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Lantana fucata

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

Description Top

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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)

Common names Top

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

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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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

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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

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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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5R,6R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44254789 Click to see C1C(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)OC5C(C(CO5)(CO)O)O)O)O)O 742.70 unknown https://doi.org/10.1021/NP9002383
[(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 C1C(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)OC5C(C(CO5)(CO)O)O)O)O)O 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 C 44254788 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
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinethiones
Mercaptopurine 667490 Click to see C1=NC2=C(N1)C(=S)N=CN2 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 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
[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 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
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 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
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/10.1590/S0102-695X2008000200010
https://doi.org/10.1055/S-2006-957374
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Scutellarein 4'-methyl ether 11174076 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 300.26 unknown https://doi.org/10.1021/NP9002383
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 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 COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 360.30 unknown https://doi.org/10.1021/NP9002383
5,3',5'-Trihydroxy-6,7,4'-trimethoxyflavone 21581557 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)O)OC)O)O)OC 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 COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1021/NP9002383

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