Neolitsea dealbata - Unknown
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Internal ID UUID644047603f230098710626
Scientific name Neolitsea dealbata
Authority (R.Br.) Merr.
First published in J. Arnold Arbor. 29: 200 (1948)

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Synonyms Top

Scientific name Authority First published in
Litsea baueri Endl. Iconogr. Gen. Pl. 4: t. 44 (1838)
Litsea dealbata (R.Br.) Nees Syst. Laur. : 630 (1836)
Litsea rufa Nees Syst. Laur. : 631 (1836)
Malapoenna dealbata (R.Br.) Kuntze Revis. Gen. Pl. 2: 571 (1891)
Tetradenia baueri (Endl.) Pax Nat. Pflanzenfam. [Engler & Prantl] 3(Abt. 2, Lief. 29): 119, fig. 72. 1889 [Mar 1889]
Bryantea dealbata (R.Br.) Raf. Sylva Tellur. : 165 (1838)
Tetranthera dealbata R.Br. Prodr. Fl. Nov. Holland. : 403 (1810)
Litsea dealbata var. glabrata Meisn. Prodromus 15(1) 1864
Litsea dealbata var. incisa Meisn. Prodromus 15(1) 1864
Litsea dealbata var. rufa Benth. Flora Australiensis 5 1870

Common names Top

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Language Common/alternative name
English bolly gum
English hairy-leaved bolly gum
English white bolly gum

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001071634
Tropicos 17805226
KEW urn:lsid:ipni.org:names:466955-1
The Plant List tro-17805226
Open Tree Of Life 893264
Observations.org 458643
NCBI Taxonomy 344104
IUCN Red List 158692171
IPNI 466955-1
iNaturalist 369555
GBIF 4180000
Freebase /m/02rp635
Elurikkus 481918
Wikipedia Neolitsea_dealbata
CMAUP NPO11152

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
Impacts of Myrtle Rust Induced Tree Mortality on Species and Functional Richness within Seedling Communities of a Wet Sclerophyll Forest in Eastern Australia Stevenson K, Pegg G, Wills J, Herbohn J, Firn J Plants (Basel) 12-May-2023
PMCID:PMC10221985
doi:10.3390/plants12101970
PMID:37653886
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
Genomic Screening to Identify Food Trees Potentially Dispersed by Precolonial Indigenous Peoples Fahey M, Rossetto M, Ens E, Ford A Genes (Basel) 08-Mar-2022
PMCID:PMC8954434
doi:10.3390/genes13030476
PMID:35328030
A higher-rank classification for rust fungi, with notes on genera Aime MC, McTaggart AR Fungal Syst Evol 13-Nov-2020
PMCID:PMC8165960
doi:10.3114/fuse.2021.07.02
PMID:34124616
Impacts of rainforest fragmentation on the composition of ground-active vertebrate communities and their patterns of seed consumption Palmer GJ, Catterall CP PLoS One 12-Sep-2018
PMCID:PMC6135387
doi:10.1371/journal.pone.0202870
PMID:30208055
Impact of Austropuccinia psidii (myrtle rust) on Myrtaceae-rich wet sclerophyll forests in south east Queensland Pegg G, Taylor T, Entwistle P, Guymer G, Giblin F, Carnegie A PLoS One 21-Nov-2017
PMCID:PMC5697815
doi:10.1371/journal.pone.0188058
PMID:29161305
Sex‐specific floral morphology, biomass, and phytohormones associated with altitude in dioecious Populus cathayana populations He J, Dong T, Huang K, Yang Y, Li D, Xu X, He X Ecol Evol 25-Apr-2017
PMCID:PMC5468146
doi:10.1002/ece3.2808
PMID:28616192
Antileishmanial Potential of Tropical Rainforest Plant Extracts Monzote L, Piñón A, Setzer WN Medicines (Basel) 19-Nov-2014
PMCID:PMC5532977
doi:10.3390/medicines1010032
PMID:28933376
Limitations to Reproductive Success in the Dioecious Tree Rhamnus davurica Wang J, Zhang C, Zhao X, Gadow KV PLoS One 06-Dec-2013
PMCID:PMC3855689
doi:10.1371/journal.pone.0081140
PMID:24324665
Chemical investigation of drug-like compounds from the Australian tree, Neolitseadealbata. Tran TD, Pham NB, Fechner G, Quinn RJ Bioorg Med Chem Lett 01-Oct-2010
doi:10.1016/J.BMCL.2010.07.100
PMID:20732809
Correlations between leaf toughness and phenolics among species in contrasting environments of Australia and New Caledonia Read J, Sanson GD, Caldwell E, Clissold FJ, Chatain A, Peeters P, Lamont BB, De Garine-Wichatitsky M, Jaffré T, Kerr S Ann Bot 19-Dec-2008
PMCID:PMC2707862
doi:10.1093/aob/mcn246
PMID:19098067
In Tropical Lowland Rain Forests Monocots have Tougher Leaves than Dicots, and Include a New Kind of Tough Leaf Dominy NJ, Grubb PJ, Jackson RV, Lucas PW, Metcalfe DJ, Svenning JC, Turner IM Ann Bot 03-Apr-2008
PMCID:PMC2710255
doi:10.1093/aob/mcn046
PMID:18387969
Monocot Leaves are Eaten Less than Dicot Leaves in Tropical Lowland Rain Forests: Correlations with Toughness and Leaf Presentation Grubb PJ, Jackson RV, Barberis IM, Bee JN, Coomes DA, Dominy NJ, De La Fuente MA, Lucas PW, Metcalfe DJ, Svenning JC, Turner IM, Vargas O Ann Bot 02-Apr-2008
PMCID:PMC2710256
doi:10.1093/aob/mcn047
PMID:18387972
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340

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
(11R,12R)-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 72194492 Click to see C[N+]1(CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3)[O-] 295.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
(12R)-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 73348116 Click to see C[N+]1(CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3)[O-] 295.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
(12R)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-17-ol 46947263 Click to see C1CNC2CC3=C(C=C(C=C3)O)C4=C2C1=CC5=C4OCO5 281.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol 248507 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
1,10-Dimethoxy-6a-alpha-noraporphine-2,9-diol 628557 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
1,2-Methylenedioxy-9-hydroxy-10-methoxynoraporphine 5089476 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
3,5-Dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-17-ol 71199252 Click to see C1CNC2CC3=C(C=C(C=C3)O)C4=C2C1=CC5=C4OCO5 281.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Actinodaphnine 160502 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Octyl docosanoate 80081 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCC 452.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
alpha-Amyrin palmitate 10394654 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmastanol 241572 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-juziphine 14526074 Click to see CN1CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O 299.40 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
(R)-Juziphine 14526072 Click to see CN1CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O 299.40 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Norjuziphine, (+/-)- 21635162 Click to see COC1=C(C2=C(CCNC2CC3=CC=C(C=C3)O)C=C1)O 285.34 unknown https://doi.org/10.1016/J.BMCL.2010.07.100
Norjuziphine, (S)- 15690956 Click to see COC1=C(C2=C(CCNC2CC3=CC=C(C=C3)O)C=C1)O 285.34 unknown https://doi.org/10.1016/J.BMCL.2010.07.100

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