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Mitraria coccinea

Mitraria coccinea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Mitraria coccinea - 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 UUID6440467e42fba563218280
Scientific name Mitraria coccinea
Authority Cav.
First published in Anales Ci. Nat. 3: 281 (1801)

Description Top

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Synonyms Top

Scientific name Authority First published in
Diplocalyx pallidus C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 576 (1845)
Diplocalyx tomentellus C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 576 (1845)
Gesneria chilensis Molina Sag. Stor. Nat. Chili , ed. 2: 140 (1810)
Mitraria pallida Hanst. Linnaea 34: 419 (1865)

Common names Top

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Language Common/alternative name
Chinese 红钟苣苔
Chinese 蔓岩桐

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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No forms added yet.

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
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001064550
Tropicos 14000262
KEW urn:lsid:ipni.org:names:381777-1
The Plant List tro-14000262
Open Tree Of Life 1067288
NCBI Taxonomy 49015
IPNI 381777-1
iNaturalist 527646
GBIF 5591192
EPPO MITCO
EOL 5027977
USDA GRIN 24502

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
The functional mechanism behind the latitudinal pattern of liana diversity: Freeze–thaw embolism reduces the ecological performance of liana species Lobos‐Catalán P, Jiménez‐Castillo M Ecol Evol 19-Sep-2023
PMCID:PMC10509155
doi:10.1002/ece3.10486
PMID:37736281
Frugivore-Mediated Selection in A Habitat Transformation Scenario Fontúrbel FE, Medel R Sci Rep 28-Mar-2017
PMCID:PMC5368566
doi:10.1038/srep45371
PMID:28349942
The temporal build-up of hummingbird/plant mutualisms in North America and temperate South America Abrahamczyk S, Renner SS BMC Evol Biol 10-Jun-2015
PMCID:PMC4460853
doi:10.1186/s12862-015-0388-z
PMID:26058608
Internal Habitat Quality Determines the Effects of Fragmentation on Austral Forest Climbing and Epiphytic Angiosperms Magrach A, Larrinaga AR, Santamaría L PLoS One 31-Oct-2012
PMCID:PMC3485344
doi:10.1371/journal.pone.0048743
PMID:23119096
Ecophysiological Traits May Explain the Abundance of Climbing Plant Species across the Light Gradient in a Temperate Rainforest Gianoli E, Saldaña A, Jiménez-Castillo M PLoS One 07-Jun-2012
PMCID:PMC3369858
doi:10.1371/journal.pone.0038831
PMID:22685611
Changes in Patch Features May Exacerbate or Compensate for the Effect of Habitat Loss on Forest Bird Populations Magrach A, Larrinaga AR, Santamaría L PLoS One 28-Jun-2011
PMCID:PMC3125244
doi:10.1371/journal.pone.0021596
PMID:21738723
Climbing plants in a temperate rainforest understorey: searching for high light or coping with deep shade? Valladares F, Gianoli E, Saldaña A Ann Bot 17-Jun-2011
PMCID:PMC3143042
doi:10.1093/aob/mcr132
PMID:21685433
Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Schäferhoff B, Fleischmann A, Fischer E, Albach DC, Borsch T, Heubl G, Müller KF BMC Evol Biol 12-Nov-2010
PMCID:PMC2992528
doi:10.1186/1471-2148-10-352
PMID:21073690
Mitrariosides, Five Bitter Labdane Glycosides from <i>Mitraria coccinea</i> (Gesneriaceae) Luz Clarena Cárdenas, Jaime Rodríguez, Ricardo Riguera, Maria Cristina Chamy Wiley 19-Jul-2007
doi:10.1002/JLAC.1992199201113
Nectar Concentration and Composition of 26 Species from the Temperate Forest of South America CHALCOFF VR, AIZEN MA, GALETTO L Ann Bot 01-Mar-2006
PMCID:PMC2803636
doi:10.1093/aob/mcj043
PMID:16373370

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4R,5R,6S)-2-[(E)-5-[(1S,4S,4aR,5R,8aR)-4-hydroxy-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-methyloxane-3,4,5-triol 162931638 Click to see CC1C(C(C(C(O1)OCC=C(C)CCC2C(=C)CC(C3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C)O)O)O)O 630.80 unknown https://doi.org/10.1002/JLAC.1992199201113
(2R,3R,4R,5R,6S)-2-[(E)-5-[(1S,4S,4aR,5R,8aR)-4-hydroxy-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-methyloxane-3,4,5-triol 15659906 Click to see CC1C(C(C(C(O1)OCC=C(C)CCC2C(=C)CC(C3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C)O)O)O)O 630.80 unknown https://doi.org/10.1002/JLAC.1992199201113
(2R,3R,4R,5R,6S)-2-[[(1R,4aR,5S,8S,8aR)-8-hydroxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-methyloxane-3,4,5-triol 15659909 Click to see CC1C(C(C(C(O1)OCC2(CCCC3(C2C(CC(=C)C3CCC(=CCO)C)O)C)C)O)O)O 468.60 unknown https://doi.org/10.1002/JLAC.1992199201113
(2R,3R,4S,5S,6R)-2-[(E)-5-[(1S,4S,4aR,5R,8aR)-4-hydroxy-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 15659907 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CC(C3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C)O 646.80 unknown https://doi.org/10.1002/JLAC.1992199201113
(2R,3R,4S,5S,6R)-2-[[(1R,4aR,5S,8S,8aR)-8-hydroxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 15659908 Click to see CC(=CCO)CCC1C(=C)CC(C2C1(CCCC2(C)COC3C(C(C(C(O3)CO)O)O)O)C)O 484.60 unknown https://doi.org/10.1002/JLAC.1992199201113
2-[[8-hydroxy-5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162999714 Click to see CC(=CCO)CCC1C(=C)CC(C2C1(CCCC2(C)COC3C(C(C(C(O3)CO)O)O)O)C)O 484.60 unknown https://doi.org/10.1002/JLAC.1992199201113
2-[[8-hydroxy-5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-methyloxane-3,4,5-triol 163050756 Click to see CC1C(C(C(C(O1)OCC2(CCCC3(C2C(CC(=C)C3CCC(=CCO)C)O)C)C)O)O)O 468.60 unknown https://doi.org/10.1002/JLAC.1992199201113
2-[5-[4-hydroxy-5,8a-dimethyl-2-methylidene-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162926493 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CC(C3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C)O 646.80 unknown https://doi.org/10.1002/JLAC.1992199201113
2-[5-[4-hydroxy-5,8a-dimethyl-2-methylidene-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-methyloxane-3,4,5-triol 162931637 Click to see CC1C(C(C(C(O1)OCC=C(C)CCC2C(=C)CC(C3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C)O)O)O)O 630.80 unknown https://doi.org/10.1002/JLAC.1992199201113
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1002/JLAC.1992199201113
Calceolarioside C 45360240 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 610.60 unknown https://doi.org/10.1002/JLAC.1992199201113
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1002/JLAC.1992199201113

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