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Stevia origanoides

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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 UUID643fd2bc1b4ef205023719
Scientific name Stevia origanoides
Authority Kunth
First published in Nov. Gen. Sp. 4(15): 115 (ed. fol.) (1818)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stevia dissitifolia DC. Prodr. 5: 121 (1836)
Stevia scabridula B.L.Rob. Contr. Gray Herb. 90: 19, 119 (1930)

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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No germination or propagation data was added yet.

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 Northwest
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000126198
Tropicos 2708375
KEW urn:lsid:ipni.org:names:251483-1
The Plant List gcc-87241
Open Tree Of Life 282029
NCBI Taxonomy 558494
IPNI 251483-1
iNaturalist 280191
GBIF 3125643
EOL 6247949
CMAUP NPO24626

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
Pest categorisation of Coleosporium eupatorii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Maiorano A, Pautasso M, Reignault PL EFSA J 24-May-2023
PMCID:PMC10208091
doi:10.2903/j.efsa.2023.8020
PMID:37234271
Heliangolides from Stevia origanoides J. S. Calderón, L. Quijano, F. Gómez, T. Ríos American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50051A039
The Flavonoids of Stevia microchaeta, Stevia monardifolia, and Stevia origanoides Amriteswori Rajbhandari, Margaret F. Roberts American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50039A036
Longipinene derivatives from Stevia origanoides Carlos M. Cerda-García-Rojas, Eugenio Sánchez-Arreola, Pedro Joseph-Nathan, Luisa U. Román, Juan D. Hernandez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95095-7

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4-Acetyloxy-3,7,9-trimethyl-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl)methyl 2-methylbut-2-enoate 163075109 Click to see CC=C(C)C(=O)OCC1(C(CCC2(C3C1C2C(=O)C=C3C)C)OC(=O)C)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
[(1R,2S,3S,4R,6R,7R,8R)-4-acetyloxy-3,7,9-trimethyl-6-(3-methylbut-2-enoyloxy)-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl]methyl (Z)-2-methylbut-2-enoate 162910241 Click to see CC=C(C)C(=O)OCC1(C(CC(C2(C3C1C2C(=O)C=C3C)C)OC(=O)C=C(C)C)OC(=O)C)C 472.60 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
[(1R,2S,3S,4R,6R,7R,8R)-4-acetyloxy-3,7,9-trimethyl-6-[(Z)-2-methylbut-2-enoyl]oxy-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl]methyl (Z)-2-methylbut-2-enoate 163070488 Click to see CC=C(C)C(=O)OCC1(C(CC(C2(C3C1C2C(=O)C=C3C)C)OC(=O)C(=CC)C)OC(=O)C)C 472.60 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
[(1R,2S,3S,4R,7R,8R)-4-acetyloxy-3,7,9-trimethyl-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl]methyl (Z)-2-methylbut-2-enoate 163075110 Click to see CC=C(C)C(=O)OCC1(C(CCC2(C3C1C2C(=O)C=C3C)C)OC(=O)C)C 374.50 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
[4-Acetyloxy-3,7,9-trimethyl-6-(2-methylbut-2-enoyloxy)-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl]methyl 2-methylbut-2-enoate 163070487 Click to see CC=C(C)C(=O)OCC1(C(CC(C2(C3C1C2C(=O)C=C3C)C)OC(=O)C(=CC)C)OC(=O)C)C 472.60 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
[4-Acetyloxy-3,7,9-trimethyl-6-(3-methylbut-2-enoyloxy)-11-oxo-3-tricyclo[5.4.0.02,8]undec-9-enyl]methyl 2-methylbut-2-enoate 162910240 Click to see CC=C(C)C(=O)OCC1(C(CC(C2(C3C1C2C(=O)C=C3C)C)OC(=O)C=C(C)C)OC(=O)C)C 472.60 unknown https://doi.org/10.1016/S0031-9422(00)95095-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6E,9S,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-(acetyloxymethyl)-4-hydroxybut-2-enoate 15572109 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)COC(=O)C)C(=C)C(=O)O2)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP50051A039
[(3aS,11aS)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-(hydroxymethyl)but-2-enoate 137706452 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O2)C)OC(=O)C 420.50 unknown https://doi.org/10.1021/NP50051A039
Eucannabinolide-19-O-acetate 6440423 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCOC(=O)C)CO)C(=C)C(=O)O2)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP50051A039
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Canophyllal 12302400 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C 440.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1021/NP50039A036
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP50039A036

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