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Lavandula dentata

Lavandula dentata - 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 UUID643fe08ecf9e7845573558
Scientific name Lavandula dentata
Authority L.
First published in Sp. Pl. : 572 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lavandula dentata var. rendalliana Bolle Bonplandia (Hannover) 8: 280. 1860
Lavandula pinnata Moench Suppl. Meth. : 135 (1802)
Stoechas dentata Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Lavandula dentata f. multibracteolata Sennen Diagn. Nouv. 113 1936
Lavandula dentata var. balearica Ging. Hist. Nat. Lavand. 139. 1826
Lavandula dentata f. pinnatilobulata Sennen Diagn. Nouv. 113 1936
Lavandula dentata f. rosea Maire Cat. Pl. Maroc 3: 622 1934
Lavandula dentata f. albiflora Maire Cat. Pl. Maroc 3: 622 1934

Common names Top

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Language Common/alternative name
English toothed lavender
English french lavender
Spanish espliego dentado
Spanish garlanda
Spanish cantueso rizado
Spanish cantueso dentado
Spanish alhucema inglesa
Spanish alhucema rizada
Arabic خزامى مسننة
br lavand-spagn
Catalan espígol retallat
Catalan gal·landa
Catalan espígol dentat
Czech levandule zoubkatá
German grüner zahn-lavendel
German gezähnter lavendel
German französischer lavendel
Persian لاواندولا دنتاتا
Finnish nyhälaventeli
French lavande dentée
Galician lavanda dentada
Galician lavanda francesa
Italian spigo-nardo
Russian Лаванда зубчатая
Slovak levanduľa zúbkatá
Swedish kamlavendel
Turkish fransız lavantası
Urdu اسطو خودوس ہسپانوی
Chinese 齿叶薰衣草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Lavandula dentata var. candicans Batt. Fl. Alger 2: 666 (1888)
Lavandula dentata var. dentata Unknown

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
  • Africa
    • Macaronesia
      • Canary Islands
      • Cape Verde
      • Madeira
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Palestine
  • Australasia
    • Australia
      • Norfolk Island
    • New Zealand
      • New Zealand North
  • Europe
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000224153
UNII ISP4E5T96U
Tropicos 17603649
INPN 105304
Flora of Italy 4661
KEW urn:lsid:ipni.org:names:449031-1
The Plant List kew-109005
PFAF Lavandula dentata
Open Tree Of Life 5800970
Observations.org 119261
NCBI Taxonomy 1441374
IPNI 449031-1
iNaturalist 71134
GBIF 7307829
Freebase /m/0cny593
EPPO LAVDE
EOL 3013094
Elurikkus 586298
USDA GRIN 21678
Wikipedia Lavandula_dentata
CMAUP NPO19626

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
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Comprehensive Insights into Ochratoxin A: Occurrence, Analysis, and Control Strategies Ben Miri Y, Benabdallah A, Chentir I, Djenane D, Luvisi A, De Bellis L Foods 12-Apr-2024
PMCID:PMC11049263
doi:10.3390/foods13081184
PMID:38672856
Exploring the multifaceted bioactivities of Lavandula pinnata L. essential oil: promising pharmacological activities Haddou M, Elbouzidi A, Taibi M, Baraich A, Loukili EH, Bellaouchi R, Saalaoui E, Asehraou A, Salamatullah AM, Bourhia M, Nafidi HA, Addi M, Guerrouj BE, Chaabane K Front Chem 08-Apr-2024
PMCID:PMC11041020
doi:10.3389/fchem.2024.1383731
PMID:38660570
Applied insight: studying reducing the carbon footprint of the drying process and its environmental impact and financial return Ibrahim A, Amer A, Elsebaee I, Sabahe A, Amer MA Front Bioeng Biotechnol 14-Mar-2024
PMCID:PMC10979823
doi:10.3389/fbioe.2024.1355133
PMID:38558793
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Antibacterial activity of plant extracts against Streptococcus equi subsp. zooepidemicus isolates from guinea pigs with lymphadenitis in Ecuador Ordóñez YF, Miranda E, López MF, Ordóñez PE Heliyon 02-Feb-2024
PMCID:PMC10862515
doi:10.1016/j.heliyon.2024.e25226
PMID:38352743
Chemical Composition and Biological Properties of New Romanian Lavandula Species Marchidan IG, Ortan A, Marcu Spinu S, Avramescu SM, Avram I, Fierascu RC, Babeanu N Antioxidants (Basel) 16-Dec-2023
PMCID:PMC10741150
doi:10.3390/antiox12122127
PMID:38136246
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Macaronesian Plants as Promising Biopesticides against the Crop Pest Ceratitis capitata Tavares WR, Jiménez IA, Oliveira L, Kuhtinskaja M, Vaher M, Rosa JS, Seca AM, Bazzocchi IL, Barreto MD Plants (Basel) 10-Dec-2023
PMCID:PMC10747946
doi:10.3390/plants12244122
PMID:38140449
Plant-Associated Bacillus thuringiensis and Bacillus cereus: Inside Agents for Biocontrol and Genetic Recombination in Phytomicrobiome Sorokan A, Gabdrakhmanova V, Kuramshina Z, Khairullin R, Maksimov I Plants (Basel) 30-Nov-2023
PMCID:PMC10707757
doi:10.3390/plants12234037
PMID:38068672
Which Plant Species for Green Roofs in the Mediterranean Environment? Leotta L, Toscano S, Romano D Plants (Basel) 27-Nov-2023
PMCID:PMC10708222
doi:10.3390/plants12233985
PMID:38068621
Phytochemical analysis, GC–MS profile and determination of antibacterial, antifungal, anti-inflammatory, antioxidant activities of peel and seeds extracts (chloroform and ethyl acetate) of Tamarindus indica L Tavanappanavar AN, Mulla SI, Shekhar Seth C, Bagewadi ZK, Rahamathulla M, Muqtader Ahmed M, Ayesha Farhana S Saudi J Biol Sci 25-Nov-2023
PMCID:PMC10730893
doi:10.1016/j.sjbs.2023.103878
PMID:38125735
Development of Essential Oil-Loaded Polymeric Nanocapsules as Skin Delivery Systems: Biophysical Parameters and Dermatokinetics Ex Vivo Evaluation Silva-Flores PG, Galindo-Rodríguez SA, Pérez-López LA, Álvarez-Román R Molecules 18-Oct-2023
PMCID:PMC10609357
doi:10.3390/molecules28207142
PMID:37894621
Nanoemulsion of Lavandula angustifolia Essential Oil/Gold Nanoparticles: Antibacterial Effect against Multidrug-Resistant Wound-Causing Bacteria Fadel BA, Elwakil BH, Fawzy EE, Shaaban MM, Olama ZA Molecules 09-Oct-2023
PMCID:PMC10574385
doi:10.3390/molecules28196988
PMID:37836831
Pharmacological activities of chemically characterized essential oils from Haplophyllum tuberculatum (Forssk.) Agour A, Mssillou I, Allali A, Chebaibi M, El Abdali Y, El Barnossi A, Bin Jardan YA, Wondmie GF, Nafidi HA, Bourhia M, Bari A, Lyoussi B, Derwich E Front Chem 06-Oct-2023
PMCID:PMC10587419
doi:10.3389/fchem.2023.1251449
PMID:37867997

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
> Alkaloids and derivatives
[(1S,3R,13S,14S,17S,18R,19R,20R,21S,22S,23R,24R,25S)-19,21,24-triacetyloxy-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 102317474 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)O)OC(=O)C)COC(=O)C)OC(=O)C)O)C 721.70 unknown via CMAUP database
Aquifoliunine E-I 70684079 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C 867.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> 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/S10600-007-0236-5
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/S10600-007-0236-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 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/10.1007/S10600-007-0236-5
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-007-0236-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10724415 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O)O 902.80 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10919701 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 5487339 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Alcesefoliside 11828754 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-007-0236-5
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-007-0236-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1007/S10600-007-0236-5

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