Flindersia acuminata - Unknown
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Internal ID UUID64401cc2706b9168284572
Scientific name Flindersia acuminata
Authority C.T.White
First published in Bull. Dept. Agric. Queensland 21: 5 (1919)

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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-0000691368
UNII 8729M0DKLU
Tropicos 100339279
KEW urn:lsid:ipni.org:names:773621-1
The Plant List kew-2813484
Open Tree Of Life 1076060
NCBI Taxonomy 67921
IUCN Red List 192228255
IPNI 773621-1
iNaturalist 1145762
GBIF 3835691
EOL 5621502
Wikipedia Flindersia_acuminata

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Indole: The After Next Scaffold of Antiplasmodial Agents? Surur AS, Huluka SA, Mitku ML, Asres K Drug Des Devel Ther 11-Nov-2020
PMCID:PMC7666986
doi:10.2147/DDDT.S278588
PMID:33204071
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
In-silico screening for anti-Zika virus phytochemicals Byler KG, Ogungbe IV, Setzer WN J Mol Graph Model 28-Aug-2016
PMCID:PMC7185537
doi:10.1016/j.jmgm.2016.08.011
PMID:27588363
Synthesis of flinderoles B and C by a gold-catalyzed allene hydroarylation Zeldin RM, Toste FD Chem Sci 24-Jun-2011
PMCID:PMC3389741
doi:10.1039/C1SC00290B
PMID:22773943
Antiplasmodial Natural Products Nogueira CR, Lopes LM Molecules 04-Mar-2011
PMCID:PMC6259672
doi:10.3390/molecules16032146
The Chemical Constituents of Australian Flindersia Species. XV. The Constituents of Flindersia acuminata C. T. White CT White, E Ritchie, WC Taylor, STK Vautin CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9610469
Flinderoles A-C: antimalarial bis-indole alkaloids from Flindersia species. Fernandez LS, Buchanan MS, Carroll AR, Feng YJ, Quinn RJ, Avery VM Org Lett 15-Jan-2009
doi:10.1021/OL802506N
PMID:19090698

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
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
6aalpha,7,8,10aalpha-Tetrahydro-N,7,7,9-tetramethyl-6alpha-[3-[2-(methylamino)ethyl]-1H-indol-2-yl]-6H-isoindolo[2,1-a]indole-11-(ethanamine) 101647945 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCNC)C(C1)(C)C 480.70 unknown https://doi.org/10.1021/OL802506N
N-methyl-2-[2-[(E)-2-[(1S,3S)-1-methyl-4-[2-(methylamino)ethyl]-3-(2-methylprop-1-enyl)-2,3-dihydropyrrolo[1,2-a]indol-1-yl]ethenyl]-1H-indol-3-yl]ethanamine 162871913 Click to see CC(=CC1CC(N2C1=C(C3=CC=CC=C32)CCNC)(C)C=CC4=C(C5=CC=CC=C5N4)CCNC)C 480.70 unknown https://doi.org/10.1021/OL802506N
N-methyl-2-[2-[2-[1-methyl-4-[2-(methylamino)ethyl]-3-(2-methylprop-1-enyl)-2,3-dihydropyrrolo[1,2-a]indol-1-yl]ethenyl]-1H-indol-3-yl]ethanamine 74405766 Click to see CC(=CC1CC(N2C1=C(C3=CC=CC=C32)CCNC)(C)C=CC4=C(C5=CC=CC=C5N4)CCNC)C 480.70 unknown https://doi.org/10.1021/OL802506N
N-methyl-2-[2-[7,7,9-trimethyl-11-[2-(methylamino)ethyl]-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-6-yl]-1H-indol-3-yl]ethanamine 432920 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCNC)C(C1)(C)C 480.70 unknown https://doi.org/10.1021/OL802506N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)- 3594 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1071/CH9610469
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1071/CH9610469

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