Lantana montevidensis - Unknown
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Internal ID UUID643fe0651afef838645745
Scientific name Lantana montevidensis
Authority Briq.
First published in Annuaire Conserv. Jard. Bot. Genève 7-8: 301 (1904)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lantana decumbens Sellow ex A.DC. Prodr. 11: 604 (1847)
Lantana delicatissima Poit. Rev. Hort. (Paris) , sér. 4, 1: 461 (1852)
Lantana montevidensis f. albiflora Moldenke Phytologia 2: 365 (1947)
Lantana selloi Steud. Nomencl. Bot. , ed. 2, 2: 8 (1841)
Lantana sellowiana Link & Otto Icon. Pl. Select. : 107 (1826)
Lantana sellowiana var. lanceolata Hook. in Curtis Bot. Mag. 68: t. 3941 (1842)
Lantana sellowiana f. planifolia Cham. Linnaea 7: 126 (1832)
Lantana sellowiana f. rugosa Cham. Linnaea 7: 126 (1832)
Lippia montevidensis Spreng. Syst. Veg. 2: 751 (1825)
Camara montevidensis (Spreng.) Kuntze Revis. Gen. Pl. 3(2): 250 (1898)
Camara sellowiana (Link & Otto) Kuntze Revis. Gen. Pl. 2: 504 (1891)

Common names Top

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Language Common/alternative name
English trailing shrubverbena
Arabic لانتانا مونتيفيديوية
Arabic لانتانا زاحفة
Hebrew לנטנה לילכית
Japanese コバノランタナ
Japanese 小葉のランタナ
Dutch kruipende wisselbloem
Vietnamese trâm ổi tím
Vietnamese bông ổi tím
Chinese 蔓马缨丹
Chinese 黄马缨丹

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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Distribution (via Powo/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
    • Southwestern U.S.A.
      • California
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Costa Rica
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000223286
Florida Plant Atlas 375
Flora of Alabama 3681
USDA Plants LAMO2
Tropicos 33700784
INPN 446078
Flora of Italy 11605
KEW urn:lsid:ipni.org:names:135260-2
The Plant List kew-108181
Missouri Botanical Garden 287465
Open Tree Of Life 371059
NCBI Taxonomy 1241423
Nature Serve 2.135587
IPNI 135260-2
iNaturalist 77624
GBIF 2925314
Freebase /m/047nf1t
EPPO LANMV
EOL 579777
Calflora (Californian flora) 4567
USDA GRIN 101133
Wikipedia Lantana_montevidensis
CMAUP NPO14851

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
Smart Nanomaterials in Cancer Theranostics: Challenges and Opportunities Kashyap BK, Singh VV, Solanki MK, Kumar A, Ruokolainen J, Kesari KK ACS Omega 10-Apr-2023
PMCID:PMC10134471
doi:10.1021/acsomega.2c07840
PMID:37125102
First Report on the Chemical Composition, Antioxidant Capacity, and Preliminary Toxicity to Artemia salina L. of Croton campinarensis Secco, A. Rosário & PE Berry (Euphorbiaceae) Essential Oil, and In Silico Study da Costa LS, de Moraes ÂA, Cruz JN, Mali SN, Almeida LQ, do Nascimento LD, Ferreira OO, Varela EL, Percário S, de Oliveira MS, Andrade EH Antioxidants (Basel) 06-Dec-2022
PMCID:PMC9774510
doi:10.3390/antiox11122410
PMID:36552618
Comparative LC–LTQ–MS–MS Analysis of the Leaf Extracts of Lantana camara and Lantana montevidensis Growing in Egypt with Insights into Their Antioxidant, Anti-Inflammatory, and Cytotoxic Activities El-Din MI, Fahmy NM, Wu F, Salem MM, Khattab OM, El-Seedi HR, Korinek M, Hwang TL, Osman AK, El-Shazly M, Fayez S Plants (Basel) 27-Jun-2022
PMCID:PMC9269492
doi:10.3390/plants11131699
PMID:35807651
Recent Advances in the Antiproliferative and Proapoptotic Activity of Various Plant Extracts and Constituents against Murine Malignant Melanoma Dumitraș DA, Andrei S Molecules 17-Apr-2022
PMCID:PMC9028509
doi:10.3390/molecules27082585
PMID:35458783
A Potential New Source of Therapeutic Agents for the Treatment of Mucocutaneous Leishmaniasis: The Essential Oil of Rhaphiodon echinus Oliveira CV, da Silva PA, Tintino SR, Coronel CC, Gomez MC, Rolón M, da Cunha FA, Morais-Braga MF, Coutinho HD, Siyadatpanah A, Wilairatana P, Kamdem JP, Barros LM, Duarte AE, Pereira PS Molecules 27-Mar-2022
PMCID:PMC9000529
doi:10.3390/molecules27072169
PMID:35408565
Diterpenes/Diterpenoids and Their Derivatives as Potential Bioactive Leads against Dengue Virus: A Computational and Network Pharmacology Study Khan RA, Hossain R, Siyadatpanah A, Al-Khafaji K, Khalipha AB, Dey D, Asha UH, Biswas P, Saikat AS, Chenari HA, Wilairatana P, Islam MT Molecules 11-Nov-2021
PMCID:PMC8623982
doi:10.3390/molecules26226821
PMID:34833913
Pest categorisation of Phenacoccus solenopsis Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Campese C, Czwienczek E, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Aug-2021
PMCID:PMC8371560
doi:10.2903/j.efsa.2021.6801
PMID:34429782
The Involvement of Natural Polyphenols in the Chemoprevention of Cervical Cancer Drețcanu G, Iuhas CI, Diaconeasa Z Int J Mol Sci 16-Aug-2021
PMCID:PMC8396230
doi:10.3390/ijms22168812
PMID:34445518
β-Caryophyllene, A Natural Dietary CB2 Receptor Selective Cannabinoid can be a Candidate to Target the Trinity of Infection, Immunity, and Inflammation in COVID-19 Jha NK, Sharma C, Hashiesh HM, Arunachalam S, Meeran MN, Javed H, Patil CR, Goyal SN, Ojha S Front Pharmacol 14-May-2021
PMCID:PMC8163236
doi:10.3389/fphar.2021.590201
PMID:34054510
Revisiting nature: a review of iridoids as a potential antileishmanial class Arraché Gonçalves G, Eifler-Lima VL, von Poser GL Phytochem Rev 16-Mar-2021
PMCID:PMC7960493
doi:10.1007/s11101-021-09750-8
PMID:33746658

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(+)-Rhododendrol 919204 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown via CMAUP database
4-(4-Hydroxyphenyl)-2-butanone 21648 Click to see CC(=O)CCC1=CC=C(C=C1)O 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6bR,12aS)-10-hydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163073639 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)CO)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-0035-1545209
(4aS,6aS,6bR,12aS)-14a-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,3,4,5,6,6a,7,8,8a,11,12,14b-dodecahydropicene-4a-carboxylic acid 162817004 Click to see CC1(CCC2(CCC3(C4(CCC5C(C(=O)CCC5(C4C=CC3(C2C1)O)C)(C)C)C)C)C(=O)O)C 470.70 unknown https://doi.org/10.1055/S-0035-1545209
CID 91895465 91895465 Click to see CC=C(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C 568.80 unknown https://doi.org/10.1055/S-0035-1545209
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/10.1055/S-0035-1545209
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1055/S-0035-1545209
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-0035-1545209
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 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/10.1248/BPB.25.875
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/10.1016/S0305-1978(96)00115-9
> 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/10.1248/BPB.25.875
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1248/BPB.25.875
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4',5-Dihydroxy-3',5',6,7-tetramethoxyflavone 16681753 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 374.30 unknown https://doi.org/10.1248/BPB.25.875
4',5,6-Trihydroxy-3',5',7-trimethoxyflavone 91602946 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 360.30 unknown https://doi.org/10.1248/BPB.25.875
5-Hydroxy-3',4',7-trimethoxyflavone 5272653 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1016/S0305-1978(96)00115-9
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/10.1248/BPB.25.875
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone 10020367 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC 344.30 unknown https://doi.org/10.1248/BPB.25.875
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/NP900051S
https://doi.org/10.1248/BPB.25.875
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP900051S
https://doi.org/10.1248/BPB.25.875
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1248/BPB.25.875
Nuchensin 373260 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown https://doi.org/10.1248/BPB.25.875
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0305-1978(96)00115-9
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
7,8,4'-Trihydroxyisoflavone 5466139 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
6''-O-Acetylononin 102463148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O 472.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol 177149 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database

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