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Internal ID UUID644061d12414a534436262
Scientific name Raputiarana heptaphylla
Authority (Pittier) Kallunki
First published in Monogr. Syst. Bot. Missouri Bot. Gard. 129: 803 (2014)

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Synonyms Top

Scientific name Authority First published in
Raputia heptaphylla Pittier Contr. Fl. Venez. : 5 (1921)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001342622
Tropicos 100406849
KEW urn:lsid:ipni.org:names:77147509-1
Open Tree Of Life 6126585
NCBI Taxonomy 2894648
IUCN Red List 197786825
IPNI 77147509-1
GBIF 8074722

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
Ruta angustifolia Pers. (Narrow-Leaved Fringed Rue): Pharmacological Properties and Phytochemical Profile Bailly C Plants (Basel) 13-Feb-2023
PMCID:PMC9959652
doi:10.3390/plants12040827
PMID:36840175
Quinolone: a versatile therapeutic compound class Dube PS, Legoabe LJ, Beteck RM Mol Divers 17-Dec-2022
PMCID:PMC9758687
doi:10.1007/s11030-022-10581-8
PMID:36527518
Antileishmanial activity of synthetic analogs of the naturally occurring quinolone alkaloid N-methyl-8-methoxyflindersin Torres Suarez E, Granados-Falla DS, Robledo SM, Murillo J, Upegui Y, Delgado G PLoS One 28-Dec-2020
PMCID:PMC7769561
doi:10.1371/journal.pone.0243392
PMID:33370295
Biologically Active Quinoline and Quinazoline Alkaloids Part II Shang XF, Morris-Natschke SL, Yang GZ, Liu YQ, Guo X, Xu XS, Goto M, Li JC, Zhang JY, Lee KH Med Res Rev 27-Feb-2018
PMCID:PMC6105521
doi:10.1002/med.21492
PMID:29485730
Cytotoxicity and anti-Leishmania amazonensis activity of Citrus sinensis leaf extracts Garcia AR, Amaral AC, Azevedo MM, Corte-Real S, Lopes RC, Alviano CS, Pinheiro AS, Vermelho AB, Rodrigues IA Pharm Biol 19-May-2017
PMCID:PMC6130762
doi:10.1080/13880209.2017.1325380
PMID:28524774
The Chemistry and Pharmacology of Citrus Limonoids Gualdani R, Cavalluzzi MM, Lentini G, Habtemariam S Molecules 13-Nov-2016
PMCID:PMC6273274
doi:10.3390/molecules21111530
PMID:27845763
Natural Products: Insights into Leishmaniasis Inflammatory Response Rodrigues IA, Mazotto AM, Cardoso V, Alves RL, Amaral AC, Silva JR, Pinheiro AS, Vermelho AB Mediators Inflamm 11-Oct-2015
PMCID:PMC4619978
doi:10.1155/2015/835910
PMID:26538837
seco-limonoids and quinoline alkaloids from Raputia heptaphylla and their antileishmanial activity. Coy Barrera CA, Coy Barrera ED, Granados Falla DS, Delgado Murcia G, Cuca Suarez LE Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.855
PMID:21720036

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
11-(Furan-3-yl)-4'-hydroxy-5-(2-hydroxypropan-2-yl)-2,10-dimethylspiro[12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-6,5'-oxane]-2',3,13-trione 4482268 Click to see CC12CCC3C(C14C(O4)C(=O)OC2C5=COC=C5)(C(=O)CC(C36COC(=O)CC6O)C(C)(C)O)C 488.50 unknown https://doi.org/10.1248/CPB.59.855
Ichangin 441801 Click to see CC12CCC3C(C14C(O4)C(=O)OC2C5=COC=C5)(C(=O)CC(C36COC(=O)CC6O)C(C)(C)O)C 488.50 unknown https://doi.org/10.1248/CPB.59.855
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
6-Methyl-[1]benzofuro[2,3-b]quinolin-11-one 12621905 Click to see CN1C2=CC=CC=C2C(=O)C3=C1OC4=CC=CC=C43 249.26 unknown https://doi.org/10.1248/CPB.59.855
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1248/CPB.59.855
Flindersiamine 68221 Click to see COC1=C2C=COC2=NC3=C(C4=C(C=C31)OCO4)OC 273.24 unknown https://doi.org/10.1248/CPB.59.855
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1248/CPB.59.855
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/CPB.59.855
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
N-methyl-2-phenoxyquinolin-4(1h)-one 53348958 Click to see CN1C2=CC=CC=C2C(=O)C=C1OC3=CC=CC=C3 251.28 unknown https://doi.org/10.1248/CPB.59.855
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C 271.31 unknown https://doi.org/10.1248/CPB.59.855

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