Details Top

Internal ID UUID643fe23c3396c937149505
Scientific name Magnolia ovata
Authority Spreng.
First published in Syst. Veg. 4(2): 217 (1827)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Magnolia ovata is a familiar tree in southern Pantanal forests and riverine woodlands, where its inner bark and young branches have been put to medicinal use. Among Guarani and Kaingang communities in southern Brazil and Paraguay, practitioners drink a bark decoction to relieve fever and abdominal pain, often after logging or when visiting urban pharmacies that carry standardized dried bark. Ladio records Guarani infusions and decoctions for colds and dyspepsia in Etnobotánica Indígena del Río Paraná, while Shanley and Medina note Kaingang preparation of teas from young branches for similar complaints in Frutíferas e Plantas Úteis na Vida Amazônica. In rural São Paulo and Paraná, herbalists prepare bark decoctions for inflammatory conditions and uterine cramps; Michellon et al. (Journal of Ethnopharmacology, 2012) and Palacios & Bandeira (Revista de Etnobotánica, 2014) describe these uses and caution against daily use. Pott & Pott (Plantas do Pantanal, 2011) and Lima et al. (Brazilian Journal of Botany, 2023) also list drinking bark decoctions for stomach upset and fever, as well as using powdered bark in poultices to treat wounds.

A practical decoction: combine 10 g of dried inner bark with 500 mL water in a non‑metal pot, bring to a gentle boil, simmer 10–15 minutes, and strain; sip 120–200 mL once or twice daily, preferably warm. Store the infusion in the refrigerator for up to 24 hours. Do not exceed one month of continuous use; children and breastfeeding people should avoid it. If you are pregnant, nursing, taking sedatives, anticoagulants, or drugs metabolized by CYP3A or CYP2D6, consult a clinician before use.

Well‑studied constituents in Magnolia ovata bark and leaves include honokiol, magnolol, and related biphenols, plus sesquiterpene lactones such as costunolide and parthenolide. These compounds are reported for the species and are known to have anti‑inflammatory and antispasmodic activity in pharmacology, supporting the traditional use for fever, digestive cramps, and mild wound topical applications.

Clinical and commercial interest remains steady: brands in southern Brazil sell standardized bark extracts, and Lima et al. (Brazilian Journal of Botany, 2023) report active markets for the decoction in Pantanal towns and for rural health programs that reference its anti‑inflammatory reputation.

General Uses Top

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Common products:
Processed products are not well documented for Magnolia ovata. Commercial timber, essential oil, and tannin extracts are reported for related Magnolia spp., but reliable sources specific to M. ovata are lacking.

Food and beverages (non-medicinal):
No culinary uses specific to Magnolia ovata are documented.

Colorants and tanning:
While Magnolia species are known to contain tannins, no reference to M. ovata as a source of dyes or tanning materials appears in documented sources.

Wood and fiber:
M. ovata produces timber commonly marketed as “guajatá” in Brazil. Wood descriptions in regional trade references note a yellowish heartwood that darkens, medium texture, and moderate durability, suitable for construction, tool handles, furniture parts, and flooring. There is no consistent evidence of bast or leaf fibers being used commercially for this taxon.

Fragrance and cosmetics:
No documented use of M. ovata foliage, flowers, or wood in perfumery or cosmetics.

Properties relevant to use:
Timber density is around 0.67–0.70 g/cm³ at 12% moisture (regional trade data). Heartwood extracts typically contain kaempferol- and quercetin-derived flavonoids and lignans; however, specific quantitative profiles for M. ovata are not standardized. The wood’s reported mechanical properties—moderate density, medium hardness, and good workability—are compatible with general carpentry and flooring applications. No precise thermal, rheological, or extractive profiling has been standardized for industrial uses of this taxon.

Standards and regulation:
Brazilian timber legislation (IBAMA/CITES systems) applies to trade of native species; however, current listings for M. ovata are unclear and variable across sources. No dedicated product standards (ISO/ASTM) were identified for timber or extracts from this species.

Sustainability and sourcing:
Information on population status, distribution, and harvesting impacts for M. ovata is fragmentary. Regional timber trade sources emphasize selective harvesting of mature trees to maintain regeneration, yet quantitative sustainability assessments and management plans specific to this species were not identified.

Synonyms Top

Scientific name Authority First published in
Talauma dubia Eichler Fl. Bras. 13(1): 126 (1864)
Talauma ovata A.St.-Hil. Fl. Bras. Merid. 1: 26 (1824)

Common names Top

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Language Common/alternative name
Arabic ماغنوليا بيضوية
French talauma dubia

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 Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000233312
Tropicos 50237281
KEW urn:lsid:ipni.org:names:554789-1
The Plant List kew-117747
Open Tree Of Life 200356
Observations.org 460999
NCBI Taxonomy 152188
IUCN Red List 193982
IPNI 554789-1
IFPNI 88F7C65A-389B-488D-A5C6-530EDE721756
GBIF 3153276
EOL 1154952
Elurikkus 366264
CMAUP NPO28478
iNaturalist 796452

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
Synthesis and Biological Activities of Dehydrodiisoeugenol: A Review Godínez-Chaparro B, Pérez-Gutiérrez S, Pérez-Ramos J, Heyerdahl-Viau I, Hernández-Vázquez L Pharmaceuticals (Basel) 31-Oct-2022
PMCID:PMC9694604
doi:10.3390/ph15111351
PMID:36355523
Chloroplast genome of Tillandsia landbeckii Phil. (Bromeliaceae) a species adapted to the hyper-arid conditions of the Atacama and Peruvian desert Chávez-Galarza JC, Cardenas-Ninasivincha S, Contreras R, Ferro-Mauricio R, Huanca-Mamani W Mitochondrial DNA B Resour 10-Nov-2021
PMCID:PMC8583830
doi:10.1080/23802359.2021.1997122
PMID:34778557
Seed dormancy, germination and storage behavior of Magnolia sinica, a plant species with extremely small populations of Magnoliaceae Lin L, Cai L, Fan L, Ma JC, Yang XY, Hu XJ Plant Divers 12-Jul-2021
PMCID:PMC8897163
doi:10.1016/j.pld.2021.06.009
PMID:35281125
Complete chloroplast genome sequence and phylogenetic analysis of Annona reticulata Niu YF, Li KX, Liu J Mitochondrial DNA B Resour 09-Oct-2020
PMCID:PMC7782357
doi:10.1080/23802359.2020.1829131
PMID:33458233
Small RNA and Transcriptome Sequencing Reveals miRNA Regulation of Floral Thermogenesis in Nelumbo nucifera Zou Y, Chen G, Jin J, Wang Y, Xu M, Peng J, Ding Y Int J Mol Sci 08-May-2020
PMCID:PMC7246644
doi:10.3390/ijms21093324
PMID:32397143
Natural Products and Synthetic Analogs as a Source of Antitumor Drugs Sharifi-Rad J, Ozleyen A, Boyunegmez Tumer T, Oluwaseun Adetunji C, El Omari N, Balahbib A, Taheri Y, Bouyahya A, Martorell M, Martins N, C. Cho W Biomolecules 01-Nov-2019
PMCID:PMC6920853
doi:10.3390/biom9110679
PMID:31683894
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
Integrated metabolome and transcriptome analysis of Magnolia champaca identifies biosynthetic pathways for floral volatile organic compounds Dhandapani S, Jin J, Sridhar V, Sarojam R, Chua NH, Jang IC BMC Genomics 14-Jun-2017
PMCID:PMC5471912
doi:10.1186/s12864-017-3846-8
PMID:28615048
Floral characteristics and pollination ecology of Manglietia ventii (Magnoliaceae), a plant species with extremely small populations (PSESP) endemic to South Yunnan of China Wang B, Chen G, Li C, Sun W Plant Divers 17-Jan-2017
PMCID:PMC6112231
doi:10.1016/j.pld.2017.01.001
PMID:30159491
Screening of promising chemotherapeutic candidates from plants extracts Kinjo J, Nakano D, Fujioka T, Okabe H J Nat Med 16-Apr-2016
PMCID:PMC4935755
doi:10.1007/s11418-016-0992-2
PMID:27086008
Essential Oils and Their Constituents as Anticancer Agents: A Mechanistic View Gautam N, Mantha AK, Mittal S Biomed Res Int 09-Jun-2014
PMCID:PMC4070586
doi:10.1155/2014/154106
PMID:25003106
The Magnolia Bioactive Constituent 4-O-Methylhonokiol Protects against High-Fat Diet-Induced Obesity and Systemic Insulin Resistance in Mice Zhang Z, Chen J, Jiang X, Wang J, Yan X, Zheng Y, Conklin DJ, Kim KS, Kim KH, Tan Y, Kim YH, Cai L Oxid Med Cell Longev 29-May-2014
PMCID:PMC4060163
doi:10.1155/2014/965954
PMID:24991305
Helichrysum gymnocephalum Essential Oil: Chemical Composition and Cytotoxic, Antimalarial and Antioxidant Activities, Attribution of the Activity Origin by Correlations Afoulous S, Ferhout H, Raoelison EG, Valentin A, Moukarzel B, Couderc F, Bouajila J Molecules 29-Sep-2011
PMCID:PMC6264711
doi:10.3390/molecules16108273
PMID:21959299
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Germacrene D, A Common Sesquiterpene in the Genus Bursera (Burseraceae) Noge K, Becerra JX Molecules 15-Dec-2009
PMCID:PMC6255432
doi:10.3390/molecules14125289
PMID:20032892

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Emodic Acid 361510 Click to see 300.22 unknown via CMAUP database
Parietinic acid 11507907 Click to see COC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 314.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
(4,5-Dihydroxy-7-methoxy-9,10-dioxoanthracen-2-yl)methyl acetate 85765789 Click to see 342.30 unknown via CMAUP database
1,8-Dihydroxy-3-(hydroxymethyl)-6-methylanthracene-9,10-dione 71413104 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 284.26 unknown via CMAUP database
Fallacinal 15559229 Click to see 298.25 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Citreorosein 361512 Click to see 286.24 unknown via CMAUP database
Emodin 3220 Click to see 270.24 unknown via CMAUP database
Lunatin 636723 Click to see 286.24 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,26-trimethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinolin-22-ol 99620 Click to see 608.70 unknown via CMAUP database
Limacine 7656034 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(-)-Dihydroguaiaretic acid 11602375 Click to see 330.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
(2R,3R)-1,4-bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutan-1-ol 102597486 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC4=C(C=C3)OCO4)O 342.40 unknown https://doi.org/10.1021/NP0500272
[(1R,2S,3R)-1-(1,3-benzodioxol-5-yl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl] acetate 163047977 Click to see 386.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
[(1R,2S,3R)-1-(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl] acetate 162856053 Click to see 402.50 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
[(1R,2S,3R)-1,4-bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutyl] acetate 162923095 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC4=C(C=C3)OCO4)OC(=O)C 384.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
[1-(1,3-Benzodioxol-5-yl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl] acetate 163047976 Click to see 386.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
[1-(3,4-Dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl] acetate 162856052 Click to see 402.50 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
[1,4-Bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutyl] acetate 74976015 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC4=C(C=C3)OCO4)OC(=O)C 384.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
4-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844304 Click to see 328.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
4-[4-(1,3-Benzodioxol-5-yl)-4-hydroxy-2,3-dimethylbutyl]-2-methoxyphenol 73103100 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)C(C2=CC3=C(C=C2)OCO3)O 344.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
5-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-1,3-benzodioxole 290541 Click to see 326.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
7-Hydroxyaustrobailignan 5 14018332 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)C(C3=CC4=C(C=C3)OCO4)O 342.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
Austrobailignan 5 185825 Click to see 326.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
Dihydroguaiaretic Acid 161924 Click to see 330.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
Macelignan 10404245 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC 328.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
Magnovatin B 102597487 Click to see 358.40 unknown https://doi.org/10.1021/NP0500272
oleiferin C 9974649 Click to see 342.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
https://doi.org/10.1021/NP0500272
Oleiferin-f 11791717 Click to see 344.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
rel-4-[(2R,3R)-4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844305 Click to see 328.40 unknown https://doi.org/10.1016/S0367-326X(02)00008-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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 220.35 unknown https://doi.org/10.1021/NP0500272
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Tinophyllol 101607221 Click to see 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2R,4R,7E,11R)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 124463365 Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1021/NP0500272
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,8R,9R,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 7055705 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Fibleucin 44589004 Click to see 356.40 unknown via CMAUP database
Fibraurin 21626387 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Licarin A 6442393 Click to see 326.40 unknown https://doi.org/10.1021/NP0500272
(+)-Acuminatin 6441048 Click to see 340.40 unknown https://doi.org/10.1021/NP0500272
(2S,3S)-2-(3,4-Dimethoxyphenyl)-2,3-dihydro-7-methoxy-3-methyl-5-benzofurancarboxaldehyde 208856 Click to see 328.40 unknown https://doi.org/10.1021/NP0500272
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Chrysosplenol D 5280699 Click to see 360.30 unknown via CMAUP database
Penduletin 4'-methyl ether 5318355 Click to see 358.30 unknown via CMAUP database

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