Iris pseudacorus

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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

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Details Top

Internal ID	UUID644027ba8d414671789102
Scientific name	Iris pseudacorus
Authority	L.
First published in	Sp. Pl. : 38 (1753)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Acorus adulterinus	Garsault	Fig. Pl. Med. 1: t. 1 b. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 2. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 780.
Iris acoriformis	Boreau	Fl. Centre France , ed. 3, 2: 635 (1857)
Iris acoroides	Spach	Hist. Nat. Vég. 13: 44 (1846)
Iris bastardii	Boreau	Fl. Centre France , ed. 3, 2: 635 (1857)
Iris curtopetala	F.Delaroche	Liliac. 6: t. 340 1811
Iris flava	Tornab.	Fl. Sicul. : 212 (1887)
Iris lutea	Lam.	Fl. Franç. (Lamarck) 3: 496. 1779 [1778 publ. after 21 Mar 1779]
Iris pallidior	Hill	Brit. Herb. : 473 (1756)
Iris paludosa	Pers.	Syn. Pl. 1: 52 (1805)
Iris palustris	Gaterau	Descr. Pl. Montauban : 31 (1789)
Iris sativa	Mill.	Gard. Dict. ed. 8 : n.º 15 (1768)
Limniris pseudoacorus	Fuss	Fl. Transsilv. : 636 (1866)
Limnirion pseudacorus	(L.) Opiz	Seznam : 59 (1852)
Moraea candolleana	Spreng.	Syst. Veg. 1: 164 (1824)
Pseudo-iris palustris	Medik.	Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. 6: 417 (1790)
Vieusseuxia iridioides	Link	Enum. Hort. Berol. Alt. 1: 56. 1821 [16 Mar-30 Jun 1821]
Xiphion acoroides	Alef.	Bot. Zeitung (Berlin) 21: 297 (1863)
Xyridion pseudacorus	Klatt	Bot. Zeitung (Berlin) 30: 500 (1872)
Xiphion pseudoacorus	Schrank	Fl. Monac. 1: t. 99 (1811)
Xyridion acoroideum	Klatt	Bot. Zeitung (Berlin) 30: 500 (1872)
Iris pseudacorus f. nyaradyana	Prodán	Fl. Reipubl. Popul. Roman. 11: 852 1966
Iris pseudacorus f. longiacuminata	Prodán	Bul. Grad. Bot. Univ. Cluj 15: 67 1935
Iris pseudacorus var. acoroides	(Spach) Baker	Handb. Irid. 11. 1892
Iris pseudacorus var. bastardii	(Boreau) Nyman	Consp. Fl. Eur. 702. 1882
Iris pseudacorus var. acoriformis	(Boreau) Nyman	Consp. Fl. Eur. 702. 1882
Iris pseudacorus subsp. bastardii	(Boreau) K.Richt.	Pl. Eur. 1: 257. 1890 (1890)
Iris pseudacorus subsp. acoriformis	(Boreau) K.Richt.	Pl. Eur. 1: 257. 1890 (1890)
Iris pseudacorus var. ochroleuca	Peterm.	Flora 27: 344. 1844
Iris pseudacorus f. submersa	Glück	Biol. Morphol. Untersuch. Wasser- Sumpfgew. 3: 13 1911
Iris pseudacorus var. citrina	Hook.	Brit. Fl. 18. 1830
Iris curtopetala	Redouté	Liliac. 6: t. 340 (1811)
Iris pseudacorus var. longifolia	DC.	Fl. Franç. , ed. 3, 3: 237 (1805)

Common names Top

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Filter by language:

Language	Common/alternative name
English	yellow flag, yellow iris
English	yellow iris
English	yellow flag
English	water flag
Spanish	iris acoriformis
Spanish	xyridion pseudacorus
Spanish	iris flava
Spanish	iris paludosa
Spanish	iris sativa
Spanish	moraea candolleana
Spanish	xyridion acoroideum
Spanish	acaro bastardo
Spanish	acoro acuatico amarillo
Spanish	acoro acuático amarillo
Spanish	acoro bastardo
Spanish	Ácoro bastardo
Spanish	acoro falso
Spanish	acoro palustre
Spanish	Ácoro palustre
Spanish	acorus adulterinus
Spanish	alsusena
Spanish	azucena amarilla
Spanish	brimbio
Spanish	colchicum falcifolium
Spanish	espadana amarilla
Spanish	espadaña amarilla
Spanish	espadana de flor amarilla
Spanish	espadaña de flor amarilla
Spanish	espadana fina
Spanish	espadanal
Spanish	falso acoro
Spanish	falso ácoro
Spanish	falso-acoro
Spanish	gladiolo de agua
Spanish	iris acoroides
Spanish	iris amarillo
Spanish	iris bastardii
Spanish	iris curtopetala
Spanish	iris lutea
Spanish	iris pallidior
Spanish	iris palustris
Spanish	jarro de oro
Spanish	limnirion pseudacorus
Spanish	limniris pseudacorus
Spanish	lirio amarillo de agua
Spanish	lirio amarillo de lagunas
Spanish	lirio borde
Spanish	lirio de la marisma
Spanish	lirio espadanal amarillo
Spanish	lirio espadañal amarillo
Spanish	lirio pajizo
Spanish	lirio salvaje amarillo
Spanish	lirios de campo
Spanish	liris de la espadana de flor amarilla
Spanish	liris de la espadaña de flor amarilla
Spanish	pseudo iris palustris
Spanish	pseudo-iris palustris
Spanish	pseudoacoro
Spanish	raiz de lirio amarillo
Spanish	raíz de lirio amarillo
Spanish	vieusseuxia iridioides
Spanish	xiphion acoroides
Spanish	xiphion pseudacorus
Arabic	سوسن أصفر
Arabic	سياف
Azerbaijani	sarı süsən
azb	ساری سوسن
Belarusian	касач жоўты
Bulgarian	блатна перуника
br	elestr
Catalan	coltell groc
Catalan	iris des marais
Catalan	iris jaune
Catalan	lliri groc
Czech	kosatec žlutý
Welsh	gellesgen
Welsh	gellesg
Danish	gul sværdlilje
Danish	gul iris
German	gelbe schwertlilie
German	wasser-schwertlilie
German	iris des marais
German	iris jaune
German	sumpfschwertlilie
German	wasserschwertlilie
German	sumpf-schwertlilie
Estonian	kollane võhumõõk
Basque	lirio hori
Persian	پرچم زرد
Finnish	keltakurjenmiekka
Finnish	kurjenmiekka
French	iris des marais
French	iris jaune
French	iris d'eau
frr	güül wüfen
frr	güül wüf
fy	floddermûtse
fy	bargeblom
fy	bargesnyl
fy	earrebarreblom
fy	earrebarresnyl
fy	barchjeblom
Irish	feileastram
Galician	lirio amarelo
Manx	cleeshag
Hebrew	אירוס ענף
Croatian	Žuta perunika
Upper Sorbian	wódna dźiwja lilija
Upper Sorbian	wódna łučna lilija
Upper Sorbian	wódna škleńčica
Hungarian	mocsári nőszirom
Hungarian	sárga nőszirom
Icelandic	sverðlilja
Italian	giaggiolo acquatico
Italian	iris d'acqua
Japanese	キショウブ
Georgian	წყლის ზამბახი
Cornish	elester
Lithuanian	iris des marais
Lithuanian	iris jaune
Lithuanian	geltonasis vilkdalgis
Norwegian Bokmål	sverdlilje
nds	leus
Dutch	gele lis
Dutch	gele iris
Norwegian Nynorsk	sverdlilje
Polish	kosaciec żółty
Romanian	iris galben
Romanian	stânjenel galben
Romanian	stînjenel galben
Russian	ирис аировидный
Russian	ирис болотный
Russian	ирис водяной
Russian	ирис желтый
Russian	ирис жёлтый
Russian	ирис ложноаирный
Russian	ирис ложноаировый
se	fiskisiris
Slovak	kosatec žltý
Slovenian	vodna perunika
smn	fiskiskuorgâmiekki
Swedish	bäckasvärla
Swedish	iris des marais
Swedish	iris jaune
Swedish	svärdlilja
Swedish	svärdslilja
Turkish	bataklık süseni
Ukrainian	півник болотяний
Ukrainian	півники болотні
Chinese	黄菖蒲
Chinese	黄鸢尾
Chinese	黃菖蒲

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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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

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.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

sow fresh or soak old seed; prechill 4 weeks or place outdoors over winter and bring indoors once germinated to avoid temperature shock; transplant at 4 leaves

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Madeira
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
- Siberia
  - West Siberia
- Western Asia
  - East Aegean Islands
  - Iran
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - India

Australasia click to expand
- New Zealand
  - New Zealand North

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Wisconsin
- Northeastern U.S.A.
  - Maine
  - Massachusetts
  - New Hampshire
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Washington
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
- Western Canada
  - British Columbia
  - Manitoba

Southern America click to expand
- Southern South America
  - Argentina Northeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000783754
UNII	859OM32O9Y
Florida Plant Atlas	1975
Flora of Alabama	4314
Canadensys	6184
USDA Plants	IRPS
Tropicos	16600257
INPN	103772
KEW	urn:lsid:ipni.org:names:438992-1
The Plant List	kew-322261
Plantarium	20799
Missouri Botanical Garden	281137
PFAF	Iris pseudacorus
Open Tree Of Life	43059
Observations.org	6903
NCBI Taxonomy	82213
NBN Atlas	NBNSYS0000002269
Nature Serve	2.149941
IUCN Red List	163999
IPNI	438992-1
iNaturalist	47779
GBIF	5298231
Freebase	/m/07yrgc
WisFlora	3942
FEIS	plants/forb/iripse
EPPO	IRIPS
EOL	491653
Elurikkus	5252
Calflora (Californian flora)	4358
USDA GRIN	20385
Wikipedia	Iris_pseudacorus

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

Purification Effect of Water Eutrophication Using the Mosaic System of Submerged–Emerged Plants and Growth Response

Chang B, Xu Y, Zhang Z, Wang X, Jin Q, Wang Y

Plants (Basel)

19-Feb-2024

PMCID:	PMC10891872
doi:	10.3390/plants13040560
PMID:	38498525

Pollutant accumulation and microbial community evolution in rain gardens with different drainage types at field scale

Zhang Z, Zhang Y, Li J, Sun Y, Liu Z

Sci Rep

16-Jan-2024

PMCID:	PMC10792081
doi:	10.1038/s41598-023-48255-6
PMID:	38228664

The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species

Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M

Sci Rep

21-Dec-2023

PMCID:	PMC10739867
doi:	10.1038/s41598-023-49696-9
PMID:	38129458

Ameliorating Effects of Graphene Oxide on Cadmium Accumulation and Eco-Physiological Characteristics in a Greening Hyperaccumulator (Lonicera japonica Thunb.)

Liu Z, Lu Q, Zhao Y, Wei J, Liu M, Duan X, Lin M

Plants (Basel)

20-Dec-2023

PMCID:	PMC10780341
doi:	10.3390/plants13010019
PMID:	38202327

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

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

The Application of Arbuscular Mycorrhizal Fungi as Microbial Biostimulant, Sustainable Approaches in Modern Agriculture

Sun W, Shahrajabian MH

Plants (Basel)

29-Aug-2023

PMCID:	PMC10490045
doi:	10.3390/plants12173101
PMID:	37687348

New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America

Turner NJ

Plants (Basel)

28-Aug-2023

PMCID:	PMC10490097
doi:	10.3390/plants12173087
PMID:	37687334

Nanoemulsions of synthetic rhamnolipids act as plant resistance inducers without damaging plant tissues or affecting soil microbiota

Mottola M, Bertolino MC, Kourdova LT, Valdivia Pérez JA, Bogino MF, Nocelli NE, Chaveriat L, Martin P, Vico RV, Fabro G, Fanani ML

Front Plant Sci

22-Aug-2023

PMCID:	PMC10478713
doi:	10.3389/fpls.2023.1195718
PMID:	37674738

Revisiting the Green Synthesis of Nanoparticles: Uncovering Influences of Plant Extracts as Reducing Agents for Enhanced Synthesis Efficiency and Its Biomedical Applications

Singh H, Desimone MF, Pandya S, Jasani S, George N, Adnan M, Aldarhami A, Bazaid AS, Alderhami SA

Int J Nanomedicine

18-Aug-2023

PMCID:	PMC10444627
doi:	10.2147/IJN.S419369
PMID:	37621852

Tectorigenin: A Review of Its Sources, Pharmacology, Toxicity, and Pharmacokinetics

Rong J, Fu F, Han C, Wu Y, Xia Q, Du D

Molecules

05-Aug-2023

PMCID:	PMC10421414
doi:	10.3390/molecules28155904
PMID:	37570873

Impact of the Invasive Alien Macrophyte Ludwigia hexapetala on Freshwater Ecosystems: Evidence from Field Data

Pelella E, Questino B, Luzi B, Mariani F, Ceschin S

Biology (Basel)

31-May-2023

PMCID:	PMC10295687
doi:	10.3390/biology12060794
PMID:	37372079

Damselflies (Coenagrionidae) have been avoiding leaf veins during oviposition for at least 52 million years

Romero-Lebrón E, Fernández-Monescillo M, Matushkina N, Delclòs X, Gleiser RM

iScience

12-May-2023

PMCID:	PMC10220475
doi:	10.1016/j.isci.2023.106865
PMID:	37250779

Effects of Graphene Oxide on the Growth and Photosynthesis of the Emergent Plant Iris pseudacorus

Zhou Z, Li J, Li C, Guo Q, Hou X, Zhao C, Wang Y, Chen C, Wang Q

Plants (Basel)

23-Apr-2023

PMCID:	PMC10180715
doi:	10.3390/plants12091738
PMID:	37176796

Halophytic Clonal Plant Species: Important Functional Aspects for Existence in Heterogeneous Saline Habitats

Ievinsh G

Plants (Basel)

21-Apr-2023

PMCID:	PMC10144567
doi:	10.3390/plants12081728
PMID:	37111952

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
> Alkaloids and derivatives / Morphinans
Cephamuline	15966187	Click to see CN1CCC23CC(=O)C(=C(C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	359.40	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
> Benzenoids / Phenols / Methoxyphenols
2-[(E)-heptadec-10-enyl]-6-methoxy-benzene-1,4-diol	5459106	Click to see CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)O	376.60	unknown	https://doi.org/10.1002/HLCA.19920750509
3-[(Z)-heptadec-10-enyl]-5-methoxyphenol	101919836	Click to see CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)O	360.60	unknown	https://doi.org/10.1002/HLCA.19920750509
3-Heptadecyl-4,5-dimethoxyphenol	71666296	Click to see CCCCCCCCCCCCCCCCCC1=C(C(=CC(=C1)O)OC)OC	392.60	unknown	https://doi.org/10.1002/HLCA.19920750509
3-Methoxy-5-pentadecylphenol	46189014	Click to see CCCCCCCCCCCCCCCC1=CC(=CC(=C1)OC)O	334.50	unknown	https://doi.org/10.1002/HLCA.19920750509
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2Z)-2-[(1S,3S,5R,6S,10R)-1,6-dihydroxy-10-(3-hydroxypropyl)-6-methyl-3-[(1E,3E,5E)-2,6,10-trimethylundeca-1,3,5,9-tetraenyl]-2-oxaspiro[4.5]decan-9-ylidene]propanal	163185828	Click to see CC(=CCCC(=CC=CC(=CC1CC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)C(O1)O)C)C)C	486.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
(2Z)-2-[(2S,3R,4R)-2-(3-hydroxypropyl)-3,4-dimethyl-3-[(3E,6E,8S)-4,8,12-trimethyltrideca-3,6,11-trienyl]cyclohexylidene]propan-1-ol	163045823	Click to see CC1CCC(=C(C)CO)C(C1(C)CCC=C(C)CC=CC(C)CCC=C(C)C)CCCO	444.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
(2Z)-2-[(2S,3R,4R)-2-(3-hydroxypropyl)-3,4-dimethyl-3-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]cyclohexylidene]propanal	162899258	Click to see CC1CCC(=C(C)C=O)C(C1(C)CCC=C(C)CCC=C(C)CCC=C(C)C)CCCO	442.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
(2Z)-2-[(3R,5S,6R,10S)-10-hydroxy-6-(3-hydroxypropyl)-10-methyl-3-[(1E,3E,5E)-2,6,10-trimethylundeca-1,3,5,9-tetraenyl]-2-oxaspiro[4.5]decan-7-ylidene]propanal	162949567	Click to see CC(=CCCC(=CC=CC(=CC1CC2(CO1)C(C(=C(C)C=O)CCC2(C)O)CCCO)C)C)C	470.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
(2Z)-2-[(3S,4S,5S,6R,10S)-4,10-dihydroxy-3-[(3E,5Z)-6-(hydroxymethyl)-10-methylundeca-1,3,5,9-tetraen-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal	162977641	Click to see CC(=CCCC(=CC=CC(=C)C1CCC2(C1O)C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C	486.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
[(2Z,4E)-6-[(3S,4S,5S,6R,7Z,10S)-4,10-dihydroxy-6-(3-hydroxypropyl)-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-3-yl]-2-(4-methylpent-3-enyl)hepta-2,4,6-trienyl] acetate	162935270	Click to see CC(=CCCC(=CC=CC(=C)C1CCC2(C1O)C(C(=C(C)C=O)CCC2(C)O)CCCO)COC(=O)C)C	528.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
[6-[4,10-Dihydroxy-6-(3-hydroxypropyl)-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-3-yl]-2-(4-methylpent-3-enyl)hepta-2,4,6-trienyl] acetate	3759412	Click to see CC(=CCCC(=CC=CC(=C)C1CCC2(C1O)C(C(=C(C)C=O)CCC2(C)O)CCCO)COC(=O)C)C	528.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
2-[1,6-Dihydroxy-10-(3-hydroxypropyl)-6-methyl-3-(2,6,10-trimethylundeca-1,3,5,9-tetraenyl)-2-oxaspiro[4.5]decan-9-ylidene]propanal	3405533	Click to see CC(=CCCC(=CC=CC(=CC1CC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)C(O1)O)C)C)C	486.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
2-[10-Hydroxy-6-(3-hydroxypropyl)-10-methyl-3-(2,6,10-trimethylundeca-1,3,5,9-tetraenyl)-2-oxaspiro[4.5]decan-7-ylidene]propanal	73819162	Click to see CC(=CCCC(=CC=CC(=CC1CC2(CO1)C(C(=C(C)C=O)CCC2(C)O)CCCO)C)C)C	470.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
2-[2-(3-Hydroxypropyl)-3,4-dimethyl-3-(4,8,12-trimethyltrideca-3,6,11-trienyl)cyclohexylidene]propan-1-ol	163045822	Click to see CC1CCC(=C(C)CO)C(C1(C)CCC=C(C)CC=CC(C)CCC=C(C)C)CCCO	444.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
2-[2-(3-Hydroxypropyl)-3,4-dimethyl-3-(4,8,12-trimethyltrideca-3,7,11-trienyl)cyclohexylidene]propanal	162899257	Click to see CC1CCC(=C(C)C=O)C(C1(C)CCC=C(C)CCC=C(C)CCC=C(C)C)CCCO	442.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
2-[4-Hydroxy-2-(3-hydroxypropyl)-3-(5-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dimethylcyclohexylidene]propanal	75069326	Click to see CC(=CCCC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)O)C)C	474.70	unknown	https://doi.org/10.1515/ZNC-1992-1-205
2-[4,10-Dihydroxy-3-[6-(hydroxymethyl)-10-methylundeca-1,3,5,9-tetraen-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal	495072	Click to see CC(=CCCC(=CC=CC(=C)C1CCC2(C1O)C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C	486.70	unknown	https://doi.org/10.1002/JLAC.1990199001105
3-[(1R,2S,3S,6Z)-3-hydroxy-2,3-dimethyl-6-(1-oxopropan-2-ylidene)-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]cyclohexyl]propyl decanoate	162915953	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C1(C)CCC=C(C)CCC=C(C)CCC=C(C)C)(C)O	613.00	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[(1S,2R,3R,6Z)-2-[(3E,5R,7E)-5-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl]-2,3-dimethyl-6-(1-oxopropan-2-ylidene)cyclohexyl]propyl decanoate	162997086	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C1(C)CCC=C(C)C(CC=C(C)CCC=C(C)C)O)C	613.00	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[(3R,4R,5S,6R,7Z,10S)-3-[(2E,4E,6E)-1-acetyloxy-6,10-dimethylundeca-2,4,6,9-tetraen-2-yl]-4,10-dihydroxy-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-6-yl]propyl decanoate	162998341	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C12CCC(C2O)C(=CC=CC(=CCC=C(C)C)C)COC(=O)C)(C)O	683.00	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[(3R,4R,5S,6R,7Z,10S)-3-[(3E,5E)-6,10-dimethylundeca-1,3,5,9-tetraen-2-yl]-4,10-dihydroxy-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-6-yl]propyl decanoate	162949266	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C12CCC(C2O)C(=C)C=CC=C(C)CCC=C(C)C)(C)O	624.90	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[(3R,4R,5S,6R,7Z,10S)-4,10-dihydroxy-3-[(2E,4E,6E)-1-hydroxy-6,10-dimethylundeca-2,4,6,9-tetraen-2-yl]-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-6-yl]propyl decanoate	163188332	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C12CCC(C2O)C(=CC=CC(=CCC=C(C)C)C)CO)(C)O	640.90	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[2-(5-Hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl)-2,3-dimethyl-6-(1-oxopropan-2-ylidene)cyclohexyl]propyl decanoate	162997085	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C1(C)CCC=C(C)C(CC=C(C)CCC=C(C)C)O)C	613.00	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[3-(6,10-Dimethylundeca-1,3,5,9-tetraen-2-yl)-4,10-dihydroxy-10-methyl-7-(1-oxopropan-2-ylidene)spiro[4.5]decan-6-yl]propyl decanoate	162949265	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C12CCC(C2O)C(=C)C=CC=C(C)CCC=C(C)C)(C)O	624.90	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
3-[3-Hydroxy-2,3-dimethyl-6-(1-oxopropan-2-ylidene)-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)cyclohexyl]propyl decanoate	162915952	Click to see CCCCCCCCCC(=O)OCCCC1C(=C(C)C=O)CCC(C1(C)CCC=C(C)CCC=C(C)CCC=C(C)C)(C)O	613.00	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
Iridal	5318463	Click to see CC(=CCCC(=CCCC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)C)C	458.70	unknown	https://doi.org/10.1007/S11101-013-9333-1
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4S)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	44481270	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258201/
Violaxanthin	448438	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C	600.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258201/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
1H-Pyrrole-2-carboxylic acid, 4,5-dihydro-5-oxo-	9543309	Click to see C1C=C(NC1=O)C(=O)O	127.10	unknown	https://doi.org/10.1016/S0305-1978(02)00228-4
Methyl 2-oxo-1,3-dihydropyrrole-5-carboxylate	163192669	Click to see COC(=O)C1=CCC(=O)N1	141.12	unknown	https://doi.org/10.1016/S0305-1978(02)00228-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
3-[[1-(4-Aminobutylamino)-1-oxo-3-phenylpropan-2-yl]carbamoyl]oxirane-2-carboxylic acid	19423296	Click to see C1=CC=C(C=C1)CC(C(=O)NCCCCN)NC(=O)C2C(O2)C(=O)O	349.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258201/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2-Hydroxy-5-methoxy-3-pentadecyl[1,4]benzoquinone	4984595	Click to see CCCCCCCCCCCCCCCC1=C(C(=O)C=C(C1=O)OC)O	364.50	unknown	https://doi.org/10.1002/HLCA.19920750509
2-Methoxy-6-nonadecylcyclohexa-2,5-diene-1,4-dione	21592368	Click to see CCCCCCCCCCCCCCCCCCCC1=CC(=O)C=C(C1=O)OC	404.60	unknown	https://doi.org/10.1002/HLCA.19920750509
Irisoquin	127797	Click to see CCCCCCCCCCCCCCCCCCC1=C(C(=O)C=C(C1=O)OC)O	406.60	unknown	https://doi.org/10.1002/HLCA.19920750509
Irisquinone	5318483	Click to see CCCCCCC=CCCCCCCCCCC1=CC(=O)C=C(C1=O)OC	374.60	unknown	https://doi.org/10.1002/HLCA.19920750509
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
remangiflavanone A	10763962	Click to see CC(=C)CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C)C	408.50	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	162844791	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3O	272.25	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
5,7,2'-Trihydroxyflavanone	179999	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3O	272.25	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-alpinone	46883390	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
(2S,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	14794884	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
(2S,3R)-3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	12305771	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
Alpinone	5317747	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
Folerogenin	5319509	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3-Dihydroxy-2-methoxy-11H-benzofuro[2,3-b][1]benzopyran-11-one	5491552	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=CC=CC=C4O3)O	298.25	unknown	https://doi.org/10.1016/0031-9422(91)83613-P https://doi.org/10.1016/0031-9422(91)84117-B
1,3,7-Trihydroxy-2-methoxy-[1]benzofuro[2,3-b]chromen-11-one	14804073	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(O3)C(=CC=C4)O)O	314.25	unknown	https://doi.org/10.1016/0031-9422(91)84117-B https://doi.org/10.1016/0031-9422(91)83613-P
1,3,7-Trihydroxy-8-methoxy-(1)benzofuro(2,3-b)chromen-11-one	5491447	Click to see COC1=C(C2=C(C=C1)C3=C(O2)OC4=CC(=CC(=C4C3=O)O)O)O	314.25	unknown	https://doi.org/10.1016/0031-9422(91)83613-P
11H-Benzofuro(2,3-b)(1)benzopyran-11-one, 1, 3,8-trihydroxy-2-methoxy-	5491554	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(O3)C=C(C=C4)O)O	314.25	unknown	https://doi.org/10.1016/0031-9422(91)83613-P https://doi.org/10.1016/0031-9422(91)84117-B
4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(2-hydroxyphenyl)-	5488561	Click to see C1=CC=C(C(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
5,7,2'-Trihydroxy-6-methoxyisoflavone	5491551	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=CC=C3O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
Ayamenin B	5324348	Click to see C1=CC=C2C(=C1)C3=C(O2)OC4=CC(=CC(=C4C3=O)O)O	268.22	unknown	https://doi.org/10.1016/0031-9422(91)83613-P https://doi.org/10.1016/0031-9422(91)84117-B
Ayamenin C	5491553	Click to see C1=CC2=C(C(=C1)O)OC3=C2C(=O)C4=C(C=C(C=C4O3)O)O	284.22	unknown	https://doi.org/10.1016/0031-9422(91)84117-B https://doi.org/10.1016/0031-9422(91)83613-P
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
Lupinalbin A	5324349	Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)C4=C(C=C(C=C4O3)O)O	284.22	unknown	https://doi.org/10.1016/0031-9422(91)84117-B https://doi.org/10.1016/0031-9422(91)83613-P
Tectorigenin	5281811	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one	25231268	Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C4C=CC(OC4=C(C(=C3C2=O)O)CC=C(C)C)(C)C)O)C	472.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258201/
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Iridin	5281777	Click to see COC1=CC(=CC(=C1OC)O)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	https://doi.org/10.1007/S11101-013-9333-1 https://doi.org/10.21608/BFSA.1993.70202
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol	5319744	Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
Iristectorigenin A	5491637	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O	330.29	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Irigenin	5464170	Click to see COC1=CC(=CC(=C1OC)O)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O	360.30	unknown	https://doi.org/10.1007/S11101-013-9333-1 https://doi.org/10.21608/BFSA.1993.70202
Iristectorigenin B	5488781	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O	330.29	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
Pratensein	5281803	Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O	284.26	unknown	https://doi.org/10.1016/0031-9422(91)84117-B
Irisolidone	5281781	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O	314.29	unknown	https://doi.org/10.21608/BFSA.1993.70202
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Irilin A	5491550	Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=CC=C3O)O)OC	314.29	unknown	https://doi.org/10.1016/0031-9422(91)84117-B

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Iris pseudacorus

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