Papaver arenarium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Papaver arenarium - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64400208e13b9399693452
Scientific name Papaver arenarium
Authority M.Bieb.
First published in Fl. Taur.-Caucas. 3: 364 (1819)

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic خشخاش رملي

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Turkmenistan
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000480334
Tropicos 24000367
KEW urn:lsid:ipni.org:names:673404-1
The Plant List kew-2560669
Open Tree Of Life 5727880
Observations.org 120372
NBN Atlas NBNSYS0200002789
IPNI 673404-1
GBIF 7315108
Elurikkus 587461
USDA GRIN 419473
Wikipedia Papaver_arenarium

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
The structure of arenine I. A. Israilov, M. A. Manushakyan, M. S. Yunusov, V. A. Mnatsakanyan, S. Yu. Yunusov Springer Science and Business Media LLC 01-Dec-2004
doi:10.1007/BF00713355
Alkaloids ofPapaver arenarium I. S. Israilov, M. A. Manushakyan, V. A. Mnatsakanyan, M. S. Yunusov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00574795
Alkaloids of Papaver arenarium and P. commutatum V. A. Mnatsakanyan, M. A. Manushakyan, N. E. Mesropyan Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00573572
Alkaloids ofPapaver orientale I. A. Israilov, O. N. Denisenko, M. S. Yunusov, D. A. Murav'eva, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565244
Alkaloids from Papaver cylindricum. Sariyar G Planta Med 01-Nov-1982
doi:10.1055/S-2007-971208
PMID:17396967

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1007/BF00574795
12H-Benzo[a]-1,3-benzodioxolo[4,5-g]quinolizin-9-ol, 6,6a,11,14-tetrahydro-8-methoxy- 590762 Click to see COC1=C(C=C2CCN3CC4=C(CC3C2=C1)C=CC5=C4OCO5)O 325.40 unknown https://doi.org/10.1055/S-2007-971208
Chelianthifoline 5117621 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1055/S-2007-971208
https://doi.org/10.1007/BF00574795
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[1-(1,3-benzodioxol-5-ylmethyl)-6-methoxyisoquinolin-7-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162930350 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC4=C(C=C3)OCO4)OC5C(C(C(C(O5)CO)O)O)O 471.50 unknown https://doi.org/10.1007/BF00574795
2-[1-(1,3-Benzodioxol-5-ylmethyl)-6-methoxyisoquinolin-7-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162930349 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC4=C(C=C3)OCO4)OC5C(C(C(C(O5)CO)O)O)O 471.50 unknown https://doi.org/10.1007/BF00574795
> Organoheterocyclic compounds / Isoquinolines and derivatives
7-Hydroxy-6-methoxy-1-(3,4-methylenedioxybenzyl) isoquinoline 21763772 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC4=C(C=C3)OCO4)O 309.30 unknown https://doi.org/10.1007/BF00574795
https://doi.org/10.1055/S-2007-971208
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
1-(1,3-Benzodioxol-5-ylmethyl)-6-methoxy-4-(1-methylpyrrolidin-2-yl)isoquinolin-7-ol 163010607 Click to see CN1CCCC1C2=CN=C(C3=CC(=C(C=C32)OC)O)CC4=CC5=C(C=C4)OCO5 392.40 unknown https://doi.org/10.1007/BF00565244
https://doi.org/10.1007/BF00574795
1-(1,3-benzodioxol-5-ylmethyl)-6-methoxy-4-[(2S)-1-methylpyrrolidin-2-yl]isoquinolin-7-ol 101324776 Click to see CN1CCCC1C2=CN=C(C3=CC(=C(C=C32)OC)O)CC4=CC5=C(C=C4)OCO5 392.40 unknown https://doi.org/10.1007/BF00565244
https://doi.org/10.1007/BF00574795
https://doi.org/10.1055/S-2007-971208
https://doi.org/10.1007/BF00713355
1-(1,3-Benzodioxol-5-ylmethyl)-6,7-dimethoxy-4-(1-methylpyrrolidin-2-yl)isoquinoline 13945379 Click to see CN1CCCC1C2=CN=C(C3=CC(=C(C=C32)OC)OC)CC4=CC5=C(C=C4)OCO5 406.50 unknown https://doi.org/10.1007/BF00574795
Macrostomine 185760 Click to see CN1CCCC1C2=CN=C(C3=CC(=C(C=C32)OC)OC)CC4=CC5=C(C=C4)OCO5 406.50 unknown https://doi.org/10.1007/BF00574795
https://doi.org/10.1055/S-2007-971208
https://doi.org/10.1007/BF00573572

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