Darlingia darlingiana

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Internal ID UUID644015d154f64651373786
Scientific name Darlingia darlingiana
Authority (F.Muell.) L.A.S.Johnson
First published in Contr. New South Wales Natl. Herb. 3: 93 (1962)

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Synonyms Top

Scientific name Authority First published in
Knightia darlingii F.Muell. Fragm. 5: 152 (1866)
Darlingia spectatissima F.Muell. Fragm. (Mueller) 5(37): 152. 1866 [Feb 1866]
Helicia darlingiana F.Muell. Fragm. 5: 24 (1865)

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Language Common/alternative name
Chinese 布朗榄仁栎
Chinese 布朗银桦

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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-0000638150
Tropicos 100320589
KEW urn:lsid:ipni.org:names:703378-1
The Plant List kew-2757491
Open Tree Of Life 414374
Observations.org 503521
NCBI Taxonomy 488357
IUCN Red List 112604702
IPNI 703378-1
iNaturalist 518848
GBIF 3999874
Freebase /m/0pcjv5j
EOL 5510497
Elurikkus 449118
Wikipedia Darlingia_darlingiana

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
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
The role of big trees and abundant species in driving spatial patterns of species richness in an Australian tropical rainforest Murphy HT, Bradford MG Ecol Evol 20-Sep-2022
PMCID:PMC9486822
doi:10.1002/ece3.9324
PMID:36188495
A cyclic dipeptide from the Chilean hazelnut cotyledons (Gevuina avellana Mol., Proteaceae) Schmeda-Hirschmann G, de Andrade JP, Jiménez-Aspee F, Mieres-Castro D Sci Rep 27-Apr-2020
PMCID:PMC7184718
doi:10.1038/s41598-020-63983-9
PMID:32341441
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
Rates of molecular evolution and diversification in plants: chloroplast substitution rates correlate with species-richness in the Proteaceae Duchene D, Bromham L BMC Evol Biol 13-Mar-2013
PMCID:PMC3600047
doi:10.1186/1471-2148-13-65
PMID:23497266
Alkaloids of Darlingia darlingiana IRC Bick, JW Gillard, H Leow CSIRO Publishing 07-Aug-2006
doi:10.1071/CH9792523
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
Tropane alkaloids from Darlingia darlingiana Peter L. Katavic, Mark S. Butler, Ronald J. Quinn, Paul I. Forster, Gordon P. Guymer Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00263-0

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
(3E,5E)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-2-one 163186899 Click to see 255.35 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-4-phenylbut-3-en-2-one 86113873 Click to see 229.32 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-6-phenylhexa-3,5-dien-2-one 86113878 Click to see 255.35 unknown https://doi.org/10.1071/CH9792523
> Benzenoids / Benzene and substituted derivatives / Styrenes
(2R,3E,5E)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-2-ol 163185611 Click to see 257.37 unknown https://doi.org/10.1071/CH9792523
(2R,3E,5Z)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexa-3,5-dien-2-ol 163194291 Click to see 257.37 unknown https://doi.org/10.1071/CH9792523
(E,2R)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhex-5-en-2-ol 163185836 Click to see CN1CCCC1CC(CCC=CC2=CC=CC=C2)O 259.40 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-6-phenylhex-5-en-2-ol 162859223 Click to see 259.40 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-6-phenylhexa-3,5-dien-2-ol 162904734 Click to see 257.37 unknown https://doi.org/10.1071/CH9792523
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2R)-1-[(2R)-1-methylpyrrolidin-2-yl]-6-phenylhexan-2-ol 162979944 Click to see 261.40 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-6-phenylhexan-2-ol 162979943 Click to see 261.40 unknown https://doi.org/10.1071/CH9792523
> Organoheterocyclic compounds / Cycloheptapyrans
(1S,9R)-4,5,12-trimethyl-6-oxa-12-azatricyclo[7.2.1.02,7]dodeca-2(7),4-dien-3-one 11622645 Click to see CC1=C(OC2=C(C1=O)C3CCC(C2)N3C)C 219.28 unknown https://doi.org/10.1071/CH9792523
https://doi.org/10.1016/S0031-9422(99)00263-0
4,5,12-Trimethyl-12-oxido-6-oxa-12-azoniatricyclo[7.2.1.02,7]dodeca-2(7),4-dien-3-one 101037026 Click to see 235.28 unknown https://doi.org/10.1016/S0031-9422(99)00263-0
Darlingine 333105 Click to see CC1=C(OC2=C(C1=O)C3CCC(C2)N3C)C 219.28 unknown https://doi.org/10.1016/S0031-9422(99)00263-0
https://doi.org/10.1071/CH9792523
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(1S,2R,7S,9R)-4,5,12-trimethyl-6-oxa-12-azatricyclo[7.2.1.02,7]dodec-4-en-3-one 162986018 Click to see 221.29 unknown https://doi.org/10.1071/CH9792523
4,5,12-Trimethyl-6-oxa-12-azatricyclo[7.2.1.02,7]dodec-4-en-3-one 101417642 Click to see CC1=C(OC2CC3CCC(C2C1=O)N3C)C 221.29 unknown https://doi.org/10.1071/CH9792523
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-1-[(2R)-1-methylpyrrolidin-2-yl]-4-phenylbut-3-en-2-one 102021151 Click to see 229.32 unknown https://doi.org/10.1071/CH9792523
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(E,2R)-1-[(2R)-1-methylpyrrolidin-2-yl]-4-phenylbut-3-en-2-ol 102021150 Click to see CN1CCCC1CC(C=CC2=CC=CC=C2)O 231.33 unknown https://doi.org/10.1071/CH9792523
1-(1-Methylpyrrolidin-2-yl)-4-phenylbut-3-en-2-ol 163083073 Click to see CN1CCCC1CC(C=CC2=CC=CC=C2)O 231.33 unknown https://doi.org/10.1071/CH9792523

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