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Sideritis sventenii

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID643fecdf5f2bb182809497
Scientific name Sideritis sventenii
Authority (G.Kunkel) Mend.-Heuer
First published in Vieraea 5(1-2): 74. 1975

Description Top

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Synonyms Top

Scientific name Authority First published in
Leucophae sventenii G.Kunkel Cuad. Bot. Canaria 18-19: 69 (1973)

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000310483
Tropicos 100259007
KEW urn:lsid:ipni.org:names:459108-1
The Plant List kew-191679
Open Tree Of Life 792852
Observations.org 146726
NCBI Taxonomy 403032
IPNI 459109-1
iNaturalist 940253
GBIF 3888608
Elurikkus 434157
USDA GRIN 475192

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)!
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Title Authors Publication Released IDs
Diterpenes from Sideritis sventenii and S. cystosiphon Braulio M. Fraga, Melchor G. Hernández, JoséM.H. Santana, JoséM. Arteaga Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85122-V
Flavonoid aglycones from some canary islands species of sideritis. Fernandez C, Fraga BM, Hernandez MG, Arteaga JM J Nat Prod 01-May-1988
doi:10.1021/NP50057A027
PMID:21401173

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
(1R,2S,4R,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 163009392 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)C=O)O)C)CO 318.40 unknown https://doi.org/10.1016/0031-9422(90)85122-V
(1R,2S,4R,5S,9R,10S,13R)-5,14-bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 163014760 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
(1R,2S,4R,5S,9S,10S,13R)-2-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162916334 Click to see CC12CCCC(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(90)85122-V
(1R,4S,5S,9S,10S)-2-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 138114075 Click to see CC12CCCC(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(90)85122-V
(4beta,7beta)-Kaur-15-ene-7,17,18-triol 12315544 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
[(1R,2S,4R,5S,9R,10S,13R)-5,14-bis(hydroxymethyl)-5,9-dimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 163038411 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C4)CO)C)(C)CO 362.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
[14-Formyl-5-(hydroxymethyl)-5,9-dimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 14487051 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C4)C=O)C)(C)CO 360.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 14487053 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)C=O)O)C)CO 318.40 unknown https://doi.org/10.1016/0031-9422(90)85122-V
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
5,14-Bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 12315543 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
7beta,19-Dihydroxykaur-15-ene-17-carbaldehyde 14890430 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CC=O)O)C)CO 332.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
ent-16-Kauren-19-ol 529650 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
Kaura-16-ene-7beta,19-diol 7-acetate 101615200 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4)C)(C)CO 346.50 unknown https://doi.org/10.1016/0031-9422(90)85122-V
Sventenic acid 14487041 Click to see CC12CCCC(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(90)85122-V
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[DL-Abu-DL-Val-DL-N(Me)Ala-bAla-DL-OLeu-DL-Pro] 75049028 Click to see CCC1C(=O)NC(C(=O)N(C(C(=O)NCCC(=O)OC(C(=O)N2CCCC2C(=O)N1)CC(C)C)C)C)C(C)C 551.70 unknown https://doi.org/10.1016/0031-9422(90)85122-V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/0031-9422(90)85122-V
https://doi.org/10.1021/NP50057A027

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