Podophyllum pleianthum

Details Top

Internal ID UUID64404fe245f18611978591
Scientific name Podophyllum pleianthum
Authority Hance
First published in J. Bot. 21: 175 (1883)

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.

Podophyllum peltatum L. has a well‑documented record of preparation as poultices and topical decoctions among indigenous peoples of eastern North America. Among the Cherokee of the southeastern United States, leaf pastes were applied to tumors and skin conditions (University of Michigan Ethnobotany Database), and the Iroquois of the Northeast used a whole‑plant decoction as a wash for ulcers and cutaneous growths (University of Michigan Ethnobotany Database). The Lenape (Delaware) of the Mid‑Atlantic also reported use of the whole plant in wash or poultice form for growths and tumors, and the Winnebago and Menominee of the Great Lakes employed the mashed or boiled plant topically on swellings (University of Michigan Ethnobotany Database). In these traditions, the plant part was most often the aerial parts (leaves, stems) or occasionally the rhizome/root, typically crushed and moistened as a direct application to lesions.

In a modern context, a basic cold compress of 5 g of fresh aerial parts in 250 mL of cool water, steeped for 10 minutes, may be applied topically to inflamed or swelling areas. A 1:5 ethanol tincture of the plant—5 g of dried aerial parts macerated in 25 mL of 40–50% ethanol for 7–10 days, shaken daily—provides a standardized topical preparation. The plant is potentially toxic if ingested due to podophyllotoxin, and pregnant or nursing people should not handle or ingest preparations (National Center for Complementary and Integrative Health, 2020).

Well‑established constituents for the species include podophyllotoxin and its glycosides, and related lignans such as quercetin and kaempferol glycosides, supporting the traditional use for warty and growth‑related skin conditions. Current work focuses on podophyllotoxin as a precursor for anticancer drug derivatives, and tinctures and crude preparations for dermatological use are available in specialty herbal markets.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Dysosma chengii (S.S.Chien) M.Hiroe Pl. Basho's & Buson's Hokku Lit. 8: 328 (1973)
Dysosma hispida (K.S.Hao) M.Hiroe Pl. Basho's & Buson's Hokku Lit. 8: 329 (1973)
Dysosma pleiantha Woodson Ann. Missouri Bot. Gard. 15: 339 (1928)
Podophyllum onzoi Hayata Icon. Pl. Formosan. 5: 2 (1915)
Podophyllum pleianthum var. album Masam. Annual Rep. Taihoku Bot. Gard. 2: 81 1932
Podophyllum hispidum K.S.Hao Repert. Spec. Nov. Regni Veg. 36: 223 (1934)
Podophyllum chengii S.S.Chien Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. 10: 108 (1936)

Common names Top

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Language Common/alternative name
Chinese 六角莲
Chinese 六角蓮

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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Germination/Propagation Top

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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
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.
hydrophilic

Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001146536
Tropicos 3500420
KEW urn:lsid:ipni.org:names:107600-1
Missouri Botanical Garden 277809
IPNI 107601-1
GBIF 3981308
USDA GRIN 406972
Wikipedia Podophyllum_pleianthum
CMAUP NPO27244
Open Tree Of Life 570386

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)!
Title Authors Publication Released IDs
Ultrahigh pressure extraction of lignan compounds from Dysosma versipellis and purification by high-speed counter-current chromatography. Zhu Q, Liu F, Xu M, Lin X, Wang X J Chromatogr B Analyt Technol Biomed Life Sci 15-Sep-2012
doi:10.1016/J.JCHROMB.2012.08.016
PMID:22939268
Isopicropodophyllone from Podophyllum pleianthum Frederic C. Chang, Chiao-kuo Chang*, V. Nambi Aiyar Elsevier BV 12-Feb-2003
doi:10.1016/S0031-9422(00)98653-9
Tumour-inhibitory aryltetralin lignans from Podophyllum pleianthum David E. Jackson, Paul M. Dewick Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83052-6
Supercritical carbon dioxide extraction of podophyllotoxin from Dysosma pleiantha roots. Choi YH, Kim JY, Ryu JH, Yoo KP, Chang YS, Kim J Planta Med 01-Jun-1998
doi:10.1055/S-2006-957493
PMID:17253269
Podophyllotoxin intoxication: toxic effect of Bajiaolian in herbal therapeutics. Kao WF, Hung DZ, Tsai WJ, Lin KP, Deng JF Hum Exp Toxicol 01-Nov-1992
doi:10.1177/096032719201100607
PMID:1361136

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 / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol 19818056 Click to see COC1=C(C=CC(=C1)O)N 139.15 unknown via CMAUP database
Feruloyltyramine 5280537 Click to see 313.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
4'-Demethyldehydropodophyllotoxin 15232507 Click to see COC1=CC(=CC(=C1O)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O 396.30 unknown via CMAUP database
Dehydropodophyllotoxin 5316463 Click to see 410.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
4'-Demethyldeoxypodophyllotoxin 160705 Click to see 384.40 unknown via CMAUP database
9-Hydroxy-5-(3,4,5-trimethoxyphenyl)-3,5,5a,8,8a,9-hexahydro-[2]benzofuro[6,5-f][1,2]benzodioxol-6-one 45358776 Click to see 414.40 unknown via CMAUP database
CID 11384371 11384371 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 412.40 unknown via CMAUP database
d,l-Isopodophyllotoxone 323439 Click to see 412.40 unknown https://doi.org/10.1016/S0031-9422(00)98653-9
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1016/S0031-9422(00)83052-6
Isopicropodophyllone 11189106 Click to see 412.40 unknown https://doi.org/10.1016/S0031-9422(00)83052-6
https://doi.org/10.1016/S0031-9422(00)98653-9
Picropodopyllotoxone 3083574 Click to see 412.40 unknown via CMAUP database
Podophyllotoxone 443014 Click to see 412.40 unknown https://doi.org/10.1016/S0031-9422(00)83052-6
https://doi.org/10.1016/S0031-9422(00)98653-9
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
4'-Demethylpodophyllotoxin 122667 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(00)83052-6
https://doi.org/10.1016/J.JCHROMB.2012.08.016
Lignans 443013 Click to see 414.40 unknown via CMAUP database
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1055/S-2006-957493
https://doi.org/10.1016/S0031-9422(00)83052-6
https://doi.org/10.1177/096032719201100607
Podophyllotoxin, glucoside 294472 Click to see 576.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(4S,5R,9S)-8-hydroxy-5,9,13-trimethyl-11-oxatetracyclo[7.2.2.01,4.04,8]tridecane-2,12-dione 6852268 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene 6419724 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 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
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol 46833330 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone 21633629 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C 558.50 unknown via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone 10769263 Click to see 563.00 unknown via CMAUP database
Physalin F 49864133 Click to see 526.50 unknown via CMAUP database
Physalin G 56683730 Click to see 526.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid 21573758 Click to see 459.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573757 Click to see 445.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573755 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1 429.60 unknown via CMAUP database
N-Methylsolasodine 21573751 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C 427.70 unknown via CMAUP database
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21573761 Click to see 900.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102058012 Click to see 722.90 unknown via CMAUP database
Degalactotigonin 162401 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1035.20 unknown via CMAUP database
Khasianine 21573759 Click to see 721.90 unknown via CMAUP database
Nigrumnin I 10820113 Click to see 1151.30 unknown via CMAUP database
nigrumnin II 10630134 Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1181.30 unknown via CMAUP database
Solamargine 73611 Click to see 868.10 unknown via CMAUP database
Solanigroside C 16083118 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O 1111.20 unknown via CMAUP database
Solanigroside D 16083121 Click to see 1181.30 unknown via CMAUP database
Solanigroside E 16083119 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1=O)O 1197.30 unknown via CMAUP database
Solanigroside G 16083120 Click to see 1051.20 unknown via CMAUP database
Solanigroside H 16083123 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1047.20 unknown via CMAUP database
Solasonine 119247 Click to see 884.10 unknown via CMAUP database
Uttroside B 44566638 Click to see 1215.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
alpha-Glycine 5257127 Click to see 75.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Qui3Me(b1-4)Oli3Me(a)-O-Et 101490302 Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC 350.40 unknown via CMAUP database
Qui3Me(b1-4)Oli3Me(b)-O-Et 101490301 Click to see 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
2-(1H-Indol-3-yl)ethyl acetate 588705 Click to see CC(=O)OCCC1=CNC2=CC=CC=C21 203.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 159894 Click to see 238.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 101243377 Click to see 933.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
CID 44258797 44258797 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database

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