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Lippia turbinata

Lippia turbinata - Unknown
Part: Unknown
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 UUID643fe197c38ad928552088
Scientific name Lippia turbinata
Authority Griseb.
First published in Abh. Königl. Ges. Wiss. Göttingen 19: 243 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lippia aprica Phil. Anales Univ. Chile 91: 415 (1895)
Lippia disepala Phil. Anales Univ. Chile 90: 622 (1895)
Lippia globiflora f. glabriuscula Kuntze Revis. Gen. Pl. 3[3]: 252. 1898 [28 Sep 1898]
Lippia turbinata f. angustifolia Osten ex Moldenke Lilloa 5: 431 (1940)
Lippia turbinata f. magnifolia Moldenke Phytologia 10: 172 (1964)

Common names Top

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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
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile North
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000229205
Tropicos 33700309
KEW urn:lsid:ipni.org:names:863862-1
The Plant List kew-113805
Open Tree Of Life 288152
NCBI Taxonomy 925360
IPNI 863862-1
iNaturalist 431235
GBIF 7297680
EPPO LIPTU
EOL 5389215
iNaturalist 431232

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
Comprehensive Insights into Ochratoxin A: Occurrence, Analysis, and Control Strategies Ben Miri Y, Benabdallah A, Chentir I, Djenane D, Luvisi A, De Bellis L Foods 12-Apr-2024
PMCID:PMC11049263
doi:10.3390/foods13081184
PMID:38672856
Phytochemical Profile and In Vitro Bioactivities of Wild Asparagus stipularis Hamdi A, Jaramillo-Carmona S, Rodríguez-Arcos R, Jiménez-Araujo A, Karray Bouraoui N, Guillén-Bejarano R Molecules 10-Feb-2024
PMCID:PMC10892698
doi:10.3390/molecules29040817
PMID:38398569
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
Exploring the volatile metabolites of three Chorisia species: Comparative headspace GC–MS, multivariate chemometrics, chemotaxonomic significance, and anti-SARS-CoV-2 potential Refaat Fahim J, Darwish AG, El Zawily A, Wells J, Abourehab MA, Yehia Desoukey S, Zekry Attia E Saudi Pharm J 22-Mar-2023
PMCID:PMC10172601
doi:10.1016/j.jsps.2023.03.012
PMID:37181141
Essential Oils Encapsulated in Zeolite Structures as Delivery Systems (EODS): An Overview Ferreira AP, Almeida-Aguiar C, Costa SP, Neves IC Molecules 03-Dec-2022
PMCID:PMC9740572
doi:10.3390/molecules27238525
PMID:36500617
Antifungal Activity of Essential Oil and Plant-Derived Natural Compounds against Aspergillus flavus Tian F, Woo SY, Lee SY, Park SB, Zheng Y, Chun HS Antibiotics (Basel) 01-Dec-2022
PMCID:PMC9774910
doi:10.3390/antibiotics11121727
PMID:36551384
In Vitro Anticancer Activity of Mucoadhesive Oral Films Loaded with Usnea barbata (L.) F. H. Wigg Dry Acetone Extract, with Potential Applications in Oral Squamous Cell Carcinoma Complementary Therapy Popovici V, Matei E, Cozaru GC, Bucur L, Gîrd CE, Schröder V, Ozon EA, Musuc AM, Mitu MA, Atkinson I, Rusu A, Petrescu S, Mitran RA, Anastasescu M, Caraiane A, Lupuliasa D, Aschie M, Badea V Antioxidants (Basel) 28-Sep-2022
PMCID:PMC9598167
doi:10.3390/antiox11101934
PMID:36290658
Evaluation of the toxicology, anti-lipase, and antioxidant effects of Callistemon citrinus in rats fed with a high fat-fructose diet Ortega-Pérez LG, Piñón-Simental JS, Magaña-Rodríguez OR, Lopéz-Mejía A, Ayala-Ruiz LA, García-Calderón AJ, Godínez-Hernández D, Rios-Chavez P Pharm Biol 07-Aug-2022
PMCID:PMC9361760
doi:10.1080/13880209.2022.2099907
PMID:35938503
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
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
Chemical Composition and Antibacterial Activity of Lippia multiflora Moldenke Essential Oil from Different Regions of Angola Samba N, Aitfella-Lahlou R, Nelo M, Silva L, Coca. R, Rocha P, López Rodilla JM Molecules 31-Dec-2020
PMCID:PMC7795161
doi:10.3390/molecules26010155
PMID:33396345
Phytogenic Additives Can Modulate Rumen Microbiome to Mediate Fermentation Kinetics and Methanogenesis Through Exploiting Diet–Microbe Interaction Hassan FU, Arshad MA, Ebeid HM, Rehman MS, Khan MS, Shahid S, Yang C Front Vet Sci 12-Nov-2020
PMCID:PMC7688522
doi:10.3389/fvets.2020.575801
PMID:33263013
Antibacterial, Antifungal, Antimycotoxigenic, and Antioxidant Activities of Essential Oils: An Updated Review Mutlu-Ingok A, Devecioglu D, Dikmetas DN, Karbancioglu-Guler F, Capanoglu E Molecules 14-Oct-2020
PMCID:PMC7587387
doi:10.3390/molecules25204711
PMID:33066611

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 / Triterpenoids
(1S,2R,6R,11S,14S,15R,18S,20S)-20-hydroxy-8,8,14,15,19,19-hexamethyl-10-(2-methylbut-2-enoyloxy)-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 129316669 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/10.1021/NP000267B
(1S,2S,6S,10R,11S,14S,15R,18R,20S)-20-hydroxy-8,8,14,15,19,19-hexamethyl-10-[(2R)-2-methylbutanoyl]oxy-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 162888789 Click to see CCC(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C 570.80 unknown https://doi.org/10.1021/NP000267B
(1S,2S,6S,10R,11S,14S,15R,18R)-20-hydroxy-8,8,14,15,19,19-hexamethyl-10-[(Z)-2-methylbut-2-enoyl]oxy-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 6475941 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/10.1021/NP000267B
(1S,2S,6S,9S,10S,11S,14S,15R,18R,20S)-9,20-dihydroxy-8,8,14,15,19,19-hexamethyl-10-[(E)-2-methylbut-2-enoyl]oxy-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 21592383 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)O 584.80 unknown https://doi.org/10.1021/NP000267B
(1S,2S,6S,9S,10S,11S,14S,15R,18R,20S)-9,20-dihydroxy-8,8,14,15,19,19-hexamethyl-10-[(Z)-2-methylbut-2-enoyl]oxy-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 21592382 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)O 584.80 unknown https://doi.org/10.1021/NP000267B
2,2,6a,6b,9,9,12a-heptamethyl-4-(2-methylbut-2-enoyloxy)-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid 409532 Click to see CC=C(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)(C)C 552.80 unknown https://doi.org/10.1021/NP000267B
20-Hydroxy-8,8,14,15,19,19-hexamethyl-10-(2-methylbut-2-enoyloxy)-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 500192 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/10.1021/NP000267B
20-Hydroxy-8,8,14,15,19,19-hexamethyl-10-(2-methylbutanoyloxy)-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 73809343 Click to see CCC(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C 570.80 unknown https://doi.org/10.1021/NP000267B
20-Hydroxy-8,8,14,15,19,19-hexamethyl-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 15560078 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP000267B
3beta,25-Epoxy-3-hydroxy-22beta-[(3-methyl-1-oxo-2-butenyl)oxy]oleana-12-ene-28-oic acid 495632 Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)C 568.80 unknown https://doi.org/10.1021/NP000267B
9,20-Dihydroxy-8,8,14,15,19,19-hexamethyl-10-(2-methylbut-2-enoyloxy)-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 73718671 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)O 584.80 unknown https://doi.org/10.1021/NP000267B
9,20-Dihydroxy-8,8,14,15,19,19-hexamethyl-10-(3-methylbut-2-enoyloxy)-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-11-carboxylic acid 73809342 Click to see CC(=CC(=O)OC1C(C(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)O)C 584.80 unknown https://doi.org/10.1021/NP000267B
CID 3003153 3003153 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP000267B
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/10.1021/NP000267B
Lantanilic acid 101316804 Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)C 568.80 unknown https://doi.org/10.1021/NP000267B
Lantanolic acid 15560079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP000267B
Olean-12-en-28-oic acid, 3,25-epoxy-3,21-dihydroxy-22-[(3-methyl-1-oxo-2-butenyl)oxy]-, (3beta,21alpha,22beta)- 21592381 Click to see CC(=CC(=O)OC1C(C(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)O)C 584.80 unknown https://doi.org/10.1021/NP000267B
Rehmannic acid 6436598 Click to see CC=C(C)C(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)(C)C 552.80 unknown https://doi.org/10.1021/NP000267B
> Organoheterocyclic compounds / Tetrahydroisoquinolines
6'-Methylspiro[6,9-dihydro-[1,3]dioxolo[4,5-h]isochromene-7,5'-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline] 21632927 Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(CO4)C6=C(C=C5)OCO6)OCO3 353.40 unknown https://doi.org/10.1021/NP000267B

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