Loasa acerifolia - Unknown
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Internal ID UUID64404790dd212353329586
Scientific name Loasa acerifolia
Authority Domb. ex Juss.
First published in Ann. Mus. Natl. Hist. Nat. 5: 24 (1804)

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Scientific name Authority First published in
Loasa lechleriana Miq. Berberid. Amer. Austral. : 55 (1857)
Loasa solanifolia Gay Fl. Chil. 2: 449 (1847)
Loasa furcata Phil. Anales Univ. Chile 27: 328 (1865)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

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Database ID/link to page
World Flora Online wfo-0001073577
Tropicos 18900082
KEW urn:lsid:ipni.org:names:545159-1
The Plant List tro-18900082
Open Tree Of Life 442680
NCBI Taxonomy 230024
IPNI 545159-1
GBIF 4021796
EOL 5740464

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Delayed differentiation of epidermal cells walls can underlie pedomorphosis in plants: the case of pedomorphic petals in the hummingbird-pollinated Caiophora hibiscifolia (Loasaceae, subfam. Loasoideae) species Strelin MM, Zattara EE, Ullrich K, Schallenberg-Rüdinger M, Rensing S EvoDevo 03-Jan-2022
PMCID:PMC8725396
doi:10.1186/s13227-021-00186-x
PMID:34980236
Exploring the ontogenetic scaling hypothesis during the diversification of pollination syndromes in Caiophora (Loasaceae, subfam. Loasoideae) Strelin MM, Benitez-Vieyra S, Fornoni J, Klingenberg CP, Cocucci AA Ann Bot 06-Apr-2016
PMCID:PMC4845809
doi:10.1093/aob/mcw035
PMID:27056974
Loasafolioside, a minor iridoid dimer from the leaves of Loasa acerifolia1The investigation here presented is part of a joint venture between the Institute of Systematic Botany and the Institute of Pharmaceutical Biology, Munich, for the investigation of the biology and systematics of Loasaceae and a screening program for antiinflammatory plant drugs from ethnopharmacology.1 Andreas A Müller, Maximilian Weigend Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(98)00560-3
Iridoid glucosides—chemotaxonomic markers in Loasoideae A.A. Müller, J.K. Kufer, K.G. Dietl, S.A. Reiter, J. Grau, M. Weigend Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00744-4
A dimeric iridoid from loasa acerifolia. Müller AA, Kufer JK, Dietl KG, Weigend M Phytochemistry 20-Nov-1998
doi:10.1016/S0031-9422(98)00194-0
PMID:11711085
Iridoids from Loasa acerifolia. Müller AA, Weigend M Phytochemistry 01-Sep-1998
doi:10.1016/S0031-9422(97)01000-5
PMID:9745765

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 glycosides
methyl (3R,4R,4aS,6R,7R,7aS)-6-[2-[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-3-hydroxy-7-methyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyran-4-carboxylate 162979300 Click to see CC1C(CC2C1COC(C2C(=O)OC)O)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C 616.60 unknown https://doi.org/10.1016/S0031-9422(98)00560-3
methyl (4R,4aS,6S,7R,7aS)-6-[2-[3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-3-hydroxy-7-methyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyran-4-carboxylate 100989554 Click to see CC1C(CC2C1COC(C2C(=O)OC)O)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C 616.60 unknown https://doi.org/10.1016/S0031-9422(98)00744-4
methyl (4S,4aS,6S,7R,7aS)-6-[2-[(2S,3R,4R)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-7-methyl-3-oxo-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-4-carboxylate 163190614 Click to see CC1C(CC2C1COC(=O)C2C(=O)OC)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C 614.60 unknown https://doi.org/10.1016/S0031-9422(98)00194-0
methyl 1,6-bis[[2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy]-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163047543 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC(=O)CC5C(C(OC=C5C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)C=C 1000.90 unknown https://doi.org/10.1016/S0031-9422(97)01000-5
methyl 6-[2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-3-hydroxy-7-methyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyran-4-carboxylate 162979299 Click to see CC1C(CC2C1COC(C2C(=O)OC)O)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C 616.60 unknown https://doi.org/10.1016/S0031-9422(98)00560-3
methyl 6-[2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-7-methyl-3-oxo-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-4-carboxylate 163099371 Click to see CC1C(CC2C1COC(=O)C2C(=O)OC)OC(=O)CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C 614.60 unknown https://doi.org/10.1016/S0031-9422(98)00194-0
Secoxyloganin 162868 Click to see COC(=O)C1=COC(C(C1CC(=O)O)C=C)OC2C(C(C(C(O2)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(98)00194-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl (1S,6S,7R)-6-[2-[(2S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 102586546 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)CC4C(C(OC=C4C(=O)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C 776.70 unknown https://doi.org/10.1016/S0031-9422(97)01000-5

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