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Flourensia oolepis

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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 UUID643fc91a843d8427461400
Scientific name Flourensia oolepis
Authority S.F.Blake
First published in Contr. U.S. Natl. Herb. 20: 406. 1921

Description Top

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Synonyms Top

Scientific name Authority First published in
Flourensia grindelioides S.Moore J. Bot. 64: 192 (1926)

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000027768
Tropicos 2706207
KEW urn:lsid:ipni.org:names:277225-2
The Plant List gcc-12684
Open Tree Of Life 7605022
NCBI Taxonomy 2604036
IPNI 105235-2
iNaturalist 791162
GBIF 3094568

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
Rosmarinic Acid Present in Lepechinia floribunda and Lepechinia meyenii as a Potent Inhibitor of the Adenylyl Cyclase gNC1 from Giardia lamblia Zurita A, Vega Hissi E, Cianci Romero A, Luján AM, Salido S, Yaneff A, Davio C, Cobo J, Carpinella MC, Enriz RD Plants (Basel) 26-Feb-2024
PMCID:PMC10935199
doi:10.3390/plants13050646
PMID:38475493
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
Antibacterial potential of chalcones and its derivatives against Staphylococcus aureus da Silva L, Donato IA, Gonçalves CA, Scherf JR, dos Santos HS, Mori E, Coutinho HD, da Cunha FA 3 Biotech 01-Dec-2022
PMCID:PMC9712905
doi:10.1007/s13205-022-03398-7
PMID:36466769
Extracts from Argentinian native plants reverse fluconazole resistance in Candida species by inhibiting the efflux transporters Mdr1 and Cdr1 Gil F, Laiolo J, Bayona-Pacheco B, Cannon RD, Ferreira-Pereira A, Carpinella MC BMC Complement Med Ther 12-Oct-2022
PMCID:PMC9555179
doi:10.1186/s12906-022-03745-4
PMID:36224581
Oxonitrogenated Derivatives of Eremophilans and Eudesmans: Antiproliferative and Anti-Trypanosoma cruzi Activity Beer MF, Reta GF, Puerta A, Bivona AE, Alberti AS, Cerny N, Malchiodi EL, Tonn CE, Padrón JM, Sülsen VP, Donadel OJ Molecules 10-May-2022
PMCID:PMC9143450
doi:10.3390/molecules27103067
PMID:35630539
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
Physicochemical Properties of Biochar Produced from Goldenrod Plants Łapczyńska-Kordon B, Ślipek Z, Słomka-Polonis K, Styks J, Hebda T, Francik S Materials (Basel) 02-Apr-2022
PMCID:PMC9000654
doi:10.3390/ma15072615
PMID:35407947
Pinocembrin suppresses proliferation and enhances apoptosis in lung cancer cells in vitro by restraining autophagy Gong H Bioengineered 04-Sep-2021
PMCID:PMC8806703
doi:10.1080/21655979.2021.1972779
PMID:34486470
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Mechanism Underlying the Reversal of Drug Resistance in P-Glycoprotein-Expressing Leukemia Cells by Pinoresinol and the Study of a Derivative González ML, Vera DM, Laiolo J, Joray MB, Maccioni M, Palacios SM, Molina G, Lanza PA, Gancedo S, Rumjanek V, Carpinella MC Front Pharmacol 25-Apr-2017
PMCID:PMC5403950
doi:10.3389/fphar.2017.00205
PMID:28487651
Assessment of the Potential Biological Activity of Low Molecular Weight Metabolites of Freshwater Macrophytes with QSAR Kurashov EA, Fedorova EV, Krylova JV, Mitrukova GG Scientifica (Cairo) 20-Apr-2016
PMCID:PMC4854990
doi:10.1155/2016/1205680
PMID:27200207
Antibacterial and Cytotoxic Activity of Compounds Isolated from Flourensia oolepis Joray MB, Trucco LD, González ML, Napal GN, Palacios SM, Bocco JL, Carpinella MC Evid Based Complement Alternat Med 27-Dec-2015
PMCID:PMC4706877
doi:10.1155/2015/912484
PMID:26819623
Pinocembrin: A Novel Natural Compound with Versatile Pharmacological and Biological Activities Rasul A, Millimouno FM, Ali Eltayb W, Ali M, Li J, Li X Biomed Res Int 05-Aug-2013
PMCID:PMC3747598
doi:10.1155/2013/379850
PMID:23984355
Screening of Uruguayan plants for deterrent activity against insects Castillo L, González-Coloma A, González A, Díaz M, Santos E, Alonso-Paz E, Bassagoda MJ, Rossini C Ind Crops Prod 01-Jan-2009
PMCID:PMC2779539
doi:10.1016/j.indcrop.2008.05.004
PMID:20046902
Sesquiterpenoids and flavonoids from Flourensia oolepis Eduardo Guerreiro, Juan Kavka, Oscar S. Giordano, Eduardo G. Gros Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(79)80148-X

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 / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid 496073 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(79)80148-X
Ilicic acid 11876195 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(79)80148-X
Ilicol 44559657 Click to see CC12CCCC(C1CC(CC2)C(=C)CO)(C)O 238.37 unknown https://doi.org/10.1016/0031-9422(79)80148-X
> Organoheterocyclic compounds / Benzofurans
Euparin 119039 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 216.23 unknown https://doi.org/10.1016/0031-9422(79)80148-X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1016/0031-9422(79)80148-X
2',4'-Dihydroxychalcone 5376979 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1016/0031-9422(79)80148-X

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