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Internal ID UUID643fd99e84832941721019
Scientific name Acacia crombiei
Authority C.T.White
First published in Proc. Roy. Soc. Queensland53: 213 (1942)

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Synonyms Top

Scientific name Authority First published in
Acacia crombei C.T.White
Racosperma crombiei (C.T.White) Pedley Bot. J. Linn. Soc.92: 247 (1986)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
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Database ID/link to page
World Flora Online wfo-0000186425
Tropicos 13037680
KEW urn:lsid:ipni.org:names:470082-1
The Plant List ild-32865
Open Tree Of Life 3918220
IPNI 470082-1
GBIF 2978630
EOL 643963
Wikipedia Acacia_crombiei

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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)!
Title Authors Publication Released IDs
Metabolites from the purple heartwood of mimosoideae. Part 3. Acacia crombei C. T. White: structure and partial synthesis of crombenin, a natural spiropeltogynoid Edward V. Brandt, Daneel Ferreira, David G. Roux Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19810001879

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
5,6-Dihydroxyisobenzofuran-1(3H)-one 20622260 Click to see 166.13 unknown https://doi.org/10.1039/P19810001879
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R,4R)-4,4',6,6',7-pentahydroxyspiro[1,4-dihydroisochromene-3,2'-1-benzofuran]-3'-one 163089804 Click to see 332.26 unknown https://doi.org/10.1039/P19810001879
Crombenin 42607794 Click to see 332.26 unknown https://doi.org/10.1039/P19810001879
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,7,3',4'-Tetrahydroxyflavanone 246330 Click to see 288.25 unknown https://doi.org/10.1039/P19810001879
Fustin 5317435 Click to see 288.25 unknown https://doi.org/10.1039/P19810001879
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(2R,3S,4S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7-triol 442398 Click to see 290.27 unknown https://doi.org/10.1039/P19810001879
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,7-triol 3508976 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/P19810001879
Fisetinidol-4alpha-ol 164762 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/P19810001879
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown https://doi.org/10.1039/P19810001879
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(6aR,12aR)-2,3,8,10-tetrahydroxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 101324791 Click to see C1C2=CC(=C(C=C2C3C(O1)C(=O)C4=C(C=C(C=C4O3)O)O)O)O 316.26 unknown https://doi.org/10.1039/P19810001879
(6aR,7R,12aS)-5,6a,7,12a-tetrahydroisochromeno[4,3-b]chromene-2,3,7,10-tetrol 162959016 Click to see 302.28 unknown https://doi.org/10.1039/P19810001879
(6aR,7S,12aS)-5,6a,7,12a-tetrahydroisochromeno[4,3-b]chromene-2,3,7,10-tetrol 162959014 Click to see 302.28 unknown https://doi.org/10.1039/P19810001879
(6aS,12aS)-2,3,10-trihydroxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 163195626 Click to see 300.26 unknown https://doi.org/10.1039/P19810001879
2,3,10-trihydroxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 12314040 Click to see 300.26 unknown https://doi.org/10.1039/P19810001879
2,3,8,10-tetrahydroxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 162851878 Click to see 316.26 unknown https://doi.org/10.1039/P19810001879
2,3,8,10-Tetrahydroxy[2]benzopyrano[4,3-b][1]benzopyran-7(5H)-one 44260087 Click to see 314.25 unknown https://doi.org/10.1039/P19810001879
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/P19810001879
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/P19810001879

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