Podophyllum peltatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Podophyllum peltatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643ff82bcebca193407934
Scientific name Podophyllum peltatum
Authority L.
First published in Sp. Pl. : 505 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Podophyllum callicarpum Raf. Fl. Ludov. : 14 (1817)
Podophyllum montanum Raf. Med. Fl. 2: 59 (1830)
Anapodophyllum peltatum Moench Methodus : 277 (1794)

Common names Top

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Language Common/alternative name
English mayapple
English american mandrake
English may apple
Arabic اليبروح
Arabic اللفاح
Arabic تفاح مايو
Arabic تفاحة مايو
Arabic تفاح هندي
Arabic بودوفلون درقي
Arabic التفاح الهندي
Arabic البودوفلون الدرقي
Azerbaijani qalxanabənzər podofil
Bulgarian щитовиден подофил
Catalan podofil
Catalan podòfil
Czech noholist štítnatý
Danish prærie-fodblad
German schildförmiges fußblatt
German amerikanischer maiapfel
German entenfuß
German gewöhnlicher maiapfel
Finnish amerikanjalkalehti
French podophylle pelté
Japanese アメリカハッカクレン
Japanese ポドフィルム
Japanese ポドフィルム根
Japanese ポドフィルム脂
Japanese 亜米利加八角蓮
Nepali लघुपत्र
Polish stopkowiec tarczowaty
Polish stopkowiec
Russian Подофилл щитовидный
Russian Майское яблоко
Chinese 足叶草
Chinese 北美桃儿七

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • 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-0000397408
UNII 5Y42EY8SM7
Florida Plant Atlas 3636
Flora of Alabama 1146
Canadensys 3672
USDA Plants POPE
Tropicos 3500162
KEW urn:lsid:ipni.org:names:107599-1
The Plant List kew-2412818
Missouri Botanical Garden 277777
Open Tree Of Life 928422
NCBI Taxonomy 35933
Nature Serve 2.157183
IPNI 107599-1
iNaturalist 49288
GBIF 3033839
Freebase /m/062y27
WisFlora 4553
EPPO PDLPE
EOL 596250
US Library of Congress sh85103689
USDA GRIN 29138
Wikipedia Podophyllum_peltatum

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
Traditional ethnobotanical knowledge and ethnomedicinal use of plants in the Tropical Rift Valley of Ethiopia Wendimu A, Tekalign W, Bojago E, Abrham Y Heliyon 13-Mar-2024
PMCID:PMC10955238
doi:10.1016/j.heliyon.2024.e27528
PMID:38515698
The therapeutic potential of natural metabolites in targeting endocrine-independent HER-2-negative breast cancer Püsküllüoğlu M, Michalak I Front Pharmacol 04-Mar-2024
PMCID:PMC10944949
doi:10.3389/fphar.2024.1349242
PMID:38500769
Transcriptomic Insights and Cytochrome P450 Gene Analysis in Kadsura coccinea for Lignan Biosynthesis Fu H, Guo C, Peng J, Shao F, Sheng S, Wang S Genes (Basel) 21-Feb-2024
PMCID:PMC10969973
doi:10.3390/genes15030270
PMID:38540329
Carnosic Acid against Lung Cancer: Induction of Autophagy and Activation of Sestrin-2/LKB1/AMPK Signalling O’Neill EJ, Sze NS, MacPherson RE, Tsiani E Int J Mol Sci 06-Feb-2024
PMCID:PMC10888478
doi:10.3390/ijms25041950
PMID:38396629
Anticancer Drug Discovery Based on Natural Products: From Computational Approaches to Clinical Studies Chunarkar-Patil P, Kaleem M, Mishra R, Ray S, Ahmad A, Verma D, Bhayye S, Dubey R, Singh HN, Kumar S Biomedicines 16-Jan-2024
PMCID:PMC10813144
doi:10.3390/biomedicines12010201
PMID:38255306
The CYP80A and CYP80G Are Involved in the Biosynthesis of Benzylisoquinoline Alkaloids in the Sacred Lotus (Nelumbo nucifera) Hao C, Yu Y, Liu Y, Liu A, Chen S Int J Mol Sci 05-Jan-2024
PMCID:PMC10815925
doi:10.3390/ijms25020702
PMID:38255776
Illicium verum anticancer activity against MDA-MB-231 cell line Pahore AK, Khan S, Karim N Pak J Med Sci 01-Jan-2024
PMCID:PMC10772409
doi:10.12669/pjms.40.1.7860
PMID:38196489
Two New Compounds from the Endophytic Fungi of Dryopteris crassirhizoma and Their Antimicrobial Activities Hai P, Gao Y, Yang L, Chen N, Jia H, Wang M, Li H, Jiang W, Yang J, Li R Molecules 12-Dec-2023
PMCID:PMC10745856
doi:10.3390/molecules28248043
PMID:38138533
Health-Promoting Effects of Bioactive Compounds from Plant Endophytic Fungi Wijesekara T, Xu B J Fungi (Basel) 08-Oct-2023
PMCID:PMC10608072
doi:10.3390/jof9100997
PMID:37888253
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Expression Profiles of Long Non-Coding RNAs in the Articular Cartilage of Rats Exposed to T-2 Toxin Yu F, Wang M, Luo K, Sun L, Yu S, Zuo J, Wang Y Int J Mol Sci 05-Sep-2023
PMCID:PMC10530968
doi:10.3390/ijms241813703
PMID:37762015
Virtual Screening of Different Subclasses of Lignans with Anticancer Potential and Based on Genetic Profile Maia MD, Mendonça-Junior FJ, Rodrigues GC, da Silva AS, de Oliveira NI, da Silva PR, Felipe CF, Gurgel AP, Nayarisseri A, Scotti MT, Scotti L Molecules 11-Aug-2023
PMCID:PMC10459202
doi:10.3390/molecules28166011
PMID:37630263
Exploration of potential molecular mechanisms and genotoxicity of anti-cancer drugs using next generation knowledge discovery methods Pushparaj PN, Rasool M, Naseer MI, Gauthaman K Pak J Med Sci 01-Jul-2023
PMCID:PMC10364265
doi:10.12669/pjms.39.4.7427
PMID:37492288
Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK Biomolecules 25-Jun-2023
PMCID:PMC10377637
doi:10.3390/biom13071038
PMID:37509074

Phytochemical Profile Top

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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 / Benzene and substituted derivatives / Biphenols
Garcibiphenyl C 134817091 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=C(C=C2)O 246.26 unknown https://doi.org/10.1246/CL.1982.1539
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Tetradehydropodophyllotoxin 5316463 Click to see COC1=CC(=CC(=C1OC)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O 410.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.08-1296A
> Lignans, neolignans and related compounds / Aryltetralin lignans
[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (5R,6R,7R)-7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylate 162987245 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC4=C(C=C23)OCO4)CO)C(=O)OC5C(C(C(C(O5)CO)O)O)O 578.60 unknown https://doi.org/10.1002/HLCA.19630460632
beta-D-Glucopyranose, 1-[5,6,7,8-tetrahydro-7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)naphtho[2,3-d]-1,3-dioxole-6-carboxylate], (5alpha,6alpha,7beta)- 12311207 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC4=C(C=C23)OCO4)CO)C(=O)OC5C(C(C(C(O5)CO)O)O)O 578.60 unknown https://doi.org/10.1002/HLCA.19630460632
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
5-[4-(3,4-Dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 9902716 Click to see CC(CC1=CC(=C(C=C1)OC)O)C(C)CC2=CC(=C(C=C2)OC)OC 344.40 unknown https://doi.org/10.1246/CL.1982.1539
> Lignans, neolignans and related compounds / Lignan glycosides
(5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 11972430 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O 562.50 unknown https://doi.org/10.1016/0031-9422(90)85342-D
https://doi.org/10.1002/HLCA.19570400525
9-(4-hydroxy-3,5-dimethoxyphenyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 294474 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O 562.50 unknown https://doi.org/10.1016/0031-9422(90)85342-D
https://doi.org/10.1002/HLCA.19570400525
beta-Peltatin-beta-D-glucoside 6325789 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O 576.50 unknown https://doi.org/10.1016/0031-9422(90)85342-D
https://doi.org/10.1002/HLCA.19570400525
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin 2203 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1135/CCCC19590314
https://doi.org/10.1016/0031-9422(81)80129-X
https://doi.org/10.3891/ACTA.CHEM.SCAND.08-1296A
https://doi.org/10.1016/S0031-9422(00)82628-X
https://doi.org/10.3987/COM-91-5862
(5aS,8aR,9R)-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-[2]benzofuro[5,6-f][1,3]benzodioxole-5,8-dione 13473531 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 398.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
(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 COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 414.40 unknown https://doi.org/10.1021/NP50024A015
https://doi.org/10.1007/BF02866546
https://doi.org/10.1002/PCA.2800060207
https://doi.org/10.1021/NP960155D
https://doi.org/10.1021/JM960023H
https://doi.org/10.1016/0031-9422(91)84194-W
https://doi.org/10.1016/0021-9673(95)00433-5
https://doi.org/10.1055/S-2002-26740
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 COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 400.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
https://doi.org/10.1021/JA01203A515
4'-Demethyldeoxypodophyllotoxin 160705 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 384.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
5-(4-hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one 1689 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 384.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
8-(4-Hydroxy-3,5-dimethoxyphenyl)-5,12,14-trioxatetracyclo(7.7.0.0(3,7).0(11,15))hexadeca-1(16),9(10),11(15)-triene-2,6-dione 468871 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 398.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
9-(4-Hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-[2]benzofuro[5,6-f][1,3]benzodioxole-5,8-dione 13473529 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 398.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
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/10.1021/NP50024A015
https://doi.org/10.1021/JA01203A515
https://doi.org/10.1007/BF02866546
https://doi.org/10.1002/PCA.2800060207
https://doi.org/10.1021/NP960155D
https://doi.org/10.1021/JM960023H
https://doi.org/10.1016/0031-9422(91)84194-W
https://doi.org/10.1016/B978-0-12-013320-8.50007-1
https://doi.org/10.1016/0021-9673(95)00433-5
https://doi.org/10.1016/0031-9422(86)80071-1
https://doi.org/10.1055/S-2002-26740
https://doi.org/10.1016/S0031-9422(00)82628-X
beta-Peltatin 92122 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 414.40 unknown https://doi.org/10.1021/NP50024A015
https://doi.org/10.1007/BF02866546
https://doi.org/10.1002/PCA.2800060207
https://doi.org/10.1021/NP960155D
https://doi.org/10.1021/JM960023H
https://doi.org/10.1016/0031-9422(91)84194-W
https://doi.org/10.1016/B978-0-12-013320-8.50007-1
https://doi.org/10.1016/0021-9673(95)00433-5
https://doi.org/10.1016/0031-9422(86)80071-1
https://doi.org/10.1055/S-2002-26740
https://doi.org/10.1016/S0031-9422(00)82628-X
beta-Peltatin A 2363 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 414.40 unknown https://doi.org/10.1016/S0031-9422(00)82628-X
d,l-Isopodophyllotoxone 323439 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/S0031-9422(00)82628-X
https://doi.org/10.1016/0031-9422(81)80129-X
https://doi.org/10.3987/COM-91-5862
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/10.3891/ACTA.CHEM.SCAND.08-1296A
https://doi.org/10.1021/JM960023H
https://doi.org/10.1016/S0031-9422(00)82628-X
https://doi.org/10.3987/COM-91-5862
https://doi.org/10.1021/NP50024A015
https://doi.org/10.1016/0031-9422(81)80129-X
https://doi.org/10.1135/CCCC19590314
Isopicropodophyllone 11189106 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/S0031-9422(00)82628-X
Podophyllotoxone 443014 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/10.3987/COM-91-5862
https://doi.org/10.1016/S0031-9422(00)82628-X
https://doi.org/10.1016/0031-9422(81)80129-X
> 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 COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 400.40 unknown https://doi.org/10.3987/COM-91-5862
https://doi.org/10.1002/BMC.1595
https://doi.org/10.1016/S0031-9422(00)82628-X
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/BMC.1595
https://doi.org/10.1002/PCA.2800060207
https://doi.org/10.1021/NP960155D
https://doi.org/10.3987/COM-91-5862
https://doi.org/10.1016/S0031-9422(00)82628-X
4'-Demthylpodophyllotoxin beta-D-glucoside 170385 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 562.50 unknown https://doi.org/10.1002/HLCA.19570400525
5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 4865 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/10.1016/J.ULTSONCH.2011.08.010
https://doi.org/10.1021/NP060174F
https://doi.org/10.3987/COM-91-5862
https://doi.org/10.1016/S0031-9422(00)82628-X
Epipodophyllotoxin 105111 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/10.1021/NP960155D
Picropodophyllin 72435 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/10.1021/NP50024A015
Picropodophyllin, 4'-demethyl-B-D-glucoside 345517 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 562.50 unknown https://doi.org/10.1002/HLCA.19570400525
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/10.1021/JM960023H
https://doi.org/10.1021/NP50095A008
https://doi.org/10.1016/S0031-9422(00)82628-X
https://doi.org/10.1055/S-2002-26740
https://doi.org/10.1016/0021-9673(95)00433-5
https://doi.org/10.1016/0031-9422(91)84194-W
https://doi.org/10.1021/NP960155D
https://doi.org/10.3987/COM-91-5862
https://doi.org/10.1055/S-2001-10636
https://doi.org/10.1080/01483918508067160
https://doi.org/10.1021/NP060174F
https://doi.org/10.1021/NP50024A015
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1195461/
https://doi.org/10.1007/BF02866546
https://doi.org/10.1016/J.ULTSONCH.2011.08.010
https://doi.org/10.3987/COM-92-6177
https://doi.org/10.1016/B978-0-12-013320-8.50007-1
https://doi.org/10.1021/NP50120A008
https://doi.org/10.1002/PCA.2800060207
Podophyllotoxin glucoside 161177 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 576.50 unknown https://doi.org/10.1002/HLCA.19570400525
Podophyllotoxin, glucoside 294472 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 576.50 unknown https://doi.org/10.1002/HLCA.19570400525
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[4,5-Dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl] 11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162943369 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4)C)(CCC7C6(CC(C(C7(C)CO)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)O 1121.30 unknown https://doi.org/10.1016/0031-9422(90)85342-D
https://doi.org/10.1002/HLCA.19570400525
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
1-[(3S,8R,9S,10R,12R,13S,14S,17R)-3,12,14-trihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone 24882901 Click to see CC(=O)C1CCC2(C1(C(CC3C2CC=C4C3(CCC(C4)O)C)O)C)O 348.50 unknown https://doi.org/10.1246/CL.1982.1539
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[5-[3,4-Dihydroxy-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 72775092 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)OC 1211.30 unknown https://doi.org/10.1246/CL.1982.1539
> 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/10.3987/COM-91-5862
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3987/COM-91-5862
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
[5-[2-amino-1-[[3,4-dihydroxy-6-[(2-oxoazepan-3-yl)carbamoyl]-3,4-dihydro-2H-pyran-2-yl]oxy]-2-oxoethyl]-2-(2,4-dioxopyrimidin-1-yl)-4-methoxyoxolan-3-yl] carbamate 139583784 Click to see COC1C(C(OC1C(C(=O)N)OC2C(C(C=C(O2)C(=O)NC3CCCCNC3=O)O)O)N4C=CC(=O)NC4=O)OC(=O)N 612.50 unknown https://doi.org/10.1246/CL.1982.1539
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(10R)-3-hydroxy-23,24-dimethoxy-10-methyl-9,20-dioxa-6-azaheptacyclo[15.12.0.02,14.04,12.06,10.019,28.021,26]nonacosa-1(17),2,4(12),13,15,19(28),21,23,25-nonaene-5,18,27,29-tetrone 124464535 Click to see CC12CC3=C(C(=C4C(=C3)C=CC5=C4C(=O)C6=C(C5=O)OC7=CC(=C(C=C7C6=O)OC)OC)O)C(=O)N1CCO2 527.50 unknown https://doi.org/10.1246/CL.1982.1539
> Organoheterocyclic compounds / Lactams / Beta lactams / Penams / Penicillins
Amoxicillin, L- 32324 Click to see CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C 365.40 unknown https://doi.org/10.1007/BF02866546
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC1195461/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC1195461/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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 https://doi.org/10.1007/BF02144742
Astragalin 5282102 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 https://doi.org/10.1007/BF02144742

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