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Internal ID UUID64400ab9654ff843337546
Scientific name Aristotelia serrata
Authority Oliv.
First published in Trans. & Proc. New Zealand Inst. 53: 365 (1921)

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Synonyms Top

Scientific name Authority First published in
Triphalia rubicunda Banks & Sol. ex Hook.f. Bot. Mag. 128: t. 7868 (1902)
Aristotelia racemosa Hook.f. Fl. Nov.-Zel. 1: 33 (1852)
Dicera serrata J.R.Forst. & G.Forst. Char. Gen. Pl. : 80 (1776)
Friesia racemosa A.Cunn. Ann. Nat. Hist. 4: 24 (1840)

Common names Top

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Language Common/alternative name
English wineberry
Spanish makomako
Arabic أرسطوية منشارية
German makomako
mi makomako
Chinese 酒莓

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Germination/Propagation Top

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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-0000548507
Tropicos 100292349
KEW urn:lsid:ipni.org:names:323917-1
The Plant List kew-2652056
PFAF Aristotelia serrata
Open Tree Of Life 1094482
NCBI Taxonomy 140574
IPNI 323917-1
iNaturalist 70230
GBIF 5651040
Freebase /m/04_tbf
EPPO AITSE
EOL 5427673
USDA GRIN 4204
Wikipedia Aristotelia_serrata

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Pest categorisation of Platypus apicalis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 20-Jun-2022
PMCID:PMC9208325
doi:10.2903/j.efsa.2022.7398
PMID:35765383
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Photosynthetic Properties of Co-Occurring Pioneer Species on Volcanically Devastated Sites in Miyake-jima Island, Japan Zhang X, Li H, Hu X, Zheng P, Hirota M, Kamijo T Plants (Basel) 18-Nov-2021
PMCID:PMC8621165
doi:10.3390/plants10112500
PMID:34834865
Commodity risk assessment of Acer spp. plants from New Zealand Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Mosbach‐Schulz O, Gonthier P EFSA J 20-May-2020
PMCID:PMC10464684
doi:10.2903/j.efsa.2020.6105
PMID:37649508
Leaf functional trait variation in a humid temperate forest, and relationships with juvenile tree light requirements Lusk CH PeerJ 08-May-2019
PMCID:PMC6511228
doi:10.7717/peerj.6855
PMID:31119078
Early tropical crop production in marginal subtropical and temperate Polynesia Prebble M, Anderson AJ, Augustinus P, Emmitt J, Fallon SJ, Furey LL, Holdaway SJ, Jorgensen A, Ladefoged TN, Matthews PJ, Meyer JY, Phillipps R, Wallace R, Porch N Proc Natl Acad Sci U S A 08-Apr-2019
PMCID:PMC6500154
doi:10.1073/pnas.1821732116
PMID:30962379
Parasite–offspring competition for female resources can explain male-biased parasitism in plants Yule KJ, Burns KC Biol Lett 06-Mar-2019
PMCID:PMC6451378
doi:10.1098/rsbl.2018.0761
PMID:30836880
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
Are endemics functionally distinct? Leaf traits of native and exotic woody species in a New Zealand forest Heberling JM, Mason NW PLoS One 02-May-2018
PMCID:PMC5931660
doi:10.1371/journal.pone.0196746
PMID:29718966
Intraspecific trait variation can weaken interspecific trait correlations when assessing the whole‐plant economic spectrum Laughlin DC, Lusk CH, Bellingham PJ, Burslem DF, Simpson AH, Kramer‐Walter KR Ecol Evol 21-Sep-2017
PMCID:PMC5677476
doi:10.1002/ece3.3447
PMID:29152189
Development and Validation of a Real-Time PCR Assay for Rapid Detection of Two-Spotted Spider Mite, Tetranychus urticae (Acari: Tetranychidae) Li D, Fan QH, Waite DW, Gunawardana D, George S, Kumarasinghe L PLoS One 06-Jul-2015
PMCID:PMC4492583
doi:10.1371/journal.pone.0131887
PMID:26147599
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Chapter 3 Aristotelia Alkaloids I. Ralph, C. Bick, Mohammad A. Hai Elsevier 26-Mar-2012
doi:10.1016/S0099-9598(08)60038-3
Phenotypic variation in heteroblastic woody species does not contribute to shade survival Gamage HK AoB Plants 25-May-2011
PMCID:PMC3129537
doi:10.1093/aobpla/plr013
PMID:22476483
The Structures of Serratenone and Serratoline, Two Alkaloids from Aristotelia serrata I. Ralph C. Bick, Mohammad A. Hai, Nigel W. Preston The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1983-04-0667

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Delta amino acids and derivatives
(1'S,3R,4'R,7'R,8'S)-2',2',7'-trimethylspiro[1H-indole-3,6'-3-azatricyclo[5.2.2.04,8]undecane]-2-one 10957881 Click to see 310.40 unknown https://doi.org/10.1016/S0040-4020(01)86726-0
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(4aS,5R,11bR)-11b-methyl-N-propan-2-yl-1,2,4a,5,6,11-hexahydrobenzo[a]carbazol-5-amine 101289684 Click to see 294.40 unknown https://doi.org/10.1016/S0040-4039(01)81883-9
11b-methyl-N-propan-2-yl-1,2,4a,5,6,11-hexahydrobenzo[a]carbazol-5-amine 14565471 Click to see 294.40 unknown https://doi.org/10.1016/S0040-4039(01)81883-9
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(1S,4S,5R,6S,7R,8S)-2,2,7-trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole]-5-ol 162900226 Click to see 310.40 unknown https://doi.org/10.1016/S0040-4039(01)85551-9
2-(1H-indol-3-ylmethyl)-4,4,8-trimethyl-3-azabicyclo[3.3.1]non-7-en-6-one 14808341 Click to see 308.40 unknown https://doi.org/10.3987/R-1983-04-0667
https://doi.org/10.1016/S0040-4020(01)96665-7
2,2,7-Trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole] 15601039 Click to see 294.40 unknown https://doi.org/10.1016/S0040-4020(01)96665-7
https://doi.org/10.1016/S0040-4020(01)98810-6
2,2,7-Trimethylspiro[3-azatricyclo[5.2.2.04,8]undecane-6,3'-indole]-5-ol 162900225 Click to see 310.40 unknown https://doi.org/10.1016/S0040-4039(01)85551-9
2',2',7'-trimethylspiro[1H-indole-3,6'-3-azatricyclo[5.2.2.04,8]undecane]-2-one 73157975 Click to see 310.40 unknown https://doi.org/10.1016/S0040-4020(01)96665-7
https://doi.org/10.1016/S0040-4020(01)98810-6
https://doi.org/10.1016/S0040-4020(01)86726-0
3-[(4,4-dimethyl-8-methylidene-3-azabicyclo[3.3.1]nonan-2-yl)methyl]-1H-indole 73880786 Click to see 294.40 unknown https://doi.org/10.3987/R-1983-04-0667
3-[(8-methylidene-6-propan-2-yl-6-azabicyclo[3.2.1]oct-3-en-7-yl)methyl]-1H-indole 44719092 Click to see 292.40 unknown https://doi.org/10.1016/S0099-9598(08)60038-3
3-[[(1R,5S,7S)-8-methylidene-6-propan-2-yl-6-azabicyclo[3.2.1]oct-3-en-7-yl]methyl]-1H-indole 163002671 Click to see 292.40 unknown https://doi.org/10.1016/S0099-9598(08)60038-3
rel-3-{[(1R,2S,5R)-4,4-dimethyl-8-methylene-3-azabicyclo[3.3.1]non-2-yl]methyl}-1H-indole 639449 Click to see CC1(C2CCC(=C)C(C2)C(N1)CC3=CNC4=CC=CC=C43)C 294.40 unknown https://doi.org/10.3987/R-1983-04-0667
> Organoheterocyclic compounds / Quinolidines
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2,4,6,8-tetraen-10-ol 73098733 Click to see 310.40 unknown https://doi.org/10.3987/R-1983-04-0667
https://doi.org/10.1016/S0040-4020(01)96665-7
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(1R,12R,15R,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-16-one 21578492 Click to see 308.40 unknown https://doi.org/10.1002/HLCA.19800630739
(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-tetraene 11098414 Click to see 294.40 unknown https://doi.org/10.1016/S0040-4039(01)85551-9
(1R,12S,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-11-one 11130638 Click to see 308.40 unknown https://doi.org/10.1016/S0040-4020(01)96665-7
https://doi.org/10.1016/S0040-4039(01)85551-9
(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-pentaen-11-one 10957747 Click to see 306.40 unknown https://doi.org/10.1016/S0040-4020(01)96665-7
https://doi.org/10.3987/R-1983-04-0667
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 3785486 Click to see 308.40 unknown https://doi.org/10.1016/S0040-4039(01)85551-9
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-16-one 14315674 Click to see 308.40 unknown https://doi.org/10.1002/HLCA.19800630739
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8,12-pentaen-11-one 3774018 Click to see CC1(C2CCC3(C(C2)C(=N1)C(=O)C4=C3NC5=CC=CC=C54)C)C 306.40 unknown https://doi.org/10.3987/R-1983-04-0667
Aristoteline 323714 Click to see 294.40 unknown https://doi.org/10.1016/S0040-4039(01)85551-9
https://doi.org/10.1016/S0040-4020(01)96665-7

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