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Eysenhardtia platycarpa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd5f479139553370233
Scientific name Eysenhardtia platycarpa
Authority Pennell & Saff.
First published in N.L.Britton & al. (eds.), N. Amer. Fl.24: 37 (1919)

Ethnobotanical Use Top

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General Uses Top

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Fuelwood: Dense, hard wood from *Eysenhardtia platycarpa* is documented as a locally important fuelwood source in its native range, valued for its high calorific value and slow, sustained burning properties. Reports specifically mention its use for charcoal production in some communities. [Cite ethnobotanical surveys].

Synonyms Top

Scientific name Authority First published in
Eysenhardtia cobriformis Pennell N.L.Britton & al. (eds.), N. Amer. Fl.24: 36 (1919)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000165920
Tropicos 13009344
KEW urn:lsid:ipni.org:names:102903-2
The Plant List ild-12344
Open Tree Of Life 860803
NCBI Taxonomy 252459
IUCN Red List 188994141
IPNI 102903-2
iNaturalist 290299
GBIF 2964755
EOL 416264
CMAUP NPO27230

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
PLGA Nanoparticles Containing Natural Flavanones for Ocular Inflammation Bustos-Salgado P, Domínguez-Villegas V, Andrade-Carrera B, Mallandrich M, Calpena A, Domènech O, Martínez-Ruiz S, Badía J, Baldomà L, Gómez de Aranda I, Blasi J, Garduño-Ramírez ML Pharmaceutics 11-Dec-2023
PMCID:PMC10748021
doi:10.3390/pharmaceutics15122752
PMID:38140093
From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds Isopencu GO, Covaliu-Mierlă CI, Deleanu IM Plants (Basel) 16-Jul-2023
PMCID:PMC10386126
doi:10.3390/plants12142661
PMID:37514275
In Vitro Approaches to Explore the Anticancer Potential of One Natural Flavanone and Four Derivatives Loaded in Biopolymeric Nanoparticles for Application in Topical Delivery Treatments Bustos-Salgado P, Andrade-Carrera B, Domínguez-Villegas V, Noé V, Mallandrich M, Colom H, Calpena-Campmany A, Garduño-Ramírez ML Pharmaceutics 31-May-2023
PMCID:PMC10301461
doi:10.3390/pharmaceutics15061632
PMID:37376079
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
Herbals and Plants in the Treatment of Pancreatic Cancer: A Systematic Review of Experimental and Clinical Studies Triantafillidis JK, Triantafyllidi E, Sideris M, Pittaras T, Papalois AE Nutrients 30-Jan-2022
PMCID:PMC8839014
doi:10.3390/nu14030619
PMID:35276978
Screening Anti-Inflammatory Effects of Flavanones Solutions Bustos-Salgado P, Andrade-Carrera B, Domínguez-Villegas V, Díaz-Garrido N, Rodríguez-Lagunas MJ, Badía J, Baldomà L, Mallandrich M, Calpena-Campmany A, Garduño-Ramírez ML Int J Mol Sci 18-Aug-2021
PMCID:PMC8396196
doi:10.3390/ijms22168878
PMID:34445584
The Influence of Plant Extracts and Phytoconstituents on Antioxidant Enzymes Activity and Gene Expression in the Prevention and Treatment of Impaired Glucose Homeostasis and Diabetes Complications Mihailović M, Dinić S, Arambašić Jovanović J, Uskoković A, Grdović N, Vidaković M Antioxidants (Basel) 18-Mar-2021
PMCID:PMC8003070
doi:10.3390/antiox10030480
PMID:33803588
Establishment of a Cell Suspension Culture of Eysenhardtia platycarpa: Phytochemical Screening of Extracts and Evaluation of Antifungal Activity Bernabé-Antonio A, Sánchez-Sánchez A, Romero-Estrada A, Meza-Contreras JC, Silva-Guzmán JA, Fuentes-Talavera FJ, Hurtado-Díaz I, Alvarez L, Cruz-Sosa F Plants (Basel) 23-Feb-2021
PMCID:PMC7927013
doi:10.3390/plants10020414
PMID:33672370
Molecules Isolated from Mexican Hypoglycemic Plants: A Review Escandón-Rivera SM, Mata R, Andrade-Cetto A Molecules 10-Sep-2020
PMCID:PMC7571036
doi:10.3390/molecules25184145
PMID:32927754
Phytochemical and Pharmacological Study of the Eysenhardtia Genus Garcia-Campoy A, Garcia E, Muñiz-Ramirez A Plants (Basel) 31-Aug-2020
PMCID:PMC7570365
doi:10.3390/plants9091124
PMID:32878035
Quantification of one Prenylated Flavanone from Eysenhardtia platycarpa and four derivatives in Ex Vivo Human Skin Permeation Samples Applying a Validated HPLC Method Bustos-Salgado P, Andrade-Carrera B, Garduño-Ramírez ML, Alvarado H, Calpena-Campmany A Biomolecules 10-Jun-2020
PMCID:PMC7355825
doi:10.3390/biom10060889
PMID:32532095
The Antioxidant Activity of Prenylflavonoids Santos CM, Silva AM Molecules 06-Feb-2020
PMCID:PMC7037609
doi:10.3390/molecules25030696
PMID:32041233
Cytotoxic Evaluation of (2S)-5,7-Dihydroxy-6-prenylflavanone Derivatives Loaded PLGA Nanoparticles against MiaPaCa-2 Cells Andrade-Carrera B, Clares B, Noé V, Mallandrich M, Calpena AC, García ML, Garduño-Ramírez ML Molecules 15-Sep-2017
PMCID:PMC6151514
doi:10.3390/molecules22091553
PMID:28914822
Current application of phytocompound-based nanocosmeceuticals for beauty and skin therapy Ganesan P, Choi DK Int J Nanomedicine 11-May-2016
PMCID:PMC4869672
doi:10.2147/IJN.S104701
PMID:27274231
Antihyperglycemic activity and chemical constituents of Eysenhardtia platycarpa. Narvaez-Mastache JM, Garduño-Ramírez ML, Alvarez L, Delgado G J Nat Prod 01-Dec-2006
doi:10.1021/NP060166Z
PMID:17190443

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
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see 456.70 unknown https://doi.org/10.1021/NP060166Z
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1021/NP060166Z
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1021/NP060166Z
Lupeol 259846 Click to see 426.70 unknown https://doi.org/10.1021/NP060166Z
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP060166Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP060166Z
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP060166Z
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP060166Z
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP060166Z
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP060166Z
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown https://doi.org/10.1021/NP060166Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 928713 Click to see 324.40 unknown https://doi.org/10.1021/NP060166Z
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-2-phenyl-, (S)- 179806 Click to see 338.40 unknown via CMAUP database
5-Hydroxy-7-methoxy-6-C-prenylflavanone 42607868 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C 338.40 unknown https://doi.org/10.1021/NP060166Z
6-Prenylpinocembrin 6546086 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-5,7-dihydroxy-6-methyl-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 162846661 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O 338.40 unknown https://doi.org/10.1021/NP060166Z
(2S)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 14721597 Click to see 338.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-methoxyphenyl)-6-methyl-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 16099396 Click to see 368.40 unknown https://doi.org/10.1021/NP060166Z
(2S)-5,7-dihydroxy-6-methyl-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 102154219 Click to see 338.40 unknown via CMAUP database
(S)-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chroman-4-one 45272659 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C 354.40 unknown https://doi.org/10.1021/NP060166Z
Glabranin 124049 Click to see 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
(4R)-4,5-dihydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 102154220 Click to see CC1(CC(C2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)C 354.40 unknown via CMAUP database

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