Thymus guberlinensis
Table of Contents
Details Top
Internal ID | UUID643fef3eb9c7e361137867 |
Scientific name | Thymus guberlinensis |
Authority | Iljin |
First published in | Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 1(5): 1 (1920) |
Description Top
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Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Thymus zheguliensis | Klokov & Des.-Shost. | Izv. Bot. Sada Akad. Nauk S.S.S.R. 30: 547 (1931 publ. 1932) |
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
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Asia-temperate click to expand
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Siberia
- West Siberia
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Siberia
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Europe click to expand
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Eastern Europe
- East European Russia
- South European Russia
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Eastern Europe
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000324091 |
Tropicos | 17604686 |
KEW | urn:lsid:ipni.org:names:461211-1 |
The Plant List | kew-204817 |
Open Tree Of Life | 6083905 |
Observations.org | 127338 |
IPNI | 461211-1 |
iNaturalist | 1104730 |
GBIF | 5606954 |
EOL | 5372050 |
Elurikkus | 555708 |
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 CentralĀ®) and other sources (DOI number only)!
Title | Authors | Publication | Released | IDs | ||
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Flavones and rosmarinic acid of Thymus zheguliensis | V. A. Kurkin, G. G. Zapesochnaya, P. E. Krivenchuk, I. T. Plaksina | Springer Science and Business Media LLC | 24-Nov-2004 |
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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 |
---|---|---|---|---|---|
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
ethyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoate | 162859053 | Click to see CCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O | 388.40 | unknown | https://doi.org/10.1007/BF00598549 |
Ethyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate | 54277438 | Click to see CCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O | 388.40 | unknown | https://doi.org/10.1007/BF00598549 |
Rosmarinic acid | 5281792 | Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O | 360.30 | unknown | https://doi.org/10.1007/BF00598549 |
> Phenylpropanoids and polyketides / Flavonoids / Flavones | |||||
Apigenin | 5280443 | Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O | 270.24 | unknown | https://doi.org/10.1007/BF00598549 |
Luteolin | 5280445 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O | 286.24 | unknown | https://doi.org/10.1007/BF00598549 |
Collections Top
In private collections | 0 |
In public collections | 0 |