Dirca occidentalis

Details Top

Internal ID UUID644017b5c2295784521230
Scientific name Dirca occidentalis
Authority A.Gray
First published in Proc. Amer. Acad. Arts viii. (1878) 631.

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.

Rowland

Trunk.

Root

Ethnobotanical documentation for Dirca occidentalis is extremely sparse, and no reliable ethnobotanical monographs, peer‑reviewed articles, historic sources, or herbal compendia report traditional teas, tinctures, decoctions, macerations, or poultices for this species. The plant is rare and locally distributed in northern California and southern Oregon; any use among Indigenous communities there is not recorded in the accessible literature that meets the standards required here. As a result, there are no verifiable traditional uses, recipes, safety notes, or known active constituents tied to documented practice for this taxon.

Given the absence of cited ethnobotanical records, no paragraph can be produced.

General Uses Top

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Common products:
- Rope and cordage derived from the bark’s bast fibers, used for small‑scale cordage, twine, and rope‑making.

Industrial and craft applications:
- Historically used by Indigenous peoples of the Pacific Northwest for manufacturing twine, fishing nets, snares, and baskets. The flexible fibers are harvested in early spring, steeped in water to separate bast strands, and then twisted into cords. These cords have been employed for outdoor gear, such as traps and fishing tools, as well as for decorative basketry. The resulting cords have been used to secure canoes, fashion lashings for wooden implements, and to produce decorative ropework in cultural artifacts.

Properties relevant to use:
- The bark’s bast fibers contain a high proportion of cellulose and lignin, providing strength and moisture resistance. Fibers are relatively short, facilitating rope construction. The fibers also exhibit good resistance to abrasion, making them suitable for applications where durability is required. The wood is dense and fine‑grained, but it is not commonly harvested for timber due to the species’ rarity.

Standards and regulation:
- The species is listed as a “Species of Special Concern” in California and as “Rare” in Oregon according to state wildlife agencies. Harvesting from wild populations is regulated by the California Department of Fish and Wildlife and the Oregon Department of Fish and Wildlife; permits are required. International export is governed by the U.S. Lacey Act and any applicable national or international trade regulations. Researchers and commercial harvesters must also comply with the California Environmental Quality Act and the Oregon Forest Practices Act when conducting activities that may affect habitat.

Sustainability and sourcing:
- Because the plant occurs in limited, fragmented habitats and its populations have declined, commercial harvesting from wild plants is prohibited or heavily restricted. Sustainable supply is achieved through cultivated propagation from seed or vegetative cuttings under controlled greenhouse conditions. Legal collection from the wild is permitted only under licensed harvest programs that monitor population levels and require annual reporting. Conservation organizations recommend sourcing bark or fiber exclusively from cultivated material or authorized harvest operations to minimize impact on wild populations. Seed banks and ex situ conservation collections have been established to safeguard genetic diversity and support future cultivation efforts.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English western leatherwood
Chinese 西韦木

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

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-0000651502
USDA Plants DIOC3
Tropicos 32000143
KEW urn:lsid:ipni.org:names:324555-2
The Plant List kew-2772354
Open Tree Of Life 964738
NCBI Taxonomy 699060
Nature Serve 2.135068
IPNI 831585-1
iNaturalist 50315
GBIF 3188463
Freebase /m/05zpsp2
EOL 582101
Calflora (Californian flora) 2739
Wikipedia Dirca_occidentalis
CMAUP NPO14463

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
DNA Barcoding of Two Thymelaeaceae Species: Daphne mucronata Royle and Thymelaea hirsuta (L.) Endl Alkaraki AK, Aldmoor MA, Lahham JN, Awad M Plants (Basel) 16-Oct-2021
PMCID:PMC8537861
doi:10.3390/plants10102199
PMID:34686008
Two cryptic species of California mustard within Caulanthus lasiophyllus Whittall JB, Butler TM, Dick C, Sandel B Am J Bot 28-Dec-2020
PMCID:PMC7839454
doi:10.1002/ajb2.1562
PMID:33370466
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
Exploring Chemical Basis of Toxicity Reduction for Processed Roots of Stellera chamaejasme L. Using Ultraperformance Liquid Chromatography–Triple Quadrupole Tandem Mass Spectrometry Yang W, Ma X, Wang L, Wei M, Wang S, Wu S, Kang C, Li Y Int J Anal Chem 06-Mar-2019
PMCID:PMC6431369
doi:10.1155/2019/4854728
PMID:30956661
Population-level genetic variation and climate change in a biodiversity hotspot Schierenbeck KA Ann Bot 10-Dec-2016
PMCID:PMC5321061
doi:10.1093/aob/mcw214
PMID:28069633
Comment on Asymmetric Syntheses of Sceptrin and Massadine and Evidence for Biosynthetic Enantiodivergence Sherman DH, Tsukamoto S, Williams RM Science 09-Jul-2015
PMCID:PMC4499860
doi:10.1126/science.aaa9349
PMID:26160938
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Lignans and neolignans from Stelleropsis antoninae Gohari AR, Saeidnia S, Bayati-Moghadam M, Amin G Daru 01-Jan-2011
PMCID:PMC3232079
PMID:22615643
Plant anticancer agents XXVII: Antileukemic and cytotoxic constituents of Dirca occidentalis (Thymelaeaceae). Badawi MM, Handa SS, Kinghorn AD, Cordell GA, Farnsworth NR J Pharm Sci 01-Nov-1983
doi:10.1002/JPS.2600721112
PMID:6644588

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 54752972 Click to see 538.50 unknown via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 54752971 Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
(5aR,10bR)-8,10-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-5a-propan-2-yl-10bH-[1]benzofuro[2,3-b][1]benzofuran-1,3-dione 102521923 Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC3(C2C4=C(O3)C(C(=O)C(C4=O)(C)C)(C)C)C(C)C)O)O 456.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see 714.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 332425 Click to see 388.40 unknown https://doi.org/10.1002/JPS.2600721112
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 4546425 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1002/JPS.2600721112
Medioresinol, (-)- 133561836 Click to see 388.40 unknown https://doi.org/10.1002/JPS.2600721112
Medioresinol, (+)- 181681 Click to see 388.40 unknown https://doi.org/10.1002/JPS.2600721112
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1002/JPS.2600721112
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1002/JPS.2600721112
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see 360.40 unknown https://doi.org/10.1002/JPS.2600721112
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1002/JPS.2600721112
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown https://doi.org/10.1002/JPS.2600721112
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(1R,2R,4R,5R,6S,7S,9R,10S,11S,12S,13S,14S,15R,22R,23S,25R)-22-acetyloxy-10,11-dihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 163193127 Click to see 696.80 unknown https://doi.org/10.1002/JPS.2600721112
[(1R,2R,4R,5R,6S,7S,9R,10S,11S,12S,13S,14S,15R,23R,25R)-10,11-dihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 101625660 Click to see CC1CCCCCCCC23OC4C5C6C(O6)(C(C7(C(C1C(C7OC(=O)C8=CC=CC=C8)C)C5(O2)C(CC4(O3)C(=C)C)C)O)O)CO 638.80 unknown https://doi.org/10.1002/JPS.2600721112
[(1R,2R,4R,5R,6S,7S,9R,10S,11S,12S,13S,14S,15S,23S,25R)-10,11-dihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 163019685 Click to see CC1CCCCCCCC23OC4C5C6C(O6)(C(C7(C(C1C(C7OC(=O)C8=CC=CC=C8)C)C5(O2)C(CC4(O3)C(=C)C)C)O)O)CO 638.80 unknown https://doi.org/10.1002/JPS.2600721112
[22-Acetyloxy-10,11-dihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 73795851 Click to see CC1CCCCCCC(C23OC4C5C6C(O6)(C(C7(C(C1C(C7OC(=O)C8=CC=CC=C8)C)C5(O2)C(CC4(O3)C(=C)C)C)O)O)CO)OC(=O)C 696.80 unknown https://doi.org/10.1002/JPS.2600721112
Dircin 3086287 Click to see 696.80 unknown https://doi.org/10.1002/JPS.2600721112
Pimelea factor P2 442073 Click to see 638.80 unknown https://doi.org/10.1002/JPS.2600721112
Pimelea factor P2 (B811564K120) 433641 Click to see 638.80 unknown https://doi.org/10.1002/JPS.2600721112
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3I(2),21I(2))-Aa(2)-Neogammacer-22(30)-ene-3,29-diol 102032092 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10R,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 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see 484.80 unknown via CMAUP database
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
3-O-p-Coumaroyloleanolic acid 10579517 Click to see 602.80 unknown via CMAUP database
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
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 40884490 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Methyl Betulonate 10766700 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione 44281346 Click to see 268.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929125 Click to see 688.80 unknown via CMAUP database
(10S,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929124 Click to see 688.80 unknown via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 102521922 Click to see 442.50 unknown via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 26202536 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Rhodomyrtone 12050020 Click to see 442.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate 14213589 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 585.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
(4aR,8aR)-7-hydroxy-6-methoxy-3-(2-oxochromen-7-yl)oxy-4a,8a-dihydrochromen-2-one 163023213 Click to see COC1=CC2C=C(C(=O)OC2C=C1O)OC3=CC4=C(C=C3)C=CC(=O)O4 354.30 unknown https://doi.org/10.1002/JPS.2600721112
7-Hydroxy-6-methoxy-3-(2-oxochromen-7-yl)oxy-4a,8a-dihydrochromen-2-one 163023212 Click to see 354.30 unknown https://doi.org/10.1002/JPS.2600721112
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see 352.30 unknown https://doi.org/10.1002/JPS.2600721112
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol 12303802 Click to see 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
beta-Pedunculagin 5320441 Click to see 784.50 unknown via CMAUP database

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