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Stevia yaconensis

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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 UUID643fcc73894d1476976532
Scientific name Stevia yaconensis
Authority Hieron.
First published in Bot. Jahrb. Syst. 22(4-5): 724 (1897)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Stevia yaconensis var. aristifera B.L.Rob. Contr. Gray Herb. 90: 21, 62 (1930)
Stevia yaconensis var. saltensis B.L.Rob. Contr. Gray Herb. 90: 21, 62 (1930)
Stevia yaconensis var. subeglandulosa Hieron. Bot. Jahrb. Syst. 40(3): 366 (1908)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000062887
KEW urn:lsid:ipni.org:names:245568-2
The Plant List gcc-1988
Open Tree Of Life 7604542
iNaturalist 1080038
GBIF 6064716

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)!
Title Authors Publication Released IDs
Heliangolides from Stevia yaconensis var. Aristifera Roberto R. Gil, Juan C. Oberti, Alicia B. Gutiérrez, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85351-F
10-Epideoxycumambrin b and other constituents of Stevia yaconensis var. subeglandulosa Virginia E. Sosa, Juan C. Oberti, Roberto R. Gil, Edmundo A. Rúveda, Virgil L. Goedken, Alicia B, Gutiérrez, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97888-9
The first 12.8β-germacrolide and other constituents from bolivian Stevia species C. Zdero, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80673-3

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 / Kaurane diterpenoids
(1S,4S,5R,9R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadec-10-ene-5-carboxylic acid 137705080 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(=C)C4)(C)C(=O)O 300.40 unknown https://doi.org/10.1016/0031-9422(88)80673-3
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(88)80673-3
CID 161387 161387 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(=C)C4)(C)C(=O)O 300.40 unknown https://doi.org/10.1016/0031-9422(88)80673-3
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(88)80673-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)80673-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-Ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one 14038379 Click to see CC1C2CC(C(CC2OC1=O)(C)C=C)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)85351-F
Callitrin 14038380 Click to see CC1C2CC(C(CC2OC1=O)(C)C=C)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)85351-F
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(+)-Costunolide; Costus lactone 12304109 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(88)80673-3
(3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-7-yl) acetate 162884293 Click to see CC1C2CC=C(C(CC=C(CC2OC1=O)C)OC(=O)C)C 292.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(88)80673-3
(3S,3aS,6R,9E,11aS)-3,6,10-trimethyl-3,3a,4,5,6,8,11,11a-octahydrocyclodeca[b]furan-2,7-dione 163008055 Click to see CC1CCC2C(C(=O)OC2CC(=CCC1=O)C)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85351-F
[(3R,3aR,5Z,7S,9E,11aR)-3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-7-yl] acetate 15143889 Click to see CC1C2CC=C(C(CC=C(CC2OC1=O)C)OC(=O)C)C 292.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
3,6,10-Trimethyl-3,3a,4,5,6,8,11,11a-octahydrocyclodeca[b]furan-2,7-dione 163008054 Click to see CC1CCC2C(C(=O)OC2CC(=CCC1=O)C)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85351-F
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(88)80673-3
Ludartin 14355826 Click to see CC1=C2CC3C(C2C4C(CC1)C(=C)C(=O)O4)(O3)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)97888-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1-Methyl-5-methylidene-2-oxo-1,3a,4,5a,6,8a,9,9a-octahydroazuleno[6,7-b]furan-8-yl)methyl acetate 163027110 Click to see CC1C2CC3C(CC=C3COC(=O)C)C(=C)CC2OC1=O 290.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
(1S,2S,10S,12R,14S)-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 15559180 Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4 246.30 unknown https://doi.org/10.1016/0031-9422(88)80673-3
(3aS,6aR,9aR,9bS)-9-methyl-3,6-dimethylidene-3a,4,5,6a,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 11746867 Click to see CC1=CC(=O)C2C1C3C(CCC2=C)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/0031-9422(88)80673-3
[(1R,3aR,5aR,8aR,9aR)-1-methyl-5-methylidene-2-oxo-1,3a,4,5a,6,8a,9,9a-octahydroazuleno[6,7-b]furan-8-yl]methyl acetate 101589356 Click to see CC1C2CC3C(CC=C3COC(=O)C)C(=C)CC2OC1=O 290.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
Estafiatin 566474 Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4 246.30 unknown https://doi.org/10.1016/0031-9422(88)80673-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3,8,12-Trimethyl-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-7-yl) acetate 162939585 Click to see CC1C2CC=C(C(CC3C(O3)(CC2OC1=O)C)OC(=O)C)C 308.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
[(1S,3S,5R,7R,8Z,11S,12S)-3,8,12-trimethyl-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-7-yl] acetate 162939587 Click to see CC1C2CC=C(C(CC3C(O3)(CC2OC1=O)C)OC(=O)C)C 308.40 unknown https://doi.org/10.1016/0031-9422(90)85351-F
10-Epi-8-deoxy-cumambrin B 46887018 Click to see CC1=CCC2C1C3C(CCC2)C(=C)C(=O)O3 218.29 unknown https://doi.org/10.1016/S0031-9422(00)97888-9
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1016/S0031-9422(00)97888-9

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