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Quassia bidwillii

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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 UUID6440220a67d6d092078540
Scientific name Quassia bidwillii
Authority (Hook.f.) Noot.
First published in Blumea 11: 519 (1963)

Description Top

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Synonyms Top

Scientific name Authority First published in
Samadera bidwillii Oliv. Hooker's Icon. Pl. 25: t. 2449 (1896)
Simaba bidwillii (Hook.f.) Feuillet Bull. Jard. Bot. Natl. Belg. 53: 510 (1983)

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000733357
Tropicos 100349403
KEW urn:lsid:ipni.org:names:814009-1
The Plant List kew-2868418
IPNI 814009-1
GBIF 3709122

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)!
Title Authors Publication Released IDs
The secondary metabolites of aff. Samadera SAC-2825: An australian simaroubaceae with unusual chemistry Simon Gibbons, Lyn Craven, Clyde Dunlop, Alexander I. Gray, Thomas G. Hartley, Peter G. Waterman Elsevier BV 01-May-2003
doi:10.1016/S0031-9422(96)00708-X
An insecticidal quassinoid from the new Australian species Quassia sp. aff. bidwillii Zahid Latif, Lyn Craven, T.G Hartley, Brian R Kemp, Janet Potter, Martin J Rice, Roger D Waigh, Peter G Waterman Elsevier BV 26-Jul-2002
doi:10.1016/S0305-1978(99)00042-3

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
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Epieudesmin 7299790 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
(-)-Sesamin 382073 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
(+)-Epieudesmine 7000209 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
(+)-Fargesin 5320622 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
(3R,3aS,6R,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 325601 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
5-[(3aR,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 137705003 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
5-[(3R,3aR,6S,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 11210905 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Asarinin 101612 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Eudesmin 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Fargesin 10926754 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1S,4R,5R,6R,7S,8R,11S,13R,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-acetyloxy-2-methylbutanoate 162943631 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)OC(=O)C 538.60 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Chaparrinone 73154 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O 378.40 unknown https://doi.org/10.1016/S0305-1978(99)00042-3
Glaucarubine-2'-acetate 326462 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)OC(=O)C 538.60 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Evodia fruit 235284 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one 163033172 Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O 328.40 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Methoxy-10-methyl-acridin-9-one 468117 Click to see CN1C2=C(C(=CC=C2)OC)C(=O)C3=CC=CC=C31 239.27 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
1,8-Dihydroxyacridin-9(10H)-one 49863128 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(N2)C=CC=C3O 227.21 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
[2-(10-Acetyloxyundecyl)-4-oxoquinolin-1-yl]methyl acetate 85724273 Click to see CC(CCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1COC(=O)C)OC(=O)C 429.50 unknown https://doi.org/10.1016/S0031-9422(96)00708-X
[2-[(10R)-10-acetyloxyundecyl]-4-oxoquinolin-1-yl]methyl acetate 162962967 Click to see CC(CCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1COC(=O)C)OC(=O)C 429.50 unknown https://doi.org/10.1016/S0031-9422(96)00708-X

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