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Atherosperma moschatum

Atherosperma moschatum - Unknown
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Author: Public Domain - WikiMedia
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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 UUID64400bb3abdc5348322872
Scientific name Atherosperma moschatum
Authority Labill.
First published in Nov. Holl. Pl. 2: 74 (1806)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English blackheart sassafras
English southern sassafras
Finnish australiansassafras
Russian Атеросперма
Swedish svart sassafras
Vietnamese atherosperma tasmanicum

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Atherosperma moschatum subsp. integrifolium (A.Cunn. ex Tul.) Schodde Fl. Australia 2: 456 (2007)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000555572
Tropicos 50146097
KEW urn:lsid:ipni.org:names:581759-1
The Plant List kew-2664805
Open Tree Of Life 831123
NCBI Taxonomy 88856
IUCN Red List 61985299
IPNI 581759-1
iNaturalist 323237
GBIF 7264506
EPPO AOPMO
USDA GRIN 5970

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
Diet Is a Stronger Covariate than Exercise in Determining Gut Microbial Richness and Diversity Yun EJ, Imdad S, Jang J, Park J, So B, Kim JH, Kang C Nutrients 16-Jun-2022
PMCID:PMC9229834
doi:10.3390/nu14122507
PMID:35745235
Differential effects of ecosystem engineering by the superb lyrebird Menura novaehollandiae and herbivory by large mammals on floristic regeneration and structure in wet eucalypt forests Maisey AC, Haslem A, Leonard SW, Bennett AF Ecol Evol 02-Jun-2022
PMCID:PMC9163197
doi:10.1002/ece3.8956
PMID:35784040
Identifying thresholds in the impacts of an invasive groundcover on native vegetation O’Loughlin LS, Panetta FD, Gooden B Sci Rep 15-Oct-2021
PMCID:PMC8520009
doi:10.1038/s41598-021-98667-5
PMID:34654864
Temporal patterns of forest seedling emergence across different disturbance histories Bowd EJ, McBurney L, Blair DP, Lindenmayer DB Ecol Evol 26-Jun-2021
PMCID:PMC8293764
doi:10.1002/ece3.7568
PMID:34306621
Novel 3D geometry and models of the lower regions of large trees for use in carbon accounting of primary forests Dean C, Kirkpatrick JB, Osborn J, Doyle RB, Fitzgerald NB, Roxburgh SH AoB Plants 28-Feb-2018
PMCID:PMC5861447
doi:10.1093/aobpla/ply015
PMID:29593855
Habitat type and dispersal mode underlie the capacity for plant migration across an intermittent seaway Worth JR, Holland BR, Beeton NJ, Schönfeld B, Rossetto M, Vaillancourt RE, Jordan GJ Ann Bot 27-Jul-2017
PMCID:PMC5737502
doi:10.1093/aob/mcx086
PMID:28961707
Warming puts the squeeze on photosynthesis – lessons from tropical trees Dusenge ME, Way DA J Exp Bot 30-May-2017
PMCID:PMC5447882
doi:10.1093/jxb/erx114
Plant Traits Demonstrate That Temperate and Tropical Giant Eucalypt Forests Are Ecologically Convergent with Rainforest Not Savanna Tng DY, Jordan GJ, Bowman DM PLoS One 17-Dec-2013
PMCID:PMC3866143
doi:10.1371/journal.pone.0084378
PMID:24358359
Light requirements of Australian tropical vs. cool-temperate rainforest tree species show different relationships with seedling growth and functional traits Lusk CH, Kelly JW, Gleason SM Ann Bot 21-Dec-2012
PMCID:PMC3579444
doi:10.1093/aob/mcs289
PMID:23264237
Interacting Factors Driving a Major Loss of Large Trees with Cavities in a Forest Ecosystem Lindenmayer DB, Blanchard W, McBurney L, Blair D, Banks S, Likens GE, Franklin JF, Laurance WF, Stein JA, Gibbons P PLoS One 05-Oct-2012
PMCID:PMC3465306
doi:10.1371/journal.pone.0041864
PMID:23071486
ContentSnapshots N/A Ann Bot 01-Nov-2011
PMCID:PMC3197465
doi:10.1093/aob/mcr270
Low but structured chloroplast diversity in Atherosperma moschatum (Atherospermataceae) suggests bottlenecks in response to the Pleistocene glacials Worth JR, Marthick JR, Jordan GJ, Vaillancourt RE Ann Bot 18-Aug-2011
PMCID:PMC3197450
doi:10.1093/aob/mcr220
PMID:21856633
Tlie alkaloids of Atherosperma moschatum Labill. II. Non-phenolic alkaloids IRC Bick, GK Douglas CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9651997
The alkaloids of Atherosperma moschatum Labill. I. Isolation of the alkaloids and structure of Berbamine IRC Bick, PS Clezy, ED Crow CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9560111
CLXXIV.—The essential oil of the leaves of atherosperma moschatum(“Australian Sassafras”) Margaret E. Scott Royal Society of Chemistry (RSC) 02-Apr-2004
doi:10.1039/CT9120101612

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 / 6,6a-secoaporphines
Atherosperminine 96918 Click to see CN(C)CCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC 309.40 unknown https://doi.org/10.1071/CH9651997
https://doi.org/10.1071/CH9560111
n,n-Dimethyl-2-(2,3,4-trimethoxyphenanthren-1-yl)ethanamine 261479 Click to see CN(C)CCC1=C2C=CC3=CC=CC=C3C2=C(C(=C1OC)OC)OC 339.40 unknown https://doi.org/10.1071/CH9651997
> Alkaloids and derivatives / Aporphines
Atherospermidine 77514 Click to see COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2 305.30 unknown https://doi.org/10.1071/CH9651997
https://doi.org/10.1071/CH9560111
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1071/CH9560111
https://doi.org/10.1071/CH9651997
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1039/CT9120101612
> Lignans, neolignans and related compounds
(1R,14S)-20,25-dimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene-9,21-diol 162895634 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)O)OC 580.70 unknown https://doi.org/10.1071/CH9651997
1-Isotetrandrine 457825 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1071/CH9560111
20,25-Dimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene-9,21-diol 425996 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)O)OC 580.70 unknown https://doi.org/10.1071/CH9651997
6,6',7-Trimethoxy-2,2'-dimethylberbaman-12-ol 10170 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1071/CH9560111
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1071/CH9560111
Isotetrandrine 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1071/CH9560111
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1039/CT9120101612
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1039/CT9120101612
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1039/CT9120101612
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1039/CT9120101612
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown https://doi.org/10.1039/CT9120101612
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Ramonanin D 53355807 Click to see COC1=C(C=CC(=C1)C2C(=C)C3(CCC4=C(C3)C(OC4C5=CC(=C(C=C5)O)OC)C6=CC(=C(C=C6)O)OC)C(O2)C7=CC(=C(C=C7)O)OC)O 680.70 unknown https://doi.org/10.1071/CH9651997

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