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Thymus bashkiriensis

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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 UUID643fef3200ef8186076339
Scientific name Thymus bashkiriensis
Authority Klokov & Des.-Shost.
First published in Izv. Bot. Sada Akad. Nauk S.S.S.R. 30: 533 (1931 publ. 1932)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • East European Russia
      • South European Russia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000323739
KEW urn:lsid:ipni.org:names:460928-1
The Plant List kew-204480
Open Tree Of Life 6083824
Observations.org 122993
IPNI 460928-1
iNaturalist 1074801
GBIF 5607656
Elurikkus 555837

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
Components of the epigeal part of Thymus bashkiriensis V. A. Kurkin, V. B. Braslavskii, P. E. Krivenchuk, T. I. Plaksina Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00633407

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 / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF00633407
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF00633407
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(3R)-3-(3,4-dihydroxyphenyl)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoic acid 163185213 Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1007/BF00633407
3-(3,4-Dihydroxyphenyl)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 77583661 Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1007/BF00633407
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/BF00633407
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00633407
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00633407
> 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/BF00633407
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/BF00633407

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