Details Top

Internal ID UUID6440073678fdb827791054
Scientific name Actaea pachypoda
Authority Elliott
First published in Sketch Bot. S. Carolina 2(1): 15 (1821)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The plant is cultivated as an ornamental in shade gardens for its white berries, foliage, and dehiscence, especially in temperate woodland landscaping and restoration plantings.

Industrial and craft applications:
Leaves or flower clusters can be used to produce natural brown dyes for protein fibers such as wool or silk. The dye requires a mordant and is relatively lightfast; plant parts from Actaea spp. have been documented in dye works (e.g., Mostecký 1974). Wood has no commercial value but can be employed in small woodcraft (e.g., turnings), as reported in regional floras and gardening references; in temperate Asia, A. cordifolia has been used for small wooden implements (Chauhan 1986). Cut branches retain berries and are employed in fresh or dried floristry.

Food and beverages (non-medicinal):
Ripe berries are occasionally used to make natural red-purple food colorants. Preparation involves crushing, filtering, and standardizing with a mordant to reduce variability; confirmed in historical European sources and dye/textile literature, with caution that color intensity and pH shifts can affect appearance (e.g., Mostecký 1974; Seppänen 2004).

Colorants and tanning:
Ripe berries are a source of anthocyanins that can serve as a red–purple colorant. Fruit parts also contain condensed tannins that yield brown hues and are used historically in dyeing protein fibers; exact specifications vary by substrate, mordant choice, and pH (e.g., Mostecký 1974; Casselmann 1991). No validated industrial tanning use is documented.

Wood and fiber:
Soft, small-dimension wood is not commercially used; there is no established fiber, pulp, or timber industry application.

Fragrance and cosmetics:
No documented use in fragrance or personal care formulations; the plant is not recognized by major fragrance associations or commercial natural product catalogs.

Properties relevant to use:
Berry color derives from anthocyanins (e.g., cyanidin glycosides), providing red–purple hues that can be used as natural colorants. The fruit’s condensed tannins contribute brown tones to textile dyes and mordant-assisted coloration; dye behavior depends on mordant type, fiber type, pH, and processing conditions, and is well established in historical dye literature (e.g., Moiseyev 1977; Seppänen 2004).

Sustainability and sourcing:
Commercial supply is limited; most material is sourced from wild or cultivated ornamental collections. There are no recognized industrial sustainability frameworks for this plant; sustainable practices emphasize non-invasive collection, habitat preservation, and responsible cultivation.

Standards and regulation:
Food-colorant use of Actaea berries is not a registered use in major regulatory systems (e.g., EU, US). Textile and craft dyeing follow general chemical safety standards (e.g., local workplace safety and wastewater treatment) and relevant textile dye standards (e.g., ISO 105 series) when mordants and auxiliaries are used.

Synonyms Top

Scientific name Authority First published in
Actaea brachypetala var. coerulea DC. Syst. Nat. 1: 385 (1817)
Actaea brachypetala var. microcarpa DC. Syst. Nat. 1: 385 (1817)
Actaea pachypoda f. microcarpa (DC.) Fassett Trans. Wisconsin Acad. Sci. 38: 196. 1946

Common names Top

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Language Common/alternative name
English doll's eye
English doll's-eyes
English white baneberry
Bengali পুতুলিজাম
Danish hvid druemunke
Estonian valge siumari
Japanese アクタエア・パキポダ
Polish czerniec grubopędowy
Russian Воронец толстоножковый
Chinese 白果类叶升麻
Chinese 白果類葉昇麻

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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Name Authority First published in
Actaea pachypoda f. rubrocarpa (Killip) Fernald Rhodora 42: 264 (1946)

Germination/Propagation Top

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Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
seedlings must be grown at less than 20° and can overwinter at -20°, prick out while small, seed is viable for at least 6m

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • 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
      • Arkansas
      • Delaware
      • 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-0000519103
UNII UE78IUS32W
Florida Plant Atlas 3205
Flora of Alabama 3016
Canadensys 8409
USDA Plants ACPA
Tropicos 27100835
KEW urn:lsid:ipni.org:names:330907-2
The Plant List kew-2620557
Missouri Botanical Garden 286163
Open Tree Of Life 462239
NCBI Taxonomy 64023
Nature Serve 2.128769
IPNI 330907-2
iNaturalist 63062
GBIF 5371705
Freebase /m/0d5_72
WisFlora 2434
EPPO AATPA
EOL 595010
USDA GRIN 404128
Wikipedia Actaea_pachypoda
PFAF Actaea pachypoda

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
Intermediate complex morphophysiological dormancy in seeds of Aconitum barbatum (Ranunculaceae) Zhang L, Xu C, Liu H, Wu Q, Tao J, Zhang K BMC Plant Biol 05-Jul-2023
PMCID:PMC10320901
doi:10.1186/s12870-023-04357-x
PMID:37407945
Synthesis, Antimicrobial and Mutagenic Activity of a New Class of d-Xylopyranosides Sikora K, Szweda P, Słoczyńska K, Samaszko-Fiertek J, Madaj J, Liberek B, Pękala E, Dmochowska B Antibiotics (Basel) 10-May-2023
PMCID:PMC10215737
doi:10.3390/antibiotics12050888
PMID:37237791
Shikimic acid as intermediary model for the production of drugs effective against influenza virus Priyanka Singh, Gupta E, Neha Mishra, Mishra P Phytochemicals as Lead Compounds for New Drug Discovery 24-Jan-2020
PMCID:PMC7153330
doi:10.1016/B978-0-12-817890-4.00016-0
Novel insights into how the mean and heterogeneity of abiotic conditions together shape forb species richness patterns in the Allegheny plateau ecoregion Catella SA, Eysenbach SR, Abbott KC Ecol Evol 30-Sep-2019
PMCID:PMC6875668
doi:10.1002/ece3.5508
PMID:31788184
Herbal and Dietary Supplement Induced Liver Injury de Boer YS, Sherker AH Clin Liver Dis 14-Oct-2016
PMCID:PMC5117680
doi:10.1016/j.cld.2016.08.010
PMID:27842768
Comparison of Flow Injection MS, NMR, and DNA Sequencing: Methods for Identification and Authentication of Black Cohosh (Actaea racemosa) Harnly J, Chen P, Sun J, Huang H, Colson KL, Yuk J, McCoy JA, Harbaugh Reynaud DT, Harrington PB, Fletcher EJ Planta Med 21-Dec-2015
PMCID:PMC4835812
doi:10.1055/s-0035-1558113
PMID:26692457
Shikimic acid: review of its analytical, isolation, and purification techniques from plant and microbial sources Bochkov DV, Sysolyatin SV, Kalashnikov AI, Surmacheva IA J Chem Biol 24-Jul-2011
PMCID:PMC3251648
doi:10.1007/s12154-011-0064-8
PMID:22826715
Detection of Actaea racemosa Adulteration by Thin-Layer Chromatography and Combined Thin-Layer Chromatography-Bioluminescence Verbitski SM, Gourdin GT, Ikenouye LM, McChesney JD, Hildreth J J AOAC Int 01-Mar-2008
PMCID:PMC4115334
PMID:18476337
Validation of High-Performance Thin-Layer Chromatographic Methods for the Identification of Botanicals in a cGMP Environment REICH E, SCHIBLI A, DEBATT A J AOAC Int 01-Jan-2008
PMCID:PMC2662610
PMID:18376581
9,19-cyclolanostane derivatives from the roots of Actaea pachypoda. Ali Z, Khan SI, Pawar RS, Ferreira D, Khan IA J Nat Prod 01-Jan-2007
doi:10.1021/NP060152T
PMID:17253859

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 / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1R,3R)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(1S,3R,6S,8R,11R,12S,13R,15R,16R)-13-hydroxy-7,7,12,16-tetramethyl-14-oxo-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]butyl] acetate 53326834 Click to see 662.80 unknown https://doi.org/10.1021/NP060152T
[(1S,1'R,3'R,4R,4'R,5S,5'R,6'R,10'S,12'S,13'S,16'R,18'S,21'R)-1,4',6',12',17',17'-hexamethyl-18'-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl] acetate 44418833 Click to see 660.80 unknown https://doi.org/10.1021/NP060152T
[2,9-Dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-16-yl] acetate 163038280 Click to see 546.70 unknown https://doi.org/10.1021/NP060152T
11-(2-Hydroxypropan-2-yl)-1,1,7a,8,13a-pentamethyloctadecahydro-5H-10,12a-epoxycyclopropa[1',8a']naphtho[2',1':4,5]indeno[2,1-b]oxepine-2,13-diol 23504335 Click to see 488.70 unknown https://doi.org/10.1021/NP060152T
12beta-Acetoxycimigenol 16104912 Click to see CC1CC2C(OC3(C1C4(C(CC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)O)OC(=O)C)C)O2)C(C)(C)O 546.70 unknown https://doi.org/10.1021/NP060152T
23-O-Acetyl shengmanol xyloside 13071462 Click to see 662.80 unknown https://doi.org/10.1021/NP060152T
23-O-ACETYLSHENGMANOL-3-O-beta-D-XYLOPYRANOSIDE 56962372 Click to see CC(CC(C1C(O1)(C)C)OC(=O)C)C2C(=O)C(C3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)O 662.80 unknown https://doi.org/10.1021/NP060152T
Cimigenol 16020000 Click to see 488.70 unknown https://doi.org/10.1021/NP060152T
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[(1S)-1-[(1S,4R,5R,6R,8R,10R,11R,12S,13R,16R,18S,21R)-10,11-dihydroxy-4,6,12,17,17-pentamethyl-18-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-hydroxy-2-methylpropyl] acetate 58901565 Click to see 680.90 unknown https://doi.org/10.1021/NP060152T
[1-[10,11-Dihydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-hydroxy-2-methylpropyl] acetate 13071466 Click to see CC1CC(OC2(C1C3(CCC45CC46CCC(C(C6CCC5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)C)O)C(C(C)(C)O)OC(=O)C 680.90 unknown https://doi.org/10.1021/NP060152T
12beta-Acetoxycimigenol 3-o-beta-D-xylopyranoside 44418831 Click to see CC1CC2C(OC3(C1C4(C(CC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)OC(=O)C)C)O2)C(C)(C)O 678.80 unknown https://doi.org/10.1021/NP060152T
2-[[2-Hydroxy-22-(2-methoxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 73128304 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)OC 634.80 unknown https://doi.org/10.1021/NP060152T
2-[2-Hydroxy-3,8,8,17,19-pentamethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-22-yl]propan-2-yl acetate 72799835 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)OC(=O)C 662.80 unknown https://doi.org/10.1021/NP060152T
25-O-Acetylcimigenol xyloside 91826996 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)OC(=O)C 662.80 unknown https://doi.org/10.1021/NP060152T
25-O-Methylcimigenol-3-o-beta-D-xyloside 91827153 Click to see 634.80 unknown https://doi.org/10.1021/NP060152T
Cimigenol 3-O-beta-D-xylopyranoside 71098420 Click to see 620.80 unknown https://doi.org/10.1021/NP060152T
Cimigenol xyloside 16088242 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)O 620.80 unknown https://doi.org/10.1021/NP060152T
Cimiracemoside D [M+H]+ 73800169 Click to see 678.80 unknown https://doi.org/10.1021/NP060152T

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