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Thymus saturejoides

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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 UUID643fef533cba4640963796
Scientific name Thymus saturejoides
Authority Coss. & Balansa
First published in Bull. Soc. Bot. France 20: 253 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Origanum saturejodes Kuntze Revis. Gen. Pl. 2: 528 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Thymus saturejoides subsp. commutatus Batt. Bull. Soc. Bot. France 58: 436 (1911)
Thymus saturejoides subsp. pseudomastichina (Ball) Dobignard J. Bot. Soc. Bot. France 28: 23 (2004)
Thymus saturejoides subsp. saturejoides Unknown

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000324708
Tropicos 50194500
KEW urn:lsid:ipni.org:names:461627-1
The Plant List kew-205412
Open Tree Of Life 905407
NCBI Taxonomy 751874
IUCN Red List 139600868
IPNI 461627-1
iNaturalist 789307
GBIF 7306681

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Chemical Characterization and Antifungal Activity of Blue Tansy (Tanacetum annuum) Essential Oil and Crude Extracts against Fusarium oxysporum f. sp. albedinis, an Agent Causing Bayoud Disease of Date Palm Ettakifi H, Abbassi K, Maouni S, Erbiai EH, Rahmouni A, Legssyer M, Saidi R, Lamrani Z, Esteves da Silva JC, Pinto E, Maouni A Antibiotics (Basel) 16-Sep-2023
PMCID:PMC10526058
doi:10.3390/antibiotics12091451
PMID:37760747
Identification of phytochemical, antioxidant, anticancer and antimicrobial potential of Calotropis procera leaf aqueous extract Ahmad Nejhad A, Alizadeh Behbahani B, Hojjati M, Vasiee A, Mehrnia MA Sci Rep 07-Sep-2023
PMCID:PMC10485245
doi:10.1038/s41598-023-42086-1
PMID:37679486
Evaluation of the constituent compounds, antioxidant, anticancer, and antimicrobial potential of Prangos ferulacea plant extract and its effect on Listeria monocytogenes virulence gene expression Jalil Sarghaleh S, Alizadeh Behbahani B, Hojjati M, Vasiee A, Noshad M Front Microbiol 10-Jul-2023
PMCID:PMC10364450
doi:10.3389/fmicb.2023.1202228
PMID:37492261
In Vitro Propagation of Origanum scabrum (Boiss. & Heldr.): An Endemic Medicinal Plant of Greece Alexopoulos AA, Kartsonas E, Karras S, Mavrommati E, Petropoulos SA, Papafotiou M Plants (Basel) 26-May-2023
PMCID:PMC10255548
doi:10.3390/plants12112118
PMID:37299098
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
Six Spain Thymus essential oils composition analysis and their in vitro and in silico study against Streptococcus mutans Park SY, Raka RN, Hui XL, Song Y, Sun JL, Xiang J, Wang J, Jin JM, Li XK, Xiao JS, Wu H BMC Complement Med Ther 05-Apr-2023
PMCID:PMC10074788
doi:10.1186/s12906-023-03928-7
PMID:37020229
Essential oil of Cymbopogon martini, source of geraniol, as a potential antibacterial agent against Bacillus subtilis, a pathogen of the bakery industry Santamarta S, Aldavero AC, Rojo MA F1000Res 24-Mar-2023
PMCID:PMC9936101
doi:10.12688/f1000research.54196.1
PMID:36817513
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263
Thymus serpyllum Exhibits Anti-Diabetic Potential in Streptozotocin-Induced Diabetes Mellitus Type 2 Mice: A Combined Biochemical and In Vivo Study Azhar J, John P, Bhatti A Nutrients 29-Aug-2022
PMCID:PMC9460602
doi:10.3390/nu14173561
PMID:36079819
The Potential of Lamiaceae Herbs for Mitigation of Overweight, Obesity, and Fatty Liver: Studies and Perspectives Diab F, Zbeeb H, Baldini F, Portincasa P, Khalil M, Vergani L Molecules 08-Aug-2022
PMCID:PMC9370348
doi:10.3390/molecules27155043
PMID:35956991
Role of ethno-phytomedicine knowledge in healthcare of COVID-19: advances in traditional phytomedicine perspective Nasir Ahmed M, Hughes K Beni Suef Univ J Basic Appl Sci 04-Aug-2022
PMCID:PMC9362587
doi:10.1186/s43088-022-00277-1
PMID:35966214
Essential Oils in Respiratory Mycosis: A Review Zuzarte M, Salgueiro L Molecules 28-Jun-2022
PMCID:PMC9268412
doi:10.3390/molecules27134140
PMID:35807386
Correlation between the chemical composition and the antimicrobial properties of seven samples of essential oils of endemic Thymes in Morocco against multi-resistant bacteria and pathogenic fungi Drioiche A, Zahra Radi F, Ailli A, Bouzoubaa A, Boutakiout A, Mekdad S, AL Kamaly O, Saleh A, Maouloua M, Bousta D, Sahpaz S, EL Makhoukhi F, Zair T Saudi Pharm J 22-Jun-2022
PMCID:PMC9508645
doi:10.1016/j.jsps.2022.06.022
PMID:36164579

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1080/10412905.1993.9698169
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF60206A038
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2,6-Dimethyl-3-propan-2-ylphenol 21908410 Click to see CC1=C(C(=C(C=C1)C(C)C)C)O 164.24 unknown https://doi.org/10.1080/10412905.1993.9698169
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/JF60206A038
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1021/JF60206A038
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see CC1(C2CCC1(C(C2)CC(=O)O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698169
(1R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol 12315149 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1021/JF60206A038
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60206A038
4,6,6-Trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]bicyclo[3.1.1]hept-4-en-2-ol 56924154 Click to see CC1=C2CC(C2(C)C)CC1C3(CC4CC(=C3C)C4(C)C)C5C(C6CC(=C5C)C6(C)C)O 420.70 unknown https://doi.org/10.1021/JF60206A038
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF60206A038
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/JF60206A038
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1993.9698169
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/JF60206A038
Dihydrocarvone 24473 Click to see CC1CCC(CC1=O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
> 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/10.1021/JF60206A038
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1055/S-2007-969583
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1055/S-2007-969583
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
8-Methoxycirsilineol 181092 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown https://doi.org/10.1055/S-2007-969583
Thymonin 442662 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)O 360.30 unknown https://doi.org/10.1055/S-2007-969583
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1055/S-2007-969583

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