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Stevia pilosa

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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 UUID643fcd1ca74ff527718222
Scientific name Stevia pilosa
Authority Lag.
First published in Gen. Sp. Pl. : 26 (1816)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stevia conferta var. pilosa (Lag.) DC. Prodr. 5: 116 (1836)
Stevia purpurea var. dianthoides Sch.Bip. Linnaea 25: 285 (1853)
Stevia conferta var. puberula DC. Prodr. 5: 116 (1836)
Stevia conferta DC. Prodr. 5: 116 (1836)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000069352
Tropicos 2716352
KEW urn:lsid:ipni.org:names:251507-1
The Plant List gcc-26179
Open Tree Of Life 282022
NCBI Taxonomy 558497
IPNI 251507-1
iNaturalist 289380
GBIF 3125526
EOL 6247923

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
Anti-Cancer Properties of Stevia rebaudiana; More than a Sweetener Iatridis N, Kougioumtzi A, Vlataki K, Papadaki S, Magklara A Molecules 17-Feb-2022
PMCID:PMC8874712
doi:10.3390/molecules27041362
PMID:35209150
Stevia Eupatoria and Stevia Pilosa Extracts Inhibit the Proliferation and Migration of Prostate Cancer Cells Martínez-Rojo E, Cariño-Cortés R, Berumen LC, García-Alcocer G, Escobar-Cabrera J Medicina (Kaunas) 23-Feb-2020
PMCID:PMC7074313
doi:10.3390/medicina56020090
PMID:32102219
Delineation of attenuation of oxidative stress and mutagenic stress by Murraya exotica L. leaves Kaur D, Kaur A, Arora S Springerplus 11-Jul-2016
PMCID:PMC4940350
doi:10.1186/s40064-016-2709-0
PMID:27462485
Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity Del-Toro-Sánchez CL, Bautista-Bautista N, Blasco-Cabal JL, Gonzalez-Ávila M, Gutiérrez-Lomelí M, Arriaga-Alba M Evid Based Complement Alternat Med 23-Jul-2014
PMCID:PMC4135139
doi:10.1155/2014/273878
PMID:25152760
Sesquiterpene Lactones from Gynoxys verrucosa and their Anti-MRSA Activity Ordóñez PE, Quave CL, Reynolds WF, Varughese KI, Berry B, Breen PJ, Malagón O, Smeltzer MS, Compadre CM J Ethnopharmacol 12-Jul-2011
PMCID:PMC3159821
doi:10.1016/j.jep.2011.07.012
PMID:21782013
Conformational Analysis of Achillin and Leukodin Mariano Martinez V., Alejandra Muñoz-Zamora, Pedro Joseph-Nathan American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50056A005
Absolute configuration of the alpha-methylbutyryl residue in longipinene derivatives from Stevia pilosa. Alvarez-García R, Torres-Valencia JM, Román LU, Hernández JD, Cerda-García-Rojas CM, Joseph-Nathan P Phytochemistry 01-Mar-2005
doi:10.1016/J.PHYTOCHEM.2004.12.001
PMID:15771882

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 / Monoterpenoids / Bicyclic monoterpenoids
(3,3,7,9-Tetramethyl-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl) 2-methylbut-2-enoate 163018132 Click to see CC=C(C)C(=O)OC1CCC2(C3C(C2C(=O)C=C3C)C1(C)C)C 316.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2R,3S,4S,5S,7S,8R)-3-hydroxy-2,6,6,9-tetramethyl-5-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (2S)-2-methylbutanoate 102465396 Click to see CCC(C)C(=O)OC1C(C2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C)O 432.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2R,3S,4S,5S,7S,8R)-3-hydroxy-2,6,6,9-tetramethyl-5-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (E)-2-methylbut-2-enoate 162984441 Click to see CC=C(C)C(=O)OC1C(C2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C)O 430.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2R,4S,5S,7S,8R)-2,6,6,9-tetramethyl-5-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (2S)-2-methylbutanoate 163042341 Click to see CCC(C)C(=O)OC1CC2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C 416.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2R,4S,5S,7S,8R)-2,6,6,9-tetramethyl-5-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (E)-2-methylbut-2-enoate 163064357 Click to see CC=C(C)C(=O)OC1CC2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C 414.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2S,4R,7R,8R)-3,3,7,9-tetramethyl-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (Z)-2-methylbut-2-enoate 163018133 Click to see CC=C(C)C(=O)OC1CCC2(C3C(C2C(=O)C=C3C)C1(C)C)C 316.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[(1R,2S,4S,5R,6S,7R,8R)-5-acetyloxy-3,3,7,9-tetramethyl-6-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (Z)-2-methylbut-2-enoate 163051574 Click to see CC=C(C)C(=O)OC1C(C(C2(C3C(C2C(=O)C=C3C)C1(C)C)C)OC(=O)C(=CC)C)OC(=O)C 472.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[2,6,6,9-Tetramethyl-5-(2-methylbut-2-enoyloxy)-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] 2-methylbut-2-enoate 163064356 Click to see CC=C(C)C(=O)OC1CC2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C 414.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[2,6,6,9-Tetramethyl-5-(2-methylbut-2-enoyloxy)-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] 2-methylbutanoate 163042340 Click to see CCC(C)C(=O)OC1CC2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C 416.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[3-Hydroxy-2,6,6,9-tetramethyl-5-(2-methylbut-2-enoyloxy)-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] 2-methylbut-2-enoate 162984439 Click to see CC=C(C)C(=O)OC1C(C2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C)O 430.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
[3-Hydroxy-2,6,6,9-tetramethyl-5-(2-methylbut-2-enoyloxy)-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] 2-methylbutanoate 162936050 Click to see CCC(C)C(=O)OC1C(C2(C3C(C2C(=O)C=C3C)C(C1OC(=O)C(=CC)C)(C)C)C)O 432.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Acetic acid, (13-tetradecene-2,4-diynyloxy)- 177349 Click to see C=CCCCCCCCC#CC#CCOCC(=O)O 262.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.001
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Desacetoxymatricarin 167683 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1021/NP50056A005

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