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Internal ID UUID644001cc2309a398353447
Scientific name Piper glabratum
Authority (Kunth) Steud.
First published in Nomencl. Bot. ed. 2, 2: 341 1841

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Synonyms Top

Scientific name Authority First published in
Piper ledebourii C.DC. Prodr. 16(1): 281 (1869)
Steffensia glabrata Kunth Linnaea 13: 632 (1840)
Artanthe glabrata Miq. Syst. Piperac. : 481 (1844)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay
    • Western South America
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000478951
Tropicos 25003483
KEW urn:lsid:ipni.org:names:681516-1
The Plant List kew-2558055
Open Tree Of Life 416677
NCBI Taxonomy 405326
IPNI 681516-1
GBIF 4189094

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 Ethanolic Extract of Piper glabratum Kunth Is Teratogenic and Interferes with the Ossification Process of Swiss Mice Fetuses Nunes RC, Neves SC, Salustriano FR, Vilela ML, do Nascimento VA, Arunachalam K, Gomes RD, Kassuya CA, Mota JD, Oliveira RJ Pharmaceuticals (Basel) 11-Mar-2023
PMCID:PMC10051201
doi:10.3390/ph16030430
PMID:36986529
Flavonoids from Piper Species as Promising Antiprotozoal Agents against Giardia intestinalis: Structure-Activity Relationship and Drug-Likeness Studies Ticona JC, Bilbao-Ramos P, Amesty Á, Flores N, Dea-Ayuela MA, Bazzocchi IL, Jiménez IA Pharmaceuticals (Basel) 10-Nov-2022
PMCID:PMC9695682
doi:10.3390/ph15111386
PMID:36355559
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Prototyping a Knowledge-Based System to Identify Botanical Extracts for Plant Health in Sub-Saharan Africa Silvie PJ, Martin P, Huchard M, Keip P, Gutierrez A, Sarter S Plants (Basel) 29-Apr-2021
PMCID:PMC8146496
doi:10.3390/plants10050896
PMID:33946682
Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) on the “Offensive” in Africa: Prospects for Integrated Management Initiatives Tarusikirwa VL, Machekano H, Mutamiswa R, Chidawanyika F, Nyamukondiwa C Insects 06-Nov-2020
PMCID:PMC7694550
doi:10.3390/insects11110764
PMID:33171892
Essential Oils as a Feed Additives: Pharmacokinetics and Potential Toxicity in Monogastric Animals Horky P, Skalickova S, Smerkova K, Skladanka J Animals (Basel) 13-Jun-2019
PMCID:PMC6617186
doi:10.3390/ani9060352
PMID:31200591
Piper Species: A Comprehensive Review on Their Phytochemistry, Biological Activities and Applications Salehi B, Zakaria ZA, Gyawali R, Ibrahim SA, Rajkovic J, Shinwari ZK, Khan T, Sharifi-Rad J, Ozleyen A, Turkdonmez E, Valussi M, Tumer TB, Monzote Fidalgo L, Martorell M, Setzer WN Molecules 07-Apr-2019
PMCID:PMC6479398
doi:10.3390/molecules24071364
PMID:30959974
Extract of Nicotiana tabacum as a potential control agent of Grapholita molesta (Lepidoptera: Tortricidae) Sarker S, Lim UT PLoS One 23-Aug-2018
PMCID:PMC6107112
doi:10.1371/journal.pone.0198302
PMID:30138428
Essential Oils from Neotropical Piper Species and Their Biological Activities da Silva JK, da Trindade R, Alves NS, Figueiredo PL, Maia JG, Setzer WN Int J Mol Sci 14-Dec-2017
PMCID:PMC5751174
doi:10.3390/ijms18122571
PMID:29240662
Amides from Piper as a Diuretic: Behind the Ethnopharmacological Uses of Piper glabratum Kunth Prando TB, Baciquete TD, Vieira JA, Bressan J, Gasparotto FM, Jesus DR, Cardozo Junior EL, Lourenço EL, Gasparotto Junior A Evid Based Complement Alternat Med 01-Jul-2014
PMCID:PMC4102017
doi:10.1155/2014/615109
PMID:25101133
Natural Products as a Source for Treating Neglected Parasitic Diseases Ndjonka D, Rapado LN, Silber AM, Liebau E, Wrenger C Int J Mol Sci 06-Feb-2013
PMCID:PMC3588050
doi:10.3390/ijms14023395
PMID:23389040
Plant-Derived Antimalarial Agents: New Leads and Efficient Phytomedicines. Part II. Non-Alkaloidal Natural Products Batista R, de Jesus Silva Júnior A, de Oliveira AB Molecules 13-Aug-2009
PMCID:PMC6254980
doi:10.3390/molecules14083037
PMID:19701144
Benzoic acid derivatives from Piper species and their antiparasitic activity. Flores N, Jiménez IA, Giménez A, Ruiz G, Gutiérrez D, Bourdy G, Bazzocchi IL J Nat Prod 01-Sep-2008
doi:10.1021/NP800104P
PMID:18712933

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Nervogenic acid 5320129 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C(=O)O)C 274.35 unknown https://doi.org/10.1021/NP800104P
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4-methoxy-5-(3-methylbut-2-enyl)benzoic acid 25111595 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)C=CC(C)(C)O)OC)C 304.40 unknown https://doi.org/10.1021/NP800104P
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-dihydroxy-5-(2-hydroxy-3-methylbut-3-enyl)benzoate 102411349 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)CC(C(=C)C)O 266.29 unknown https://doi.org/10.1021/NP800104P
ethyl 3,4-dihydroxy-5-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 163007224 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)CC(C(=C)C)O 266.29 unknown https://doi.org/10.1021/NP800104P
Ethyl 4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)benzoate 102411350 Click to see CCOC(=O)C1=CC(=C(C=C1)O)CC(C(=C)C)O 250.29 unknown https://doi.org/10.1021/NP800104P
ethyl 4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 163016924 Click to see CCOC(=O)C1=CC(=C(C=C1)O)CC(C(=C)C)O 250.29 unknown https://doi.org/10.1021/NP800104P
Methyl 3-(2-acetyloxy-3-methylbut-3-enyl)-4,5-dihydroxybenzoate 102411351 Click to see CC(=C)C(CC1=C(C(=CC(=C1)C(=O)OC)O)O)OC(=O)C 294.30 unknown https://doi.org/10.1021/NP800104P
methyl 3-[(2R)-2-acetyloxy-3-methylbut-3-enyl]-4,5-dihydroxybenzoate 163025320 Click to see CC(=C)C(CC1=C(C(=CC(=C1)C(=O)OC)O)O)OC(=O)C 294.30 unknown https://doi.org/10.1021/NP800104P
Methyl 3,4-dihydroxy-5-(2-hydroxy-3-methylbut-3-enyl)benzoate 25058113 Click to see CC(=C)C(CC1=C(C(=CC(=C1)C(=O)OC)O)O)O 252.26 unknown https://doi.org/10.1021/NP800104P
methyl 3,4-dihydroxy-5-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 163091108 Click to see CC(=C)C(CC1=C(C(=CC(=C1)C(=O)OC)O)O)O 252.26 unknown https://doi.org/10.1021/NP800104P
Methyl 4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)benzoate 13846908 Click to see CC(=C)C(CC1=C(C=CC(=C1)C(=O)OC)O)O 236.26 unknown https://doi.org/10.1021/NP800104P
Methyl 4-hydroxy-3-(3'-methyl-2'-butenyl)benzoate 127925 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)OC)O)C 220.26 unknown https://doi.org/10.1021/NP800104P
methyl 4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 92466200 Click to see CC(=C)C(CC1=C(C=CC(=C1)C(=O)OC)O)O 236.26 unknown https://doi.org/10.1021/NP800104P
Methyl 4-hydroxy-3-pent-3-en-2-ylbenzoate 163194076 Click to see CC=CC(C)C1=C(C=CC(=C1)C(=O)OC)O 220.26 unknown https://doi.org/10.1021/NP800104P

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