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Sideritis caesarea

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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 UUID643feccf3881e708030889
Scientific name Sideritis caesarea
Authority H.Duman, Aytaç & Bașer
First published in Turkish J. Bot. 22: 51 (1998)

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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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-0000309917
Tropicos 100258538
KEW urn:lsid:ipni.org:names:1013701-1
The Plant List kew-191132
Open Tree Of Life 6081597
IPNI 1013701-1
iNaturalist 940326
GBIF 3892068

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
Complete 13C NMR assignments for ent-kaurane diterpenoids from Sideritis species. Halfon B, Gören AC, Ertaş A, Topçu G Magn Reson Chem 01-May-2011
doi:10.1002/MRC.2747
PMID:21491485
An ent-kaurane from Sideritis huber-morathii K.Husnu Can Baser, Maria Luisa Bondi, Maurizio Bruno, Nese Kirimer, Franco Piozzi, Gulendam Tumen, Nadia Vassallo Elsevier BV 05-Apr-2003
doi:10.1016/S0031-9422(96)00371-8

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,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 101306818 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4O)O)C)CO 320.50 unknown https://doi.org/10.1002/MRC.2747
(1R,2S,4S,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 162942250 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4=O)O)C)CO 318.40 unknown https://doi.org/10.1002/MRC.2747
[(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/10.1002/MRC.2747
[15-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 56663970 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4O)C)(C)CO 362.50 unknown https://doi.org/10.1002/MRC.2747
[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 CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C5(C4O5)C)C)(C)CO 362.50 unknown https://doi.org/10.1002/MRC.2747
https://doi.org/10.1016/S0031-9422(96)00371-8
[5-(Hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12315547 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/S0031-9422(96)00371-8
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 14239632 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4O)O)C)CO 320.50 unknown https://doi.org/10.1002/MRC.2747
Epoxysiderol 102445841 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C5(C4O5)C)C)(C)CO 362.50 unknown https://doi.org/10.1002/MRC.2747
https://doi.org/10.1016/S0031-9422(96)00371-8
Siderol 12315548 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/S0031-9422(96)00371-8

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