Details Top

Internal ID UUID64405725ee52f129828671
Scientific name Podophyllum delavayi
Authority Franch.
First published in Bull. Mus. Hist. Nat. (Paris) 1: 63 (1895)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Dried rhizome of Podophyllum delavayi is harvested and marketed as bulk raw material for the extraction of podophyllotoxin, a lignan used as a precursor in the industrial synthesis of anticancer agents (e.g., etoposide, teniposide). The product is supplied as ground rhizome powder or as a concentrated ethanol‑methanol extract.

Industrial and craft applications:
The principal industrial use is the isolation of podophyllotoxin from the rhizomes via solvent extraction (commonly ethanol or methanol) followed by chromatographic purification for fine‑chemical and biopharmaceutical manufacturing. The plant is cultivated specifically for its high podophyllotoxin yield, supporting a supply chain for anti‑cancer drug intermediates.

Properties relevant to use:
The rhizome contains up to 2–5 % (w/w) dry‑weight podophyllotoxin, a dibenzylbutane lignan with high lipophilicity, a characteristic UV absorption (λmax ≈ 290 nm), and good solubility in organic solvents—features that enable efficient extraction and downstream purification. Related lignans (e.g., deoxypodophyllotoxin) present similar physicochemical behavior, allowing simultaneous isolation during standard processing.

Standards and regulation:
Bulk Podophyllum rhizome raw material must comply with pharmacopeial standards. The European Pharmacopoeia (Ph. Eur.) monograph “Podophyllum rhizome” specifies a minimum podophyllotoxin content of ≥ 2 % for dried material and limits for heavy metals and microbial contamination. Extracted podophyllotoxin is further regulated under ICH Q3A guidelines for impurity profiling in pharmaceutical intermediates.

Sustainability and sourcing:
Wild populations of P. delavayi are vulnerable to over‑harvest because rhizomes are the harvested part, reducing plant regeneration. Conservation assessments list the species as near‑threatened in parts of its native range in China. Sustainable sourcing initiatives include cultivation trials in southern China that achieve comparable podophyllotoxin yields and the development of in‑vitro micropropagation protocols to reduce pressure on wild populations.

Synonyms Top

Scientific name Authority First published in
Dysosma veitchii var. longipetala J.L.Wu & P.Zhuang Pl. Mt. Emei : 484 (2007)
Dysosma delavayi (Franch.) Hu Bull. Fan Mem. Inst. Biol. , Bot. 8: 37 (1937)
Dysosma veitchii (Hemsl. & E.H.Wilson) L.K.Fu ex T.S.Ying Acta Phytotax. Sin. 17(1): 20 (1979)
Podophyllum delavayi var. longipetalum J.L.Wu & P.Zhuang ex J.M.H.Shaw New Plantsman 6(3): 163 (1999).
Podophyllum veitchii Hemsl. & E.H.Wilson Bull. Misc. Inform. Kew 1906: 152 (1906)

Common names Top

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Language Common/alternative name
Vietnamese dysosma delavayi

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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Sow at 4°C for 3 weeks, then increase to 20°C.
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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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001258038
Tropicos 50186767
KEW urn:lsid:ipni.org:names:107585-1
IPNI 107585-1
GBIF 7300339
Freebase /m/0d6bfw
Elurikkus 585094
USDA GRIN 435138
Wikipedia Podophyllum_delavayi
CMAUP NPO6669

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
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

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 / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one 10523042 Click to see 368.40 unknown via CMAUP database
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one 20056151 Click to see 384.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3-hydroxy-4-methoxyphenyl)methyl]-2H-furan-5-one 21592358 Click to see 370.40 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Chinensin 5315827 Click to see 364.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C 11796268 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
4-[(3S,3aS,6S,6aS)-6-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxy-phenol 12309695 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown via CMAUP database
(3R,4R)-3-(4-Hydroxy-3-methoxy-benzyl)-4-(4-hydroxy-3,5-dimethoxybenzyl)dihydrofuran-2(3H)-one 10249666 Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC 388.40 unknown via CMAUP database
(3R,4R)-3-[(3,4-dimethoxyphenyl)methyl]-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 11164637 Click to see 372.40 unknown via CMAUP database
(3R,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methyl]oxolan-2-one 101630410 Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 356.40 unknown via CMAUP database
(3R,4R)-4-[(3-hydroxy-4-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101097988 Click to see 358.40 unknown via CMAUP database
(3R,4R)-4-[(3,4-dihydroxyphenyl)methyl]-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 14682324 Click to see 358.40 unknown via CMAUP database
(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-3-hydroxyoxolan-2-one 14630578 Click to see 386.40 unknown via CMAUP database
(3S,4S)-3-hydroxy-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101681939 Click to see 404.40 unknown via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]oxolan-2-one 101630409 Click to see 354.40 unknown via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylidene]oxolan-2-one 6506046 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown via CMAUP database
(3Z,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one 643806 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O 356.40 unknown via CMAUP database
[(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-2-oxooxolan-3-yl] acetate 14630580 Click to see CC(=O)OC1(C(COC1=O)CC2=CC3=C(C=C2)OCO3)CC4=CC(=C(C=C4)OC)OC 428.40 unknown via CMAUP database
Arctigenin methyl ether 384877 Click to see 386.40 unknown via CMAUP database
Arctigenin, (+)- 28125531 Click to see 372.40 unknown via CMAUP database
Bursehernin 94504 Click to see 370.40 unknown via CMAUP database
Epinortrachelogenin 14159539 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Hydroxymatairesinol 10948757 Click to see 374.40 unknown via CMAUP database
Isosalicifolin 638390 Click to see 356.40 unknown via CMAUP database
Kaerophyllin 6440534 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Salicifolin 101681940 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O 356.40 unknown via CMAUP database
Thujaplicatin methyl ether 192827 Click to see COC1=CC(=CC(=C1O)OC)CC2C(COC2=O)CC3=CC(=C(C=C3)O)OC 388.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(3R,3aR,6aR)-3-(1,3-benzodioxol-5-yl)-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one 16038940 Click to see 248.23 unknown via CMAUP database
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
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5S,5aR,8aR,9R)-5-hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 500181 Click to see 400.40 unknown https://doi.org/10.1016/J.JCHROMB.2012.08.016
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633130/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,6,7-Trimethoxycoumarin 148724 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC 236.22 unknown via CMAUP database
5,7-Dimethoxycoumarin 2775 Click to see 206.19 unknown via CMAUP database
6,7,8-Trimethoxycoumarin 3083928 Click to see 236.22 unknown via CMAUP database
Methylumbelliferone 10748 Click to see 176.17 unknown via CMAUP database
Scoparone 8417 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database

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