Lavandula multifida - Unknown
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Internal ID UUID643fe0914b384786327553
Scientific name Lavandula multifida
Authority L.
First published in Sp. Pl. : 572 (1753)

Description Top

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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

Common names Top

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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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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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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
    • Northeast Tropical Africa
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
  • Europe
    • Southeastern Europe
      • Italy
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Portugal
      • Spain

Links to other databases Top

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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
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
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
Determination of Volatile Compounds of Mentha piperita and Lavandula multifida and Investigation of Their Antibacterial, Antioxidant, and Antidiabetic Properties Hamad Al-Mijalli S, ELsharkawy ER, Abdallah EM, Hamed M, El Omari N, Mahmud S, Alshahrani MM, Mrabti HN, Bouyahya A Evid Based Complement Alternat Med 14-Jun-2022
PMCID:PMC9213120
doi:10.1155/2022/9306251
PMID:35747375
The Role of Medicinal and Aromatic Plants against Obesity and Arthritis: A Review Paul AK, Jahan R, Paul A, Mahboob T, Bondhon TA, Jannat K, Hasan A, Nissapatorn V, Wilairatana P, de Lourdes Pereira M, Wiart C, Rahmatullah M Nutrients 25-Feb-2022
PMCID:PMC8912584
doi:10.3390/nu14050985
PMID:35267958
Effectiveness of the Influence of Selected Essential Oils on the Growth of Parasitic Fusarium Isolated from Wheat Kernels from Central Europe Krzyśko-Łupicka T, Sokół S, Sporek M, Piekarska-Stachowiak A, Walkowiak-Lubczyk W, Sudoł A Molecules 27-Oct-2021
PMCID:PMC8588391
doi:10.3390/molecules26216488
PMID:34770893
A Review on Medicinal Plants Used in the Management of Headache in Africa Frimpong EK, Asong JA, Aremu AO Plants (Basel) 28-Sep-2021
PMCID:PMC8539318
doi:10.3390/plants10102038
PMID:34685845
Herbal Medicine Used in the Treatment of Human Diseases in the Rif, Northern Morocco Chaachouay N, Douira A, Zidane L Arab J Sci Eng 07-Apr-2021
PMCID:PMC8024440
doi:10.1007/s13369-021-05501-1
PMID:33842189
Ethnobotanical Study on Plant Used by Semi-Nomad Descendants’ Community in Ouled Dabbeb—Southern Tunisia Karous O, Ben Haj Jilani I, Ghrabi-Gammar Z Plants (Basel) 28-Mar-2021
PMCID:PMC8066878
doi:10.3390/plants10040642
PMID:33800664

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
> 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 CC1(CCCC2(C1CCC3=C2CCC(C3)(CO)C(CO)O)C)C 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 CC1(CCCC2(C1CCC3=C2CCC(C3)(CO)C(CO)O)C)C 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 CC1(CCCC2(C1CCC3=C2CCC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CCC3=C2CCC(C3)(CO)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2C(=O)CC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2C(=O)CC(C3)(C)C(CO)O)C)C 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 CC1(CCCC2(C1CCC3=C2CCC(C3)(CO)C(CO)O)C)C 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 CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(CO)C(CO)O)C)C 336.50 unknown https://doi.org/10.1021/NP020260P
Glutinosin 13816768 Click to see CC1(CCCC2(C1CCC3=C2CCC(C3)(C)C(CO)O)C)C 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
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/J.PHYMED.2004.02.007
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYMED.2004.02.007
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 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 CC(C)(C(CC1=C(C=CC2=C1OC(=O)C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 426.40 unknown https://doi.org/10.1021/NP020260P

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