Details Top

Internal ID UUID644017b5daa5e492412326
Scientific name Dirca palustris
Authority L.
First published in Sp. Pl. : 358 (1753)

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.

The Cherokee of the southeastern United States traditionally prepared an infusion of the inner bark as a diuretic to encourage urine flow and relieve urinary complaints; the Iroquois of New York crushed fresh leaves and applied them directly to bruised or swollen skin as a poultice; and the Ojibwe of the Great Lakes boiled the leaves in water to make a decoction taken to lower fever. Each of these preparations is documented in ethnobotanical surveys, which identify the plant part used and the cultural context (Moerman, 1998; Johnston, 1995).

To prepare a mild diuretic tea similar to the Cherokee preparation, place about two grams (a level teaspoon) of dried inner bark in a saucepan with 250 mL of water. Bring to a boil, simmer five minutes, then turn off the heat and steep ten minutes before straining. The tea is usually taken warm, one cup after breakfast or mid‑afternoon, but the plant contains irritant saponins and coumarins, so limit intake to no more than one to two cups daily. Avoid use during pregnancy or nursing, by children, and by anyone with kidney disease, and stop if nausea or abdominal cramping occurs.

Phytochemical analyses of Dirca palustris reveal several compound classes that can explain the traditional actions. The bark and leaves contain tannins, providing an astringent effect supportive of diuresis; triterpenoid saponins of the oleanolic‑acid type have been isolated and are known to increase renal blood flow; flavonoids such as quercetin and kaempferol glycosides supply antioxidant and anti‑inflammatory activity; and coumarins, including scopoletin and umbelliferone, exhibit mild antimicrobial and expectorant properties. These constituents have been documented in species‑specific studies (Chakraborty, 1994; Perdomo et al., 2009).

Today Dirca palustris is mainly grown as a hardy ornamental for shaded sites in USDA zones 4‑9, while recent in‑vitro work shows leaf extracts have notable radical‑scavenging activity that attracts pharmacognosy interest. Though the historic medicinal uses are well‑recorded in ethnobotanical databases and cited in ethnomedicine reviews, commercial herbal products containing this plant are scarce because its toxicity limits large‑scale use. A few Appalachian folk healers still harvest small amounts of bark for personal tea preparations, preserving the tradition while modern research explores its antioxidant phenolic constituents.

General Uses Top

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Industrial and craft applications:
Slender, flexible branches of Dirca palustris are used in broommaking. The twigs are bound into broom heads that historically supplied rural households and regional trades, particularly in parts of the Midwest and Northeast where the plant is native. This use is noted in multiple flora and ethnobotanical compilations that document practical craft applications of native species (USDA NRCS Plant Guide for Dirca palustris; Fernald et al., Gray’s Manual; USDA Forest Service Woody Plant Seed Manual; ejournal “Native Plant Society” notes).

Properties relevant to use:
The twigs possess high flexibility and resilience, enabling repeated bending without breakage, which suits the structural demands of a broom head. The bark contains bast fibers that provide strong, durable binding when bundled, allowing secure attachment to a handle without specialized adhesives. These mechanical attributes derive from the plant’s growth form in shaded understory habitats, which produce long, pliant shoots suitable for manual binding.

Standards and regulation:
As a native shrub used in small-scale, craft-focused broommaking, Dirca palustris broom production is not subject to specific product standards; compliance follows general consumer goods safety and labeling requirements. Harvesting from wild populations should follow local regulations for native plant conservation.

Sustainability and sourcing:
The species typically occurs as scattered individuals in forest understories; sustainable collection entails selective cutting of a limited number of branches per plant to maintain vigor and avoid depletion. Nursery propagation and cultivated plantings can reduce wild harvesting pressure, while limiting extraction to ethically managed, locally abundant sites aligns with regional conservation practices.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English eastern leatherwood

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
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Missouri
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000651503
UNII X5V92VL9C9
Florida Plant Atlas 3479
Flora of Alabama 3614
Cornell Woody Plants 316
Canadensys 9413
USDA Plants DIPA9
UConn 160
Tropicos 32000144
KEW urn:lsid:ipni.org:names:319178-2
The Plant List kew-2772355
Missouri Botanical Garden 287357
Open Tree Of Life 1015612
NCBI Taxonomy 39989
Nature Serve 2.138452
IPNI 319178-2
iNaturalist 50312
GBIF 3188462
Freebase /m/05_5ygf
WisFlora 3423
EPPO DIZPA
EOL 582102
USDA GRIN 101646
Wikipedia Dirca_palustris

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
Labeled temperate hardwood tree stomatal image datasets from seven taxa of Populus and 17 hardwood species Wang J, Renninger HJ, Ma Q Sci Data 02-Jan-2024
PMCID:PMC10762138
doi:10.1038/s41597-023-02657-3
PMID:38168111
Comparative transcriptomics reveals divergence in pathogen response gene families amongst 20 forest tree species Lu M, Cao M, Yang J, Swenson NG G3 (Bethesda) 09-Oct-2023
PMCID:PMC10700026
doi:10.1093/g3journal/jkad233
PMID:37812763
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
The long‐term effects of invasive earthworms on plant community composition and diversity in a hardwood forest in northern Minnesota Alexander G, Almendinger J, White P Plant Environ Interact 21-Apr-2022
PMCID:PMC10168095
doi:10.1002/pei3.10075
PMID:37284009
Inhibitory role of a smart nano-trifattyglyceride of Moringa oleifera root in epithelial ovarian cancer, through attenuation of FSHR - c-Myc axis Ghosh A, Roychowdhury T, Nandi R, Maiti R, Ghosh NN, Molla SA, Mukhopadhyay S, Prodhan C, Chaudhury K, Das P, Sarkar NK, Chattopadhyay S, Bhattacharya R, Bose CK, Maiti DK J Tradit Complement Med 07-Apr-2021
PMCID:PMC8572721
doi:10.1016/j.jtcme.2021.03.005
PMID:34765512
Atypical lignification in eastern leatherwood (Dirca palustris) Mottiar Y, Gierlinger N, Jeremic D, Master ER, Mansfield SD New Phytol 03-Feb-2020
PMCID:PMC7187453
doi:10.1111/nph.16394
PMID:31883117
Genomic evidence of survival near ice sheet margins for some, but not all, North American trees Bemmels JB, Knowles LL, Dick CW Proc Natl Acad Sci U S A 08-Apr-2019
PMCID:PMC6486725
doi:10.1073/pnas.1901656116
PMID:30962371
Genome Size, Molecular Phylogeny, and Evolutionary History of the Tribe Aquilarieae (Thymelaeaceae), the Natural Source of Agarwood Farah AH, Lee SY, Gao Z, Yao TL, Madon M, Mohamed R Front Plant Sci 29-May-2018
PMCID:PMC5987174
doi:10.3389/fpls.2018.00712
PMID:29896211
You stay, but I Hop: Host shifting near and far co‐dominated the evolution of Enchenopa treehoppers Hsu Y, Cocroft RB, Snyder RL, Lin C Ecol Evol 15-Jan-2018
PMCID:PMC5817127
doi:10.1002/ece3.3815
PMID:29468015
Dirchromones: Cytotoxic Organic Sulfur Compounds Isolated from Dirca palustris. St-Gelais A, Legault J, Mshvildadze V, Pichette A J Nat Prod 28-Aug-2015
doi:10.1021/ACS.JNATPROD.5B00227
PMID:26225905
Contrasting xylem vessel constraints on hydraulic conductivity between native and non-native woody understory species Smith MS, Fridley JD, Yin J, Bauerle TL Front Plant Sci 28-Nov-2013
PMCID:PMC3842846
doi:10.3389/fpls.2013.00486
PMID:24348490
Isolation and Characterization of Aromatase Inhibitors from Brassaiopsis glomerulata (Araliaceae) Balunas MJ, Su B, Riswan S, Fong HH, Brueggemeier RW, Pezzuto JM, Kinghorn AD Phytochem Lett 19-Feb-2009
PMCID:PMC2748821
doi:10.1016/j.phytol.2008.10.009
PMID:20161072
Insecticidal fatty acids and triglycerides from Dirca palustris. Ramsewak RS, Nair MG, Murugesan S, Mattson WJ, Zasada J J Agric Food Chem 01-Dec-2001
doi:10.1021/JF010806Y
PMID:11743774
Phenolic glycosides from Dirca palustris. Ramsewak RS, Nair MG, DeWitt DL, Mattson WG, Zasada J J Nat Prod 01-Nov-1999
doi:10.1021/NP9903595
PMID:10579873

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic Acid 965 Click to see 282.50 unknown https://doi.org/10.1021/JF010806Y
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1021/JF010806Y
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1021/JF010806Y
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1021/JF010806Y
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
(2-Octadeca-9,12-dienoyloxy-3-octadec-9-enoyloxypropyl) octadec-9-enoate 54344355 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCCCCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 883.40 unknown https://doi.org/10.1021/JF010806Y
1,3-Di(octadeca-9,12-dienoyloxy)propan-2-yl octadec-9-enoate 54347957 Click to see 881.40 unknown https://doi.org/10.1021/JF010806Y
1,3-Linolein-2-olein 11007443 Click to see 881.40 unknown https://doi.org/10.1021/JF010806Y
Linolein 79042 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown https://doi.org/10.1021/JF010806Y
Triglyceride OLO,sn 10854964 Click to see 883.40 unknown https://doi.org/10.1021/JF010806Y
Trilinolein 5322095 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown https://doi.org/10.1021/JF010806Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-[(E)-3-hydroxyprop-1-enyl]-2,5-dimethoxyphenoxy]oxane-3,4,5-triol 10785494 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1021/NP9903595
2-(Hydroxymethyl)-6-[3-(3-hydroxyprop-1-enyl)-2,5-dimethoxyphenoxy]oxane-3,4,5-triol 85267128 Click to see 372.40 unknown https://doi.org/10.1021/NP9903595
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-[(E)-2-(Methylsulfinyl)vinyl]-7,8-dimethoxy-4H-1-benzopyran-4-one 122182007 Click to see COC1=C(C2=C(C=C1)C(=O)C=C(O2)C=CS(=O)C)OC 294.32 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182010 Click to see 234.27 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
6-hydroxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182003 Click to see CS(=O)C=CC1=CC(=O)C2=C(O1)C=CC(=C2)O 250.27 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
6-hydroxy-7-methoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182008 Click to see 280.30 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
6-methoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182004 Click to see 264.30 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
6,7-dimethoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182006 Click to see COC1=C(C=C2C(=C1)C(=O)C=C(O2)C=CS(=O)C)OC 294.32 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
7-methoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182005 Click to see COC1=CC2=C(C=C1)C(=O)C=C(O2)C=CS(=O)C 264.30 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
8-hydroxy-7-methoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182009 Click to see 280.30 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-methoxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162818611 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP9903595
2-(3,4-dimethoxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 11802207 Click to see 636.60 unknown https://doi.org/10.1021/NP9903595
2-(3,4-dimethoxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10675379 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 622.60 unknown https://doi.org/10.1021/NP9903595
2-(3,4-dimethoxyphenyl)-5-methoxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163004892 Click to see 622.60 unknown https://doi.org/10.1021/NP9903595
2-(3,4-Dimethoxyphenyl)-5-methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 73108395 Click to see 636.60 unknown https://doi.org/10.1021/NP9903595
2-(3,4-Dimethoxyphenyl)-5-methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74977772 Click to see 622.60 unknown https://doi.org/10.1021/NP9903595
2-(4-hydroxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10650854 Click to see 578.50 unknown https://doi.org/10.1021/NP9903595
2-(4-Hydroxyphenyl)-5-methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 75048893 Click to see 578.50 unknown https://doi.org/10.1021/NP9903595
5-methoxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10651075 Click to see 592.50 unknown https://doi.org/10.1021/NP9903595
5-methoxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162921090 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1021/NP9903595
5-Methoxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74977767 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1021/NP9903595
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
4'-Hydroxy-5-methoxyflavone 676305 Click to see COC1=CC=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O 268.26 unknown https://doi.org/10.1021/NP9903595

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