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Flindersia fournieri

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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 UUID64401cc33f84e719753618
Scientific name Flindersia fournieri
Authority Pancher & Sebert
First published in Rev. Marit. Colon. 41: 203 (1874)

Description Top

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Synonyms Top

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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

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-0000691381
Tropicos 50203898
INPN 673133
KEW urn:lsid:ipni.org:names:578488-1
The Plant List kew-2813496
Open Tree Of Life 1076071
NCBI Taxonomy 67929
IPNI 578488-1
GBIF 3835500
EOL 5621514

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
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
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
Major Clades of Australasian Rutoideae (Rutaceae) Based on rbcL and atpB Sequences Bayly MJ, Holmes GD, Forster PI, Cantrill DJ, Ladiges PY PLoS One 13-Aug-2013
PMCID:PMC3742607
doi:10.1371/journal.pone.0072493
PMID:23967311
Correlations between leaf toughness and phenolics among species in contrasting environments of Australia and New Caledonia Read J, Sanson GD, Caldwell E, Clissold FJ, Chatain A, Peeters P, Lamont BB, De Garine-Wichatitsky M, Jaffré T, Kerr S Ann Bot 19-Dec-2008
PMCID:PMC2707862
doi:10.1093/aob/mcn246
PMID:19098067
Deux nouveaux alcaloïdes bis-indoliques de Flindersia fournieri François Tillequin, Michel Koch Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82753-3
Trois nouveaux alcaloïdes bis-indoliques de Flindersia fo urnieri François Tillequin, Michel Koch Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98496-6
Isoborrérine, nouvel alcaloïde indolo-isoprénique de Flindersia fournieri François Tillequin, Michel Koch Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83119-0

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
> Alkaloids and derivatives / Harmala alkaloids
(1S)-2-methyl-1-(2-methylprop-1-enyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole 134860448 Click to see CC(=CC1C2=C(CCN1C)C3=CC=CC=C3N2)C 240.34 unknown https://doi.org/10.1016/0031-9422(80)83119-0
Borrerine 182658 Click to see CC(=CC1C2=C(CCN1C)C3=CC=CC=C3N2)C 240.34 unknown https://doi.org/10.1016/0031-9422(80)83119-0
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(1S,9R,10S,12R,15R,16R)-12,14,14,19-tetramethyl-16-[3-[2-(methylamino)ethyl]-1H-indol-2-yl]-8,19-diazapentacyclo[7.7.3.01,9.02,7.010,15]nonadeca-2,4,6-trien-12-ol 163195553 Click to see CC1(CC(CC2C1C(C34C2(NC5=CC=CC=C53)N(CC4)C)C6=C(C7=CC=CC=C7N6)CCNC)(C)O)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)82753-3
12,14,14,19-tetramethyl-16-[3-[2-(methylamino)ethyl]-1H-indol-2-yl]-8,19-diazapentacyclo[7.7.3.01,9.02,7.010,15]nonadeca-2,4,6-trien-12-ol 163004006 Click to see CC1(CC(CC2C1C(C34C2(NC5=CC=CC=C53)N(CC4)C)C6=C(C7=CC=CC=C7N6)CCNC)(C)O)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)82753-3
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
(6R,6aS,9S,10aS)-7,7,9-trimethyl-11-[2-(methylamino)ethyl]-6-[3-[2-(methylamino)ethyl]-1H-indol-2-yl]-6a,8,10,10a-tetrahydro-6H-isoindolo[2,1-a]indol-9-ol 163193443 Click to see CC1(CC(CC2C1C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCNC)(C)O)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)82753-3
2-[(6R,6aS,10aS)-6-[3-[2-(dimethylamino)ethyl]-1H-indol-2-yl]-7,7,9-trimethyl-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-11-yl]-N-methylethanamine 163195554 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCN(C)C)C(C1)(C)C 494.70 unknown https://doi.org/10.1016/S0031-9422(00)98496-6
2-[2-[(6R,6aS,10aS)-11-[2-(dimethylamino)ethyl]-7,7,9-trimethyl-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-6-yl]-1H-indol-3-yl]-N,N-dimethylethanamine 57412131 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCN(C)C)C5=C(C6=CC=CC=C6N5)CCN(C)C)C(C1)(C)C 508.70 unknown https://doi.org/10.1016/S0031-9422(00)98496-6
2-[2-[11-[2-(dimethylamino)ethyl]-7,7,9-trimethyl-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-6-yl]-1H-indol-3-yl]-N,N-dimethylethanamine 76527499 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCN(C)C)C5=C(C6=CC=CC=C6N5)CCN(C)C)C(C1)(C)C 508.70 unknown https://doi.org/10.1016/S0031-9422(00)98496-6
2-[6-[3-[2-(dimethylamino)ethyl]-1H-indol-2-yl]-7,7,9-trimethyl-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-11-yl]-N-methylethanamine 163044220 Click to see CC1=CC2C(C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCN(C)C)C(C1)(C)C 494.70 unknown https://doi.org/10.1016/S0031-9422(00)98496-6
7,7,9-trimethyl-11-[2-(methylamino)ethyl]-6-[3-[2-(methylamino)ethyl]-1H-indol-2-yl]-6a,8,10,10a-tetrahydro-6H-isoindolo[2,1-a]indol-9-ol 162961693 Click to see CC1(CC(CC2C1C(N3C2=C(C4=CC=CC=C43)CCNC)C5=C(C6=CC=CC=C6N5)CCNC)(C)O)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)82753-3

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