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Melicope simplex

Melicope simplex - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643ffe5dea128049436748
Scientific name Melicope simplex
Authority A.Cunn.
First published in Ann. Nat. Hist. 3: 315 (1839)

Description Top

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Synonyms Top

Scientific name Authority First published in
Melicope parvula Buchanan Trans. & Proc. New Zealand Inst. 20: 255 (1887 publ. 1888)
Astorganthus huegelii Endl. Cat. Hort. Vindob. 2: 196 (1842)

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000452842
Tropicos 50232581
KEW urn:lsid:ipni.org:names:774334-1
Open Tree Of Life 554701
NCBI Taxonomy 384966
IPNI 774334-1
iNaturalist 366690
GBIF 3831445
Freebase /m/0k2j53r
Wikipedia Melicope_simplex

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
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
Complementary description of Colomerus novahebridensis Keifer (Acari, Eriophyidae), with a discussion about the constitution of the genus and its economic importance, and a tentative key to Colomerus Newkirk & Keifer species Chandrapatya A, Konvipasruang P, Flechtmann CH, de Moraes GJ Zookeys 14-Aug-2014
PMCID:PMC4141164
doi:10.3897/zookeys.434.7308
PMID:25152678
Melicope balgooyi Appelhans, W.L. Wagner & K.R. Wood, a new species and new record in Melicope section Melicope (Rutaceae) for the Austral Islands Appelhans MS, Wagner WL, Wood KR PhytoKeys 25-Jul-2014
PMCID:PMC4152893
doi:10.3897/phytokeys.39.7691
PMID:25197227
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
Identification of PPARgamma Partial Agonists of Natural Origin (II): In Silico Prediction in Natural Extracts with Known Antidiabetic Activity Guasch L, Sala E, Mulero M, Valls C, Salvadó MJ, Pujadas G, Garcia-Vallvé S PLoS One 06-Feb-2013
PMCID:PMC3566095
doi:10.1371/journal.pone.0055889
PMID:23405231
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
Two new pathogenic ascomycetes in Guignardia and Rosenscheldiella on New Zealand's pygmy mistletoes (Korthalsella: Viscaceae) Sultan A, Johnston PR, Park D, Robertson AW Stud Mycol 01-Jan-2011
PMCID:PMC3065993
doi:10.3114/sim.2011.68.11
PMID:21523197
The road from Santa Rosalia: A faster tempo of evolution in tropical climates Wright S, Keeling J, Gillman L Proc Natl Acad Sci U S A 03-May-2006
PMCID:PMC1472511
doi:10.1073/pnas.0510383103
PMID:16672371
486. Chemistry of New Zealand Melicope species. Part IV. Constituents of the bark of Melicope simplex Lindsay H. Briggs, R. H. Locker Royal Society of Chemistry (RSC) 22-Apr-2004
doi:10.1039/JR9500002376
Flavonoids of the barks of Melicope simplex and Melicope ternata Richard C. Cambie, Yijun J. Pan, Bruce F. Bowden Elsevier BV 12-May-2003
doi:10.1016/0305-1978(96)88874-0

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 / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Alloevodionol 225063 Click to see CC(=O)C1=C2C(=C(C=C1O)OC)C=CC(O2)(C)C 248.27 unknown https://doi.org/10.1016/0305-1978(96)88874-0
Evodinnol 225062 Click to see CC(=O)C1=C(C2=C(C=C1O)OC(C=C2)(C)C)OC 248.27 unknown https://doi.org/10.1016/0305-1978(96)88874-0
https://doi.org/10.1039/JR9500002376
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans / Precocenes
1-(5,7-Dimethoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone 12468042 Click to see CC(=O)C1=C(C=C(C2=C1OC(C=C2)(C)C)OC)OC 262.30 unknown https://doi.org/10.1039/JR9500002376
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Meliternatin 386320 Click to see COC1=C2C(=CC3=C1OCO3)OC(=C(C2=O)OC)C4=CC5=C(C=C4)OCO5 370.30 unknown https://doi.org/10.1039/JR9500002376
https://doi.org/10.1016/0305-1978(96)88874-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Isokanugin 386324 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC4=C(C=C3)OCO4)OC 356.30 unknown https://doi.org/10.1016/0305-1978(96)88874-0
Melisimplexin 386322 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC4=C(C=C3)OCO4)OC)OC 386.40 unknown https://doi.org/10.1039/JR9500002376
Melisimplin 5466136 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC4=C(C=C3)OCO4)O)OC 372.30 unknown https://doi.org/10.1016/0305-1978(96)88874-0
https://doi.org/10.1039/JR9500002376
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxy-3',4'-methylenedioxyflavone 5379400 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC 372.30 unknown https://doi.org/10.1016/0305-1978(96)88874-0
Meliternin 386319 Click to see COC1=CC(=C(C2=C1C(=O)C(=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0305-1978(96)88874-0
Ternatin 5459184 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC)OC)OC)O 374.30 unknown https://doi.org/10.1039/JR9500002376
https://doi.org/10.1016/0305-1978(96)88874-0

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