Podocarpus elatus - Unknown
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Internal ID UUID6440028f05c3f681364160
Scientific name Podocarpus elatus
Authority Endl.
First published in Syn. Conif. : 213 (1847)

Description Top

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Synonyms Top

Scientific name Authority First published in
Nageia elata F.Muell. Select Pl. , ed. 2: 138 (1876)
Margbensonia elata (R.Br. ex Endl.) A.V.Bobrov & Melikyan Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 103(1): 60 (1998)
Podocarpus acicularis hort. ex Carrière Traité Gén. Conif. : 456 (1855)

Common names Top

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Language Common/alternative name
English illawarra plum
English turpentine pine
English yellow pine
English plum pine
English brown pine
Arabic معلاقة باسقة
Azerbaijani hündür podokarpus
azb هۆندور پودوکارپوس
Bulgarian висок подокарп
Japanese イラワラプラム
Russian Подокарп высокий
Chinese 高大罗汉松
Chinese 高大羅漢松

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000485093
UNII H38807Y47G
Tropicos 25600127
KEW urn:lsid:ipni.org:names:120790-3
The Plant List kew-2567455
Open Tree Of Life 407274
Observations.org 498889
NCBI Taxonomy 75982
IUCN Red List 42500
IPNI 120790-3
iNaturalist 135618
GBIF 5286128
Freebase /m/0fz45h
EPPO PODET
EOL 1033639
Elurikkus 503686
USDA GRIN 29109
Wikipedia Podocarpus_elatus
CMAUP NPO862

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
Ecdysterone and Turkesterone—Compounds with Prominent Potential in Sport and Healthy Nutrition Todorova V, Ivanova S, Chakarov D, Kraev K, Ivanov K Nutrients 02-May-2024
PMCID:PMC11085066
doi:10.3390/nu16091382
PMID:38732627
Detailed Seed Cone Morpho-Anatomy Provides New Insights into Seed Cone Origin and Evolution of Podocarpaceae; Podocarpoid and Dacrydioid Clades Khan R, Hill RS, Dörken VM, Biffin E Plants (Basel) 19-Nov-2023
PMCID:PMC10674377
doi:10.3390/plants12223903
PMID:38005800
A Review of Phytochemicals and Bioactive Properties in the Proteaceae Family: A Promising Source of Functional Food Zhang J, Netzel ME, Pengelly A, Sivakumar D, Sultanbawa Y Antioxidants (Basel) 01-Nov-2023
PMCID:PMC10669417
doi:10.3390/antiox12111952
PMID:38001805
Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae Khan R, Hill RS, Liu J, Biffin E Plants (Basel) 03-Mar-2023
PMCID:PMC10005643
doi:10.3390/plants12051171
PMID:36904033
Bioassay Guided Fractionation Protocol for Determining Novel Active Compounds in Selected Australian Flora Mani J, Johnson J, Hosking H, Hoyos BE, Walsh KB, Neilsen P, Naiker M Plants (Basel) 28-Oct-2022
PMCID:PMC9654191
doi:10.3390/plants11212886
PMID:36365337
Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones Arif Y, Singh P, Bajguz A, Hayat S Int J Mol Sci 04-Aug-2022
PMCID:PMC9369314
doi:10.3390/ijms23158664
PMID:35955797
Anthocyanins in Colorectal Cancer Prevention Review Shi N, Chen X, Chen T Antioxidants (Basel) 12-Oct-2021
PMCID:PMC8533526
doi:10.3390/antiox10101600
PMID:34679735
Targeting Inflammation by Anthocyanins as the Novel Therapeutic Potential for Chronic Diseases: An Update Kozłowska A, Dzierżanowski T Molecules 20-Jul-2021
PMCID:PMC8304181
doi:10.3390/molecules26144380
PMID:34299655
The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A Acta Pharm Sin B 16-Oct-2020
PMCID:PMC8343124
doi:10.1016/j.apsb.2020.10.012
PMID:34386319
Exploiting the Biosynthetic Potency of Taxol from Fungal Endophytes of Conifers Plants; Genome Mining and Metabolic Manipulation El-Sayed AS, El-Sayed MT, Rady AM, Zein N, Enan G, Shindia A, El-Hefnawy S, Sitohy M, Sitohy B Molecules 30-Jun-2020
PMCID:PMC7412027
doi:10.3390/molecules25133000
PMID:32630044
Natural Compounds with Potential to Modulate Cancer Therapies and Self-Reactive Immune Cells Moody R, Wilson K, Jaworowski A, Plebanski M Cancers (Basel) 13-Mar-2020
PMCID:PMC7139800
doi:10.3390/cancers12030673
PMID:32183059
Medicinal Plants in the Prevention and Treatment of Colon Cancer Aiello P, Sharghi M, Mansourkhani SM, Ardekan AP, Jouybari L, Daraei N, Peiro K, Mohamadian S, Rezaei M, Heidari M, Peluso I, Ghorat F, Bishayee A, Kooti W Oxid Med Cell Longev 04-Dec-2019
PMCID:PMC7187726
doi:10.1155/2019/2075614
PMID:32377288
Andean Prumnopitys Andina (Podocarpacae) Fruit Extracts: Characterization of Secondary Metabolites and Potential Cytoprotective Effect Jiménez-Aspee F, Theoduloz C, Pormetter L, Mettke J, Ávila F, Schmeda-Hirschmann G Molecules 07-Nov-2019
PMCID:PMC6891447
doi:10.3390/molecules24224028
PMID:31703314
Niche squeeze induced by climate change of the cold-tolerant subtropical montane Podocarpus parlatorei Quiroga MP, Premoli AC, Kitzberger T R Soc Open Sci 28-Nov-2018
PMCID:PMC6281919
doi:10.1098/rsos.180513
PMID:30564385
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

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
(+)-Isodomesticine 15690954 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O 325.40 unknown via CMAUP database
(6aS)-9-Hydroxy-1,2,10-trimethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester 44206920 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)N(CCC3=C1)C(=O)OC)OC 385.40 unknown via CMAUP database
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown via CMAUP database
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown via CMAUP database
CID 91884708 91884708 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown via CMAUP database
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown via CMAUP database
methyl (6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate 44207164 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)OC)OC 399.40 unknown via CMAUP database
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown via CMAUP database
Oxonantenine 3084224 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC5=C(C=C42)OCO5)OC 335.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Litebamine 196885 Click to see CN1CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O 339.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid 5312351 Click to see CCCCCC=CCCC(=O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(1R,2R,5S)-5-Methyl-2-(1-methylethenyl)cyclohexanol 7057942 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Menthoglycol 19100 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,6S)-2,3,6,7-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 13470433 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O 496.60 unknown https://doi.org/10.1007/BF01946280
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6,7-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 13470434 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O 496.60 unknown https://doi.org/10.1007/BF01946280
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
Litseacubebic Acid 76312534 Click to see CC(=CC=CC(C)(C)O)C(=O)O 170.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one 76319759 Click to see CC1=CC(=O)OC(CC1)C(C)(C)O 184.23 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database

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