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Papaver albiflorum

Papaver albiflorum - 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 UUID64404a12ad441524695413
Scientific name Papaver albiflorum
Authority (Elkan) Pacz.
First published in Trudy Bot. Sada Imp. Yur'evsk. Univ. 6: 147 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Papaver paczoskii Mikheev Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 90(3): 91 (1985)

Common names Top

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Language Common/alternative name
Ukrainian Мак білоцвітий

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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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-0001090272
Tropicos 24000025
KEW urn:lsid:ipni.org:names:673384-1
Open Tree Of Life 5727872
IPNI 673384-1
iNaturalist 854392
GBIF 7315162

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
Alkaloids from Papaver albiflorum subsp. austromoravicum KUBÁT, P. albiflorum PACZ. subsp. albiflorum and P. lecoquii LAMOTTE Jiří Slavík, Leonora Slavíková, Ladislav Dolejš Institute of Organic Chemistry & Biochemistry 12-Aug-2011
doi:10.1135/CCCC19812587
Alkaloids from Papaver albiflorum PACZ. subsp. albiflorum and P. cf. stevenianum A. D. Mikheev Jiří Slavík, Leonora Slavíková Institute of Organic Chemistry & Biochemistry 11-Feb-2010
doi:10.1135/CCCC19901812

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 / Aporphines
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/CCCC19901812
https://doi.org/10.1135/CCCC19812587
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/CCCC19901812
https://doi.org/10.1135/CCCC19812587
> Alkaloids and derivatives / Morphinans
Morphinan, 6,7,8,14-tetradehydro-4,5-epoxy-3,6-dimethoxy-17-methyl-, (5alpha)- 408120 Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)OC)O4)OC 311.40 unknown https://doi.org/10.1135/CCCC19812587
Thebaine 5324289 Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)OC)O4)OC 311.40 unknown https://doi.org/10.1135/CCCC19812587
https://doi.org/10.1135/CCCC19901812
> Alkaloids and derivatives / Proaporphines
Mecambrine 121336 Click to see CN1CCC2=CC3=C(C4=C2C1CC45C=CC(=O)C=C5)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19901812
> 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/CCCC19901812
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/CCCC19901812
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/CCCC19901812
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/CCCC19901812
> 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/CCCC19812587
https://doi.org/10.1135/CCCC19901812
Muramine 288122 Click to see CN1CCC2=CC(=C(C=C2C(=O)CC3=C(C1)C(=C(C=C3)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1135/CCCC19901812
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/CCCC19901812
https://doi.org/10.1135/CCCC19812587
> Alkaloids and derivatives / Rhoeadine alkaloids
(1R)-11,17-dimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaen-16-ol 5320411 Click to see COC1C2=C(C=CC3=C2OCO3)C4C(O1)C5=CC(=C(C=C5CCN4)OC)O 371.40 unknown https://doi.org/10.1135/CCCC19901812
Papaverrubine E 601058 Click to see COC1C2=C(C=CC3=C2OCO3)C4C(O1)C5=CC6=C(C=C5CCN4)OCO6 369.40 unknown https://doi.org/10.1135/CCCC19901812
Porphyroxine 601829 Click to see COC1C2=C(C=CC3=C2OCO3)C4C(O1)C5=CC(=C(C=C5CCN4)OC)O 371.40 unknown https://doi.org/10.1135/CCCC19901812
Rheadine 601064 Click to see CN1CCC2=CC3=C(C=C2C4C1C5=C(C(O4)OC)C6=C(C=C5)OCO6)OCO3 383.40 unknown https://doi.org/10.1135/CCCC19812587
Rhoeadine 197775 Click to see CN1CCC2=CC3=C(C=C2C4C1C5=C(C(O4)OC)C6=C(C=C5)OCO6)OCO3 383.40 unknown https://doi.org/10.1135/CCCC19901812
https://doi.org/10.1135/CCCC19812587

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