Dirca palustris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

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

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English eastern leatherwood

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
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

Add a new one!
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic acid 965 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1021/JF010806Y
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 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 CCCCCC=CCC=CCCCCCCCC(=O)O 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 CCCCCCCCC=CCCCCCCCC(=O)OC(COC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC 881.40 unknown https://doi.org/10.1021/JF010806Y
1,3-Linolein-2-olein 11007443 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC(COC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC 881.40 unknown https://doi.org/10.1021/JF010806Y
9Z,12Z-octadecadienoic acid, 2-[[(9Z)-1-oxo-9-octadecen-1-yl]oxy]-1-[[[(9Z)-1-oxo-9-octadecen-1-yl]oxy]methyl]ethyl ester 10854964 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
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
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 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
> 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 CS(=O)C=CC1=CC(=O)C2=CC=CC=C2O1 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 COC1=C(C=C2C(=C1)OC(=CC2=O)C=CS(=O)C)O 280.30 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00227
6-methoxy-2-[(E)-2-methylsulfinylethenyl]chromen-4-one 122182004 Click to see COC1=CC2=C(C=C1)OC(=CC2=O)C=CS(=O)C 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 COC1=C(C2=C(C=C1)C(=O)C=C(O2)C=CS(=O)C)O 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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C(=C3)OC)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)OC)O)O)O)O)O)O 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 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-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 73108395 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C(=C3)OC)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)OC)O)O)O)O)O)O 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 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-(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 COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 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 COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 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 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-[(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

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.