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Podophyllum aurantiocaule

Podophyllum aurantiocaule - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405726129f2313086473
Scientific name Podophyllum aurantiocaule
Authority Hand.-Mazz.
First published in Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 61: 163 (1924 publ. 1925)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dysosma aurantiocaulis (Hand.-Mazz.) Hu Bull. Fan Mem. Inst. Biol. , Bot. 8: 37 (1937)
Dysosma furfuracea S.Y.Bao Acta Phytotax. Sin. 25: 155 (1987)
Dysosma mairei (Gagnep.) M.Hiroe Pl. Basho's & Buson's Hokku Lit. 8: 328 (1973)
Podophyllum aurantiocaule subsp. furfuraceum (S.Y.Bao) J.M.H.Shaw New Plantsman 6(3): 164 (1999):.
Podophyllum sikkimense var. majus R.Chatterjee & Mukerjee Rec. Bot. Surv. India 16(2): 48 1953
Podophyllum mairei Gagnep. Bull. Soc. Bot. France 85: 167 (1938)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Podophyllum aurantiocaule var. uniflorum J.M.H.Shaw New Plantsman 6: 163 (1999)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001258040
Tropicos 50186772
KEW urn:lsid:ipni.org:names:107581-1
IPNI 107581-1
GBIF 7300347
USDA GRIN 449152

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
Chemical Constituents of Dysosma versipellis Yue Zheng, Ji Ye, Yang-guo Xie, Hui-liang Li, Hui-zi Jin Springer Science and Business Media LLC 15-Feb-2017
doi:10.1007/S10600-017-1933-3
Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance). Yang Z, Liu X, Wang K, Cao X, Wu S J Sep Sci 01-Mar-2013
doi:10.1002/JSSC.201201038
PMID:23418155
Antifungal aryltetralin lignans from leaves of Podophyllum hexandrum Atta-ur-Rahman, M. Ashraf, M. Iqbal Choudhary, Habib-ur-Rehman, M.H. Kazmi Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00195-D

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 / 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 https://doi.org/10.1007/S10600-017-1933-3
> Lignans, neolignans and related compounds / Lignan lactones
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/10.1007/S10600-017-1933-3
Picropodopyllotoxone 3083574 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 412.40 unknown https://doi.org/10.1016/0031-9422(95)00195-D
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
4'-Demethylpodophyllotoxin 122667 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 400.40 unknown https://doi.org/10.1002/JSSC.201201038
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/10.1007/S10600-017-1933-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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://doi.org/10.1007/S10600-017-1933-3
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-017-1933-3
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-017-1933-3
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-017-1933-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-017-1933-3
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-017-1933-3

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