Flindersia bourjotiana

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Internal ID UUID64401cc2bf787976278464
Scientific name Flindersia bourjotiana
Authority F.Muell.
First published in Fragm. 9: 133 (1875)

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Synonyms Top

Scientific name Authority First published in
Flindersia tysoni C.DC. Bull. Herb. Boissier , sér. 2, 6: 986 (1906)

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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-0000691372
Tropicos 100339282
KEW urn:lsid:ipni.org:names:578484-1
The Plant List kew-2813488
Open Tree Of Life 1076054
NCBI Taxonomy 67924
IUCN Red List 199308862
IPNI 578484-1
iNaturalist 983607
GBIF 3835620
EOL 5621507
Wikipedia Flindersia_bourjotiana

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
The chemical constituents of Australian Flindersia species. XIX. Triterpenoids from the leaves of F. bourjotiana F. Muell GJW Breen, E Ritchie, WTL Sidwell, WC Taylor CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9660455
Monocot Leaves are Eaten Less than Dicot Leaves in Tropical Lowland Rain Forests: Correlations with Toughness and Leaf Presentation Grubb PJ, Jackson RV, Barberis IM, Bee JN, Coomes DA, Dominy NJ, De La Fuente MA, Lucas PW, Metcalfe DJ, Svenning JC, Turner IM, Vargas O Ann Bot 02-Apr-2008
PMCID:PMC2710256
doi:10.1093/aob/mcn047
PMID:18387972
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340

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 / Triterpenoids
(5R,9R,10R,13S,14S,17S)-17-[(2S,4R,5R)-4,5-dihydroxy-6-methylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 24854307 Click to see 456.70 unknown https://doi.org/10.1071/CH9660455
(5R,9R,10R,13S,14S,17S)-17-[(2S,4R,5S)-6-chloro-4,5-dihydroxy-6-methylheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163193434 Click to see 493.20 unknown https://doi.org/10.1071/CH9660455
17-(4,5-Dihydroxy-6-methylhept-6-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 74334034 Click to see 456.70 unknown https://doi.org/10.1071/CH9660455
17-(6-Chloro-4,5-dihydroxy-6-methylheptan-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162902094 Click to see 493.20 unknown https://doi.org/10.1071/CH9660455
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 15559505 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.1071/CH9660455
Germanicone 21594102 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.1071/CH9660455
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives
(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-4-oxopentan-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162921409 Click to see 398.60 unknown https://doi.org/10.1071/CH9660455
4,4,10,13,14-Pentamethyl-17-(4-oxopentan-2-yl)-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14828266 Click to see 398.60 unknown https://doi.org/10.1071/CH9660455

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