Aloysia gratissima - Unknown
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Details Top

Internal ID UUID644039842e403026011654
Scientific name Aloysia gratissima
Authority (Gillies & Hook.) Tronc.
First published in Darwiniana 12: 527 (1962)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lantana virgata Larrañaga Escritos D. A. Larrañaga 2: 188 (1923)
Lippia ligustrina var. lasiodonta Briq. Annuaire Conserv. Jard. Bot. Genève 7-8: 305 (1904)
Lippia ligustrina var. paraguariensis Briq. Annuaire Conserv. Jard. Bot. Genève 7-8: 305 (1904)
Lippia ligustrina var. schulzii Standl. Publ. Field Columb. Mus., Bot. Ser. 4: 256 (1929)
Lippia lycioides Steud. Nomencl. Bot. , ed. 2, 2: 54 (1841)
Verbena gratissima Gillies & Hook. Bot. Misc. 1: 160 (1829)
Verbena integerrima Larrañaga Escritos D. A. Larrañaga 1: 9 (1923)
Lippia gratissima (Gillies & Hook.) L.D.Benson in L.D. Benson & R.A. Darrow, Trees & Shrubs of Southwest. Deserts (ed. 3) 202 (1981):.
Lippia gratissima var. schulzii (Standl.) L.D.Benson Trees & Shrubs of Southw. Deserts 203. 1981
Aloysia mizquensis Ravenna Onira 10: 59 (2006)
Aloysia famatinensis Ravenna Onira 11: 15 (2007)
Aloysia floribunda M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 320 (1844)
Aloysia gratissima f. macrophylla Moldenke Phytologia 29: 75 (1974)
Aloysia gratissima var. paraguariensis (Briq.) Moldenke Phytologia 9: 500 (1964)
Aloysia ligustrina var. paraguariensis Moldenke Phytologia 1: 167 (1935)
Aloysia ligustrina var. schulzii Moldenke Phytologia 1: 95 (1934)
Aloysia lycioides Cham. Linnaea 7: 237 (1832)
Aloysia lycioides var. paraguariensis (Briq.) Moldenke Phytologia 2: 464 (1948)
Aloysia lycioides var. schulzii (Standl.) Moldenke Phytologia 2: 464 (1948)
Aloysia uruguayensis Moldenke Phytologia 1: 167 (1935)
Aloysia lycioides var. schulziana (Moldenke) Siedo

Common names Top

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Language Common/alternative name
English whitebrush
Arabic لويزة مرضية
Quechua kutu-kutu

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile Central
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000950823
USDA Plants ALGR2
Tropicos 33700918
KEW urn:lsid:ipni.org:names:9643-2
The Plant List kew-6904
Open Tree Of Life 2132
NCBI Taxonomy 105888
Nature Serve 2.142071
IPNI 9643-2
iNaturalist 56891
GBIF 5341161
EPPO ALYLY
EOL 579785
USDA GRIN 101120

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
Understanding Phakopsora pachyrhizi in soybean: comprehensive insights, threats, and interventions from the Asian perspective Hossain MM, Sultana F, Yesmin L, Rubayet MT, Abdullah HM, Siddique SS, Bhuiyan MA, Yamanaka N Front Microbiol 11-Jan-2024
PMCID:PMC10808435
doi:10.3389/fmicb.2023.1304205
PMID:38274768
Multiscale assessment of habitat selection and avoidance of sympatric carnivores by the endangered ocelot Sergeyev M, Cherry MJ, Tanner EP, Lombardi JV, Tewes ME, Campbell TA Sci Rep 01-Jun-2023
PMCID:PMC10235131
doi:10.1038/s41598-023-35271-9
PMID:37264027
Antidepressant-Like Activity of Solvent Fractions of the Root Bark of Carissa spinarum Linn. (Apocynaceae) in Rodents Involves Multiple Signaling Pathways Ali HS, Engidawork E J Exp Pharmacol 09-Dec-2022
PMCID:PMC9748120
doi:10.2147/JEP.S386015
PMID:36531440
In Vivo Antidepressant-Like Effect Assessment of Two Aloysia Species in Mice and LCMS Chemical Characterization of Ethanol Extract Taboada T, Alvarenga NL, Galeano AK, Arrúa WJ, Campuzano-Bublitz MA, Kennedy ML Molecules 13-Nov-2022
PMCID:PMC9693556
doi:10.3390/molecules27227828
PMID:36431928
The thiophene α-terthienylmethanol isolated from Tagetes minuta inhibits angiogenesis by targeting protein kinase C isozymes α and β2 Llorens de los Ríos MC, Lanza PA, Barbieri CL, González ML, Chabán MF, Soria G, Vera DM, Carpinella MC, Joray MB Front Pharmacol 12-Oct-2022
PMCID:PMC9597362
doi:10.3389/fphar.2022.1007790
PMID:36313304
Role of ethno-phytomedicine knowledge in healthcare of COVID-19: advances in traditional phytomedicine perspective Nasir Ahmed M, Hughes K Beni Suef Univ J Basic Appl Sci 04-Aug-2022
PMCID:PMC9362587
doi:10.1186/s43088-022-00277-1
PMID:35966214
Integrating Network Pharmacology, Molecular Docking, and Experimental Validation to Investigate the Mechanism of (−)-Guaiol Against Lung Adenocarcinoma Zeng Y, Pan Y, Zhang B, Luo Y, Tian J, Wang Y, Ju X, Wu J, Li Y Med Sci Monit 25-Jul-2022
PMCID:PMC9336205
doi:10.12659/MSM.937131
PMID:35871777
Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay Säumel I, Ramírez LR Data Brief 16-May-2022
PMCID:PMC9130530
doi:10.1016/j.dib.2022.108267
PMID:35647241
Oral Microbiome: Getting to Know and Befriend Neighbors, a Biological Approach Bacali C, Vulturar R, Buduru S, Cozma A, Fodor A, Chiș A, Lucaciu O, Damian L, Moldovan ML Biomedicines 14-Mar-2022
PMCID:PMC8945538
doi:10.3390/biomedicines10030671
PMID:35327473
Screening of Natural Products Inhibitors of SARS-CoV-2 Entry González-Maldonado P, Alvarenga N, Burgos-Edwards A, Flores-Giubi ME, Barúa JE, Romero-Rodríguez MC, Soto-Rifo R, Valiente-Echeverría F, Langjahr P, Cantero-González G, Sotelo PH Molecules 07-Mar-2022
PMCID:PMC8911944
doi:10.3390/molecules27051743
PMID:35268843
Biological Properties of Aloysia gratissima (Gillies & Hook.) Tronc. (Verbenaceae) Alijar Souza M, Petry F, Vidor Morgan L, Dal Magro J, Müller LG Evid Based Complement Alternat Med 19-Jan-2022
PMCID:PMC8791711
doi:10.1155/2022/1119435
PMID:35096101
One day at a time Kattner AA Biomed J 15-Jan-2022
PMCID:PMC8760849
doi:10.1016/j.bj.2022.01.009
PMID:35042016
Antibiofilm Potential of Medicinal Plants against Candida spp. Oral Biofilms: A Review Guimarães R, Milho C, Liberal Â, Silva J, Fonseca C, Barbosa A, Ferreira IC, Alves MJ, Barros L Antibiotics (Basel) 21-Sep-2021
PMCID:PMC8464735
doi:10.3390/antibiotics10091142
PMID:34572724
Chemical Composition and Immunomodulatory Activity of Essential Oils from Rhododendron albiflorum Schepetkin IA, Özek G, Özek T, Kirpotina LN, Khlebnikov AI, Quinn MT Molecules 15-Jun-2021
PMCID:PMC8232766
doi:10.3390/molecules26123652
PMID:34203809
Plant Preparations and Compounds with Activities against Biofilms Formed by Candida spp. Karpiński TM, Ożarowski M, Seremak-Mrozikiewicz A, Wolski H, Adamczak A J Fungi (Basel) 05-May-2021
PMCID:PMC8147947
doi:10.3390/jof7050360
PMID:34063007

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 / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,2R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one 10329459 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
3-Pinanone 11038 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
3,5,5-Trimethylbicyclo[2.2.1]heptan-2-one 86707 Click to see CC1C2CC(C1=O)CC2(C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Bicyclo[3.1.1]Heptan-3-One, 2,6,6-Trimethyl-, [1S-(1a,2ss,5a)]- 12311188 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
alpha-Elemene 80048 Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Ylangenol 179519 Click to see CC(C)C1CCC2(C3C1C2C(=CC3)CO)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81286-8

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