Stylophorum diphyllum - Unknown
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Internal ID UUID64404a14ac7d1600217917
Scientific name Stylophorum diphyllum
Authority (Michx.) Nutt.
First published in Gen. N. Amer. Pl. 2: 7 (1818)

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Synonyms Top

Scientific name Authority First published in
Meconopsis diphylla (Michx.) DC. Syst. Nat. 2: 88 (1821)
Meconopsis petiolata DC. Syst. Nat. 2: 87 (1821)
Stylophorum petiolatum Nutt. Gen. N. Amer. Pl. 2: 8 (1818)
Chelidonium diphyllum Michx. Fl. Bor.-Amer. 1: 309 (1803)
Chelidonium petiolatum Spreng. ex Steud. Nomencl. Bot. , ed. 2, 1: 347 (1840)
Stylophorum ohiense Spreng. Syst. Veg. 2: 570 (1825)
Meconopsis crassifolia Benth. Trans. Hort. Soc. London , ser. 2, 1: 408 (1834 publ. 1835)

Common names Top

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Language Common/alternative name
English celandine poppy
Arabic ثرمية ثنائية الأوراق
Polish styloforum dwulistne
Chinese 白屈菜罂粟

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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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Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period.
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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Indiana
      • Michigan
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Kentucky
      • Maryland
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001090305
Flora of Alabama 2818
Canadensys 7129
USDA Plants STDI3
Tropicos 24000154
KEW urn:lsid:ipni.org:names:674012-1
The Plant List tro-24000154
Missouri Botanical Garden 284856
Open Tree Of Life 565716
NCBI Taxonomy 56864
Nature Serve 2.150797
IPNI 674012-1
iNaturalist 126378
GBIF 2888466
Freebase /m/08pj6x
EPPO SFODI
EOL 596195
USDA GRIN 35870
Wikipedia Stylophorum_diphyllum

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
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
C N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771676
doi:10.1016/B978-0-7020-7463-9.50011-2
Comparative analysis of the root and leaf transcriptomes in Chelidonium majus L. Pourmazaheri H, Soorni A, Kohnerouz BB, Dehaghi NK, Kalantar E, Omidi M, Naghavi MR PLoS One 15-Apr-2019
PMCID:PMC6464174
doi:10.1371/journal.pone.0215165
PMID:30986259
Identification and expression analysis of a microRNA cluster derived from pre-ribosomal RNA in Papaver somniferum L. and Papaver bracteatum L. Davoodi Mastakani F, Pagheh G, Rashidi Monfared S, Shams-Bakhsh M PLoS One 01-Aug-2018
PMCID:PMC6070170
doi:10.1371/journal.pone.0199673
PMID:30067748
The effects of promoter variations of the N-Methylcanadine 1-Hydroxylase (CYP82Y1) gene on the noscapine production in opium poppy Abedini D, Monfared SR, Abbasi A Sci Rep 21-Mar-2018
PMCID:PMC5862900
doi:10.1038/s41598-018-23351-0
PMID:29563567
Genes encoding norcoclaurine synthase occur as tandem fusions in the Papaveraceae Li J, Lee EJ, Chang L, Facchini PJ Sci Rep 19-Dec-2016
PMCID:PMC5171800
doi:10.1038/srep39256
PMID:27991536
The developmental and genetic bases of apetaly in Bocconia frutescens (Chelidonieae: Papaveraceae) Arango-Ocampo C, González F, Alzate JF, Pabón-Mora N EvoDevo 02-Aug-2016
PMCID:PMC4971710
doi:10.1186/s13227-016-0054-6
PMID:27489612
Transcriptome analysis of 20 taxonomically related benzylisoquinoline alkaloid-producing plants Hagel JM, Morris JS, Lee EJ, Desgagné-Penix I, Bross CD, Chang L, Chen X, Farrow SC, Zhang Y, Soh J, Sensen CW, Facchini PJ BMC Plant Biol 18-Sep-2015
PMCID:PMC4575454
doi:10.1186/s12870-015-0596-0
PMID:26384972
Metabolome analysis of 20 taxonomically related benzylisoquinoline alkaloid-producing plants Hagel JM, Mandal R, Han B, Han J, Dinsmore DR, Borchers CH, Wishart DS, Facchini PJ BMC Plant Biol 15-Sep-2015
PMCID:PMC4570626
doi:10.1186/s12870-015-0594-2
PMID:26369413
Alkaloide der Mohngewächse (Papaveraceae) XX. Über die Alkaloide aus Stylophorum diphyllum (MICHX.) NUTT. J. Slavík Institute of Organic Chemistry & Biochemistry 11-Sep-2013
doi:10.1135/CCCC19612933
THE ALKALOIDS OF PAPAVERACEOUS PLANTS: XXXII. <i>STYLOPHORUM DIPHYLLUM</i> (MICHX.) NUTT., <i>DICRANOSTIGMA FRANCHETIANUM</i> (PRAIN) FEDDE AND <i>GLAUCIUM SERPIERI</i> HELDR. Richard H. F. Manske Canadian Science Publishing 24-Apr-2011
doi:10.1139/CJR42B-009
Minor alkaloids from Stylophorum diphyllum (MICHX.) NUTT. Jiří Slavík, Leonora Slavíková Institute of Organic Chemistry & Biochemistry 10-Feb-2011
doi:10.1135/CCCC19840704
Beiträge zur Chemie des Stylophorum diphyllum J. O. Schlotterbeck, H. C. Watkins Wiley 20-Jul-2007
doi:10.1002/CBER.19020350103

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
> Alkaloids and derivatives / Aporphines
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1135/CCCC19840704
Corytuberine 160500 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1135/CCCC19840704
Corytuberine, pentahydrate 347379 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1135/CCCC19840704
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1135/CCCC19840704
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1135/CCCC19840704
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-11,12-dimethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol 162929072 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C(=C4OC)OC)OCO6)O 409.40 unknown https://doi.org/10.1135/CCCC19612933
(23S)-12-methoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol 162918177 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4OC)OCO6)O 379.40 unknown https://doi.org/10.1135/CCCC19612933
(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol 163010848 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)O 349.30 unknown https://doi.org/10.1135/CCCC19612933
11,12-Dimethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol 162929071 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C(=C4OC)OC)OCO6)O 409.40 unknown https://doi.org/10.1135/CCCC19612933
12-Methoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol 162918176 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4OC)OCO6)O 379.40 unknown https://doi.org/10.1135/CCCC19612933
Sanguinarine pseudobase 14313843 Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)O 349.30 unknown https://doi.org/10.1135/CCCC19612933
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine 197810 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1135/CCCC19840704
https://doi.org/10.1002/CBER.19020350103
https://doi.org/10.1135/CCCC19612933
https://doi.org/10.1139/CJR42B-009
Chelidonine (+) 10147 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1139/CJR42B-009
https://doi.org/10.1135/CCCC19612933
https://doi.org/10.1002/CBER.19020350103
https://doi.org/10.1135/CCCC19840704
Chelidonine, (-)- 978315 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1002/CBER.19020350103
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown https://doi.org/10.1135/CCCC19840704
Chelirubine 161243 Click to see C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OC)OCO3 362.40 unknown https://doi.org/10.1135/CCCC19840704
Macarpine 440929 Click to see C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C(=C4)OC)OCO6)OC)OCO3 392.40 unknown https://doi.org/10.1135/CCCC19840704
Sanguinarium 5154 Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6 332.30 unknown https://doi.org/10.1135/CCCC19840704
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol 1152279 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1135/CCCC19840704
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1135/CCCC19840704
Bis(1,3)benzodioxolo(5,6-a:4',5'-g)quinolizinium, 6,7-dihydro-13-methyl- 147329 Click to see CC1=C2C=CC3=C(C2=C[N+]4=C1C5=CC6=C(C=C5CC4)OCO6)OCO3 334.30 unknown https://doi.org/10.1135/CCCC19840704
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown https://doi.org/10.1135/CCCC19840704
Scoulerine 22955 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1135/CCCC19840704
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1135/CCCC19612933
https://doi.org/10.1135/CCCC19840704
https://doi.org/10.1002/CBER.19020350103
Tetrahydrocoptisine 6770 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown https://doi.org/10.1135/CCCC19612933
https://doi.org/10.1135/CCCC19840704
https://doi.org/10.1002/CBER.19020350103
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown https://doi.org/10.1135/CCCC19840704
Cryptopine 72616 Click to see CN1CCC2=CC(=C(C=C2C(=O)CC3=C(C1)C4=C(C=C3)OCO4)OC)OC 369.40 unknown https://doi.org/10.1135/CCCC19840704
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1135/CCCC19840704
https://doi.org/10.1002/CBER.19020350103
https://doi.org/10.1135/CCCC19612933
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Chelidonic acid 7431 Click to see C1=C(OC(=CC1=O)C(=O)O)C(=O)O 184.10 unknown https://doi.org/10.1002/CBER.19020350103

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