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Galipea trifoliata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401d127371f185143276
Scientific name Galipea trifoliata
Authority Aubl.
First published in Hist. Pl. Guiane 2: 662 (1775)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Sciuris trifoliata Nees & Mart. Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 11: 155 (1823)
Sciuris corymbosa Spreng. Syst. Veg. 1: 38 (1824)
Galipea fissa Miq. Stirp. Surinam. Select. : 64 (1851)
Galipea stricta Rusby

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Central America
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000693919
Tropicos 28100610
INPN 734949
KEW urn:lsid:ipni.org:names:773692-1
The Plant List kew-2816448
Open Tree Of Life 3942547
NCBI Taxonomy 1331800
IUCN Red List 179315245
IPNI 773692-1
GBIF 3834253
EOL 5622628

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
Galipein, a coumarin from Galipea trifoliata K.R. Wirasutisna, J. Gleye, C. Moulis, E. Stanislas, C. Moretti Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82516-9
O-glycosyl-C-glycosylflavones from Galipea trifoliata Amri Bakhtiar, Jacqueline Gleye, Claude Moulis, Isabelle Fouraste Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86902-2
C-glycosylflavones from Galipea trifoliata Amri Bakhtiar, Jacqueline Gleye, Claude Moulis, Isabelle Fouraste, Edouard Stanislas Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85461-N

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
> Benzenoids / Anthracenes
Ramosin 363268 Click to see 672.60 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
[8-(3-Methylbut-2-enoyl)-2-oxochromen-7-yl] 3-methylbut-2-enoate 162970193 Click to see CC(=CC(=O)C1=C(C=CC2=C1OC(=O)C=C2)OC(=O)C=C(C)C)C 326.30 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
7-(3-Methylbut-2-enoxy)-8-(3-prop-1-en-2-yloxiran-2-yl)chromen-2-one 163007515 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
7-(3-methylbut-2-enoxy)-8-[(2S,3S)-3-prop-1-en-2-yloxiran-2-yl]chromen-2-one 163007517 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
7-Methoxy-8-(3-prop-1-en-2-yloxiran-2-yl)chromen-2-one 5320515 Click to see 258.27 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
7-Methoxy-8-[(2S,3S)-3-prop-1-en-2-yloxiran-2-yl]chromen-2-one 13917405 Click to see 258.27 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
Phebalosin 188300 Click to see 258.27 unknown https://doi.org/10.1016/S0031-9422(00)82516-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 369636 Click to see 446.40 unknown https://doi.org/10.1016/0031-9422(90)85461-N
6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 101422753 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 74977779 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 14730433 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
Spinosin 155692 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
Swertisin 124034 Click to see 446.40 unknown https://doi.org/10.1016/0031-9422(90)85461-N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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/10.1016/0031-9422(90)85461-N
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(90)85461-N
8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 73157712 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 73108154 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
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/10.1016/0031-9422(90)85461-N
Isospinosin 11801844 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2
Isoswertisin 44258317 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/0031-9422(90)85461-N
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/10.1016/0031-9422(90)85461-N
Vitexin 2''-O-xyloside 11972300 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(00)86902-2

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