Cosmos sulphureus

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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	UUID643fc977d6799748903854
Scientific name	Cosmos sulphureus
Authority	Cav.
First published in	Icon. 1: 56 (1791)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Bidens artemisiifolia f. grandiflora	Kuntze	Revis. Gen. Pl. 1: 321 (1891)
Cosmos artemisiifolius	(Jacq.) M.R.Almeida	Fl. Maharashtra 3A: 93 (2001) (2001)
Coreopsis artemisiifolia	Jacq.	Icon. Pl. Rar. 3: t.595 (1793) (1793)
Bidens artemisiifolia f. parviflora	Kuntze	Revis. Gen. Pl. 1: 321 (1891)
Bidens sulfurea	(Cav.) Sch.Bip.	Seem., Narr. Voy. Herald (1853) 308 1853
Bidens sulphureus	(Cav.) Sch.Bip.
Bidens sulphurea	Sch.Bip.	Bot. Voy. Herald 7-8: 308 (1856)
Cosmos aurantiacus	Klatt	Leopoldina 25: 105 (1889)
Cosmos sulphureus var. exaristatus	Sherff	Publ. Field Columb. Mus., Bot. Ser. 8: 411 (1932)
Bidens artemisiifolia subsp. intermedia	Kuntze	Revis. Gen. Pl. 1: 321 (1891)
Cosmos sulphureus var. hirsuticaulis	Sherff	Amer. J. Bot. 24: 90 (1937)
Cosmos gracilis	Sherff	Bot. Gaz. 88: 304 (1929)
Coreopsis artemisifolia	Sessé & Moc.	148 1890
Cosmea sulphurea	Willd.	Sp. Pl., ed. 4 , 3: 2250 (1803)
Coreopsis artemisiaefolia	Jacq.	Icon. Pl. Rar. 3: 16, t. 595 1786-1793

Common names Top

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Filter by language:

Language	Common/alternative name
English	sulphur cosmos
Spanish	bidens artemisiifolia
Arabic	قسموس كبريتي
Bengali	কসমস সালফিউরিয়াস
Czech	krásenka sírožlutá
German	gelbes schmuckkörbchen
German	sulfur cosmos
German	oranges schmuckkörbchen
German	gelbe kosmee
German	gelbe cosmea
Persian	گل ستارهای
Finnish	keltakosmoskukka
Finnish	keltakosmos
Hungarian	sárga pillangóvirág
Hungarian	kénsárga pillangóvirág
Japanese	キバナコスモス
Korean	노랑코스모스
Malayalam	മാങ്ങാ നാറി
Malayalam	മാങ്ങാനാറി
Malayalam	ആകാശമല്ലി
Malayalam	yellow cosmos
Malayalam	sulfur cosmos
Malayalam	manga poovu
Malayalam	കോസ്മോസ്
Malayalam	മാങ്ങനാറി
Malayalam	മാങ്ങ നാറി
Malay	pokok ulam raja kuning
Punjab	بسنتی کوسموس
Russian	Космея серно-жёлтая
Swedish	gullskära
Thai	ดาวกระจาย
Vietnamese	sao nhái vàng
Vietnamese	cúc vạn thọ tây vàng
Chinese	硫华菊
Chinese	黄秋英
Chinese	硫黄菊
Chinese	硫磺菊
Chinese	黄波斯菊
Chinese	黄花波斯菊
Chinese	硫華菊
Chinese	黃波斯菊

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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No forms added yet.

Germination/Propagation Top

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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

Africa click to expand
- Northeast Tropical Africa
  - Ethiopia
- South Tropical Africa
  - Angola
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Kwazulu-Natal
- West Tropical Africa
  - Benin
- West-central Tropical Africa
  - Central African Republic
  - Zaïre
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- Eastern Asia
  - Korea
  - Taiwan
- Middle Asia
  - Tadzhikistan
  - Uzbekistan
- Western Asia
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
- Indo-China
  - Andaman Islands
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Philippines

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland
  - South Australia
  - Western Australia

Europe click to expand
- Eastern Europe
  - South European Russia
- Middle Europe
  - Belgium
  - Poland

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Missouri
  - Oklahoma
- Northeastern U.S.A.
  - Connecticut
  - Michigan
  - New York
  - Pennsylvania
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - Florida
  - Georgia
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- South-central Pacific
  - Society Islands
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - New Caledonia
  - Niue

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - Venezuela
- Southern South America
  - Paraguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000030713
UNII	80Z6Y1813O
Florida Plant Atlas	1587
Flora of Alabama	677
USDA Plants	COSU5
Tropicos	2702337
INPN	92624
KEW	urn:lsid:ipni.org:names:198368-1
The Plant List	gcc-129696
Missouri Botanical Garden	277308
Open Tree Of Life	964332
Observations.org	146644
NCBI Taxonomy	459758
Nature Serve	2.140887
IPNI	198368-1
iNaturalist	48651
GBIF	3098951
Freebase	/m/027txv9
EPPO	CMSSU
EOL	578193
Calflora (Californian flora)	2400
USDA GRIN	11684
Wikipedia	Cosmos_sulphureus
CMAUP	NPO28990

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

Effects of common co-occurring pesticides (a neonicotinoid and fungicide) on honey bee colony health in a semi-field study

Shepherd S, Park YG, Krupke CH

Heliyon

23-Apr-2024

PMCID:	PMC11066323
doi:	10.1016/j.heliyon.2024.e29886
PMID:	38707404

Natural deep eutectic solvents-based green extraction of vanillin: optimization, purification, and bioactivity assessment

Xu L, Liaqat F, Khazi MI, Sun J, Zhu D

Front Nutr

19-Jan-2024

PMCID:	PMC10875998
doi:	10.3389/fnut.2023.1279552
PMID:	38375356

Jasmonates and salicylic acid as enigmatic orchestrators of capitula senescence in Cosmos sulphureus Cav.

Lone ML, Farooq S, ul Haq A, Altaf F, Parveen S, Tahir I

Physiol Mol Biol Plants

23-Dec-2023

PMCID:	PMC10784253
doi:	10.1007/s12298-023-01407-4
PMID:	38222281

Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses

Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

The Potentials of Ageratum conyzoides and Other Plants from Asteraceae as an Antiplasmodial and Insecticidal for Malaria Vector: An Article Review

Kusman IT, Pradini GW, Ma’ruf IF, Fauziah N, Berbudi A, Achadiyani A, Wiraswati HL

Infect Drug Resist

07-Nov-2023

PMCID:	PMC10638911
doi:	10.2147/IDR.S433328
PMID:	37954507

Bougainvillea glabra Choisy (Nyctinaginacea): review of phytochemistry and antimicrobial potential

Ornelas García IG, Guerrero Barrera AL, Avelar González FJ, Chávez Vela NA, Gutiérrez Montiel D

Front Chem

19-Oct-2023

PMCID:	PMC10620508
doi:	10.3389/fchem.2023.1276514
PMID:	37927559

Diversity, astaxanthin production, and genomic analysis of Rhodotorula paludigena SP9-15

Phuengjayaem S, Kingkaew E, Hoondee P, Rojsitthisak P, Sritularak B, Thitikornpong W, Thompho S, Pornputtapong N, Tanasupawat S

Heliyon

16-Jul-2023

PMCID:	PMC10395543
doi:	10.1016/j.heliyon.2023.e18280
PMID:	37539266

The Most Potent Natural Pharmaceuticals, Cosmetics, and Food Ingredients Isolated from Plants with Deep Eutectic Solvents

Wawoczny A, Gillner D

J Agric Food Chem

11-Jul-2023

PMCID:	PMC10375538
doi:	10.1021/acs.jafc.3c01656
PMID:	37433265

Research on dye sensitized solar cells: recent advancement toward the various constituents of dye sensitized solar cells for efficiency enhancement and future prospects

Rahman S, Haleem A, Siddiq M, Hussain MK, Qamar S, Hameed S, Waris M

RSC Adv

28-Jun-2023

PMCID:	PMC10304709
doi:	10.1039/d3ra00903c
PMID:	37388146

Distribution, Effect, and Control of Exotic Plants in Republic of Korea

Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS

Biology (Basel)

06-Jun-2023

PMCID:	PMC10294914
doi:	10.3390/biology12060826
PMID:	37372111

Efficient floral dip transformation method using Agrobacterium tumefaciens on Cosmos sulphureus Cav.

Purwantoro A, Irsyadi MB, Sawitri WD, Fatumi NC, Fajrina SN

Saudi J Biol Sci

01-Jun-2023

PMCID:	PMC10362457
doi:	10.1016/j.sjbs.2023.103702
PMID:	37485451

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications

Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK

Antibiotics (Basel)

08-Mar-2023

PMCID:	PMC10044610
doi:	10.3390/antibiotics12030543
PMID:	36978410

Characterization of Cosmos sulphureus Cav. (Asteraceae): Phytochemical Screening, Antioxidant Activity and Chromatography Analysis

Ortega-Medrano RJ, Ceja-Torres LF, Vázquez-Sánchez M, Martínez-Ávila GC, Medina-Medrano JR

Plants (Basel)

16-Feb-2023

PMCID:	PMC9967292
doi:	10.3390/plants12040896
PMID:	36840242

De novo transcriptome assembly and functional analysis reveal a dihydrochalcone 3-hydroxylase(DHC3H) of wild Malus species that produces sieboldin in vivo

Miranda S, Lagrèze J, Knoll AS, Angeli A, Espley RV, Dare AP, Malnoy M, Martens S

Front Plant Sci

16-Dec-2022

PMCID:	PMC9800874
doi:	10.3389/fpls.2022.1072765
PMID:	36589107

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
> Benzenoids / Naphthalenes / Naphthoquinones
Hydroxysesamone	135404715	Click to see CC(=CCC1=C(C2=C(C=CC(=C2C(=O)C1=O)O)O)O)C	274.27	unknown	https://doi.org/10.1002/CBER.19660990124
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3-Oxooctadeca-8,10,14,16-tetraen-12-ynyl acetate	162998804	Click to see CC=CC=CC#CC=CC=CCCCCC(=O)CCOC(=O)C	314.40	unknown	https://doi.org/10.1002/CBER.19660990124
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
2,10,12-Tridecatriene-4,6,8-triyne-1-ol	14729088	Click to see C=CC=CC#CC#CC#CC=CCO	182.22	unknown	https://doi.org/10.1002/CBER.19640970924
Trideca-2,10,12-trien-4,6,8-triyn-1-ol	71357358	Click to see C=CC=CC#CC#CC#CC=CCO	182.22	unknown	https://doi.org/10.1002/CBER.19640970924
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(2E,10E)-trideca-2,10,12-trien-4,6,8-triynal	14729086	Click to see C=CC=CC#CC#CC#CC=CC=O	180.20	unknown	https://doi.org/10.1002/CBER.19640970924
Trideca-2,10,12-trien-4,6,8-triynal	162995441	Click to see C=CC=CC#CC#CC#CC=CC=O	180.20	unknown	https://doi.org/10.1002/CBER.19640970924
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(4aS,8S,8aR)-4a-methyl-5-oxo-8-propan-2-yl-3,4,6,7,8,8a-hexahydronaphthalene-2-carbaldehyde	101505263	Click to see CC(C)C1CCC(=O)C2(C1C=C(CC2)C=O)C	234.33	unknown	https://doi.org/10.1002/HLCA.200900290
(4aS,8S,8aR)-4a-methyl-5-oxo-8-propan-2-yl-3,4,6,7,8,8a-hexahydronaphthalene-2-carboxylic acid	101505262	Click to see CC(C)C1CCC(=O)C2(C1C=C(CC2)C(=O)O)C	250.33	unknown	https://doi.org/10.1002/HLCA.200900290
4a-Methyl-5-oxo-8-propan-2-yl-3,4,6,7,8,8a-hexahydronaphthalene-2-carbaldehyde	162843663	Click to see CC(C)C1CCC(=O)C2(C1C=C(CC2)C=O)C	234.33	unknown	https://doi.org/10.1002/HLCA.200900290
4a-Methyl-5-oxo-8-propan-2-yl-3,4,6,7,8,8a-hexahydronaphthalene-2-carboxylic acid	163046039	Click to see CC(C)C1CCC(=O)C2(C1C=C(CC2)C(=O)O)C	250.33	unknown	https://doi.org/10.1002/HLCA.200900290
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/JA01259A066
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER	21722016	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	492.40	unknown	via CMAUP database
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
HYPOLAETIN 8-O-beta-D-GLUCURONIDE	14887605	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	via CMAUP database
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE 6''-METHYL ESTER	44566911	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O	476.40	unknown	via CMAUP database
theograndin I	11156985	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O	542.40	unknown	via CMAUP database
Theograndin II	11272944	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)OS(=O)(=O)O)O)O)O	558.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(3,4-Dihydroxyphenyl)-1-[2-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	57168663	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	434.40	unknown	https://doi.org/10.1021/JA01104A036 https://doi.org/10.1021/JA01259A066
Coreopsin	12303943	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	434.40	unknown	https://doi.org/10.1021/JA01259A066 https://doi.org/10.1021/JA01104A036
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
2-[(3,4-Dihydroxyphenyl)methylidene]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one	73981741	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JA01104A036
Sulfurein	10071442	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JA01104A036
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one	15939939	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/MRC.2516
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JA01259A066 https://doi.org/10.1002/MRC.2516
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308704	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1002/MRC.2516
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1002/MRC.2516
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1002/MRC.2516
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1002/MRC.2516 https://doi.org/10.1021/JA01259A066
Quercetin 3-O-rhamnoside	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/MRC.2516
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)prop-2-en-1-one	2483	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O	272.25	unknown	https://doi.org/10.1021/JA01259A066
Butein	5281222	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O	272.25	unknown	https://doi.org/10.1021/JA01259A066

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Cosmos sulphureus

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