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Ertela trifolia

Ertela trifolia - 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 UUID64401b3a7c415144881551
Scientific name Ertela trifolia
Authority Kuntze
First published in Revis. Gen. Pl. 1: 100 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Moniera trifolia L. Syst. Nat. ed. 10 , 2: 1153 (1759)
Aubletia trifoliata Pers. Syn. Pl. [Persoon] 2(2): 638. 1807
Monnieria trifolia L. Syst. Nat., ed. 10. 2: 1153. 1759 [7 Jun 1759]

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000677357
Tropicos 28101431
INPN 734944
KEW urn:lsid:ipni.org:names:96244-2
The Plant List kew-2798705
Open Tree Of Life 6126246
NCBI Taxonomy 2820928
IPNI 96244-2
iNaturalist 700596
GBIF 3832240
EPPO MNJTR
USDA GRIN 403324

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
Herbal bathing: an analysis of variation in plant use among Saramaccan and Aucan Maroons in Suriname van ‘t Klooster CI, Haabo V, Ruysschaert S, Vossen T, van Andel TR J Ethnobiol Ethnomed 15-Mar-2018
PMCID:PMC5856216
doi:10.1186/s13002-018-0216-9
PMID:29544521
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
Alcaloides β-indolopiridoquinazolínicos de Esenbeckia grandiflora mart. (Rutaceae) Ana Helena Januário, Paulo Cezar Vieira, Maria Fátima das Graças Fernandes d Silva, João Batista Fernandes, Jorge José de Brito Silva, Lucia Maria Conserva FapUNIFESP (SciELO) 03-Dec-2009
doi:10.1590/S0100-40422009000800010
Structures of Montrifoline and Delbine: Two New Furoquinoline Alkaloids from Monnieria trifolia L Jnanabrata Bhattacharyya, Leila M. Serur The Japan Institute of Heterocyclic Chemistry 10-Mar-2009
doi:10.3987/R-1981-03-0371
The Minor Alkalods of Monnieria trifolia L. Jnanabrata Bhattacharyya, Leila M. Serur The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1983-06-1063
Furoquinoline alkaloids of Ertela (Monnieria) trifolia (L.) Kuntze from the Suriname rainforest. Cao S, Al-Rehaily AJ, Brodie P, Wisse JH, Moniz E, Malone S, Kingston DG Phytochemistry 01-Jan-2008
PMCID:PMC2245804
doi:10.1016/J.PHYTOCHEM.2007.08.009
PMID:17889047
Furoquinoline Alkaloids of Ertela (Monnieria) trifolia (L.) Kuntze from the Suriname Rainforest Cao S, Al-Rehaily AJ, Brodie P, Wisse JH, Moniz E, Malone S, Kingston DG Phytochemistry 21-Sep-2007
PMCID:PMC2245804
doi:10.1016/j.phytochem.2007.08.009
PMID:17889047
C-Glycosylflavones from Monnieria trifolia A. Keita, J. Gleye, E. Stanislas, I. Fouraste American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A038
Isolation of the Alkaloids of Monnieria trifolia J. Bhattacharyya, L. M. Serur, U. O. Cheriyan American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50032A026

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
> Lignans, neolignans and related compounds / Furanoid lignans
Fargesin 10926754 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
Delbine 101352910 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)O 425.50 unknown https://doi.org/10.1021/NP50032A026
https://doi.org/10.3987/R-1983-06-1063
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one 163033172 Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O 328.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown https://doi.org/10.1021/NP50032A026
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methoxy-3-methylbutan-2-ol 163033709 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)OC 361.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutane-2,3-diol 162911907 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.3987/R-1981-03-0371
(2S)-3-chloro-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutan-2-ol 162998818 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)Cl 365.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
(2S)-3-chloro-1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbutan-2-ol 162960518 Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)Cl 365.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
4,7-Dimethoxyfuro[2,3-b]quinolin-6-ol 86002753 Click to see COC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)O 245.23 unknown https://doi.org/10.1590/S0100-40422009000800010
https://doi.org/10.3987/R-1981-03-0371
7-Isopentenyloxy-gamma-fagarine 12110169 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)C 313.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
Evoxine 73416 Click to see CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1021/NP50032A026
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1021/NP50032A026
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP50032A026
Nkolbisine 157014 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.3987/R-1981-03-0371
https://doi.org/10.1021/NP50032A026
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP50032A026
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2245804/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 133562575 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50040A038
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 138454316 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50040A038
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50040A038
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50040A038
Vicenin 3 185958 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50040A038

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