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Thymus karamarianicus

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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 UUID643fef41ade42249707295
Scientific name Thymus karamarianicus
Authority Klokov & Des.-Shost.
First published in Trudy Bot. Inst. (Baku) 2: 308 (1936)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
English karamaryanian thyme
Azerbaijani qara mərğəm kəklikotu
Azerbaijani qaramərğəm kəklikotu

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-0000324210
KEW urn:lsid:ipni.org:names:461305-1
The Plant List kew-204932
Open Tree Of Life 6083927
IUCN Red List 200564
IPNI 461305-1
iNaturalist 444345
GBIF 5606713

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
Component composition of the essential oil ofThymus karamarianucus F. Yu. Kasumov, M. T. Farkhadova Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00599279

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 / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1007/BF00599279
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1007/BF00599279
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1007/BF00599279
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00599279
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00599279
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF00599279
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1007/BF00599279
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1007/BF00599279
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1007/BF00599279

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Collections Top

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