Scientific name	Authority	First published in
Marzaria cordata	(Willd.) Raf.	Autik. Bot. : 14 (1840)
Bocconia cordata	Willd.	Sp. Pl., ed. 4 , 2: 841 (1799)
Bocconia cordata var. thunbergii	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 11 1867
Bocconia japonica	hort. ex André	Rev. Hort. [Paris]. (1866) 369.
Bocconia jedoensis	Carrière	Rev. Hort. (Paris) 37: 340 (1866)
Macleaya cordata var. yedoensis	(André) Fedde	Pflanzenr. 217 1909
Macleaya yedoensis	(Carrière) André	Rev. Hort. (Paris) 37: 369 (1866)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	plume poppy
Azerbaijani	Ürəkvari makleya
Azerbaijani	bocconia cordata
Czech	makleja srdčitá
Danish	hvid jodplante
German	weißer federmohn
German	federmohn
Finnish	herttahuisku-unikko
Upper Sorbian	pjerojty mak
Japanese	タケニグサ
Japanese	チャンパギク
Russian	Маклейя сердцевидная
Swedish	vippvallmo
Chinese	野麻杆
Chinese	黄薄荷
Chinese	黄杨杆
Chinese	博落回
Chinese	落回
Chinese	菠萝筒
Chinese	空洞草
Chinese	山火筒
Chinese	大叶莲
Chinese	喇叭筒
Chinese	喇叭竹
Chinese	号筒草
Chinese	号筒管
Chinese	号筒树
Chinese	勃逻回
Chinese	勃勒回
Chinese	三钱三
Chinese	号筒杆
Chinese	博落迴

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!

Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Taiwan

Europe click to expand
- Eastern Europe
  - Ukraine
- Middle Europe
  - Czechoslovakia
- Southeastern Europe
  - Romania

Northern America click to expand
- Eastern Canada
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - West Virginia
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Maryland
  - North Carolina
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000448644
Canadensys	7106
USDA Plants	MACO10
Tropicos	24000096
INPN	610618
KEW	urn:lsid:ipni.org:names:673258-1
The Plant List	kew-2502545
Missouri Botanical Garden	284844
PFAF	Macleaya cordata
Open Tree Of Life	96185
Observations.org	206262
NCBI Taxonomy	56857
NBN Atlas	NHMSYS0000460550
Nature Serve	2.136434
IPNI	673258-1
iNaturalist	165054
GBIF	5334194
Freebase	/m/0fmc0z
EPPO	MCYCO
EOL	594652
Elurikkus	5612
USDA GRIN	23058
Wikipedia	Macleaya_cordata
CMAUP	NPO19264

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_002174775.1	MC_HNAU_1.0	Scaffold	Chinese Academy of Agricultural Sciences	2017-06-07	503.0x	360.33 Mb

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

Integrated transcriptomic and WGCNA analyses reveal candidate genes regulating mainly flavonoid biosynthesis in Litsea coreana var. sinensis

Xie N, Guo Q, Li H, Yuan G, Gui Q, Xiao Y, Liao M, Yang L

BMC Plant Biol

01-Apr-2024

PMCID:	PMC10985888
doi:	10.1186/s12870-024-04949-1
PMID:	38561656

铁死亡在非小细胞肺癌中的作用及中药干预进展

GUO X, WANG T, XIA J, ZENG H, SHI W

Zhongguo Fei Ai Za Zhi

20-Mar-2024

PMCID:	PMC11002191
doi:	10.3779/j.issn.1009-3419.2024.101.06
PMID:	38590196

Correction: Dong et al. Identification of the Trace Components in BopuzongJian and Macleaya cordata Extract Using LC-MS Combined with a Screening Method. Molecules 2021, 26, 3851

Dong Z, Liu M, Zhong X, Ou X, Yun X, Wang M, Ren S, Qing Z, Zeng J

Molecules

13-Mar-2024

PMCID:	PMC10975988
doi:	10.3390/molecules29061268
PMID:	38543051

Extreme Reconfiguration of Plastid Genomes in Papaveraceae: Rearrangements, Gene Loss, Pseudogenization, IR Expansion, and Repeats

Cao J, Wang H, Cao Y, Kan S, Li J, Liu Y

Int J Mol Sci

14-Feb-2024

PMCID:	PMC10888665
doi:	10.3390/ijms25042278
PMID:	38396955

From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design

Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C

Molecules

09-Feb-2024

PMCID:	PMC10892999
doi:	10.3390/molecules29040815
PMID:	38398566

Bioactive Compounds from Plant Origin as Natural Antimicrobial Agents for the Treatment of Wound Infections

Pacyga K, Pacyga P, Topola E, Viscardi S, Duda-Madej A

Int J Mol Sci

08-Feb-2024

PMCID:	PMC10889580
doi:	10.3390/ijms25042100
PMID:	38396777

Importance of phytotherapy for oral health care and quality of life in adults: A scoping review

Shinkai RS, Azevedo CL, de Campos TT, Michel-Crosato E, Biazevic MG

J Dent Sci

24-Jan-2024

PMCID:	PMC11010713
doi:	10.1016/j.jds.2024.01.002
PMID:	38618093

Full-length transcriptome characterization of Platycladus orientalis based on the PacBio platform

Liao T, Zhang L, Wang Y, Guo L, Cao J, Liu G

Front Genet

18-Jan-2024

PMCID:	PMC10830785
doi:	10.3389/fgene.2024.1345039
PMID:	38304337

Effects of Neolamarckia cadamba leaves extract on microbial community and antibiotic resistance genes in cecal contents and feces of broilers challenged with lipopolysaccharides

Wang C, Wu S, Zhou W, Hu L, Hu Q, Cao Y, Wang L, Chen X, Zhang Q

Appl Environ Microbiol

17-Jan-2024

PMCID:	PMC10880616
doi:	10.1128/aem.01107-23
PMID:	38231769

Macleaya cordata isoquinoline alkaloids attenuate Escherichia coli lipopolysaccharide-induced intestinal epithelium injury in broiler chickens by co-regulating the TLR4/MyD88/NF-κB and Nrf2 signaling pathways

Liu Y, Han K, Liu H, Jia G, Comer L, Wang G, Pan Z, Zhao Y, Jiang S, Jiao N, Huang L, Yang W, Li Y

Front Immunol

17-Jan-2024

PMCID:	PMC10828024
doi:	10.3389/fimmu.2023.1335359
PMID:	38299145

CRISPR/Cas9 revolutionizes Macleaya cordata breeding: a leap in sanguinarine biosynthesis

Sun M, Zhong X, Zhou L, Liu W, Song R, Huang P, Zeng J

Hortic Res

16-Jan-2024

PMCID:	PMC10940120
doi:	10.1093/hr/uhae024
PMID:	38495029

Ecological niches and assembly dynamics of diverse microbial consortia in the gastrointestine of goat kids

Jiao J, Wu J, Zhou C, He Z, Tan Z, Wang M

ISME J

11-Jan-2024

PMCID:	PMC10872696
doi:	10.1093/ismejo/wrae002
PMID:	38365259

Sanguinarine chloride induces ferroptosis by regulating ROS/BACH1/HMOX1 signaling pathway in prostate cancer

Liu S, Tao Y, Wu S, Lin J, Fu S, Lu J, Zhang J, Fu B, Zhang E, Xu J, Wang J, Li L, Zhang L, Wang Z

Chin Med

09-Jan-2024

PMCID:	PMC10777654
doi:	10.1186/s13020-024-00881-6
PMID:	38195593

Deciphering the gut microbiome of grass carp through multi-omics approach

Li M, Liang H, Yang H, Ding Q, Xia R, Chen J, Zhou W, Yang Y, Zhang Z, Yao Y, Ran C, Zhou Z

Microbiome

03-Jan-2024

PMCID:	PMC10763231
doi:	10.1186/s40168-023-01715-7
PMID:	38167330

Alternatives to antibiotics in pig production: looking through the lens of immunophysiology

Liu HY, Zhu C, Zhu M, Yuan L, Li S, Gu F, Hu P, Chen S, Cai D

Stress Biol

02-Jan-2024

PMCID:	PMC10758383
doi:	10.1007/s44154-023-00134-w
PMID:	38163818

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
12,13-Dihydro-13-ethoxy-1,2-dimethoxy-12-methyl[1,3]benzodioxolo[5,6-c]phenanthridine	5317228	Click to see CCOC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5	393.40	unknown	via CMAUP database
14-Ethoxy-13-methyl-13,14-dihydro-[1,3]dioxolo[4',5':4,5]benzo[1,2-c][1,3]dioxolo[4,5-i]phenanthridine	5317235	Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6	377.40	unknown	via CMAUP database
Angoline	189060	Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC	379.40	unknown	https://doi.org/10.1074/JBC.273.31.19829
Bocconoline	181121	Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)CO	379.40	unknown	via CMAUP database
Dihydrosanguinarine	124069	Click to see CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6	333.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.02.007 https://doi.org/10.1016/J.MOLP.2017.05.007
> 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/10.1016/S0021-9673(99)01126-7 https://doi.org/10.1007/BF02508114 https://doi.org/10.1007/BF00563652 https://doi.org/10.1016/J.MOLP.2017.05.007
Chelerythrine hydroxide	5351594	Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5.[OH-]	365.40	unknown	via CMAUP database
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/10.1055/S-2002-34406 https://doi.org/10.1002/HLCA.19830660208
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/10.1002/HLCA.19830660208
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/10.1007/BF02508114 https://doi.org/10.1016/S0021-9673(99)01126-7 https://doi.org/10.1016/0031-9422(89)80187-6 https://doi.org/10.1002/HLCA.19830660208 https://doi.org/10.1016/J.MOLP.2017.05.007 https://doi.org/10.1007/BF00563652
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(S)-cis-N-methylstylopine	5460426	Click to see C[N+]12CCC3=CC4=C(C=C3C1CC5=C(C2)C6=C(C=C5)OCO6)OCO4	338.40	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
Canadine	34458	Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC	339.40	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
Cyclanoline	3082134	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC	342.40	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
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/10.1016/J.MOLP.2017.05.007
Stylopine	440583	Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6	323.30	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> 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/10.1002/CBER.19000330305 https://doi.org/10.1016/J.MOLP.2017.05.007 https://doi.org/10.1016/0031-9422(83)83076-3 https://doi.org/10.1080/00032718508066156 https://doi.org/10.1135/CCCC19650887
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/10.1016/J.MOLP.2017.05.007 https://doi.org/10.1002/CBER.19000330305 https://doi.org/10.1135/CCCC19650887 https://doi.org/10.1002/HLCA.19830660208 https://doi.org/10.1016/0041-0101(85)90044-3 https://doi.org/10.1016/0031-9422(83)83076-3
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine	5610	Click to see C1=CC(=CC=C1CCN)O	137.18	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
4-Hydroxyphenylacetaldehyde	440113	Click to see C1=CC(=CC=C1CC=O)O	136.15	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
4-Hydroxyphenylpyruvic acid	979	Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O	180.16	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine	681	Click to see C1=CC(=C(C=C1CCN)O)O	153.18	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalyl acetate, (-)-	442474	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	via CMAUP database
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Thujone	6553876	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
alpha-Cadinene, (+)-	12306048	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	via CMAUP database
beta-Humulene	5318102	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine	6057	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Artemisia acetate	14890510	Click to see CC(=CC(C(C)(C)C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(4S)-3,3,6-trimethylhepta-1,5-dien-4-ol	12308602	Click to see CC(=CC(C(C)(C)C=C)O)C	154.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
protopine N-oxide	13895182	Click to see C[N+]1(CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3)[O-]	369.40	unknown	https://doi.org/10.1016/0031-9422(83)83076-3
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(S)-3'-Hydroxy-N-methylcoclaurine	440591	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)O)O)OC	315.40	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
Higenamine	114840	Click to see C1CNC(C2=CC(=C(C=C21)O)O)CC3=CC=C(C=C3)O	271.31	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
Machiline	281691	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
Reticulin	10233	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/J.MOLP.2017.05.007
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
2-Methoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-1-one	9951230	Click to see CN1C=C2C(=CC=C(C2=O)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5	333.30	unknown	https://doi.org/10.1007/BF02508114
Hydroxysanguinarine	443716	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C6=C(C=C5)OCO6	347.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database

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.

Macleaya cordata

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