Acacia fasciculifera - Unknown
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Internal ID UUID643fd964e8f25260558865
Scientific name Acacia fasciculifera
Authority F.Muell. ex Benth.
First published in Fl. Austral.2: 361 (1864)

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Acacia fasciculifera is a tree endemic to parts of Queensland, Australia. It can grow up to 10-20 m in height and has light green phyllodes with a narrowly oblong to narrowly elliptic shape. It flowers in the summer months between November and March and produces cream coloured flowers in groups of two to eight. The species was first formally described by the botanist George Bentham in 1864 and is found in Queensland from Boonah in the south up to around Bowen in the north.

Synonyms Top

Scientific name Authority First published in
Racosperma fasciculiferum (F.Muell. ex Benth.) Pedley Austrobaileya2: 348 (1987)
Acacia penninervis var. stenophylla Domin Biblioth. Bot.22(89): 254 (1926)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000185303
Tropicos 13023945
KEW urn:lsid:ipni.org:names:470312-1
The Plant List ild-31509
Open Tree Of Life 633799
NCBI Taxonomy 138022
IPNI 470312-1
iNaturalist 369337
GBIF 2978396
EOL 642014
USDA GRIN 845
Wikipedia Acacia_fasciculifera

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
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
Natural Dibenzo-α-Pyrones and Their Bioactivities Mao Z, Sun W, Fu L, Luo H, Lai D, Zhou L Molecules 22-Apr-2014
PMCID:PMC6271090
doi:10.3390/molecules19045088
PMID:24759070
Metabolites from the purple heartwoods of the mimosoideae. Part 4. Acacia fasciculifera F. Muell ex. Benth: fasciculiferin, fasciculiferol, and the synthesis of 7-aryl- and 7-flavanyl-peltogynoids Fanie R. van Heerden, Edward V. Brandt, Daneel Ferreira, David G. Roux Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19810002483
Structure and synthesis of a derivative of fasciculiferin, a novel peltogynoid from Acacia fasciculifera Fanie R. van Heerden, E.Vincent Brandt, David G. Roux Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)86634-X

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
> Phenylpropanoids and polyketides / Coumarins and derivatives
3,9,10-Trihydro xydibenzo[b,d]pyran-6-one 86011171 Click to see C1=CC2=C(C=C1O)OC(=O)C3=C2C(=C(C=C3)O)O 244.20 unknown https://doi.org/10.1039/P19810002483
3,9,10-Trimethoxybenzo[c]chromen-6-one 86011203 Click to see COC1=CC2=C(C=C1)C3=C(C=CC(=C3OC)OC)C(=O)O2 286.28 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3S,4R)-4-[(2R,3R,4R)-3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868664 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
[(2R,3S,4R)-4-[(2R,3R,4S)-3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868665 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
[4-[3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868663 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 12308746 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown https://doi.org/10.1039/P19810002483
4'-Epibileucofisetinidin 102115500 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown https://doi.org/10.1039/P19810002483
Bileucofisetinidin 101297694 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown https://doi.org/10.1039/P19810002483
> 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/P19810002483
Tetrahydroxyflavanone 246330 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/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
2-(3,4-Dimethoxyphenyl)-7-methoxy-3,4-chromanediol 602147 Click to see COC1=CC2=C(C=C1)C(C(C(O2)C3=CC(=C(C=C3)OC)OC)O)O 332.30 unknown https://doi.org/10.1039/P19810002483
Fisetinidol-4beta-ol 442398 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 290.27 unknown https://doi.org/10.1039/P19810002483
Fisetinidol-4beta-ol 7,3',4'-trimethyl ether 14991957 Click to see COC1=CC2=C(C=C1)C(C(C(O2)C3=CC(=C(C=C3)OC)OC)O)O 332.30 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1039/P19810002483
> 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/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(3,4-dimethoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 92974069 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC(=C(C=C3)OC)OC 314.30 unknown https://doi.org/10.1039/P19810002483
3',4',7-Trimethoxyflavanone 9818297 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC(=C(C=C3)OC)OC 314.30 unknown https://doi.org/10.1039/P19810002483
7,3',4'-Trimethoxyflavone 154227 Click to see COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC(=C(C=C3)OC)OC 312.30 unknown https://doi.org/10.1039/P19810002483
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/P19810002483
> 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/P19810002483
(5R)-2,3,5,10-tetrahydroxy-5H-isochromeno[4,3-b]chromen-7-one 162955121 Click to see C1=CC2=C(C=C1O)OC3=C(C2=O)OC(C4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1039/P19810002483
(5S)-2,3,5,10-tetrahydroxy-5H-isochromeno[4,3-b]chromen-7-one 162955122 Click to see C1=CC2=C(C=C1O)OC3=C(C2=O)OC(C4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1039/P19810002483
(5S)-5-ethoxy-2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162842651 Click to see CCOC1C2=CC(=C(C=C2C3=C(O1)C(=O)C4=C(O3)C=C(C=C4)OC)OC)OC 384.40 unknown https://doi.org/10.1016/S0040-4039(01)86634-X
(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/P19810002483
(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/P19810002483
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/P19810002483
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/P19810002483
3,4,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 163057116 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C4=C(CO3)C(=C(C=C4)OC)OC 340.30 unknown https://doi.org/10.1039/P19810002483
5-ethoxy-2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162842650 Click to see CCOC1C2=CC(=C(C=C2C3=C(O1)C(=O)C4=C(O3)C=C(C=C4)OC)OC)OC 384.40 unknown https://doi.org/10.1016/S0040-4039(01)86634-X
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/P19810002483
Fasciculiferin 44260090 Click to see C1=CC2=C(C=C1O)OC3=C(C2=O)OC(C4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1039/P19810002483

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