCID:PMC10255795
doi:10.3390/plants12112185
PMID:37299163
Variation of soil physicochemical properties of different vegetation restoration types on subtropical karst area in southern China Xiao C, You R, Zhu N, Mi X, Gao L, Zhou X, Zhou G PLoS One 16-Mar-2023
PMCID:PMC10019609
doi:10.1371/journal.pone.0282620
PMID:36928208
Unique gene duplications and conserved microsynteny potentially associated with resistance to wood decay in the Lauraceae Tian XC, Guo JF, Yan XM, Shi TL, Nie S, Zhao SW, Bao YT, Li ZC, Kong L, Su GJ, Mao JF, Lin J Front Plant Sci 08-Mar-2023
PMCID:PMC10030967
doi:10.3389/fpls.2023.1122549
PMID:36968354
Bioactive PI3-kinase/Akt/mTOR Inhibitors in Targeted Lung Cancer Therapy Ghareghomi S, Atabaki V, Abdollahzadeh N, Ahmadian S, Hafez Ghoran S Adv Pharm Bull 09-Oct-2021
PMCID:PMC9871280
doi:10.34172/apb.2023.003
PMID:36721812
Conflicting phylogenetic signals in plastomes of the tribe Laureae (Lauraceae) Xiao TW, Xu Y, Jin L, Liu TJ, Yan HF, Ge XJ PeerJ 15-Oct-2020
PMCID:PMC7568859
doi:10.7717/peerj.10155
PMID:33088627
The Litsea genome and the evolution of the laurel family Chen YC, Li Z, Zhao YX, Gao M, Wang JY, Liu KW, Wang X, Wu LW, Jiao YL, Xu ZL, He WG, Zhang QY, Liang CK, Hsiao YY, Zhang DY, Lan SR, Huang L, Xu W, Tsai WC, Liu ZJ, Van de Peer Y, Wang YD Nat Commun 03-Apr-2020
PMCID:PMC7125107
doi:10.1038/s41467-020-15493-5
PMID:32245969
Antitumoral Properties of Natural Products Fabiani R Molecules 03-Feb-2020
PMCID:PMC7037154
doi:10.3390/molecules25030650
PMID:32028725
Characterization of 20 complete plastomes from the tribe Laureae (Lauraceae) and distribution of small inversions Jo S, Kim YK, Cheon SH, Fan Q, Kim KJ PLoS One 01-Nov-2019
PMCID:PMC6824564
doi:10.1371/journal.pone.0224622
PMID:31675370
Plastome sequences help to improve the systematic position of trinerved Lindera species in the family Lauraceae Tian X, Ye J, Song Y PeerJ 07-Oct-2019
PMCID:PMC6786250
doi:10.7717/peerj.7662
PMID:31608166
Characterization of two complete chloroplast genomes of Lindera megaphylla (Lauraceae) Jiang K, Wang ZW, Huang WC, Hu YH Mitochondrial DNA B Resour 09-Sep-2019
PMCID:PMC7706839
doi:10.1080/23802359.2019.1660275
PMID:33365758
Comparative chloroplast genomics and phylogenetics of nine Lindera species (Lauraceae) Zhao ML, Song Y, Ni J, Yao X, Tan YH, Xu ZF Sci Rep 11-Jun-2018
PMCID:PMC5995902
doi:10.1038/s41598-018-27090-0
PMID:29891996
Selection of Native Tree Species for Subtropical Forest Restoration in Southwest China Lu Y, Ranjitkar S, Harrison RD, Xu J, Ou X, Ma X, He J PLoS One 19-Jan-2017
PMCID:PMC5245873
doi:10.1371/journal.pone.0170418
PMID:28103281
Studies on the Alkaloids of Formosan Lauraceous Plants XIX Alkaloids of lindera oldhamii hemsl. (2) Ih‐Sheng Chen Wiley 04-Jun-2015
doi:10.1002/JCCS.197700006
Transient Receptor Potential Channels as Targets for Phytochemicals Premkumar LS ACS Chem Neurosci 13-Jun-2014
PMCID:PMC4240255
doi:10.1021/cn500094a
PMID:24926802

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
> Alkaloids and derivatives / Aporphines
(+/-)-Dicentrine 630859 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1055/S-2006-957411
https://doi.org/10.1055/S-2006-960135
1,11-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol 75000759 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC)OC)O 327.40 unknown https://doi.org/10.1021/NP50108A001
Cassameridine 12302502 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C5C(=CC6=C4OCO6)C=CN=C5C3=O 319.30 unknown https://doi.org/10.1021/NP50123A013
Dehydrodicentrine 3084326 Click to see CN1CCC2=CC3=C(C4=C5C=C(C(=CC5=CC1=C24)OC)OC)OCO3 337.40 unknown https://doi.org/10.1021/NP50123A013
Dicentrine 101300 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP50123A013
Dicentrinone 177744 Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown https://doi.org/10.1021/NP50108A001
https://doi.org/10.1021/NP50123A013
N-Methylnandigerine 3083908 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)O)OC)OCO3 325.40 unknown https://doi.org/10.1055/S-2006-960135
https://doi.org/10.1021/NP50108A001
O-Methylbulbocapnine 10246564 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)OC)OCO3 339.40 unknown https://doi.org/10.1021/NP50123A013
https://doi.org/10.1021/NP50108A001
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown https://doi.org/10.1002/JCCS.197700006
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1021/NP50108A001
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
3,4-Dihydro-7-hydroxy-6-methoxy-1(2H)-isoquinolinone 10262007 Click to see COC1=C(C=C2C(=C1)CCNC2=O)O 193.20 unknown https://doi.org/10.1021/NP50108A001
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP50123A013
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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 https://doi.org/10.1021/NP50123A013
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/NP50123A013

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