Common products:
No distinct, widely recognized commercial or industrial product is reported for Lavandula multifida in the literature. The species is primarily documented as ornamental.

Industrial and craft applications:
No established industrial or craft uses are reported.

Food and beverages (non-medicinal):
No specific culinary uses are documented for this taxon.

Colorants and tanning:
No use for dyes, inks, or tannins is documented.

Wood and fiber:
No fiber, timber, or wood products are reported.

Fragrance and cosmetics:
No documented use in perfumes, aromatherapy, or cosmetics is found in reliable references.

Properties relevant to use:
Not applicable.

Standards and regulation:
Not applicable.

Sustainability and sourcing:
Not applicable.

Synonyms Top

Scientific name	Authority	First published in
Lavandula multipartita	Christm.	Vollst. Pflanzensyst. 4: 43 (1779)
Lavandula pinnatifida	Webb	Iter Hispan. : 19 (1838)
Lavandula multifida var. homotricha	Sauvage	Bull. Soc. Sci. Nat. Maroc 35-37(2): 392. 1947
Lavandula multifida var. intermedia	Ball	J. Linn. Soc., Bot. 16: 608. 1878
Lavandula multifida var. monostachya	Lundmark	Lavandula 14. 1780
Lavandula multifida f. pallescens	Maire	Bull. Soc. Hist. Nat. Afrique N. 25: 314 1934
Lavandula multifida var. heterotricha	Sauvage	Bull. Soc. Sci. Nat. Maroc 35-37(2): 392. 1947
Lavandula multifida f. albiflora	H.Lindb.	Acta Soc. Sci. Fenn., Ser. B, Opera Biol. 1(2): 129 (1932)
Lavandula multifida f. glabrifolia	Pau	Mem. Real Soc. Esp. Hist. Nat. 12: 372 (1924)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	cantueso
Spanish	confitera
Spanish	alhucema
Spanish	alhucemilla
Spanish	aljucema
Spanish	cantagüeso
Spanish	uceda
Spanish	ucema
Arabic	خزام
Arabic	لوندة
Arabic	خزامى
br	lavand-delioù-raden
Estonian	lõhislehine lavendel
Russian	Лаванда многонадрезная
Chinese	多裂薰衣草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northeast Tropical Africa
  - Sudan
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
  - Western Sahara

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
- Southwestern Europe
  - Baleares
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000224197
Tropicos	17604982
Flora of Italy	4664
KEW	urn:lsid:ipni.org:names:449064-1
The Plant List	kew-109049
Missouri Botanical Garden	281617
Open Tree Of Life	879752
Observations.org	135017
NCBI Taxonomy	260634
IPNI	449064-1
iNaturalist	82918
GBIF	3891203
Freebase	/m/05mxny3
EPPO	LAVMU
EOL	5369193
Elurikkus	215073
USDA GRIN	21682
Wikipedia	Lavandula_multifida

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

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

Ecological and Syntaxonomic Analysis of the Communities of Glebionis coronaria and G. discolor (Malvion neglectae) in the European Mediterranean Area

Cano E, Cano-Ortiz A, Quinto Canas R, Piñar Fuentes JC, Rodrigues Meireles C, Raposo M, Pinto Gomes C, Laface VL, Spampinato G, Musarella CM

Plants (Basel)

20-Feb-2024

PMCID:	PMC10934477
doi:	10.3390/plants13050568
PMID:	38475415

Biochemical Composition, Antioxidant Capacity and Protective Effects of Three Fermented Plants Beverages on Hepatotoxicity and Nephrotoxicity Induced by Carbon Tetrachloride in Mice

Gadhoumi H, Dhouafli Z, Yeddes W, serairi beji R, Miled K, Trifi M, Chirchi A, Saidani Tounsi M, Hayouni EA

Indian J Microbiol

26-Dec-2023

PMCID:	PMC10924858
doi:	10.1007/s12088-023-01172-8
PMID:	38468731

The significance of essential oils and their antifungal properties in the food industry: A systematic review

Abdi-Moghadam Z, Mazaheri Y, Rezagholizade-shirvan A, Mahmoudzadeh M, Sarafraz M, Mohtashami M, Shokri S, Ghasemi A, Nickfar F, Darroudi M, Hossieni H, Hadian Z, Shamloo E, Rezaei Z

Heliyon

29-Oct-2023

PMCID:	PMC10637975
doi:	10.1016/j.heliyon.2023.e21386
PMID:	37954273

Antibiofilm Effect of Lavandula multifida Essential Oil: A New Approach for Chronic Infections

Alves-Silva J, Zuzarte M, Cavaleiro C, Salgueiro L

Pharmaceutics

15-Aug-2023

PMCID:	PMC10458520
doi:	10.3390/pharmaceutics15082142
PMID:	37631356

Quality-by-Design-Assisted Optimization of Carvacrol Oil-Loaded Niosomal Gel for Anti-Inflammatory Efficacy by Topical Route

Ghazwani M, Hani U, Alam A, Alqarni MH

Gels

10-May-2023

PMCID:	PMC10217970
doi:	10.3390/gels9050401
PMID:	37232993

Synergistic Interaction between Boesenbergia rotunda (L.) Mansf. Essential Oil and Cloxacillin on Methicillin-Resistant Staphylococcus aureus (MRSA) Inhibition

Apinundecha C, Teethaisong Y, Suknasang S, Ayamuang IO, Eumkeb G

Evid Based Complement Alternat Med

16-Apr-2023

PMCID:	PMC10129417
doi:	10.1155/2023/3453273
PMID:	37114143

The Antioxidant Properties of Lavandula multifida Extract Contribute to Its Beneficial Effects in High-Fat Diet-Induced Obesity in Mice

Molina-Tijeras JA, Ruiz-Malagón AJ, Hidalgo-García L, Diez-Echave P, Rodríguez-Sojo MJ, Cádiz-Gurrea MD, Segura-Carretero A, del Palacio JP, González-Tejero MR, Rodríguez-Cabezas ME, Gálvez J, Rodríguez-Nogales A, Vezza T, Algieri F

Antioxidants (Basel)

29-Mar-2023

PMCID:	PMC10135096
doi:	10.3390/antiox12040832
PMID:	37107207

Design and Synthesis of Novel Antimicrobial Agents

Breijyeh Z, Karaman R

Antibiotics (Basel)

22-Mar-2023

PMCID:	PMC10045396
doi:	10.3390/antibiotics12030628
PMID:	36978495

Exploring Iberian Peninsula Lamiaceae as Potential Therapeutic Approaches in Wound Healing

Marques MP, Mendonça L, Neves BG, Varela C, Oliveira P, Cabral C

Pharmaceuticals (Basel)

24-Feb-2023

PMCID:	PMC10056130
doi:	10.3390/ph16030347
PMID:	36986446

Molecular Responses of Vegetable, Ornamental Crops, and Model Plants to Salinity Stress

Toscano S, Romano D, Ferrante A

Int J Mol Sci

06-Feb-2023

PMCID:	PMC9965374
doi:	10.3390/ijms24043190
PMID:	36834600

A New Lavender (Lavandula multifida L.) Ecotype from Arid Tunisia, with Differential Essential Oil Composition and Higher Antimicrobial Potential

Tofah ML, Mseddi K, Al-Abbasi OK, Ben Yazid A, Khechine A, Gdoura R, Khannous L

Life (Basel)

30-Dec-2022

PMCID:	PMC9866874
doi:	10.3390/life13010103
PMID:	36676052

Phytochemical Profiling, Antioxidant and Anti-Inflammatory Activity of Plants Belonging to the Lavandula Genus

Dobros N, Zawada KD, Paradowska K

Molecules

28-Dec-2022

PMCID:	PMC9821988
doi:	10.3390/molecules28010256
PMID:	36615453

Effects of Coleus amboinicus L. Essential Oil and Ethanolic Extracts on Planktonic Cells and Biofilm Formation of Microsporum canis Isolated from Feline Dermatophytosis

Leesombun A, Thanapakdeechaikul K, Suwannawiang J, Mukto P, Sungpradit S, Bangphoomi N, Changbunjong T, Thongjuy O, Weluwanarak T, Boonmasawai S

Antibiotics (Basel)

01-Dec-2022

PMCID:	PMC9774219
doi:	10.3390/antibiotics11121734
PMID:	36551390

Essential Oils in Respiratory Mycosis: A Review

Zuzarte M, Salgueiro L

Molecules

28-Jun-2022

PMCID:	PMC9268412
doi:	10.3390/molecules27134140
PMID:	35807386

Phytochemical Profile Top

Add a new one!

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R)-1-[(4bS)-2-(hydroxymethyl)-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol	163194370	Click to see	322.50	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
(1S)-1-[(2R,4bS,8aS)-2-(hydroxymethyl)-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol	163005745	Click to see	322.50	unknown	https://doi.org/10.1021/NP020260P
(1S)-1-[(2S,4bS,8aS)-2,4b,8,8-tetramethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol	163007824	Click to see	306.50	unknown	https://doi.org/10.1021/NP020260P
(1S)-1-[(4bS)-2-(hydroxymethyl)-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol	163005744	Click to see	322.50	unknown	https://doi.org/10.1021/NP020260P
(2S,4bS,8aS)-2-[(1S)-1,2-dihydroxyethyl]-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione	162956567	Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)CC(C3)(C)C(CO)O)C)C	334.40	unknown	https://doi.org/10.1021/NP020260P
(4aS,7R,10aS)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	21602085	Click to see	320.50	unknown	https://doi.org/10.1021/NP020260P
(4aS,7R,10aS)-7-[(1S)-1,2-dihydroxyethyl]-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	162931652	Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(CO)C(CO)O)C)C	336.50	unknown	https://doi.org/10.1021/NP020260P
(4aS,7S)-7-(1,2-dihydroxyethyl)-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	101218944	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
(4aS,7S)-7-(1,2-dihydroxyethyl)-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	101218946	Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(CO)C(CO)O)C)C	336.50	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
(4aS)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	162970389	Click to see	320.50	unknown	https://doi.org/10.1021/NP020260P
(4aS)-7-[(1S)-1,2-dihydroxyethyl]-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	162931653	Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(CO)C(CO)O)C)C	336.50	unknown	https://doi.org/10.1021/NP020260P
(4bS)-2-[(1R)-1,2-dihydroxyethyl]-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione	163189021	Click to see	334.40	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
(4bS)-2-[(1S)-1,2-dihydroxyethyl]-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione	162956568	Click to see	334.40	unknown	https://doi.org/10.1021/NP020260P
1-[2-(hydroxymethyl)-4b,8,8-trimethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol	85374634	Click to see	322.50	unknown	https://doi.org/10.1021/NP020260P
2-(1,2-dihydroxyethyl)-2,4b,8,8-tetramethyl-3,5,6,7,8a,9-hexahydro-1H-phenanthrene-4,10-dione	73798355	Click to see CC1(CCCC2(C1CC(=O)C3=C2C(=O)CC(C3)(C)C(CO)O)C)C	334.40	unknown	https://doi.org/10.1021/NP020260P
7-(1,2-Dihydroxyethyl)-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	73798356	Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C(CO)O)C)C	320.50	unknown	https://doi.org/10.1021/NP020260P
7-(1,2-Dihydroxyethyl)-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one	85394620	Click to see	336.50	unknown	https://doi.org/10.1021/NP020260P
Glutinosin	13816768	Click to see	306.50	unknown	https://doi.org/10.1021/NP020260P https://doi.org/10.1016/J.PHYMED.2004.02.007
> 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/10.1016/J.PHYMED.2004.02.007
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R)-2-(hydroxymethyl)-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)oxane-3,4,5-triol	163186770	Click to see CC1=C(C(=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)O)O	328.36	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
Maslinic Acid	73659	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(4aR,6bR,10S,12aR)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	163188842	Click to see CC1(CCC2(CCC3C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C	442.70	unknown	https://doi.org/10.1016/J.PHYMED.2004.02.007
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	101915811	Click to see	426.40	unknown	https://doi.org/10.1021/NP020260P

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Lavandula multifida

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top