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Melicope confusa

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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 UUID6440557b9a512728434520
Scientific name Melicope confusa
Authority (Merr.) T.S.Liu
First published in Illustr. Native & Introd. Lign. Pl. Taiwan 2: 876 (1961)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cissus frutescens Blanco Fl. Filip. : 70 (1837)
Euodia confusa Merr. Philipp. J. Sci. 20: 391 (1922)

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-0001242474
Tropicos 50118989
KEW urn:lsid:ipni.org:names:774267-1
The Plant List tro-50118989
Observations.org 368120
IUCN Red List 156220123
IPNI 774267-1
GBIF 3833576
Freebase /m/012bdm6t
EOL 5618942
Elurikkus 421170
Wikipedia Melicope_confusa
Open Tree Of Life 5762631

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
Furoquinoline alkaloids from the leaves ofMelicope confusa Sam Sik Kang, Won Sick Woo Springer Science and Business Media LLC 31-May-2008
doi:10.1007/BF02857699
Furoquinolines with antiplatelet aggregation activity from leaves of Melicope confusa. Chen KS, Chang YL, Teng CM, Chen CF, Wu YC Planta Med 01-Feb-2000
doi:10.1055/S-0029-1243116
PMID:10705744
[Studies on the alkaloids of Melicope confusa (Merr.) Liu]. Yang TH, Lu ST, Wang SJ, Wang TW, Lin JH Yakugaku Zasshi 01-Jul-1971
doi:10.1248/YAKUSHI1947.91.7_782
PMID:5105486

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 / Quinolines and derivatives / Furanoquinolines
4-Methoxyfuro(2,3-b)quinolin-7-ol 135438120 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3)O 215.20 unknown https://doi.org/10.1007/BF02857699
https://doi.org/10.1055/S-0029-1243116
4,6-Dimethoxyfuro[2,3-b]quinolin-7(9h)-one 135538731 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)O 245.23 unknown https://doi.org/10.1007/BF02857699
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one 165368 Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC 245.23 unknown https://doi.org/10.1007/BF02857699
Evolitrine 196980 Click to see COC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC 229.23 unknown https://doi.org/10.1055/S-0029-1243116
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://doi.org/10.1007/BF02857699
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_782
https://doi.org/10.1007/BF02857699
https://doi.org/10.1055/S-0029-1243116
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_782
https://doi.org/10.1007/BF02857699
https://doi.org/10.1055/S-0029-1243116

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