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Espeletia schultzii

Espeletia schultzii - 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 UUID643fcd1779499504270434
Scientific name Espeletia schultzii
Authority Wedd.
First published in Chlor. Andina 1: 63 (1856)

Description Top

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Synonyms Top

Scientific name Authority First published in
Espeletia corymbosa Sch.Bip. ex Wedd. Chlor. Andina 1: 63 (1856)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000069144
USDA Plants ESSC
Tropicos 2705617
KEW urn:lsid:ipni.org:names:205179-1
The Plant List gcc-25982
Open Tree Of Life 111377
NCBI Taxonomy 185154
IPNI 205179-1
iNaturalist 336649
GBIF 3105097
Freebase /m/012sp6hj
USDA GRIN 416337
Wikipedia Espeletia_schultzii

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
Alpha-Phellandrene and Alpha-Phellandrene-Rich Essential Oils: A Systematic Review of Biological Activities, Pharmaceutical and Food Applications Radice M, Durofil A, Buzzi R, Baldini E, Martínez AP, Scalvenzi L, Manfredini S Life (Basel) 14-Oct-2022
PMCID:PMC9605662
doi:10.3390/life12101602
PMID:36295037
Natural Products against Sand Fly Vectors of Leishmaniosis: A Systematic Review Pugliese M, Gaglio G, Passantino A, Brianti E, Napoli E Vet Sci 30-Jul-2021
PMCID:PMC8402801
doi:10.3390/vetsci8080150
PMID:34437471
Oxidative Stress Responses of Some Endemic Plants to High Altitudes by Intensifying Antioxidants and Secondary Metabolites Content Hashim AM, Alharbi BM, Abdulmajeed AM, Elkelish A, Hozzein WN, Hassan HM Plants (Basel) 09-Jul-2020
PMCID:PMC7412441
doi:10.3390/plants9070869
PMID:32659963
Near-neighbour optimal outcrossing in the bird-pollinated Anigozanthos manglesii Ayre BM, Roberts DG, Phillips RD, Hopper SD, Krauss SL Ann Bot 21-Jun-2019
PMCID:PMC6798840
doi:10.1093/aob/mcz091
PMID:31115446
The functions of foliar nyctinasty: a review and hypothesis Minorsky PV Biol Rev Camb Philos Soc 11-Jul-2018
PMCID:PMC7379275
doi:10.1111/brv.12444
PMID:29998471
Phytoregionalisation of the Andean páramo Peyre G, Balslev H, Font X PeerJ 01-Jun-2018
PMCID:PMC5985761
doi:10.7717/peerj.4786
PMID:29868254
Geography shapes the phylogeny of frailejones (Espeletiinae Cuatrec., Asteraceae): a remarkable example of recent rapid radiation in sky islands Diazgranados M, Barber JC PeerJ 02-Feb-2017
PMCID:PMC5292030
doi:10.7717/peerj.2968
PMID:28168124
A compendium of temperature responses of Rubisco kinetic traits: variability among and within photosynthetic groups and impacts on photosynthesis modeling Galmés J, Hermida-Carrera C, Laanisto L, Niinemets Ü J Exp Bot 12-Jul-2016
PMCID:PMC5014154
doi:10.1093/jxb/erw267
PMID:27406782
A new species of Coespeletia (Asteraceae, Millerieae) from Venezuela Diazgranados M, Morillo G PhytoKeys 04-Nov-2013
PMCID:PMC3881412
doi:10.3897/phytokeys.28.6378
PMID:24399890
A nomenclator for the frailejones (Espeletiinae Cuatrec., Asteraceae) Diazgranados M PhytoKeys 21-Aug-2012
PMCID:PMC3492930
doi:10.3897/phytokeys.16.3186
PMID:23233810
Total Control – Pollen Presentation and Floral Longevity in Loasaceae (Blazing Star Family) Are Modulated by Light, Temperature and Pollinator Visitation Rates Henning T, Weigend M PLoS One 20-Aug-2012
PMCID:PMC3423403
doi:10.1371/journal.pone.0041121
PMID:22916102
Photosynthetic temperature adaptation of Pinus cembra within the timberline ecotone of the Central Austrian Alps Wieser G, Oberhuber W, Walder L, Spieler D, Gruber A Ann For Sci 01-Apr-2010
PMCID:PMC3047779
doi:10.1051/forest/2009094
PMID:21379394
Cytotoxic and apoptosis-inducing effect of ent-15-oxo-kaur-16-en-19-oic acid, a derivative of grandiflorolic acid from Espeletia schultzii. Ruiz Y, Rodrígues J, Arvelo F, Usubillaga A, Monsalve M, Diez N, Galindo-Castro I Phytochemistry 01-Jan-2008
doi:10.1016/J.PHYTOCHEM.2007.07.025
PMID:17869315
Neue Hydroxyacetophenon‐Derivate aus <i>Espeletia schultzii</i> Wedd. Ferdinand Bohlmann, Nagabhushan Rao Wiley 28-Jun-2007
doi:10.1002/CBER.19731060935
Diterpene vom kaurantyp aus der composite espeletia schultzii (wedd) C.H. Brieskorn, E. Pöhlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)70745-3

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 / Diterpenoids / Kaurane diterpenoids
(1R,4R,5R,9S,10S,13R,15S)-15-acetyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 38349467 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
(1R,4R,5R,9S,10S,13R,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162965674 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
(1R,4S,5R,9S,10S,13R,15S)-15-acetyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46233536 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.025
(1S,4S,9S,10S,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane 101289537 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
ent-Kaurene 11966109 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
Kaur-16-ene 520687 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1016/S0040-4039(00)70745-3
Xylopic acid 494328 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.025
https://doi.org/10.1016/S0040-4039(00)70745-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one 3009228 Click to see CC(C)CC(=O)C1=C(C=CC(=C1)C(=O)C)OC 234.29 unknown https://doi.org/10.1002/CBER.19731060935
1-(5-Acetyl-2-methoxyphenyl)-3-methylbut-2-en-1-one 14104352 Click to see CC(=CC(=O)C1=C(C=CC(=C1)C(=O)C)OC)C 232.27 unknown https://doi.org/10.1002/CBER.19731060935

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