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Acacia victoriae

Acacia victoriae - 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 UUID643fd967afdc6188746598
Scientific name Acacia victoriae
Authority Benth.
First published in T.L.Mitchell, J. Exped. Trop. Australia: 333 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acacia sentis var. victoriae (Benth.) Domin Biblioth. Bot.22(89): 254 (1926)
Racosperma victoriae (Benth.) Pedley Bot. J. Linn. Soc.92: 249 (1986)

Common names Top

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Language Common/alternative name
English bramble acacia
Persian آکاکیا ویکتوریا
Chinese 维多利亚金合欢
Chinese 維多利亞金合歡

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Acacia victoriae subsp. arida Pedley Austrobaileya1: 271 (1979)
Acacia victoriae subsp. fasciaria Ariati Austral. Syst. Bot.20: 61 (2007)
Acacia victoriae subsp. victoriae Unknown

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Victoria
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185334
UNII L19826GVM8
USDA Plants ACVI7
Tropicos 13024685
KEW urn:lsid:ipni.org:names:471757-1
The Plant List ild-31544
PFAF Acacia victoriae
Open Tree Of Life 554923
NCBI Taxonomy 138524
IUCN Red List 193988457
IPNI 471757-1
iNaturalist 122825
GBIF 2979105
Freebase /m/08bmb7
EPPO ACAVI
EOL 643404
USDA GRIN 1028
Wikipedia Acacia_victoriae

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
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Improving the Production of Secondary Metabolites via the Application of Biogenic Zinc Oxide Nanoparticles in the Calli of Delonix elata: A Potential Medicinal Plant Tarroum M, Alfarraj NS, Al-Qurainy F, Al-Hashimi A, Khan S, Nadeem M, Salih AM, Shaikhaldein HO Metabolites 02-Aug-2023
PMCID:PMC10456625
doi:10.3390/metabo13080905
PMID:37623850
LC-MS/MS Characterization of Phenolic Metabolites and Their Antioxidant Activities from Australian Native Plants Ali A, Cottrell JJ, Dunshea FR Metabolites 24-Oct-2022
PMCID:PMC9698446
doi:10.3390/metabo12111016
PMID:36355099
Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M Molecules 16-Jun-2022
PMCID:PMC9230627
doi:10.3390/molecules27123863
PMID:35744986
Diversity of Useful Plants in Cabo Verde Islands: A Biogeographic and Conservation Perspective Duarte MC, Gomes I, Catarino S, Brilhante M, Gomes S, Rendall A, Moreno Â, Fortes AR, Ferreira VS, Baptista I, Dinis H, Romeiras MM Plants (Basel) 15-May-2022
PMCID:PMC9144021
doi:10.3390/plants11101313
PMID:35631738
Small-Molecule RAS Inhibitors as Anticancer Agents: Discovery, Development, and Mechanistic Studies Shetu SA, Bandyopadhyay D Int J Mol Sci 28-Mar-2022
PMCID:PMC8999084
doi:10.3390/ijms23073706
PMID:35409064
Multimeric Association of Purified Novel Bowman-Birk Inhibitor From the Medicinal Forage Legume Mucuna pruriens (L.) DC. Lone JK, Lekha MA, Bharadwaj RP, Ali F, Pillai MA, Wani SH, Yasin JK, Chandrashekharaiah KS Front Plant Sci 25-Nov-2021
PMCID:PMC8655843
doi:10.3389/fpls.2021.772046
PMID:34899797
Zebra finch song is a very short-range signal in the wild: evidence from an integrated approach Loning H, Griffith SC, Naguib M Behav Ecol 22-Sep-2021
PMCID:PMC8857932
doi:10.1093/beheco/arab107
PMID:35197805
Synoptic Overview of Exotic Acacia, Senegalia and Vachellia (Caesalpinioideae, Mimosoid Clade, Fabaceae) in Egypt Hassan RA, Hamdy RS Plants (Basel) 01-Jul-2021
PMCID:PMC8309130
doi:10.3390/plants10071344
PMID:34371547
Blocking K-Ras Interaction With the Plasma Membrane Is a Tractable Therapeutic Approach to Inhibit Oncogenic K-Ras Activity Henkels KM, Rehl KM, Cho KJ Front Mol Biosci 16-Jun-2021
PMCID:PMC8244928
doi:10.3389/fmolb.2021.673096
PMID:34222333
Characterization of a Bowman–Birk type trypsin inhibitor purified from seeds of Solanum surattense Herwade AP, Kasar SS, Rane NR, Ahmed S, Maras JS, Pawar PK Sci Rep 21-Apr-2021
PMCID:PMC8060351
doi:10.1038/s41598-021-87980-8
PMID:33883624
Short-beaked echidna (Tachyglossus aculeatus) home range at Fowlers Gap Arid Zone Research Station, NSW Badgery GJ, Lawes JC, Leggett KE PLoS One 16-Apr-2021
PMCID:PMC8051760
doi:10.1371/journal.pone.0242298
PMID:33861740
Mid-Infrared Spectroscopy as a Rapid Tool to Qualitatively Predict the Effects of Species, Regions and Roasting on the Nutritional Composition of Australian Acacia Seed Species Adiamo OQ, Sultanbawa Y, Cozzolino D Molecules 26-Mar-2021
PMCID:PMC8036610
doi:10.3390/molecules26071879
PMID:33810352
Dynamics of bird assemblages in response to temporally and spatially variable resources in arid Australia Pascoe BA, Pavey CR, Morton SR, Schlesinger CA Ecol Evol 17-Mar-2021
PMCID:PMC8093688
doi:10.1002/ece3.7293
PMID:33976788
Modification of Natural Proanthocyanidin Oligomers and Polymers Via Chemical Oxidation under Alkaline Conditions Imran IB, Karonen M, Salminen JP, Engström MT ACS Omega 09-Feb-2021
PMCID:PMC7906247
doi:10.1021/acsomega.0c05515
PMID:33644580

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11051331 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)O)(C)C)C(=O)O)O)C)C)C)NC(=O)C)O)O)OC8C(C(C(CO8)O)O)O)O)O 970.10 unknown https://doi.org/10.1021/NP020400V
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aS,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl]oxy-3-[(2E,6R)-6-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2E,6R)-6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-6-methyloxan-2-yl]oxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162822911 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2083.30 unknown https://doi.org/10.1021/NP020400V
[3-[5-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3-acetamido-6-[[4,5-dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl]oxy-3-[6-[3,4-dihydroxy-5-(6-hydroxy-2,6-dimethylocta-2,7-dienoyl)oxy-6-methyloxan-2-yl]oxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 3214 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)C)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2067.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC33297/
https://doi.org/10.1021/NP020400V
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC58768/
Avicin D 44566777 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2083.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC33297/
https://doi.org/10.1021/NP020400V
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC58768/
Avicin G 44566778 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)C)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2067.30 unknown https://doi.org/10.1021/NP020400V
julibroside J29 44448243 Click to see CC1C(C(C(C(O1)OC(C)(CCC=C(CO)C(=O)OC2CC3(C(CC2(C)C)C4=CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)OC9C(C(C(CO9)O)O)O)O)O)NC(=O)C)C)C(=O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C=C)O)O)O 1901.00 unknown https://doi.org/10.1021/NP020400V
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acacic acid lactone 6712546 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)O)C)C 470.70 unknown https://doi.org/10.1021/NP020400V

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