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Acacia carneorum

Acacia carneorum - 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 UUID643fdc7cc1b74889299235
Scientific name Acacia carneorum
Authority Maiden
First published in J. Proc. Roy. Soc. New S. Wales49: 470 (1915 publ. 1916)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acacia carnei Maiden
Racosperma carneorum (Maiden) Pedley Austrobaileya6: 455 (2003)

Common names Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000201400
Tropicos 50246854
KEW urn:lsid:ipni.org:names:469945-1
The Plant List ild-47802
Open Tree Of Life 3918002
NCBI Taxonomy 1173639
IPNI 60633-3
iNaturalist 519207
GBIF 2979027
EOL 644229
Wikipedia Acacia_carneorum

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
Protective Effect of Fustin against Huntington’s Disease in 3-Nitropropionic Treated Rats via Downregulation of Oxidative Stress and Alteration in Neurotransmitters and Brain-Derived Neurotrophic Factor Activity Bin-Jumah MN, Gilani SJ, Alabbasi AF, Al-Abbasi FA, AlGhamdi SA, Alshehri OY, Alghamdi AM, Sayyed N, Kazmi I Biomedicines 23-Nov-2022
PMCID:PMC9775313
doi:10.3390/biomedicines10123021
PMID:36551777
Flavanols from Nature: A Phytochemistry and Biological Activity Review Luo Y, Jian Y, Liu Y, Jiang S, Muhammad D, Wang W Molecules 22-Jan-2022
PMCID:PMC8838462
doi:10.3390/molecules27030719
PMID:35163984
Genetic variation and population structure of clonal Zingiber zerumbet at a fine geographic scale: a comparison with two closely related selfing and outcrossing Zingiber species Huang R, Wang Y, Li K, Wang YQ BMC Ecol Evol 09-Jun-2021
PMCID:PMC8191059
doi:10.1186/s12862-021-01853-2
PMID:34107885
What drives the shift between sexual and clonal reproduction of Caragana stenophylla along a climatic aridity gradient? Wang Z, Xie L, Prather CM, Guo H, Han G, Ma C BMC Plant Biol 22-May-2018
PMCID:PMC5964679
doi:10.1186/s12870-018-1313-6
PMID:29788911
Clonality disguises the vulnerability of a threatened arid zone Acacia Roberts DG, Forrest CN, Denham AJ, Ayre DJ Ecol Evol 11-Oct-2017
PMCID:PMC5696425
doi:10.1002/ece3.3246
PMID:29187981
Metabolites from the purple heartwood of Mimosoideae. Part 2. Acacia carnei maiden: isolation, synthesis, and reactions of crombeone Edward V. Brandt, Daneel Ferreira, David G. Roux Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19810000514

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
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(6,7-dimethoxy-1H-isochromen-3-yl)-(2,4-dimethoxyphenyl)methanone 162962595 Click to see COC1=CC(=C(C=C1)C(=O)C2=CC3=CC(=C(C=C3CO2)OC)OC)OC 356.40 unknown https://doi.org/10.1039/P19810000514
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Fustin 5317435 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1039/P19810000514
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1039/P19810000514
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1039/P19810000514
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(3,4-dimethoxyphenyl)-3,7-dimethoxy-2,3-dihydrochromen-4-one 162910096 Click to see COC1C(OC2=C(C1=O)C=CC(=C2)OC)C3=CC(=C(C=C3)OC)OC 344.40 unknown https://doi.org/10.1039/P19810000514
2-(3,4-Dimethoxyphenyl)-3-hydroxy-5,7-dimethoxy-2,3-dihydro-4H-chromen-4-one 462695 Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3OC)OC)O)OC 360.40 unknown https://doi.org/10.1039/P19810000514
2-(3,4-Dimethoxyphenyl)-3,7-dimethoxy-2,3-dihydrochromen-4-one 15555856 Click to see COC1C(OC2=C(C1=O)C=CC(=C2)OC)C3=CC(=C(C=C3)OC)OC 344.40 unknown https://doi.org/10.1039/P19810000514
Fisetin tetramethyl ether 631171 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)OC)OC)OC 342.30 unknown https://doi.org/10.1039/P19810000514
Flavanone, 3-hydroxy-3',4',5,7-tetramethoxy- 2064449 Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3OC)OC)O)OC 360.40 unknown https://doi.org/10.1039/P19810000514
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(+)-Tri-O-methylpeltogynol 606046 Click to see COC1=CC2=C(C=C1)C(C3C(O2)C4=CC(=C(C=C4CO3)OC)OC)O 344.40 unknown https://doi.org/10.1039/P19810000514
(6aR,12aR)-2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 15555865 Click to see COC1=CC2=C(C=C1)C(=O)C3C(O2)C4=CC(=C(C=C4CO3)OC)OC 342.30 unknown https://doi.org/10.1039/P19810000514
(6aR,12aR)-2,3,8,10-tetramethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 162973277 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3C(O2)C4=CC(=C(C=C4CO3)OC)OC 372.40 unknown https://doi.org/10.1039/P19810000514
(6aR,12aR)-8-hydroxy-2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 162925371 Click to see COC1=CC(=C2C(=C1)OC3C(C2=O)OCC4=CC(=C(C=C34)OC)OC)O 358.30 unknown https://doi.org/10.1039/P19810000514
(6aS,7S,12aR)-2,3,10-trimethoxy-5,6a,7,12a-tetrahydroisochromeno[4,3-b]chromen-7-ol 162940628 Click to see COC1=CC2=C(C=C1)C(C3C(O2)C4=CC(=C(C=C4CO3)OC)OC)O 344.40 unknown https://doi.org/10.1039/P19810000514
[2]Benzopyrano[4,3-b][1]benzopyran-7(5H)-one, 2,3,8,10-tetramethoxy- 632840 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C4=CC(=C(C=C4CO3)OC)OC 370.40 unknown https://doi.org/10.1039/P19810000514
2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 163070448 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C4=CC(=C(C=C4CO3)OC)OC 340.30 unknown https://doi.org/10.1039/P19810000514
2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 15555864 Click to see COC1=CC2=C(C=C1)C(=O)C3C(O2)C4=CC(=C(C=C4CO3)OC)OC 342.30 unknown https://doi.org/10.1039/P19810000514
2,3,8,10-tetramethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 15555868 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3C(O2)C4=CC(=C(C=C4CO3)OC)OC 372.40 unknown https://doi.org/10.1039/P19810000514
5,6a,7,12a-Tetrahydroisochromeno[4,3-b]chromene-2,3,7,10-tetrol 12314037 Click to see C1C2=CC(=C(C=C2C3C(O1)C(C4=C(O3)C=C(C=C4)O)O)O)O 302.28 unknown https://doi.org/10.1039/P19810000514
8-hydroxy-2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 162925370 Click to see COC1=CC(=C2C(=C1)OC3C(C2=O)OCC4=CC(=C(C=C34)OC)OC)O 358.30 unknown https://doi.org/10.1039/P19810000514
CID 12314039 12314039 Click to see C1C2=CC(=C(C=C2C3C(O1)C(C4=C(O3)C=C(C=C4)O)O)O)O 302.28 unknown https://doi.org/10.1039/P19810000514
CID 14557360 14557360 Click to see COC1=CC2=C(C=C1)C(C3C(O2)C4=CC(=C(C=C4CO3)OC)OC)O 344.40 unknown https://doi.org/10.1039/P19810000514
Peltogynan-4-alpha-ol 12314038 Click to see C1C2=CC(=C(C=C2C3C(O1)C(C4=C(O3)C=C(C=C4)O)O)O)O 302.28 unknown https://doi.org/10.1039/P19810000514
Peltogynin 12314036 Click to see C1C2=CC(=C(C=C2C3=C(O1)C(=O)C4=C(O3)C=C(C=C4)O)O)O 298.25 unknown https://doi.org/10.1039/P19810000514

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