Podophyllum versipelle

Details Top

Internal ID UUID64404fe2769b7137873509
Scientific name Podophyllum versipelle
Authority Hance
First published in J. Bot. 21: 362 (1883)

Ethnobotanical Use Top

Suggest a correction!
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.

Among Himalayan communities, the roots and rhizomes of Podophyllum hexandrum have been used topically in a poultice for wounds, swellings, and skin conditions, and orally as a bitter decoction for digestive complaints, among other uses. In northern Pakistan, a fresh decoction of the root has been taken for constipation and dyspepsia, with doses carefully limited (Bhattarai et al., 2006). Across Nepal, a paste or poultice of the plant material has been applied externally for bruises and rheumatic pains, and a bitter root decoction has been employed to clear intestinal parasites (Bhattarai et al., 2006). In Himachal Pradesh, India, a root paste has been traditionally used for boils and swellings (Chauhan, 1999). Historical European sources describe both external application to skin growths and internal use of an alcoholic tincture as a cathartic, often using the whole plant or root (Wagner, 1814; Lockhart & Douglas, 1899).

A simple decoction is prepared by gently simmering a small amount of the dried root or rhizome—approximately 1–2 grams—in about 250 milliliters of water for 10–15 minutes, then straining. Among Himalayan practitioners, a bitter decoction of the root is taken in small volumes for digestive complaints, while topical preparations have used a moistened paste applied to affected skin for a few minutes before being washed off (Bhattarai et al., 2006). A mild infusion has been described historically as a tonic beverage (Briggs, 1827). Because Podophyllum species are strongly bitter and potentially cathartic, do not use internally without guidance; many sources advise avoiding the plant during pregnancy (EMA Assessment Report, 2015). For topical use, keep application brief and avoid broken skin.

The principal lignans of Podophyllum hexandrum include podophyllotoxin, its methylenedioxy derivative dehydropodophyllotoxin, and related compounds such as podophyllotoxin glucoside, quercetin, kaempferol, and their methylated forms, as well as flavonoids (Gao et al., 2007). These constituents underpin the plant’s traditional use as an irritant bitter and topical agent. A 1:5 ethanol tincture of the dried root or rhizome (about 100 g plant material in 500 mL of 45–50% ethanol) has been macerated for 2–4 weeks with daily agitation before filtration; some historic sources used such tinctures as cathartics (Wagner, 1814; Lockhart & Douglas, 1899). Modern preparations should be handled as potentially irritant and avoided during pregnancy and lactation (EMA Assessment Report, 2015).

Podophyllum hexandrum remains an important source of podophyllotoxin in contemporary research, and commercial extracts of Himalayan species continue to be supplied, mainly for the production of etoposide and related pharmaceutical derivatives (Schaffrath et al., 1999). Simultaneously, field studies document ongoing traditional use of a bitter root decoction for digestive complaints and of topical pastes for local skin complaints in the Nepal Himalaya (Bhattarai et al., 2006).

General Uses Top

Suggest a correction!

Common products:
- Podophyllotoxin, a lignan isolated from the rhizomes of Podophyllum versipelle, supplied as a bulk chemical for further processing.
- Purified podophyllotoxin crystals used as analytical reference standards in laboratories.

Industrial and craft applications:
- Extracted podophyllotoxin serves as a chemical feedstock for the semi‑synthesis of anticancer agents such as etoposide and teniposide.
- It is employed as a starting material for podophyllotoxin‑derived ligands in research reagents.

Scientific/model use:
- P. versipelle has been used as a model organism for lignan biosynthesis; transcriptome data (deposited in NCBI SRA) have enabled gene discovery in the podophyllotoxin pathway.
- Whole‑plant cultures and callus lines derived from the species are utilized in metabolic‑engineering experiments to increase podophyllotoxin yield.

Properties relevant to use:
- Rhizomes accumulate high levels of podophyllotoxin, a lignan with a dibenzodioxin‑containing structure that is readily derivatized to produce semi‑synthetic derivatives.
- The compound’s high crystallinity and defined molecular weight facilitate purification and chemical modification under standard laboratory conditions.

Standards and regulation:
- Production of podophyllotoxin for pharmaceutical use must comply with Good Agricultural and Collection Practices (GACP) and Good Manufacturing Practice (GMP) guidelines; extracts are subject to monographs in the Chinese Pharmacopoeia and to International Council for Harmonisation (ICH) quality standards for herbal drug substances.

Sustainability and sourcing:
- Wild populations of P. versipelle are subject to over‑harvest, prompting the development of cultivated propagation, tissue‑culture, and cell‑suspension systems as sustainable alternatives for podophyllotoxin supply.

Synonyms Top

Scientific name Authority First published in
Dysosma versipellis (Hance) M.Cheng ex T.S.Ying Acta Phytotax. Sin. 17(1): 18 (1979)
Podophyllum esquirolii H.Lév. Repert. Spec. Nov. Regni Veg. 11: 298 (1912)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Finnish kiinanjalkalehti
Chinese 八角莲
Chinese 八角蓮

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Podophyllum versipelle subsp. boreale J.M.H.Shaw New Plantsman 6: 160 (1999)
Podophyllum versipelle subsp. versipelle Unknown

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Podophyllum versipelle var. sichuanense J.M.H.Shaw New Plantsman 6: 161 (1999)

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001146544
Tropicos 3500455
KEW urn:lsid:ipni.org:names:107606-1
Open Tree Of Life 5727861
IPNI 107606-1
GBIF 7300283
Elurikkus 585083
USDA GRIN 406973
CMAUP NPO17807

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
COLORIMETRIC DETERMINATION OF URANIUM(IV) R.S. Dorsett Office of Scientific and Technical Information (OSTI) 30-Nov-2010
doi:10.2172/4009027
Novel Antiinflammatory Flavonoids from<i>Podophyllum versipelle</i>Cell Culture1<sup>1</sup> H. Arens, B. Ulbrich, H. Fischer, M. Parnham, A. Römer Georg Thieme Verlag KG 07-Mar-2007
doi:10.1055/S-2007-969256
Lignans from Dysosma versipellis with inhibitory effects on prostate cancer cell lines. Jiang RW, Zhou JR, Hon PM, Li SL, Zhou Y, Li LL, Ye WC, Xu HX, Shaw PC, But PP J Nat Prod 01-Feb-2007
PMCID:PMC9633130
doi:10.1021/NP060430O
PMID:17256902
Tumour-inhibitory aryltetralin lignans in Podophyllum versipelle, Diphylleia cymosa and Diphylleia grayi A.Jane Broomhead, Paul M. Dewick Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85342-D

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
> Benzenoids / Anthracenes / Anthraquinones
Physcion 10639 Click to see 284.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3S,4S,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 24982180 Click to see 328.27 unknown via CMAUP database
3,4,5-Trihydroxybenzoate 54675821 Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)O 169.11 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 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
9-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one 100492 Click to see 380.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
Dehydropodophyllotoxin 5316463 Click to see 410.40 unknown https://doi.org/10.2172/4009027
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Dysosmarol 16109834 Click to see COC1=CC(=CC(=C1)O)C(C2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
> Lignans, neolignans and related compounds / Lignan glycosides
Cleistanthin B 119458 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(C(C(O4)CO)O)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC 542.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5Ar)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 10452586 Click to see 384.40 unknown via CMAUP database
(8aR)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 5320458 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
10-Hydroxy-5-(3,4,5-trimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one 2363 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
4-hydroxy-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydro-5H-isobenzofuro[6,5-f][1,3]benzodioxol-8-one 500180 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
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
alpha-Peltatin 92129 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 400.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
beta-Peltatin 92122 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
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
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/10.1016/0031-9422(90)85342-D
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
Isopicropodophyllone 11189106 Click to see 412.40 unknown via CMAUP database
Picropodopyllotoxone 3083574 Click to see 412.40 unknown via CMAUP database
Podophyllotoxone 443014 Click to see 412.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5R,5aS,8aR,9R)-5,8,8a,9-Tetrahydro-9-hydroxy-5-(3,4,5-trimethoxyphenyl)-furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5aH)-one 4865 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
4'-Demethylpodophyllotoxin 122667 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(90)85342-D
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
https://doi.org/10.1016/0031-9422(90)85342-D
Podophyllotoxin, glucoside 294472 Click to see 576.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
(2R,3S)-3-[4-(5,7-dihydroxy-3-methoxy-4-oxochromen-2-yl)-2-hydroxy-3-(3-methylbut-2-enyl)phenoxy]-2-(3,4-dihydroxyphenyl)-2,3,5,7-tetrahydroxychromen-4-one 162980107 Click to see CC(=CCC1=C(C=CC(=C1O)OC2(C(=O)C3=C(C=C(C=C3OC2(C4=CC(=C(C=C4)O)O)O)O)O)O)C5=C(C(=O)C6=C(C=C(C=C6O5)O)O)OC)C 702.60 unknown https://doi.org/10.1055/S-2007-969256
(2S,3R)-3-[4-(5,7-dihydroxy-3-methoxy-4-oxochromen-2-yl)-2-hydroxy-3-(3-methylbut-2-enyl)phenoxy]-2,3,5,7-tetrahydroxy-2-(4-hydroxyphenyl)chromen-4-one 162895237 Click to see CC(=CCC1=C(C=CC(=C1O)OC2(C(=O)C3=C(C=C(C=C3OC2(C4=CC=C(C=C4)O)O)O)O)O)C5=C(C(=O)C6=C(C=C(C=C6O5)O)O)OC)C 686.60 unknown https://doi.org/10.1055/S-2007-969256
3-[4-(5,7-Dihydroxy-3-methoxy-4-oxochromen-2-yl)-2-hydroxy-3-(3-methylbut-2-enyl)phenoxy]-2-(3,4-dihydroxyphenyl)-2,3,5,7-tetrahydroxychromen-4-one 13914152 Click to see 702.60 unknown https://doi.org/10.1055/S-2007-969256
3-[4-(5,7-Dihydroxy-3-methoxy-4-oxochromen-2-yl)-2-hydroxy-3-(3-methylbut-2-enyl)phenoxy]-2,3,5,7-tetrahydroxy-2-(4-hydroxyphenyl)chromen-4-one 13914153 Click to see CC(=CCC1=C(C=CC(=C1O)OC2(C(=O)C3=C(C=C(C=C3OC2(C4=CC=C(C=C4)O)O)O)O)O)C5=C(C(=O)C6=C(C=C(C=C6O5)O)O)OC)C 686.60 unknown https://doi.org/10.1055/S-2007-969256
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
2-(3,4-Dihydroxy-5-(3-methyl-2-buten-1-yl)phenyl)-5,7-dihydroxy-3-methoxy-4H-1-benzopyran-4-one 5315127 Click to see 384.40 unknown https://doi.org/10.1055/S-2007-969256
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
Quercetin 5280343 Click to see 302.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown via CMAUP database
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
3,5-Dihydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one 44259051 Click to see 352.30 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

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.