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Thymbra capitata

Thymbra capitata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Thymbra capitata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fef2d33405190551686
Scientific name Thymbra capitata
Authority (L.) Cav.
First published in Elench. Pl. Horti Matr. : 37 (1803)

Description Top

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Synonyms Top

Scientific name Authority First published in
Origanum capitatum Kuntze Revis. Gen. Pl. 2: 528 (1891)
Satureja capitata L. Sp. Pl. : 568 (1753)
Thymus capitatus Hoffmanns. & Link Fl. Portug. 1: 123 (1809)
Thymus creticus Garsault Fl. Lusit. 1: 174 (1804)
Coridothymus capitatus Rchb.f. Oesterr. Bot. Wochenbl. 7: 161 (1857)

Common names Top

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Language Common/alternative name
Czech mateřídouškovec vonný
German kopfiger thymian
Finnish sykerötimjami
Finnish sykerötipakki
grc θύμον
Portuguese coridothymus
Chinese 头花百里香

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000323594
Tropicos 17604934
INPN 788800
Flora of Italy 4616
KEW urn:lsid:ipni.org:names:460817-1
The Plant List kew-204339
Open Tree Of Life 27200
Observations.org 122973
NCBI Taxonomy 543980
IPNI 460816-1
iNaturalist 905463
GBIF 5607804
Freebase /m/0dgn6v0
EPPO THYCA
Elurikkus 630951

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
Potentiation of the Antimicrobial Effect of Oxytetracycline Combined with Cinnamon, Clove, Oregano, and Red Thyme Essential Oils against MDR Salmonella enterica Strains Huerta Lorenzo B, Galán-Relaño Á, Barba-Sánchez E, Romero-Salmoral A, Solarte Portilla AL, Gómez-Gascón L, Astorga Márquez RJ Animals (Basel) 30-Apr-2024
PMCID:PMC11083648
doi:10.3390/ani14091347
PMID:38731351
Antibacterial Activity of Oregano (Origanum vulgare L.) Essential Oil Vapors against Microbial Contaminants of Food-Contact Surfaces Pinto L, Cervellieri S, Netti T, Lippolis V, Baruzzi F Antibiotics (Basel) 18-Apr-2024
PMCID:PMC11047463
doi:10.3390/antibiotics13040371
PMID:38667047
Medical-Grade Honey as a Potential New Therapy for Bacterial Vaginosis Lardenoije CM, van Riel SJ, Peters LJ, Wassen MM, Cremers NA Antibiotics (Basel) 17-Apr-2024
PMCID:PMC11047503
doi:10.3390/antibiotics13040368
PMID:38667044
Plant-Based Biostimulants for Seeds in the Context of Circular Economy and Sustainability Wazeer H, Shridhar Gaonkar S, Doria E, Pagano A, Balestrazzi A, Macovei A Plants (Basel) 31-Mar-2024
PMCID:PMC11013454
doi:10.3390/plants13071004
PMID:38611532
Spray Coating of Wood with Nanoparticles from Lignin and Polylactic Glycolic Acid Loaded with Thyme Essential Oils Zikeli F, Jusic J, Palocci C, Mugnozza GS, Romagnoli M Polymers (Basel) 30-Mar-2024
PMCID:PMC11013818
doi:10.3390/polym16070947
PMID:38611206
Potential of Thuja occidentalis L. Essential Oil and Water Extracts against Field Crop Pests Gospodarek J, Krajewska A, Paśmionka IB, Bruździńska J, Tamiru G Molecules 24-Mar-2024
PMCID:PMC11013141
doi:10.3390/molecules29071457
PMID:38611736
Antilisterial Effectiveness of Origanum vulgare var. hirtum and Coridothymus capitatus Essential Oils and Hydrolates Alone and in Combination D’Amato S, Rossi C, Maggio F, Valbonetti L, Savini V, Paparella A, Serio A Foods 12-Mar-2024
PMCID:PMC10969000
doi:10.3390/foods13060860
PMID:38540850
Growth form, regeneration mode, and vegetation type explain leaf trait variability at the species and community levels in Mediterranean woody vegetation Tüfekcioğlu İ, Tavşanoğlu Ç Ecol Evol 11-Mar-2024
PMCID:PMC10927360
doi:10.1002/ece3.11145
PMID:38469041
Antibacterial Effect of Eight Essential Oils against Bacteria Implicated in Bovine Mastitis and Characterization of Primary Action Mode of Thymus capitatus Essential Oil Aouadhi C, Jouini A, Maaroufi K, Maaroufi A Antibiotics (Basel) 05-Mar-2024
PMCID:PMC10967590
doi:10.3390/antibiotics13030237
PMID:38534672
Characterization of antimicrobial multilayer film based on ethylcellulose-pectin incorporated with nanoemulsions of trans-cinnamaldehyde essential oil Baghi F, Gharsallaoui A, Dumas E, Agusti G, Ghnimi S Food Chem X 29-Feb-2024
PMCID:PMC10937108
doi:10.1016/j.fochx.2024.101261
PMID:38486619
Chemical profiling and bioactivities of essential oils from Thymus capitatus and Origanum compactum against Tribolium castaneum Annaz H, Annaz H, Ajaha A, Bouayad N, El Fakhouri K, Laglaoui A, El Bouhssini M, Sobeh M, Rharrabe K Heliyon 14-Feb-2024
PMCID:PMC10912041
doi:10.1016/j.heliyon.2024.e26102
PMID:38444480
Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L Biomedicines 04-Feb-2024
PMCID:PMC10886757
doi:10.3390/biomedicines12020365
PMID:38397967
Enhancement of Strawberry Shelf Life via a Multisystem Coating Based on Lippia graveolens Essential Oil Loaded in Polymeric Nanocapsules González-Moreno BJ, Galindo-Rodríguez SA, Rivas-Galindo VM, Pérez-López LA, Granados-Guzmán G, Álvarez-Román R Polymers (Basel) 26-Jan-2024
PMCID:PMC10857092
doi:10.3390/polym16030335
PMID:38337224
Phytochemical Profiles and Biological Activities of Plant Extracts from Aromatic Plants Cultivated in Cyprus Chrysargyris A, Petrovic JD, Tomou EM, Kyriakou K, Xylia P, Kotsoni A, Gkretsi V, Miltiadous P, Skaltsa H, Soković MD, Tzortzakis N Biology (Basel) 15-Jan-2024
PMCID:PMC10813336
doi:10.3390/biology13010045
PMID:38248476
Anti-Salmonella Activity of Thymus serpyllum Essential Oil in Sous Vide Cook–Chill Rabbit Meat Kačániová M, Čmiková N, Kluz MI, Akacha BB, Saad RB, Mnif W, Waszkiewicz-Robak B, Garzoli S, Hsouna AB Foods 08-Jan-2024
PMCID:PMC10815041
doi:10.3390/foods13020200
PMID:38254501

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Cumenes
Diisopropyl-m-cresol 169279 Click to see CC1=C(C=CC(=C1C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1995.9698524
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.020
https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic acid 8314 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1080/10412905.1995.9698524
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(x)-p-Menth-1-en-4-yl 5-isopropyl-2-methylphenyl ether 131751012 Click to see CC1=CCC(CC1)(C(C)C)OC2=C(C=CC(=C2)C(C)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(80)85019-9
1-methyl-2-[(1S)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxy-4-propan-2-ylbenzene 162919016 Click to see CC1=CCC(CC1)(C(C)C)OC2=C(C=CC(=C2)C(C)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(80)85019-9
2,4-Diisopropyl-5-methylphenol 527839 Click to see CC1=CC(=C(C=C1C(C)C)C(C)C)O 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
2,5-Diisopropylphenol 93189 Click to see CC(C)C1=CC(=C(C=C1)C(C)C)O 178.27 unknown https://doi.org/10.1016/0031-9422(80)80207-X
2,6-Diisopropyl-3-methylphenol 119956 Click to see CC1=C(C(=C(C=C1)C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)85019-9
3-Methyl-2,5-bis(1-methylethyl)phenol 20447657 Click to see CC1=CC(=CC(=C1C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
4-Methyl-2,5-diisopropylphenol 139921 Click to see CC1=CC(=C(C=C1C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
5-Methyl-2,3-diisopropylphenol 58446461 Click to see CC1=CC(=C(C(=C1)O)C(C)C)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/0031-9422(80)80207-X
https://doi.org/10.1016/0378-8741(94)90094-9
https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1002/FFJ.1029
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1080/10412905.1995.9698524
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1002/FFJ.1029
https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.020
https://doi.org/10.1016/0031-9422(80)80207-X
https://doi.org/10.1016/0378-8741(94)90094-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(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/10.1080/10412905.1995.9698524
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/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF9801670
https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698138
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(6S)-6-methyl-3-propan-2-ylcyclohex-2-en-1-one 11030021 Click to see CC1CCC(=CC1=O)C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(80)85019-9
2-Cyclohexen-1-one, 6-methyl-3-(1-methylethyl)- 10363 Click to see CC1CCC(=CC1=O)C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(80)85019-9
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Piperitenone 381152 Click to see CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1080/10412905.1995.9698524
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0031-9422(80)85019-9
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/0031-9422(80)85019-9
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see CCC(CCC(C)C)O 130.23 unknown https://doi.org/10.1080/10412905.1995.9698524
> Organic oxygen compounds / Organooxygen compounds / Enols
3-Methyl-3-propan-2-ylcyclohexa-1,5-dien-1-ol 163189860 Click to see CC(C)C1(CC=CC(=C1)O)C 152.23 unknown https://doi.org/10.1016/0378-8741(94)90094-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
Vicenin-2 3084407 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
Luteolin 7-o-rutinoside 10461109 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone 10020367 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC 344.30 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
5,6,4'-Trihydroxy-7,3'-dimethoxyflavone 10359254 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)85533-8

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