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Eupomatia laurina

Eupomatia laurina - Unknown
Part: Unknown
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 UUID64401bde1bd3e838275007
Scientific name Eupomatia laurina
Authority R.Br.
First published in Voy. Terra Austral. 2: 597 (1814)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English bolwarra
English copper laurel
English native guava
Finnish laakerikauluskukka

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000682815
Tropicos 1601396
KEW urn:lsid:ipni.org:names:72995-1
The Plant List kew-2804641
Open Tree Of Life 659249
NCBI Taxonomy 49863
IUCN Red List 144297071
IPNI 72995-1
iNaturalist 470632
GBIF 5565488
Freebase /m/0g8g8q
USDA GRIN 415601
Wikipedia Eupomatia_laurina
PaleoBotany 107791

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
From the Bush to the Brain: Preclinical Stages of Ethnobotanical Anti-Inflammatory and Neuroprotective Drug Discovery—An Australian Example Kumar P, Mathew S, Gamage R, Bodkin F, Doyle K, Rossetti I, Wagnon I, Zhou X, Raju R, Gyengesi E, Münch G Int J Mol Sci 04-Jul-2023
PMCID:PMC10342267
doi:10.3390/ijms241311086
PMID:37446262
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
A Comprehensive Review on Pharmacological Activities of Pachypodol: A Bioactive Compound of an Aromatic Medicinal Plant Pogostemon Cablin Benth Fatima S, Farzeen I, Ashraf A, Aslam B, Ijaz MU, Hayat S, Sarfraz MH, Zafar S, Zafar N, Unuofin JO, Lebelo SL, Muzammil S Molecules 14-Apr-2023
PMCID:PMC10141922
doi:10.3390/molecules28083469
PMID:37110702
Complete plastome sequence of Monoon laui (Merr.) B. Xue and R.M.K. Saunders, 2012: an endemic species in Hainan Xiu H, Sun Y, Quan Y, Fu T, Sun Q Mitochondrial DNA B Resour 07-Sep-2022
PMCID:PMC9467546
doi:10.1080/23802359.2022.2116953
PMID:36106198
Antibacterial and Antifungal Alkaloids from Asian Angiosperms: Distribution, Mechanisms of Action, Structure-Activity, and Clinical Potentials Sulaiman M, Jannat K, Nissapatorn V, Rahmatullah M, Paul AK, de Lourdes Pereira M, Rajagopal M, Suleiman M, Butler MS, Break MK, Weber JF, Wilairatana P, Wiart C Antibiotics (Basel) 24-Aug-2022
PMCID:PMC9495154
doi:10.3390/antibiotics11091146
PMID:36139926
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
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
Parallel diversifications of Cremastosperma and Mosannona (Annonaceae), tropical rainforest trees tracking Neogene upheaval of South America Pirie MD, Maas PJ, Wilschut RA, Melchers-Sharrott H, Chatrou LW R Soc Open Sci 31-Jan-2018
PMCID:PMC5792937
doi:10.1098/rsos.171561
PMID:29410860
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Antiprotozoal and Antimycobacterial Activities of Pure Compounds from Aristolochia elegans Rhizomes Jiménez-Arellanes A, León-Díaz R, Meckes M, Tapia A, Molina-Salinas GM, Luna-Herrera J, Yépez-Mulia L Evid Based Complement Alternat Med 16-Feb-2012
PMCID:PMC3292206
doi:10.1155/2012/593403
PMID:22454670
Azaphenanthrene Alkaloids with Antitumoral Activity from Anaxagorea dolichocarpa Sprague & Sandwith (Annonaceae) Lúcio AS, da Silva Almeida JR, Barbosa-Filho JM, Pita JC, Branco MV, de Fátima Formiga Melo Diniz M, de Fátima Agra M, da-Cunha EV, da Silva MS, Tavares JF Molecules 22-Aug-2011
PMCID:PMC6264400
doi:10.3390/molecules16087125
PMID:21860364
Isolation and Synthesis of Antiproliferative Eupolauridine Alkaloids of Ambavia gerrardii from the Madagascar Dry Forest Pan E, Cao S, Brodie PJ, Callmander M, Randrianaivo R, Rakotonandrasana S, Rakotobe E, Rasamison VE, TenDyke K, Shen Y, Suh EM, Kingston DG J Nat Prod 19-Apr-2011
PMCID:PMC3103620
doi:10.1021/np200093n
PMID:21504145
Constituents of Eupomatia Species. XII. Isolation of Constituents of the Tubers and Aerial Parts of Eupomatia bennettii and Determination of the Structures of New Alkaloids From the Aerial Parts of E. bennettii and Minor Alkaloids of E. laurina AR Carroll, WC Taylor CSIRO Publishing 03-Sep-2010
doi:10.1071/CH9911615
Constituents of Eupomatia Species. XI. New Eupodienone Lignans From the Flowers of Eupomatia laurina AR Carroll, WC Taylor CSIRO Publishing 03-Sep-2010
doi:10.1071/CH9901871

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / 1-azaoxoaporphines
Sampangine 387195 Click to see C1=CC=C2C(=C1)C3=NC=CC4=C3C(=NC=C4)C2=O 232.24 unknown https://doi.org/10.1076/PHBI.41.4.277.15671
> Alkaloids and derivatives / Aporphines
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown https://doi.org/10.1076/PHBI.41.4.277.15671
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/10.1076/PHBI.41.4.277.15671
https://doi.org/10.1071/CH9722659
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 15560530 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown https://doi.org/10.1071/CH9722659
Norushinsunine 5319820 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown https://doi.org/10.1071/CH9722659
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
(1',10-Dimethoxy-6,7-dimethyl-6'-oxospiro[5,6,7,8-tetrahydrocyclohepta[f][1,3]benzodioxole-9,3'-cyclohexa-1,4-diene]-5-yl) benzoate 162967603 Click to see CC1CC2(C=CC(=O)C(=C2)OC)C3=C(C4=C(C=C3C(C1C)OC(=O)C5=CC=CC=C5)OCO4)OC 476.50 unknown https://doi.org/10.1071/CH9901871
[(5S,6S,7R,9S)-1',10-dimethoxy-6,7-dimethyl-6'-oxospiro[5,6,7,8-tetrahydrocyclohepta[f][1,3]benzodioxole-9,3'-cyclohexa-1,4-diene]-5-yl] benzoate 162967604 Click to see CC1CC2(C=CC(=O)C(=C2)OC)C3=C(C4=C(C=C3C(C1C)OC(=O)C5=CC=CC=C5)OCO4)OC 476.50 unknown https://doi.org/10.1071/CH9901871
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(-)-Dihydroguaiaretic acid 11602375 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC 330.40 unknown https://doi.org/10.1071/CH9901871
Dihydroguaiaretic acid 161924 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC 330.40 unknown https://doi.org/10.1071/CH9901871
> Organoheterocyclic compounds / Benzodioxoles
(6R,7R,9R)-2',10-dimethoxy-6,7-dimethylspiro[5,6,7,8-tetrahydrocyclohepta[f][1,3]benzodioxole-9,4'-cyclohexa-2,5-diene]-1'-one 14825956 Click to see CC1CC2=CC3=C(C(=C2C4(CC1C)C=CC(=O)C(=C4)OC)OC)OCO3 356.40 unknown https://doi.org/10.1071/CH9901871
(6R,7R,9S)-2',10-dimethoxy-6,7-dimethylspiro[5,6,7,8-tetrahydrocyclohepta[f][1,3]benzodioxole-9,4'-cyclohexa-2,5-diene]-1'-one 14825957 Click to see CC1CC2=CC3=C(C(=C2C4(CC1C)C=CC(=O)C(=C4)OC)OC)OCO3 356.40 unknown https://doi.org/10.1071/CH9901871
2',10-Dimethoxy-6,7-dimethylspiro[5,6,7,8-tetrahydrocyclohepta[f][1,3]benzodioxole-9,4'-cyclohexa-2,5-diene]-1'-one 14825955 Click to see CC1CC2=CC3=C(C(=C2C4(CC1C)C=CC(=O)C(=C4)OC)OC)OCO3 356.40 unknown https://doi.org/10.1071/CH9901871
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Eupolauridine 72486 Click to see C1=CC=C2C(=C1)C3=NC=CC4=C3C2=NC=C4 204.23 unknown https://doi.org/10.1071/CH9911615
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,2S)-1-[2-(4-hydroxy-3-methoxyphenyl)-3-methyl-1-benzofuran-5-yl]propane-1,2-diol 101821079 Click to see CC1=C(OC2=C1C=C(C=C2)C(C(C)O)O)C3=CC(=C(C=C3)O)OC 328.40 unknown https://doi.org/10.1071/CH9731111
(2R,3S,4S,5S,6S)-2-methyl-6-[4-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenoxy]oxane-3,4,5-triol 163185722 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC4C(C(C(C(O4)C)O)O)O 410.50 unknown https://doi.org/10.1071/CH9722659
(2R)-1-[2-(1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]propan-2-ol 101297683 Click to see CC1=C(OC2=C1C=C(C=C2)CC(C)O)C3=CC4=C(C=C3)OCO4 310.30 unknown https://doi.org/10.1071/CH9731111
1-[2-(1,3-Benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]propan-2-ol 162959217 Click to see CC1=C(OC2=C1C=C(C=C2)CC(C)O)C3=CC4=C(C=C3)OCO4 310.30 unknown https://doi.org/10.1071/CH9731111
1-[2-(4-Hydroxy-3-methoxyphenyl)-3-methyl-1-benzofuran-5-yl]propane-1,2-diol 162926966 Click to see CC1=C(OC2=C1C=C(C=C2)C(C(C)O)O)C3=CC(=C(C=C3)O)OC 328.40 unknown https://doi.org/10.1071/CH9731111
2-(3,4-Dimethoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran 71350455 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)OC)OC 308.40 unknown https://doi.org/10.1071/CH9722659
2-(3,4-Dimethoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)benzofuran 21625895 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)OC)OC 308.40 unknown https://doi.org/10.1071/CH9722659
2-(3,4-Dimethoxyphenyl)-7-methoxy-3-methyl-5-[(E)-1-propenyl]benzofuran 10958690 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC(=C(C=C3)OC)OC 338.40 unknown https://doi.org/10.1071/CH9731111
2-(3,4-Dimethoxyphenyl)-7-methoxy-3-methyl-5-prop-1-enyl-1-benzofuran 71437667 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC(=C(C=C3)OC)OC 338.40 unknown https://doi.org/10.1071/CH9731111
2-Methoxy-4-[3-methyl-5-(1-propenyl)-2-benzofuranyl]-phenol 193821 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1071/CH9722659
2-Methyl-6-[4-(3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenoxy]oxane-3,4,5-triol 310621 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC4C(C(C(C(O4)C)O)O)O 410.50 unknown https://doi.org/10.1071/CH9722659
4-(7-Methoxy-3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 72730286 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC=C(C=C3)O 294.30 unknown https://doi.org/10.1071/CH9792317
4-[7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenol 14352596 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC=C(C=C3)O 294.30 unknown https://doi.org/10.1071/CH9792317
5-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole 261729 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1071/CH9722659
5-(7-Methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)-1,3-benzodioxole 3398496 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4 324.40 unknown https://doi.org/10.1071/CH9722659
5-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole 6051545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1071/CH9722659
Eupomatenoid 5 6443783 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1071/CH9722659
Eupomatenoid-10 71437666 Click to see CC1=C(OC2=C1C=C(C=C2)C=O)C3=CC(=C(C=C3)O)OC 282.29 unknown https://doi.org/10.1071/CH9731111
Licarin B 6441061 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4 324.40 unknown https://doi.org/10.1071/CH9722659
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown https://doi.org/10.1071/CH9731111

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