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Paepalanthus bromelioides

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 UUID6440026a711e4947319615
Scientific name Paepalanthus bromelioides
Authority Silveira
First published in Fl. Serr. Min. : 55 (1908)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Persian ذرهگل آناناسی
Chinese 凤梨食虫谷精

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000483665
Tropicos 50300638
KEW urn:lsid:ipni.org:names:180145-2
The Plant List kew-256525
Open Tree Of Life 547964
NCBI Taxonomy 885347
IPNI 180145-2
iNaturalist 1159349
GBIF 5287022
Freebase /m/068ll_
EOL 230963
Wikipedia Paepalanthus_bromelioides

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
Unprecedented variation pattern of plastid genomes and the potential role in adaptive evolution in Poales Wu H, Li DZ, Ma PF BMC Biol 29-Apr-2024
PMCID:PMC11057118
doi:10.1186/s12915-024-01890-5
PMID:38679718
Molecular Phylogenomics Reveals the Deep Evolutionary History of Carnivory across Land Plants Fleck SJ, Jobson RW Plants (Basel) 22-Sep-2023
PMCID:PMC10574757
doi:10.3390/plants12193356
PMID:37836100
Exploring the mycobiota of bromeliads phytotelmata in Brazilian Campos Rupestres dos Santos VL, Silva UC, Santos EH, Resende AA, Dias MF, Cuadros-Orellana S, Marques AR Braz J Microbiol 16-Jun-2023
PMCID:PMC10485200
doi:10.1007/s42770-023-00977-5
PMID:37322328
Therapeutic Effects of Coumarins with Different Substitution Patterns Flores-Morales V, Villasana-Ruíz AP, Garza-Veloz I, González-Delgado S, Martinez-Fierro ML Molecules 06-Mar-2023
PMCID:PMC10005689
doi:10.3390/molecules28052413
PMID:36903660
Host Plant Specificity in Web-Building Spiders Hesselberg T, Boyd KM, Styrsky JD, Gálvez D Insects 24-Feb-2023
PMCID:PMC10051880
doi:10.3390/insects14030229
PMID:36975914
Review on Compounds Isolated from Eriocaulaceae Family and Evaluation of Biological Activities by Machine Learning Moreira LL, de Menezes RP, Scotti L, Scotti MT, Lacerda Júnior V, Borges WD Molecules 24-Oct-2022
PMCID:PMC9654208
doi:10.3390/molecules27217186
PMID:36364014
The digestive systems of carnivorous plants Freund M, Graus D, Fleischmann A, Gilbert KJ, Lin Q, Renner T, Stigloher C, Albert VA, Hedrich R, Fukushima K Plant Physiol 23-May-2022
PMCID:PMC9434158
doi:10.1093/plphys/kiac232
PMID:35604105
Coumarin Derivatives in Inflammatory Bowel Disease Di Stasi LC Molecules 15-Jan-2021
PMCID:PMC7830946
doi:10.3390/molecules26020422
PMID:33467396
Yeast in plant phytotelmata: Is there a “core” community in different localities of rupestrian savannas of Brazil? Morais PB, de Sousa FM, Rosa CA Braz J Microbiol 08-May-2020
PMCID:PMC7455655
doi:10.1007/s42770-020-00286-1
PMID:32385836
Comprehensive Description of Fusarium graminearum Pigments and Related Compounds Cambaza E Foods 05-Oct-2018
PMCID:PMC6209861
doi:10.3390/foods7100165
PMID:30301164
Anti-Helicobacter pylori Activity of Isocoumarin Paepalantine: Morphological and Molecular Docking Analysis Damasceno JP, Rodrigues RP, Gonçalves RD, Kitagawa RR Molecules 12-May-2017
PMCID:PMC6154667
doi:10.3390/molecules22050786
PMID:28498343
In Vitro TNF-α Inhibitory Activity of Brazilian Plants and Anti-Inflammatory Effect of Stryphnodendron adstringens in an Acute Arthritis Model Henriques BO, Corrêa O, Azevedo EP, Pádua RM, de Oliveira VL, Oliveira TH, Boff D, Dias AC, de Souza DG, Amaral FA, Teixeira MM, Castilho RO, Braga FC Evid Based Complement Alternat Med 27-Oct-2016
PMCID:PMC5102725
doi:10.1155/2016/9872598
PMID:27867403
A novel insight into the cost–benefit model for the evolution of botanical carnivory Pavlovič A, Saganová M Ann Bot 06-May-2015
PMCID:PMC4648460
doi:10.1093/aob/mcv050
PMID:25948113
Evaluation of the Effects of Some Brazilian Medicinal Plants on the Production of TNF-α and CCL2 by THP-1 Cells Gusman GS, Campana PR, Castro LC, Castilho RO, Teixeira MM, Braga FC Evid Based Complement Alternat Med 23-Mar-2015
PMCID:PMC4386292
doi:10.1155/2015/497123
PMID:25878716
ContentSnapshots N/A Ann Bot 01-Jan-2013
PMCID:PMC3523661
doi:10.1093/aob/mcs290

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
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
8,8'-Paepalantine dimer 5473234 Click to see 602.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.01.014
Paepalantine 5472703 Click to see 302.28 unknown https://doi.org/10.1002/(SICI)1520-6866(1997)17:2<85::AID-TCM4>3.0.CO;2-A
https://doi.org/10.1016/J.PHYTOCHEM.2007.01.014
https://doi.org/10.1016/0031-9422(90)83056-7
https://doi.org/10.1016/S0031-9422(97)00952-7
https://doi.org/10.1016/S0367-326X(00)00159-3
Tf-26Vx 11962163 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.01.014
Vioxanthin 119072 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.01.014
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
10-hydroxy-5,7-dimethoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]isochromen-1-one 10027431 Click to see CC1=CC2=C(C(=C3C(=CC(=CC3=C2OC)OC)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)O1 464.40 unknown https://doi.org/10.1016/S0031-9422(97)00952-7
10-Hydroxy-5,7-dimethoxy-3-methyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]isochromen-1-one 85096569 Click to see CC1=CC2=C(C(=C3C(=CC(=CC3=C2OC)OC)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)O1 464.40 unknown https://doi.org/10.1016/S0031-9422(97)00952-7

Gallery Top

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Collections Top

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