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Piper swartzianum

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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 UUID64404a728783b999264686
Scientific name Piper swartzianum
Authority C.DC.
First published in Prodr. 16(1): 265 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper torbecanum Trel. Repert. Spec. Nov. Regni Veg. 23: 310 (1927)
Artanthe swartziana Miq. Syst. Piperac. : 490 (1844)

Common names Top

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Language Common/alternative name
English spanish elder

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
  • Southern America
    • Caribbean
      • Dominican Republic
      • Haiti
      • Puerto Rico

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001092412
USDA Plants PISW
Tropicos 25001140
KEW urn:lsid:ipni.org:names:683631-1
The Plant List tro-25001140
Open Tree Of Life 366805
NCBI Taxonomy 405344
IPNI 683631-1
GBIF 3086327
EOL 596611

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
In vitro metabolism of the alkaloid piplartine by rat liver microsomes. Marques LM, da Silva EA Jr, Gouvea DR, Vessecchi R, Pupo MT, Lopes NP, Kato MJ, de Oliveira AR J Pharm Biomed Anal 01-Jul-2014
doi:10.1016/J.JPBA.2014.02.020
PMID:24667565
Piperine production by endophytic fungus Periconia sp. isolated from Piper longum L. Verma VC, Lobkovsky E, Gange AC, Singh SK, Prakash S J Antibiot (Tokyo) 01-Jun-2011
doi:10.1038/JA.2011.27
PMID:21505472
In vitro TRPV1 activity of piperine derived amides. Correa EA, Högestätt ED, Sterner O, Echeverri F, Zygmunt PM Bioorg Med Chem 01-May-2010
doi:10.1016/J.BMC.2010.03.013
PMID:20381363
Piperamides and their derivatives as potential anti-trypanosomal agents Fernando Cotinguiba, Luis Octávio Regasini, Vanderlan da Silva Bolzani, Hosana Maria Debonsi, Gabriela Duó Passerini, Regina Maria Barretto Cicarelli, Massuo Jorge Kato, Maysa Furlan Springer Science and Business Media LLC 12-Jan-2009
doi:10.1007/S00044-008-9161-9
Isobutyl amides--potent compounds for controlling Diatraea saccharalis. Debonsi HM, Miranda JE, Murata AT, de Bortoli SA, Kato MJ, Bolzani VS, Furlan M Pest Manag Sci 01-Jan-2009
doi:10.1002/PS.1643
PMID:18785219
In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine. Bezerra DP, de Castro FO, Alves AP, Pessoa C, de Moraes MO, Silveira ER, Lima MA, Elmiro FJ, de Alencar NM, Mesquita RO, Lima MW, Costa-Lotufo LV J Appl Toxicol 01-Mar-2008
doi:10.1002/JAT.1261
PMID:17541943
New amide alkaloids from the roots of Piper nigrum. Wei K, Li W, Koike K, Pei Y, Chen Y, Nikaido T J Nat Prod 01-Jun-2004
doi:10.1021/NP030475E
PMID:15217283
Quantitative determination of anti-fungal and insecticide amides in adult plants, plantlets and callus from Piper tuberculatum by reverse-phase high-performance liquid chromatography. Navickiene HM, Bolzani Vda S, Kato MJ, Pereira AM, Bertoni BW, França SC, Furlan M Phytochem Anal 01-Sep-2003
doi:10.1002/PCA.716
PMID:14515999
Piplaroxide, an Ant-Repellent Piperidine Epoxide from <i>Piper tuberculatum</i> Mark A. Capron, David F. Wiemer American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960379W
Cepharanone B from Piper tuberculatum João Xavier de Araújo Júnior, Maria Célia de Oliveira Chaves, Emidio Vasconcelos Leitão da-Cunha, Alexander I. Gray Elsevier BV 26-Jul-2002
doi:10.1016/S0305-1978(98)00083-0
Piplartine-dimer A, a new alkaloid from Piper tuberculatum Raimundo Braz Filho, Miriam P. De Souza, Maria Elisa O. Mattos Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85125-4
Piperdardine, a piperidine alkaloid from Piper tuberculatum João Xavier De Araujo-Junior, Emidio V.L. Da-Cunha, Maria Célia De O. Chaves, Alexander I. Gray Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(96)00503-1
Antifungal amides from Piper arboreum and Piper tuberculatum. Vasques da Silva R, Navickiene HM, Kato MJ, Bolzani Vda S, Méda CI, Young MC, Furlan M Phytochemistry 01-Mar-2002
doi:10.1016/S0031-9422(01)00431-9
PMID:11853747
Two amides from Piper tuberculatum fruits. Leitão da-Cunha EV, de Oliveira Chaves MC Fitoterapia 01-Feb-2001
doi:10.1016/S0367-326X(00)00271-9
PMID:11223237
Antifungal amides from Piper hispidum and Piper tuberculatum. Navickiene HM, Alécio AC, Kato MJ, Bolzani VD, Young MC, Cavalheiro AJ, Furlan M Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00226-0
PMID:11130674

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
> Alkaloids and derivatives
Piperidine, 1-(5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl)- 4840 Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 285.34 unknown https://doi.org/10.1038/JA.2011.27
> Alkaloids and derivatives / Aristolactams
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1016/S0305-1978(98)00083-0
> Benzenoids / Phenol ethers / Anisoles
Methyl 3-(3,4,5-trimethoxyphenyl)propanoate 2797678 Click to see COC1=CC(=CC(=C1OC)OC)CCC(=O)OC 254.28 unknown https://doi.org/10.1016/S0031-9422(01)00431-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E)-N-[(2R)-butan-2-yl]deca-2,4-dienamide 154497067 Click to see CCCCCC=CC=CC(=O)NC(C)CC 223.35 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
n-Isobutyl-2,4-decadienamide 3009280 Click to see CCCCCC=CC=CC(=O)NCC(C)C 223.35 unknown https://doi.org/10.1016/S0031-9422(01)00431-9
Pellitorine 5318516 Click to see CCCCCC=CC=CC(=O)NCC(C)C 223.35 unknown https://doi.org/10.1002/PCA.716
https://doi.org/10.1016/S0367-326X(00)00271-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(2E,4E)-6-hydroxy-N-[5-[[(2E,4E)-6-hydroxy-3-methylhepta-2,4-dienoyl]amino]-2,2,4,4-tetramethyl-3-oxopentyl]-3-methylhepta-2,4-dienamide 5319747 Click to see CC(C=CC(=CC(=O)NCC(C)(C)C(=O)C(C)(C)CNC(=O)C=C(C)C=CC(C)O)C)O 448.60 unknown https://doi.org/10.1016/S0031-9422(01)00431-9
6-hydroxy-N-[5-[(6-hydroxy-3-methylhepta-2,4-dienoyl)amino]-2,2,4,4-tetramethyl-3-oxopentyl]-3-methylhepta-2,4-dienamide 78385308 Click to see CC(C=CC(=CC(=O)NCC(C)(C)C(=O)C(C)(C)CNC(=O)C=C(C)C=CC(C)O)C)O 448.60 unknown https://doi.org/10.1016/S0031-9422(01)00431-9
> Organoheterocyclic compounds / Benzodioxoles
4,5-Dihydropiperlonguminine 12682184 Click to see CC(C)CNC(=O)C=CCCC1=CC2=C(C=C1)OCO2 275.34 unknown https://doi.org/10.1002/PS.1643
5-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylpenta-2,4-dien-1-one 117669 Click to see C1CCN(C1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 271.31 unknown https://doi.org/10.1021/NP030475E
5-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)pent-2-enamide 71345969 Click to see CC(C)CNC(=O)C=CCCC1=CC2=C(C=C1)OCO2 275.34 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1007/BF02033462
5-(1,3-Benzodioxol-5-yl)penta-2,4-dienoic acid 94305 Click to see C1OC2=C(O1)C=C(C=C2)C=CC=CC(=O)O 218.20 unknown https://doi.org/10.1007/S00044-008-9161-9
5-(2H-1,3-Benzodioxol-5-YL)-1-(piperidin-1-YL)pent-2-EN-1-one 276753 Click to see C1CCN(CC1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3 287.35 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1016/J.BMC.2010.03.013
7-(1,3-Benzodioxol-5-yl)-1-piperidin-1-ylhepta-2,4-dien-1-one 85720262 Click to see C1CCN(CC1)C(=O)C=CC=CCCC2=CC3=C(C=C2)OCO3 313.40 unknown https://doi.org/10.1016/S0031-9422(96)00503-1
CID 96931 96931 Click to see CC(C)CNC(=O)C=CC1=CC2=C(C=C1)OCO2 247.29 unknown https://doi.org/10.1007/S00044-008-9161-9
Piperanine 5320618 Click to see C1CCN(CC1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3 287.35 unknown https://doi.org/10.1007/S00044-008-9161-9
https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1021/NP030475E
https://doi.org/10.1016/S0031-9422(01)00431-9
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
1-[3-(3,4,5-Trimethoxyphenyl)propanoyl]piperidin-2-one 53440296 Click to see COC1=CC(=CC(=C1OC)OC)CCC(=O)N2CCCCC2=O 321.40 unknown https://doi.org/10.1007/S00044-008-9161-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
1-[3-(3,4-Dimethoxyphenyl)prop-2-enoyl]-2,3-dihydropyridin-6-one 72737951 Click to see COC1=C(C=C(C=C1)C=CC(=O)N2CCC=CC2=O)OC 287.31 unknown https://doi.org/10.1021/NP960379W
1-[3-(3,4,5-Trimethoxy-phenyl)-acryloyl]-5,6-dihydro-1H-pyridin-2-one 643764 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O 317.34 unknown https://doi.org/10.1016/J.JPBA.2014.02.020
https://doi.org/10.1016/S0031-9422(01)00431-9
https://doi.org/10.1016/S0031-9422(00)00226-0
Piperlongumin 442653 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O 317.34 unknown https://doi.org/10.1021/NP960379W
https://doi.org/10.1002/JAT.1261
Piperlongumine 637858 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O 317.34 unknown https://doi.org/10.1002/JAT.1261
https://doi.org/10.1016/S0031-9422(01)00431-9
https://doi.org/10.1007/S00044-008-9161-9
https://doi.org/10.1016/S0031-9422(00)00226-0
https://doi.org/10.1021/NP960379W
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4,5-trimethoxyphenyl)- 7021 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)O 238.24 unknown https://doi.org/10.1016/0031-9422(81)85125-4
Methyl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate 146047 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)OC 252.26 unknown https://doi.org/10.1016/S0031-9422(01)00431-9
Methyl 3,4,5-trimethoxycinnamate 735846 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)OC 252.26 unknown https://doi.org/10.1007/S00044-008-9161-9
https://doi.org/10.1016/S0031-9422(01)00431-9

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