Aristotelia australasica - Unknown
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Internal ID UUID64400ab8a2c48152004628
Scientific name Aristotelia australasica
Authority F.Muell.
First published in Fragm. 2: 79 (1860)

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The shrub has small, white flowers and bright red berries. The berries are edible and have a sweet, tart flavor. They are often used to make jams, jellies, and wines. The leaves of the shrub are also edible and can be used to make tea.

Aristotelia australasica, also known as the mountain wineberry, is a shrub native to northern New South Wales, Australia. It has small, white flowers and bright red berries that are edible and have a sweet, tart flavor. The berries are often used to make jams, jellies, and wines, while the leaves can be used to make tea.

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000548486
Tropicos 100292342
KEW urn:lsid:ipni.org:names:833272-1
The Plant List kew-2652037
Open Tree Of Life 420802
NCBI Taxonomy 378436
IPNI 833272-1
GBIF 5651090
EOL 5427655
Wikipedia Aristotelia_australasica

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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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Structure of Aristoaristone, A New Dimeric Indole Alkaloid from<i>Aristotelia Australasica</i> J.-C. Quirion, H.-P. Husson, C. Kan, I. R. C. Bick Informa UK Limited 07-Jul-2007
doi:10.1080/10575639308043453
Novel dimeric indole alkaloids from Aristotelia australasica. Structural determination and synthesis J. C. Quirion, C. Kan, I. R. C. Bick, H. P. Husson American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JO00229A018
A revision of the structures of 17-epi-aristoteline and aristolasicone, the first two examples of inverted indole alkaloids Jean Charles Quirion, Henri Philippe Husson, Christiane Kan, Oliver Laprevote, Angele Chiaroni, Claude Riche, Stefan Burkard, Hans Juerg Borschberg, I. Ralph C. Bick American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00048A015
Aristolasol and aristolasene: Indole alkaloids from Aristotelia australasica J.C. Quirion, C. Kan-Fan, I.R.C. Bick, H.P. Husson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80064-5
Nouveaux alcaloides indoliques derives de l'aristoteline extraits d'aristotelia australasica C. Kan-Fan, J.-C. Quirion, I.R.C. Bick, H.-P. Husson Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)86726-0

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
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(1R,12R,13S,16S,18R)-20,20-dimethyl-10,19-diazapentacyclo[14.2.2.03,11.04,9.013,18]icosa-3(11),4,6,8-tetraene-12,13-diol 163188405 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C(C3O)NC5=CC=CC=C45)O)C 326.40 unknown https://doi.org/10.1016/0031-9422(88)80064-5
(1R,16R,18S)-20,20-dimethyl-10,19-diazapentacyclo[14.2.2.03,11.04,9.013,18]icosa-3(11),4,6,8,12,14-hexaene 14109885 Click to see CC1(C2CC3C(N1)CC4=C(C=C3C=C2)NC5=CC=CC=C45)C 290.40 unknown https://doi.org/10.1016/0031-9422(88)80064-5
(1R,4R,5R,7R,11S)-4,9,9-trimethylspiro[8-azatricyclo[5.3.1.04,11]undecane-5,3'-indole] 162995021 Click to see CC1(CC2CCC3(C2C(N1)CC34C=NC5=CC=CC=C45)C)C 294.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
20,20-Dimethyl-10,19-diazapentacyclo[14.2.2.03,11.04,9.013,18]icosa-3(11),4,6,8-tetraene-12,13-diol 14109882 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C(C3O)NC5=CC=CC=C45)O)C 326.40 unknown https://doi.org/10.1016/0031-9422(88)80064-5
20,20-Dimethyl-10,19-diazapentacyclo[14.2.2.03,11.04,9.013,18]icosa-3(11),4,6,8,12,14-hexaene 14109884 Click to see CC1(C2CC3C(N1)CC4=C(C=C3C=C2)NC5=CC=CC=C45)C 290.40 unknown https://doi.org/10.1016/0031-9422(88)80064-5
4,9,9-Trimethylspiro[8-azatricyclo[5.3.1.04,11]undecane-5,3'-indole] 162995020 Click to see CC1(CC2CCC3(C2C(N1)CC34C=NC5=CC=CC=C45)C)C 294.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-16-one 25085910 Click to see CC1(C2CC3C4N1C5C6=CC=CC=C6NC5(C4)C3(CC2=O)C)C 308.40 unknown https://doi.org/10.1021/JO00229A018
(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-7-[(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-16-oxo-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-5-yl]-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6(11),7,9-trien-16-one 163010647 Click to see CC1(C2CC3C4N1C5C6=C(C(=CC=C6)N7C8=CC=CC=C8C9C71CC6N9C(C7CC6C1(CC7=O)C)(C)C)NC5(C4)C3(CC2=O)C)C 614.80 unknown https://doi.org/10.1021/JO00229A018
(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-9-[(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-16-oxo-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-5-yl]-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6(11),7,9-trien-16-one 163036716 Click to see CC1(C2CC3C4N1C5C6=C(C=CC(=C6)N7C8=CC=CC=C8C9C71CC6N9C(C7CC6C1(CC7=O)C)(C)C)NC5(C4)C3(CC2=O)C)C 614.80 unknown https://doi.org/10.1021/JO00229A018
(1S,2R,4R,12S,18R)-14,14,18-trimethyl-10-[(1S,2R,4R,15S,18R)-14,14,18-trimethyl-16-oxo-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-5-yl]-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6(11),7,9-trien-16-one 102149875 Click to see CC1(C2CC3C4N1C5C6=C(C=CC=C6N7C8=CC=CC=C8C9C71CC6N9C(C7CC6C1(CC7=O)C)(C)C)NC5(C4)C3(CC2=O)C)C 614.80 unknown https://doi.org/10.1021/JO00229A018
14,14,18-Trimethyl-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-16-one 5925099 Click to see CC1(C2CC3C4N1C5C6=CC=CC=C6NC5(C4)C3(CC2=O)C)C 308.40 unknown https://doi.org/10.1021/JO00229A018
14,14,18-Trimethyl-7-(14,14,18-trimethyl-16-oxo-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-5-yl)-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6(11),7,9-trien-16-one 13895391 Click to see CC1(C2CC3C4N1C5C6=C(C(=CC=C6)N7C8=CC=CC=C8C9C71CC6N9C(C7CC6C1(CC7=O)C)(C)C)NC5(C4)C3(CC2=O)C)C 614.80 unknown https://doi.org/10.1021/JO00229A018
14,14,18-Trimethyl-9-(14,14,18-trimethyl-16-oxo-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-5-yl)-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6(11),7,9-trien-16-one 13895393 Click to see CC1(C2CC3C4N1C5C6=C(C=CC(=C6)N7C8=CC=CC=C8C9C71CC6N9C(C7CC6C1(CC7=O)C)(C)C)NC5(C4)C3(CC2=O)C)C 614.80 unknown https://doi.org/10.1021/JO00229A018
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives
2-amino-6-(2,5-dihydroxy-2-oxo-1,3,2lambda5-dioxaphosphinane-4-carbonyl)-1H-pteridin-4-one 3083002 Click to see C1C(C(OP(=O)(O1)O)C(=O)C2=CN=C3C(=N2)C(=O)N=C(N3)N)O 343.19 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(14,14-Dimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-1-yl)methanol 15601050 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)CO)C 310.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
(1R,12R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-19-one 21604798 Click to see CC1(C2CC3C(N1)CC4=C(C3(CC2=O)C)NC5=CC=CC=C45)C 308.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
https://doi.org/10.1021/JO00048A015
(1R,12S,15S,17S,19R)-19-hydroxy-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-11-one 163189183 Click to see CC1(C2CC3C(N1)C(=O)C4=C(C3(CC2O)C)NC5=CC=CC=C54)C 324.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
(1R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8,12-pentaene 11130118 Click to see CC1(C2CCC3(C(C2)C(=N1)CC4=C3NC5=CC=CC=C45)C)C 292.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
(1S,12R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraene 15601041 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)C)C 294.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
(1S,2R,4R,12S,18R)-14,14,18-trimethyl-5-[(1R,12R,15S,17S)-1,14,14-trimethyl-19-oxo-9,13-diazapentacyclo[13.2.2.02,10.03,8.012,17]nonadeca-2(10),3(8),4,6-tetraen-7-yl]-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-16-one 102149909 Click to see CC1(C2CC3C(N1)CC4=C(C3(CC2=O)C)C5=C(N4)C(=CC=C5)N6C7=CC=CC=C7C8C69CC1N8C(C2CC1C9(CC2=O)C)(C)C)C 614.80 unknown https://doi.org/10.1080/10575639308043453
[(1S,12R,15S,17S)-14,14-dimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-1-yl]methanol 163188403 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)CO)C 310.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-19-ol 15601047 Click to see CC1(C2CC3C(N1)CC4=C(C3(CC2O)C)NC5=CC=CC=C45)C 310.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8,12-pentaene 15601044 Click to see CC1(C2CCC3(C(C2)C(=N1)CC4=C3NC5=CC=CC=C45)C)C 292.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
19-Hydroxy-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-11-one 15601052 Click to see CC1(C2CC3C(N1)C(=O)C4=C(C3(CC2O)C)NC5=CC=CC=C54)C 324.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
Aristoteline 323714 Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)C)C 294.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
Aristoteline deriv B668273K008 323716 Click to see CC1(C2CC3C(N1)CC4=C(C3(CC2=O)C)NC5=CC=CC=C45)C 308.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0

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