Details Top

Internal ID UUID643fe06027ce0618203389
Scientific name Lantana fucata
Authority Lindl.
First published in Bot. Reg. 10: t. 798 (1824)

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
- Lantana fucata is cultivated as an ornamental shrub for landscaping and horticulture in subtropical and tropical regions; the plant is sold by nurseries and garden centres for garden plantings, public parks, and commercial landscaping projects.

Fragrance and cosmetics:
- Leaves and flowering tops are steam‑distilled to obtain an essential oil. The oil contains a high proportion of linalool (≈30–45 % of total volatiles), β‑caryophyllene (≈15–20 %), and geranyl acetate (≈5–10 %). This composition gives the oil a fresh, floral aroma and it is used by the fragrance industry in soaps, detergents, and perfume bases. Commercial specifications typically require a specific gravity of 0.885–0.905 g cm⁻³ at 20 °C and a linalool content of at least 30 %.

Properties relevant to use:
- The leaf surface is densely covered with glandular trichomes that store monoterpenes and sesquiterpenes, facilitating efficient steam distillation. The oil’s monoterpene‑rich profile (linalool, geraniol) is responsible for its stability in aqueous formulations and its relatively low volatility at ambient temperature, making it suitable for long‑lasting fragrance applications.

Standards and regulation:
- Essential oil of L. fucata is subject to International Fragrance Association (IFRA) standards for permissible use levels in consumer products and must comply with ISO 9235 (Essential oils – General requirements) for physical‑chemical parameters such as relative density, optical rotation, and acid value. Cosmetic use also falls under the US Food and Drug Administration (FDA) Cosmetic Act and the European Union Cosmetic Regulation (EC) No 1223/2009, which require disclosure of fragrance ingredients and adherence to maximum permissible concentrations for linalool and related terpenes.

Sustainability and sourcing:
- The species is propagated by vegetative cuttings, allowing consistent quality and rapid scaling of production without dependence on wild populations. Nurseries in Mexico and the southern United States supply horticultural material, and small‑scale essential‑oil production is typically integrated with ornamental cultivation. Sustainable horticultural practices—such as organic fertilization, water‑efficient irrigation, and integrated pest management—are recommended to maintain consistent oil yields and minimise environmental impact.

Synonyms Top

Scientific name Authority First published in
Lantana czermakii Briq. Annuaire Conserv. Jard. Bot. Genève 3: 164 (1899)
Lantana fucata f. albiflora Moldenke Phytologia 2: 468 (1948)
Lantana fucata var. antillana Moldenke Phytologia 4: 128 (1952)
Lantana fucata var. longipes Moldenke Phytologia 35: 277 (1977)
Lantana fuscata K.Koch Wochenschr. Gärtnerei Pflanzenk. 1: 322 (1858)
Lantana inconspicua Tausch Flora 19: 391 (1836)
Lantana lilacina Desf. Tabl. École Bot., ed. 3 (Cat. Pl. Horti Paris.) 392. 1829
Lantana lilacina var. media Briq. Bull. Herb. Boissier , sér. 2, 4: 1063 (1904)
Lantana lilacina var. mollis Zahlbr. Bot. Jahrb. Syst. 42: 168 (1908)
Lantana lilacina var. parvifolia Briq. Annuaire Conserv. Jard. Bot. Genève 7-8: 300 (1904)
Camara lilacina (Desf.) Kuntze Revis. Gen. Pl. 3(2): 250 (1898)
Camara lilacina f. albiflora Kuntze Revis. Gen. Pl. 3(2): 250 (1898)
Camara lilacina var. grandifolia Kuntze Revis. Gen. Pl. 3(2): 250 (1898)
Camara lilacina var. media Kuntze Revis. Gen. Pl. 3(2): 250 (1898)
Camara salviifolia Kuntze Revis. Gen. Pl. 2: 504 (1891)
Camara lilacina var. parvifolia Kuntze Revis. Gen. Pl. 4: 250 (1898)
Lantana recta Cham. Linnaea 7: 125 (1832)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic لانتانا محمرة
Portuguese cambará-roxo
Portuguese cambará
Chinese 粉花马缨丹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Jamaica
      • Venezuelan Antilles
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000223131
Tropicos 33700967
KEW urn:lsid:ipni.org:names:324303-2
The Plant List kew-108040
Open Tree Of Life 371057
NCBI Taxonomy 1241420
IPNI 324303-2
iNaturalist 545679
GBIF 2925328
EOL 579755

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 α-glucosidase inhibition by Brazilian medicinal plant extracts characterised by ultra-high performance liquid chromatography coupled to mass spectrometry Lianza M, Poli F, do Nascimento AM, Soares da Silva A, da Fonseca TS, Toledo MV, Simas RC, Chaves AR, Leitão GG, Leitão SG J Enzyme Inhib Med Chem 14-Feb-2022
PMCID:PMC8933013
doi:10.1080/14756366.2021.2022658
PMID:35152818
Antimicrobial Activity and Chemical Composition of Essential Oils from Verbenaceae Species Growing in South America Pérez Zamora CM, Torres CA, Nuñez MB Molecules 01-Mar-2018
PMCID:PMC6017629
doi:10.3390/molecules23030544
PMID:29494478
Phenylethanoid Glycosides: Research Advances in Their Phytochemistry, Pharmacological Activity and Pharmacokinetics Xue Z, Yang B Molecules 29-Jul-2016
PMCID:PMC6273160
doi:10.3390/molecules21080991
PMID:27483229
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Phenylethanoid glycosides from Lantana fucata with in vitro anti-inflammatory activity. Julião Lde S, Piccinelli AL, Marzocco S, Leitão SG, Lotti C, Autore G, Rastrelli L J Nat Prod 01-Aug-2009
doi:10.1021/NP9002383
PMID:19634889
Purification of an antibacterial compound from Lantana lilacina Aline C. Pereira, Hudson W. P. Carvalho, Geraldo H. Silva, Denilson F. Oliveira, Henrique C. P. Figueiredo, Alberto J. Cavalheiro, Douglas A. Carvalho Springer Science and Business Media LLC 07-Aug-2008
doi:10.1590/S0102-695X2008000200010
An acyclic monoterpene glucosyl ester from Lantana lilacia. Takeda Y, Takechi A, Masuda T, Otsuka H Planta Med 01-Feb-1998
doi:10.1055/S-2006-957374
PMID:17253224

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5R,6R)-4,5-bis[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 102482976 Click to see C1C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)CO)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)(CO)O 742.70 unknown https://doi.org/10.1021/NP9002383
[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74976067 Click to see 742.70 unknown https://doi.org/10.1021/NP9002383
[4,5-Bis[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74976066 Click to see C1C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)CO)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)(CO)O 742.70 unknown https://doi.org/10.1021/NP9002383
Fucatoside B 44254789 Click to see 742.70 unknown https://doi.org/10.1021/NP9002383
Fucatoside C 44254788 Click to see 742.70 unknown https://doi.org/10.1021/NP9002383
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinethiones
6-Mercaptopurine 667490 Click to see 152.18 unknown https://doi.org/10.1021/NP9002383
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74976009 Click to see 610.60 unknown https://doi.org/10.1021/NP9002383
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-4-hydroxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75225243 Click to see 624.60 unknown https://doi.org/10.1021/NP9002383
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1055/S-2006-957374
Fucatoside A 44254697 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 610.60 unknown https://doi.org/10.1021/NP9002383
Parvifloroside A 46883312 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9002383
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1055/S-2006-957374
https://doi.org/10.1590/S0102-695X2008000200010
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Scutellarein 4'-methyl ether 11174076 Click to see 300.26 unknown https://doi.org/10.1021/NP9002383
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Nepetin 5317284 Click to see 316.26 unknown https://doi.org/10.1021/NP9002383
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,3',4'-Trihydroxy-6,7,5'-trimethoxyflavone 14104185 Click to see 360.30 unknown https://doi.org/10.1021/NP9002383
5,3',5'-Trihydroxy-6,7,4'-trimethoxyflavone 21581557 Click to see 360.30 unknown https://doi.org/10.1021/NP9002383
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1021/NP9002383
Salvigenin 161271 Click to see 328.30 unknown https://doi.org/10.1021/NP9002383

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.