Scientific name	Authority	First published in
Papaver dzeghamicum	Medw.	Vestn. Tiflissk. Bot. Sada 18: 15 (1915)
Papaver grandiflorum	Moench	Methodus : 250 (1794)
Papaver paucifoliatum	(Trautv.) Fedde	Pflanzenr. , IV, 104: 366 (1909)
Papaver monanthum	Trautv.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 10: 293 (1866)
Calomecon orientalis	Spach	Hist. Nat. Vég. (Spach) 7: 9. 1838 [May 1839 publ. 4 May 1838]
Papaver intermedium	DC.
Papaver orientale var. intermedium	Grossh.
Papaver lateritium subsp. monanthum	(Trautv.) Kadereit	Edinburgh J. Bot. 53: 305 (1996)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	oriental poppy
Arabic	خشخاش مشرقي
Azerbaijani	Şərq xaşxaşı
azb	دوغو خاشخاشی
Belarusian	Мак усходні
Bulgarian	ориенталски мак
Czech	mák východní
German	türkischer mohn
German	türkenmohn
German	staudenmohn
German	stauden-mohn
German	orientalischer mohn
German	morgenländischer mohn
German	gartenmohn
German	garten-mohn
German	feuermohn
German	feuer-mohn
Estonian	idamagun
Persian	خشخاش زینتی
Finnish	idänunikko
French	pavot de tournefort
French	pavot d'orient
Upper Sorbian	narańši mak
Hungarian	díszpipacs
Hungarian	keleti pipacs
Hungarian	keleti mák
Armenian	Կակաչ արևելյան
Icelandic	tyrkjasól
Japanese	オリエンタル・ポピー
Japanese	パパヴェル・オリエンターレ
Japanese	オニゲシ
Lithuanian	rytinė aguona
Macedonian	ориентална булка
Dutch	oosterse papaver
Dutch	reuzenklaproos
Polish	mak wschodni
Russian	Мак восточный
Slovak	mak východný
Slovenian	turški mak
Swedish	orientvallmo
Turkish	gelincik, türk gelinciği
Ukrainian	Мак східний
Chinese	鬼罌粟
Chinese	东方罂粟
Chinese	鬼罂粟

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Tadzhikistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Iran
  - Turkey

Europe click to expand
- Northern Europe
  - Finland
  - Great Britain
  - Sweden
- Southeastern Europe
  - Romania

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Iowa
  - Wisconsin
- Northeastern U.S.A.
  - Michigan
  - New Jersey
  - New York
  - Pennsylvania
- Northwestern U.S.A.
  - Colorado
- Southeastern U.S.A.
  - Virginia
- Southwestern U.S.A.
  - Utah

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000480873
UNII	89MX4P9FP6
Canadensys	7118
USDA Plants	PAOR5
Tropicos	24000138
INPN	112342
Flora of Italy	12784
KEW	urn:lsid:ipni.org:names:673641-1
The Plant List	kew-2561370
Open Tree Of Life	171970
Observations.org	17140
NCBI Taxonomy	22694
NBN Atlas	NBNSYS0000034065
Nature Serve	2.137544
IPNI	673641-1
iNaturalist	166114
GBIF	2888437
Freebase	/m/05qk80
WisFlora	4416
EPPO	PAPOR
EOL	594729
Elurikkus	6096
USDA GRIN	26693
Wikipedia	Papaver_orientale

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 effects of green and chemically-synthesized copper oxide nanoparticles on the production and gene expression of morphinan alkaloids in Oriental poppy

khaldari I, Naghavi MR, Motamedi E, Zargar M

Sci Rep

12-Mar-2024

PMCID:	PMC10933268
doi:	10.1038/s41598-024-56709-8
PMID:	38472367

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

Biotechnology and In Vitro Culture as an Alternative System for Secondary Metabolite Production

Mohaddab M, El Goumi Y, Gallo M, Montesano D, Zengin G, Bouyahya A, Fakiri M

Molecules

21-Nov-2022

PMCID:	PMC9697480
doi:	10.3390/molecules27228093
PMID:	36432194

Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022

Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M

Molecules

17-Aug-2022

PMCID:	PMC9416168
doi:	10.3390/molecules27165253
PMID:	36014492

A functionally conserved STORR gene fusion in Papaver species that diverged 16.8 million years ago

Catania T, Li Y, Winzer T, Harvey D, Meade F, Caridi A, Leech A, Larson TR, Ning Z, Chang J, Van de Peer Y, Graham IA

Nat Commun

07-Jun-2022

PMCID:	PMC9174169
doi:	10.1038/s41467-022-30856-w
PMID:	35672295

Diels–Alder Adducts of Morphinan-6,8-Dienes and Their Transformations

Marton J, Fekete A, Cumming P, Hosztafi S, Mikecz P, Henriksen G

Molecules

30-Apr-2022

PMCID:	PMC9102320
doi:	10.3390/molecules27092863
PMID:	35566212

Papaver Plants: Current Insights on Phytochemical and Nutritional Composition Along with Biotechnological Applications

Butnariu M, Quispe C, Herrera-Bravo J, Pentea M, Sarac I, Küşümler AS, Özçelik B, Painuli S, Semwal P, Imran M, Gondal TA, Emamzadeh-Yazdi S, Lapava N, Yousaf Z, Kumar M, Eid AH, Al-Dhaheri Y, Suleria HA, del Mar Contreras M, Sharifi-Rad J, Cho WC

Oxid Med Cell Longev

03-Feb-2022

PMCID:	PMC9943628
doi:	10.1155/2022/2041769
PMID:	36824615

Complete chloroplast genome of Stephania tetrandra (Menispermaceae) from Zhejiang Province: insights into molecular structures, comparative genome analysis, mutational hotspots and phylogenetic relationships

Dong S, Ying Z, Yu S, Wang Q, Liao G, Ge Y, Cheng R

BMC Genomics

06-Dec-2021

PMCID:	PMC8647421
doi:	10.1186/s12864-021-08193-x
PMID:	34872502

OpiumPlex is a novel microsatellite system for profiling opium poppy (Papaver somniferum L.)

Vašek J, Čílová D, Melounová M, Svoboda P, Zdeňková K, Čermáková E, Ovesná J

Sci Rep

17-Jun-2021

PMCID:	PMC8211840
doi:	10.1038/s41598-021-91962-1
PMID:	34140548

Highly variable chloroplast genome from two endangered Papaveraceae lithophytes Corydalis tomentella and Corydalis saxicola

Ren F, Wang L, Li Y, Zhuo W, Xu Z, Guo H, Liu Y, Gao R, Song J

Ecol Evol

19-Mar-2021

PMCID:	PMC8093665
doi:	10.1002/ece3.7312
PMID:	33976800

Characterization of the complete chloroplast genome of the prickly blue poppy Meconopsis horridula Hook. f. & Thomson (Ranunculales: Papaveraceae)

Dan Q, Li Q, Li X, Suonan R, Dongzhi D, Guo X

Mitochondrial DNA B Resour

11-Mar-2021

PMCID:	PMC7954420
doi:	10.1080/23802359.2021.1882902
PMID:	33763580

Medicinal ethnobotany of wild plants: a cross-cultural comparison around Georgia-Turkey border, the Western Lesser Caucasus

Kazancı C, Oruç S, Mosulishvili M

J Ethnobiol Ethnomed

23-Nov-2020

PMCID:	PMC7681977
doi:	10.1186/s13002-020-00415-y
PMID:	33225956

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

Opium Alkaloids in Harvested and Thermally Processed Poppy Seeds

Carlin MG, Dean JR, Ames JM

Front Chem

27-Aug-2020

PMCID:	PMC7482649
doi:	10.3389/fchem.2020.00737
PMID:	33195013

Proficient dye removal from water using biogenic silver nanoparticles prepared through solid-state synthetic route

Sharbaf Moghadas MR, Motamedi E, Nasiri J, Naghavi MR, Sabokdast M

Heliyon

24-Aug-2020

PMCID:	PMC7452412
doi:	10.1016/j.heliyon.2020.e04730
PMID:	32904200

Phytochemical Profile Top

Add a new one!

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
(-)-Lirinidine	821343	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC	281.30	unknown	https://doi.org/10.1135/CCCC19861752
(6aR)-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,11-diol	162889938	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)O)O)OC	297.30	unknown	https://doi.org/10.1007/BF00565244
(6aR)-2,11-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	739273	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1135/CCCC19800914 https://doi.org/10.1002/JPS.2600660742
(6aS)-1,2,11-Trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	122216708	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)OC)OC)OC	325.40	unknown	https://doi.org/10.1007/BF00574797
(6aS)-1,2,9-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	163020962	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=CC(=C4)OC)OC)OC	325.40	unknown	https://doi.org/10.1007/BF00574797
(6aS)-1,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol	154496913	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC)OC)O	327.40	unknown	https://doi.org/10.1007/BF00574797
(6aS)-2,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	162874196	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=C(C=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1016/S0031-9422(00)80828-6
(6aS)-2,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	163025170	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=CC(=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1007/BF00579507
1,2,11-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	134848956	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)OC)OC)OC	325.40	unknown	https://doi.org/10.1007/BF00574797
1,2,9-Trimethoxyaporphine	129829837	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=CC(=C4)OC)OC)OC	325.40	unknown	https://doi.org/10.1007/BF00574797
1,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol	390656	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC)OC)O	327.40	unknown	https://doi.org/10.1007/BF00574797
2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,11-diol	162889937	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)O)O)OC	297.30	unknown	https://doi.org/10.1007/BF00565244
2,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	163025169	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=CC(=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1007/BF00579507
3,15-Dimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-16-ol	85769694	Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C=CC=C4OC)O)OC	309.40	unknown	https://doi.org/10.1007/BF00579507
3,15,16-Trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene	86250813	Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C=CC=C4OC)OC)OC	323.40	unknown	https://doi.org/10.1007/BF00574797
6-Hydroxy-2-methoxyaporphine	286866	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)O)OC	281.30	unknown	https://doi.org/10.1135/CCCC19861752
Bracteoline	133322	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC)O)OC	327.40	unknown	https://doi.org/10.1135/CCCC19911534 https://doi.org/10.1002/JPS.2600660742
CID 286864	286864	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C=C(C=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1016/S0031-9422(00)80828-6
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/CCCC19911534 https://doi.org/10.1135/CCCC19861752
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/CCCC19911534 https://doi.org/10.1135/CCCC19861752
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/CCCC19911534
Isothebaine	11281	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)OC)O)OC	311.40	unknown	https://doi.org/10.1135/CCCC19911534 https://doi.org/10.1135/CCCC19861752 https://doi.org/10.1007/BF00574797 https://doi.org/10.1002/ARDP.19142520309 https://doi.org/10.1016/S0031-9422(00)80828-6 https://doi.org/10.1002/JPS.2600660742
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/CCCC19911534
> Alkaloids and derivatives / Morphinans
(+)-Thebaine	5421845	Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)OC)O4)OC	311.40	unknown	https://doi.org/10.1002/ARDP.19142520309 https://doi.org/10.1002/ARDP.19142520310
(4R,7aR,12bS)-7-methoxy-1,2,3,4,7a,13-hexahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-9-ol	44221865	Click to see COC1=CC=C2C3CC4=C5C2(C1OC5=C(C=C4)O)CCN3	283.32	unknown	https://doi.org/10.1007/BF00569617 https://doi.org/10.1002/JPS.2600660742
(4S,7aS,12bR)-7-methoxy-3-methyl-2,4,7a,13-tetrahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-9-ol	163002904	Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)O)O4)OC	297.30	unknown	https://doi.org/10.1002/JPS.2600660742
(4S,7aS,12bR)-7,9-dimethoxy-1,2,3,4,7a,13-hexahydro-4,12-methanobenzofuro[3,2-e]isoquinoline	11044697	Click to see COC1=C2C3=C(CC4C5=CC=C(C(C53CCN4)O2)OC)C=C1	297.30	unknown	https://doi.org/10.1002/JPS.2600660742
7-Methoxy-1,2,3,4,7a,13-hexahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-9-ol	68023796	Click to see COC1=CC=C2C3CC4=C5C2(C1OC5=C(C=C4)O)CCN3	283.32	unknown	https://doi.org/10.1007/BF00569617
7,9-Dimethoxy-1,2,3,4,7a,13-hexahydro-4,12-methanobenzofuro[3,2-e]isoquinoline	12313596	Click to see COC1=C2C3=C(CC4C5=CC=C(C(C53CCN4)O2)OC)C=C1	297.30	unknown	https://doi.org/10.1002/JPS.2600660742
Morphinan-3-ol, 6,7,8,14-tetradehydro-4,5-epoxy-6-methoxy-17-methyl-, (5alpha)-	626667	Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)O)O4)OC	297.30	unknown	https://doi.org/10.1002/JPS.2600660742
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/10.1016/S0031-9422(00)81705-7 https://doi.org/10.1002/ARDP.19142520309 https://doi.org/10.1002/ARDP.19142520310
Oripavine	5462306	Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)O)O4)OC	297.30	unknown	https://doi.org/10.1135/CCCC19911534 https://doi.org/10.1021/NP50022A012 https://doi.org/10.1002/JPS.2600660742
Thebaine	5324289	Click to see CN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)OC)O4)OC	311.40	unknown	https://doi.org/10.1021/NP50022A012 https://doi.org/10.1002/JPS.2600660742 https://doi.org/10.1016/S0379-0738(97)00196-5 https://doi.org/10.1021/NP50058A030 https://doi.org/10.1135/CCCC19911534
> Alkaloids and derivatives / Phthalide isoquinolines
Noscapine	275196	Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3	413.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
> 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/CCCC19911534
(3,17,18-Trimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15,17,19-hexaen-19-yl)methanol	633984	Click to see COC1=C(C(=C2CC3C4=C(C5=C(C=C4CCN3CC2=C1)OCO5)OC)CO)OC	399.40	unknown	https://doi.org/10.1135/CCCC19861752 https://doi.org/10.1007/BF00574797 https://doi.org/10.1002/JPS.2600660742
2,11-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-9-ol	163192732	Click to see COC1=CC2=C(CCN3C2CC4=C(C3)C(=CC(=C4)OC)O)C=C1	311.40	unknown	https://doi.org/10.1016/S0367-326X(00)00193-3
Bractavine	185550	Click to see COC1=C2C(=C3CC4C5=C(C6=C(C=C5CCN4CC3=C1)OCO6)OC)COCO2	397.40	unknown	https://doi.org/10.1016/S0367-326X(00)00193-3 https://doi.org/10.1002/ARDP.19142520309 https://doi.org/10.1002/JPS.2600660742 https://doi.org/10.1007/BF00565244
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/CCCC19911534
Mecambridine	161692	Click to see COC1=C(C(=C2CC3C4=C(C5=C(C=C4CCN3CC2=C1)OCO5)OC)CO)OC	399.40	unknown	https://doi.org/10.1135/CCCC19861752 https://doi.org/10.1007/BF00574797 https://doi.org/10.1007/BF00565244 https://doi.org/10.1002/JPS.2600660742
Palmatine	19009	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC	352.40	unknown	https://doi.org/10.1135/CCCC19911534
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/CCCC19911534
> 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/CCCC19861752
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/10.1002/ARDP.19142520310 https://doi.org/10.1002/JPS.2600660742 https://doi.org/10.1135/CCCC19861752
> Alkaloids and derivatives / Rhoeadine alkaloids
(1R,11S,13S)-11,16,17-trimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene	12309624	Click to see COC1C2=C(C=CC3=C2OCO3)C4C(O1)C5=CC(=C(C=C5CCN4)OC)OC	385.40	unknown	https://doi.org/10.1135/CCCC19911534
(1R,11S)-11,16,17-trimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene	5320410	Click to see COC1C2=C(C=CC3=C2OCO3)C4C(O1)C5=CC(=C(C=C5CCN4)OC)OC	385.40	unknown	https://doi.org/10.1135/CCCC19911534
(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/CCCC19911534
(1S,11R,18S)-4,5,15,16-tetramethoxy-10-methyl-19-oxa-10-azatetracyclo[9.8.0.02,7.012,17]nonadeca-2,4,6,12(17),13,15-hexaen-18-ol	12305770	Click to see CN1CCC2=CC(=C(C=C2C3C1C4=C(C(O3)O)C(=C(C=C4)OC)OC)OC)OC	401.50	unknown	https://doi.org/10.1135/CCCC19911534 https://doi.org/10.1002/JPS.2600660742
4,5,15,16,18-Pentamethoxy-19-oxa-10-azatetracyclo[9.8.0.02,7.012,17]nonadeca-2,4,6,12(17),13,15-hexaene	162890172	Click to see COC1C2=C(C=CC(=C2OC)OC)C3C(O1)C4=CC(=C(C=C4CCN3)OC)OC	401.50	unknown	https://doi.org/10.1135/CCCC19911534
Alpinigenine	613751	Click to see CN1CCC2=CC(=C(C=C2C3C1C4=C(C(O3)O)C(=C(C=C4)OC)OC)OC)OC	401.50	unknown	https://doi.org/10.1002/JPS.2600660742
CID 166983	166983	Click to see CN1CCC2=CC(=C(C=C2C3C1C4=C(C(O3)O)C(=C(C=C4)OC)OC)OC)OC	401.50	unknown	https://doi.org/10.1135/CCCC19911534 https://doi.org/10.1055/S-2007-971507 https://doi.org/10.1002/JPS.2600660742
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/CCCC19911534
> Benzenoids / Phenanthrenes and derivatives
(1R,9S)-6-[[(1R,9S)-4,13-dimethoxy-17-methyl-12-oxo-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-3-yl]oxy]-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-12-one	102402012	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)OC5=CC(=C(C6=C5CC7C8=CC(=O)C(=CC86CCN7C)OC)O)OC)OC	652.70	unknown	https://doi.org/10.1021/NP50071A044
(1S,9R)-6-[[(1R,9S)-4,13-dimethoxy-17-methyl-12-oxo-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-3-yl]oxy]-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-12-one	163008646	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)OC5=CC(=C(C6=C5CC7C8=CC(=O)C(=CC86CCN7C)OC)O)OC)OC	652.70	unknown	https://doi.org/10.1021/NP50071A025
3-Hydroxy-4,13-dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-12-one	12313590	Click to see COC1=C(C2=C(CC3C4=CC(=O)C(=CC42CCN3)OC)C=C1)O	313.30	unknown	https://doi.org/10.1021/NP50058A030
Salutaridine	5408233	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7 https://doi.org/10.1021/NP50058A030 https://doi.org/10.1016/0031-9422(77)80115-5 https://doi.org/10.1055/S-2006-961487
Sinoacutine	625160	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1016/0031-9422(77)80115-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S)-docosane-1,3-diol	163097968	Click to see CCCCCCCCCCCCCCCCCCCC(CCO)O	342.60	unknown	https://doi.org/10.1016/0031-9422(96)00180-X
(3S)-tetracosane-1,3-diol	162986314	Click to see CCCCCCCCCCCCCCCCCCCCCC(CCO)O	370.70	unknown	https://doi.org/10.1016/0031-9422(96)00180-X
Docosane-1,3-diol	11963186	Click to see CCCCCCCCCCCCCCCCCCCC(CCO)O	342.60	unknown	https://doi.org/10.1016/0031-9422(96)00180-X
Tetracosane-1,3-diol	11963188	Click to see CCCCCCCCCCCCCCCCCCCCCC(CCO)O	370.70	unknown	https://doi.org/10.1016/0031-9422(96)00180-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
9,15,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10-dione	162821265	Click to see CC12CC(=O)CC34C1C5C(C67C3C(C(C(=C)C6)C(=O)C7(C4N5C2)O)O)O	357.40	unknown	https://doi.org/10.1007/BF00579507
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
mono-O-(3,7,11-trimethyldodeca-2,6,10-trienoyl)glycerol	73798421	Click to see CC(=CCCC(=CCCC(=CC(=O)OCC(CO)O)C)C)C	310.40	unknown	https://doi.org/10.1135/CCCC19861752 https://doi.org/10.1135/CCCC19800914 https://doi.org/10.1007/BF00574797 https://doi.org/10.1002/JPS.2600660742
> Organoheterocyclic compounds / Dihydroisoquinolines
Cotarninium	160909	Click to see C[N+]1=CC2=C(C3=C(C=C2CC1)OCO3)OC	220.24	unknown	https://doi.org/10.1021/NP50071A025
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+)-Papaveroxinoline	14106962	Click to see CC(=O)OC(C1C2=C(C3=C(C=C2CCN1C)OCO3)OC)C4=C(C(=C(C=C4)OC)OC)CO	459.50	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
(1R)-1-[(4-hydroxy-3-methoxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol	101306759	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC	329.40	unknown	https://doi.org/10.1007/BF00574797
(5S)-5-[[2-(hydroxymethyl)-3,4-dimethoxyphenyl]methyl]-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-4-ol	162860951	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)CO)O)OCO3	387.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
[(R)-[2-(hydroxymethyl)-3,4-dimethoxyphenyl]-[(5R)-4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl] acetate	124355609	Click to see CC(=O)OC(C1C2=C(C3=C(C=C2CCN1C)OCO3)OC)C4=C(C(=C(C=C4)OC)OC)CO	459.50	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
[2,3-dimethoxy-6-[(4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenyl]methanol	4235574	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)CO)OC)OCO3	401.50	unknown	https://doi.org/10.1016/0031-9422(77)80115-5 https://doi.org/10.1016/S0031-9422(00)81705-7
2,3-dimethoxy-6-[(4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]benzaldehyde	162937121	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)C=O)OC)OCO3	399.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
2,3-dimethoxy-6-[(4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]benzoic acid	53463181	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)C(=O)O)OC)OCO3	415.40	unknown	https://doi.org/10.1016/0031-9422(77)80115-5 https://doi.org/10.1016/S0031-9422(00)81705-7
2,3-dimethoxy-6-[[(5S)-4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]benzaldehyde	162937122	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)C=O)OC)OCO3	399.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
5-[[2-(hydroxymethyl)-3,4-dimethoxyphenyl]methyl]-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-4-ol	162860950	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)CO)O)OCO3	387.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7
7-Isoquinolinol, 1,2,3,4-tetrahydro-1-((4-hydroxy-3-methoxyphenyl)methyl)-6-methoxy-2-methyl-, (+-)-	14357386	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC	329.40	unknown	https://doi.org/10.1007/BF00574797
Macrantaline	188465	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)CO)OC)OCO3	401.50	unknown	https://doi.org/10.1016/0031-9422(77)80115-5 https://doi.org/10.1016/S0031-9422(00)81705-7
Macrantoridine	182492	Click to see CN1CCC2=CC3=C(C(=C2C1CC4=C(C(=C(C=C4)OC)OC)C(=O)O)OC)OCO3	415.40	unknown	https://doi.org/10.1016/0031-9422(77)80115-5 https://doi.org/10.1016/S0031-9422(00)81705-7
Narcotinediol	98447	Click to see CN1CCC2=CC3=C(C(=C2C1C(C4=C(C(=C(C=C4)OC)OC)CO)O)OC)OCO3	417.50	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7 https://doi.org/10.1021/NP50058A030
Papaveroxidine	189458	Click to see CC(=O)OC(C1C2=C(C3=C(C=C2CCN1C)OCO3)OC)C4=C(C(=C(C=C4)OC)OC)C(=O)O	473.50	unknown	https://doi.org/10.1021/NP50058A030
Papaveroxine	129011755	Click to see CN1CCC2=CC3=C(C(=C2C1C(C4=C(C(=C(C=C4)OC)OC)C=O)O)OC)OCO3	415.40	unknown	https://doi.org/10.1021/NP50058A030
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
6-Methyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-4-one	12305571	Click to see CN1CCC2=CC3=C(C(=O)C2=C1)OCO3	205.21	unknown	https://doi.org/10.1021/NP50071A025
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(5R)-4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-ol	25271644	Click to see CN1CCC2=CC3=C(C(=C2C1O)OC)OCO3	237.25	unknown	https://doi.org/10.1021/NP50071A025
Cotarnine	6715	Click to see CN1CCC2=CC3=C(C(=C2C1O)OC)OCO3	237.25	unknown	https://doi.org/10.1021/NP50071A025
Narcotine hemiacetal	90657121	Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(O4)O)C(=C(C=C5)OC)OC)OC)OCO3	415.40	unknown	https://doi.org/10.1016/S0031-9422(00)81705-7 https://doi.org/10.1021/NP50058A030
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/ARDP.19142520309

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Papaver orientale

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top