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Piper scutatum

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 UUID68f9141ddadbb679313246
Scientific name Piper scutatum
Authority Raddi
First published in Nuovo Giorn. Lett., Sci. 17(40): 3 1828

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Piper scutifolium Yunck. Bol. Inst. Bot. (São Paulo) 3: 123 (1966)

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

Links to other databases Top

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Database ID/link to page
Tropicos 50256748
KEW urn:lsid:ipni.org:names:199146-2
The Plant List tro-50256748
Open Tree Of Life 915638
NCBI Taxonomy 538347
IPNI 199146-2
GBIF 4190234
World Flora Online wfo-1200067985

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
Structural insights on the interaction potential of natural leads against major protein targets of SARS-CoV-2: Molecular modelling, docking and dynamic simulation studies Skariyachan S, Gopal D, Muddebihalkar AG, Uttarkar A, Niranjan V Comput Biol Med 13-Mar-2021
PMCID:PMC7954774
doi:10.1016/j.compbiomed.2021.104325
PMID:33751995
Participatory methods on the recording of traditional knowledge about medicinal plants in Atlantic forest, Ubatuba, São Paulo, Brazil Sauini T, Stern da Fonseca-Kruel V, Baptistela Yazbek P, Matta P, Cassas F, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Angelica Silva Gomes M, José Francischetti Garcia R, Honda S, Felipe Domingues Passero L, Esteves Conde B, Rodrigues E PLoS One 07-May-2020
PMCID:PMC7205242
doi:10.1371/journal.pone.0232288
PMID:32379779
Efficacy of some natural compounds as antifungal agents Vengurlekar S, Sharma R, Trivedi P Pharmacogn Rev 01-Jul-2012
PMCID:PMC3459460
doi:10.4103/0973-7847.99942
PMID:23055634
Antifungal activity of natural and synthetic amides from Piper species Joaquim V. Marques, Alberto de Oliveira, Ludmila Raggi, Maria C. M. Young, Massuo J. Kato FapUNIFESP (SciELO) 24-Feb-2011
doi:10.1590/S0103-50532010001000003
Antifungal amides from Piper scutifolium and Piper hoffmanseggianum. Marques JV, Kitamura RO, Lago JH, Young MC, Guimarães EF, Kato MJ J Nat Prod 01-Dec-2007
doi:10.1021/NP070347G
PMID:18031016

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 / Phenol ethers / Anisoles
6-(4-methoxyphenyl)-N-(2-methylpropyl)hexa-2,4-dienamide 161479 Click to see 273.37 unknown https://doi.org/10.1021/NP070347G
Piperovatine 5374352 Click to see 273.37 unknown https://doi.org/10.1021/NP070347G
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Aspergoterpenin B 146684129 Click to see 296.31 unknown https://doi.org/10.1590/S0103-50532010001000003
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 71716352 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://doi.org/10.1021/NP070347G
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
N-[(3Z)-3-(2-amino-4-oxo-1H-imidazol-5-ylidene)propyl]-4,5-dibromo-1H-pyrrole-2-carboxamide 10069822 Click to see 405.05 unknown https://doi.org/10.1021/NP070347G
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
Methyl 3-[5-(1,3-benzodioxol-5-yl)penta-2,4-dienoylamino]-2,2-dimethylpropanoate 163099862 Click to see CC(C)(CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2)C(=O)OC 331.40 unknown https://doi.org/10.1590/S0103-50532010001000003
> Organoheterocyclic compounds / Benzodioxoles
[1-[5-(1,3-Benzodioxol-5-yl)penta-2,4-dienoylamino]-2-methylpropan-2-yl] acetate 163037031 Click to see 331.40 unknown https://doi.org/10.1021/NP070347G
5-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)penta-2,4-dienamide 276752 Click to see CC(C)CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2 273.33 unknown https://doi.org/10.1590/S0103-50532010001000003
https://doi.org/10.1021/NP070347G
Corcovadine 44445528 Click to see CC(=O)OC(C)(C)CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2 331.40 unknown https://doi.org/10.1021/NP070347G
Piperlonguminine 5320621 Click to see CC(C)CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2 273.33 unknown https://doi.org/10.1590/S0103-50532010001000003
https://doi.org/10.1021/NP070347G
Scutifolamide A 24763329 Click to see CC(C)CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2 273.33 unknown https://doi.org/10.1021/NP070347G

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