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Thymus broussonetii

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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 UUID643fef347d787603465055
Scientific name Thymus broussonetii
Authority Boiss.
First published in Voy. Bot. Espagne 2: 492 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Origanum broussonetii 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 broussonetii subsp. broussonetii Unknown
Thymus broussonetii subsp. hannonis (Maire) R.Morales Anales Jard. Bot. Madrid 51: 226 (1993 publ. 1994)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000323793
Tropicos 50194497
KEW urn:lsid:ipni.org:names:460973-1
The Plant List kew-204533
Open Tree Of Life 303780
NCBI Taxonomy 751869
IPNI 460973-1
iNaturalist 1120536
GBIF 7307695

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
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
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
Antibacterial Activity of Essential Oils Combinations based on Thymus broussonnetii, and Their Synergism with some Antibiotics Amassmoud O, Abbad I, Iriti M, Hassani L, Mezrioui N, Abbad A Curr Microbiol 01-Nov-2023
PMCID:PMC10620311
doi:10.1007/s00284-023-03510-x
PMID:37910319
Next-generation nanomaterials: advancing ocular anti-inflammatory drug therapy Wei J, Mu J, Tang Y, Qin D, Duan J, Wu A J Nanobiotechnology 19-Aug-2023
PMCID:PMC10440041
doi:10.1186/s12951-023-01974-4
PMID:37598148
Recent advances to combat ESKAPE pathogens with special reference to essential oils Panda SK, Buroni S, Swain SS, Bonacorsi A, da Fonseca Amorim EA, Kulshrestha M, da Silva LC, Tiwari V Front Microbiol 06-Dec-2022
PMCID:PMC9763703
doi:10.3389/fmicb.2022.1029098
PMID:36560948
Chemical Composition, Antioxidant and Antibacterial Activities of Thymus broussonetii Boiss and Thymus capitatus (L.) Hoffmann and Link Essential Oils Tagnaout I, Zerkani H, Hadi N, El Moumen B, El Makhoukhi F, Bouhrim M, Al-Salahi R, Nasr FA, Mechchate H, Zair T Plants (Basel) 31-Mar-2022
PMCID:PMC9003487
doi:10.3390/plants11070954
PMID:35406936
Impact of Plant-Based Foods and Nutraceuticals on Toxoplasma gondii Cysts: Nutritional Therapy as a Viable Approach for Managing Chronic Brain Toxoplasmosis Tan S, Tong WH, Vyas A Front Nutr 25-Feb-2022
PMCID:PMC8914227
doi:10.3389/fnut.2022.827286
PMID:35284438
Antibiotic resistance modifying ability of phytoextracts in anthrax biological agent Bacillus anthracis and emerging superbugs: a review of synergistic mechanisms Dassanayake MK, Khoo TJ, An J Ann Clin Microbiol Antimicrob 02-Dec-2021
PMCID:PMC8641154
doi:10.1186/s12941-021-00485-0
PMID:34856999
GIS-Facilitated Seed Germination and Multifaceted Evaluation of the Endangered Abies marocana Trab. (Pinaceae) Enabling Conservation and Sustainable Exploitation Hatzilazarou S, El Haissoufi M, Pipinis E, Kostas S, Libiad M, Khabbach A, Lamchouri F, Bourgou S, Megdiche-Ksouri W, Ghrabi-Gammar Z, Aslanidou V, Greveniotis V, Sakellariou MA, Anestis I, Tsoktouridis G, Krigas N Plants (Basel) 27-Nov-2021
PMCID:PMC8707146
doi:10.3390/plants10122606
PMID:34961077
Evaluation of Origanum vulgare Essential Oil and Its Active Ingredients as Potential Drugs for the Treatment of Toxoplasmosis Yao N, Xu Q, He JK, Pan M, Hou ZF, Liu DD, Tao JP, Huang SY Front Cell Infect Microbiol 22-Nov-2021
PMCID:PMC8645793
doi:10.3389/fcimb.2021.793089
PMID:34881197
Phytochemistry and Pharmacology of Thymus broussonetii Boiss Naceiri Mrabti H, Doudach L, El Menyiy N, Bourhia M, Mohammad Salamatullah A, Reda Kachmar M, Belmehdi O, El Moudden H, Naceiri Mrabti N, Harhar H, El Omari N, Bouyahya A Evid Based Complement Alternat Med 04-Sep-2021
PMCID:PMC8437615
doi:10.1155/2021/6350035
PMID:34527064
Anti-inflammatory and analgesic properties of Moroccan medicinal plants: Phytochemistry, in vitro and in vivo investigations, mechanism insights, clinical evidences and perspectives Bouyahya A, Guaouguaou FE, El Omari N, El Menyiy N, Balahbib A, El-Shazly M, Bakri Y J Pharm Anal 13-Jul-2021
PMCID:PMC9073245
doi:10.1016/j.jpha.2021.07.004
PMID:35573886
Influence of monoterpenoids on the growth of freshwater cyanobacteria Balcerzak L, Lochyński S, Lipok J Appl Microbiol Biotechnol 23-Jun-2021
PMCID:PMC8285344
doi:10.1007/s00253-021-11260-8
PMID:34164714
Herbal Products and Their Active Constituents Used Alone and in Combination with Antifungal Drugs against Drug-Resistant Candida sp. Herman A, Herman AP Antibiotics (Basel) 31-May-2021
PMCID:PMC8229001
doi:10.3390/antibiotics10060655
PMID:34072664
Ethnobotanical Survey of Medicinal Plants Used by Traditional Healers to Treat Diabetes in the Taza Region of Morocco Naceiri Mrabti H, Bouyahya A, Naceiri Mrabti N, Jaradat N, Doudach L, Faouzi ME Evid Based Complement Alternat Med 24-Apr-2021
PMCID:PMC8093047
doi:10.1155/2021/5515634
PMID:33986815

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 / Polycyclic hydrocarbons
beta-Patchoulene 101731 Click to see CC1CCC2=C1CC3CCC2(C3(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
Isoledene 530426 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
> 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.PHYMED.2010.03.020
https://doi.org/10.1016/J.PHYMED.2011.12.003
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3-Ethenyl-3,7-dimethyloct-6-enoic acid 13128171 Click to see CC(=CCCC(C)(CC(=O)O)C=C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698169
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698169
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698169
> 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/10.1080/10412905.1993.9698169
https://doi.org/10.1016/J.PHYMED.2011.12.003
https://doi.org/10.1016/J.PHYMED.2010.03.020
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1080/10412905.1993.9698169
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1016/J.PHYMED.2011.12.003
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Thujene 637518 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
(2S,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol 12315151 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
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/10.1080/10412905.1993.9698169
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
https://doi.org/10.1080/10412905.1993.9698169
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
https://doi.org/10.1016/J.PHYMED.2010.03.020
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
> 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/10.1080/10412905.1993.9698169
cis-Dihydrocarvone 443181 Click to see CC1CCC(CC1=O)C(=C)C 152.23 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
https://doi.org/10.1016/J.PHYMED.2010.03.020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene 12306052 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
https://doi.org/10.1016/J.PHYMED.2010.03.020
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
beta-Gurjunene 6450812 Click to see CC1CCC2C(C2(C)C)C3C1CCC3=C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003
Isospathulenol 102303030 Click to see CC1=C2CCC(C2C3C(C3(C)C)CC1)(C)O 220.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
https://doi.org/10.1016/J.PHYMED.2011.12.003
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2010.03.020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2011.12.003

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