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Sideritis arguta

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643feccd5ea21377108477
Scientific name Sideritis arguta
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 4: 32 (1859)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000309870
KEW urn:lsid:ipni.org:names:458808-1
The Plant List kew-191090
Open Tree Of Life 6081581
IPNI 458808-1
iNaturalist 940339
GBIF 3892400

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
Antioxidant and anticholinesterase activity evaluation of ent-kaurane diterpenoids from Sideritis arguta. Ertaş A, Oztürk M, Boğa M, Topçu G J Nat Prod 27-Mar-2009
doi:10.1021/NP800671P
PMID:19215141

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,4S,5S,9R,10S,13R,14S,16R)-5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-ol 12315550 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1021/NP800671P
(1R,2S,4S,5S,9R,10S,13R,15R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 162957616 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4O)O)C)CO 320.50 unknown https://doi.org/10.1021/NP800671P
(1R,2S,4S,5S,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 101306818 Click to see 320.50 unknown https://doi.org/10.1021/NP800671P
(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 20055664 Click to see 304.50 unknown https://doi.org/10.1021/NP800671P
(2-Acetyloxy-14-hydroxy-5,9,14-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate 56663964 Click to see 406.60 unknown https://doi.org/10.1021/NP800671P
[(1R,2S,4S,5S,9R,10S,13R,14R)-2-acetyloxy-14-hydroxy-5,9,14-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 101465568 Click to see 406.60 unknown https://doi.org/10.1021/NP800671P
[(1S,2S,4S,5S,9R,10S,13R,15R)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162996402 Click to see 362.50 unknown https://doi.org/10.1021/NP800671P
[(1S,2S,4S,5S,9R,10S,13R,15S)-15-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101316941 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4O)C)(C)CO 362.50 unknown https://doi.org/10.1021/NP800671P
[(1S,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 163090957 Click to see 346.50 unknown https://doi.org/10.1021/NP800671P
[(1S,2S,4S,5S,9R,10S)-5-(hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 163194159 Click to see 346.50 unknown https://doi.org/10.1021/NP800671P
[15-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 56663970 Click to see 362.50 unknown https://doi.org/10.1021/NP800671P
[5-(Hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-yl] acetate 131752043 Click to see 362.50 unknown https://doi.org/10.1021/NP800671P
[5-(Hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12315547 Click to see 346.50 unknown https://doi.org/10.1021/NP800671P
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see 304.50 unknown https://doi.org/10.1021/NP800671P
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 14239632 Click to see 320.50 unknown https://doi.org/10.1021/NP800671P
7-Epi candicandiol 45267086 Click to see 304.50 unknown https://doi.org/10.1021/NP800671P
Diacetyldistanol 45270503 Click to see CC(=O)OCC1(CCCC2(C1CC(C34C2CCC(C3)C(C4)(C)O)OC(=O)C)C)C 406.60 unknown https://doi.org/10.1021/NP800671P
Epoxysiderol 102445841 Click to see 362.50 unknown https://doi.org/10.1021/NP800671P
Eubotriol 45269663 Click to see 320.50 unknown https://doi.org/10.1021/NP800671P
Siderol 12315548 Click to see 346.50 unknown https://doi.org/10.1021/NP800671P
Sideroxol 45269664 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1021/NP800671P
Ucriol 12315549 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1021/NP800671P

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