Scientific name	Authority	First published in
Iris germanica subsp. pallida	(Lam.) O.Bolòs & Vigo	Fl. Països Catalans 4: 159 (2001)
Iris pallide-caerulaea	Pers.	Syn. Pl. 1: 51 (1805)
Iris pallida var. rosea	Prodán	Bul. Grad. Bot. Univ. Cluj 25: 204. 1945
Iris pallida var. odoratissima	(Jacq.) Nyman	Consp. Fl. Eur. 700. 1882
Iris australis var. mandraliscae	(Tod.) Nyman	Consp. Fl. Eur. 700. 1882
Iris australis var. tinaei	(Tod.) Nyman	Consp. Fl. Eur. 700. 1882
Iris pallida subsp. mandraliscae	(Tod.) K.Richt.	Pl. Eur. 1: 256. 1890 (1890)
Iris pallida subsp. tinaei	(Tod.) K.Richt.	Pl. Eur. 1: 256. 1890 (1890)
Iris pallida subsp. sicula	(Tod.) K.Richt.	Pl. Eur. 1: 256. 1890 (1890)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sweet iris
Arabic	السوسن الفلورنسي
Arabic	سوسن شاحب
Azerbaijani	solğun süsən
azb	سولغون سوسن
Czech	kosatec bledý
German	iripallidal
German	bleiche schwertlilie
Persian	زنبق رنگپریده
Finnish	tuoksukurjenmiekka
Croatian	blijeda perunika
Upper Sorbian	blěda škleńčica
Hungarian	dalmát nőszirom
Lithuanian	blyškusis vilkdalgis
Macedonian	Перуника
Russian	Ирис бледный
Swedish	silveriris
Chinese	香根鸢尾
Chinese	香根鳶尾

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Iris pallida subsp. cengialti	(Ambrosi ex A.Kern.) Foster	Gard. Chron. , n.s., 25: 555 (1886)
Iris pallida subsp. illyrica	(Tomm. ex Vis.) K.Richt.	Pl. Eur. 1: 255 (1890)
Iris pallida subsp. pallida		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands

Asia-temperate click to expand
- Western Asia
  - Lebanon-Syria
  - Palestine

Asia-tropical click to expand
- Indian Subcontinent
  - West Himalaya

Europe click to expand
- Middle Europe
  - Czechoslovakia
- Southeastern Europe
  - Albania
  - Bulgaria
  - Italy
  - Romania
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - France
  - Sardegna

Northern America click to expand
- North-central U.S.A.
  - Missouri
- Northeastern U.S.A.
  - Indiana
- Southeastern U.S.A.
  - Georgia
  - Kentucky
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000783695
UNII	TW26GFZ22V
Canadensys	6182
USDA Plants	IRPA2
Tropicos	16602434
INPN	103763
Flora of Italy	7036
KEW	urn:lsid:ipni.org:names:438939-1
The Plant List	kew-322201
Missouri Botanical Garden	281278
PFAF	Iris pallida
Open Tree Of Life	259588
Observations.org	137266
NCBI Taxonomy	29817
Nature Serve	2.157919
IPNI	438939-1
iNaturalist	164131
GBIF	5298086
Freebase	/m/02wwgtd
EPPO	IRIPA
EOL	490956
USDA GRIN	20378
Wikipedia	Iris_pallida
CMAUP	NPO1358

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_029216955.1	ASM2921695v1	Scaffold	Novartis AG	2023-03-15	65.0x	12.56 Gb

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

An Overview of Biofilm-Associated Infections and the Role of Phytochemicals and Nanomaterials in Their Control and Prevention

Damyanova T, Dimitrova PD, Borisova D, Topouzova-Hristova T, Haladjova E, Paunova-Krasteva T

Pharmaceutics

24-Jan-2024

PMCID:	PMC10892570
doi:	10.3390/pharmaceutics16020162
PMID:	38399223

Influence of β-Ionone in the Phytotoxicity of the Rhizome of Iris pallida Lam

Sothearith Y, Appiah KS, Sophea C, Smith J, Samal S, Motobayashi T, Fujii Y

Plants (Basel)

22-Jan-2024

PMCID:	PMC10819377
doi:	10.3390/plants13020326
PMID:	38276783

Association Analysis of Transcriptome and Targeted Metabolites Identifies Key Genes Involved in Iris germanica Anthocyanin Biosynthesis

Zhao X, Wu Y, Zhang X, Tian F, Yu F, Li X, Huang D

Int J Mol Sci

17-Nov-2023

PMCID:	PMC10671556
doi:	10.3390/ijms242216462
PMID:	38003651

Genome assembly of the bearded iris, Iris pallida Lam.

Bruccoleri RE, Oakeley EJ, Faust AM, Altorfer M, Dessus-Babus S, Burckhardt D, Oertli M, Naumann U, Petersen F, Wong J

GigaByte

05-Oct-2023

PMCID:	PMC10565908
doi:	10.46471/gigabyte.94
PMID:	37829656

Characterization of the Slovene Autochthonous Rose Hybrid Rosa pendulina × spinosissima (Rosa reversa Waldst. and Kit) Using Biochemical Patterns of the Plant Blossoms

Kunc N, Hudina M, Bavcon J, Vreš B, Luthar Z, Gostinčar K, Mikulič-Petkovšek M, Osterc G, Ravnjak B

Plants (Basel)

22-Jan-2023

PMCID:	PMC9920101
doi:	10.3390/plants12030505
PMID:	36771590

Biotechnological Approaches to Producing Natural Antioxidants: Anti-Ageing and Skin Longevity Prospects

Bouzroud S, El Maaiden E, Sobeh M, Merghoub N, Boukcim H, Kouisni L, El Kharrassi Y

Int J Mol Sci

11-Jan-2023

PMCID:	PMC9867058
doi:	10.3390/ijms24021397
PMID:	36674916

Iris Pallida Extract Alleviates Cortisol-Induced Decrease in Type 1 Collagen and Hyaluronic Acid Syntheses in Human Skin Cells

Choo JH, Lee HG, Lee SY, Kang NG

Curr Issues Mol Biol

01-Jan-2023

PMCID:	PMC9857657
doi:	10.3390/cimb45010025
PMID:	36661511

New Insights on Biofilm Antimicrobial Strategies

Melo LD, Azevedo NF

Antibiotics (Basel)

09-Apr-2021

PMCID:	PMC8069210
doi:	10.3390/antibiotics10040407
PMID:	33918561

Qualitative and Quantitative Analysis of Ukrainian Iris Species: A Fresh Look on Their Antioxidant Content and Biological Activities

Mykhailenko O, Korinek M, Ivanauskas L, Bezruk I, Myhal A, Petrikaitė V, El-Shazly M, Lin GH, Lin CY, Yen CH, Chen BH, Georgiyants V, Hwang TL

Molecules

08-Oct-2020

PMCID:	PMC7582944
doi:	10.3390/molecules25194588
PMID:	33050063

Phytochemical Composition and In Vitro Biological Activity of Iris spp. (Iridaceae): A New Source of Bioactive Constituents for the Inhibition of Oral Bacterial Biofilms

Hoang L, Beneš F, Fenclová M, Kronusová O, Švarcová V, Řehořová K, Baldassarre Švecová E, Vosátka M, Hajšlová J, Kaštánek P, Viktorová J, Ruml T

Antibiotics (Basel)

11-Jul-2020

PMCID:	PMC7399867
doi:	10.3390/antibiotics9070403
PMID:	32664528

Plant In Vitro Systems as a Sustainable Source of Active Ingredients for Cosmeceutical Application

Marchev AS, Georgiev MI

Molecules

25-Apr-2020

PMCID:	PMC7248771
doi:	10.3390/molecules25092006
PMID:	32344812

Synthetic terpenoids in the world of fragrances: Iso E Super® is the showcase

Stepanyuk A, Kirschning A

Beilstein J Org Chem

31-Oct-2019

PMCID:	PMC6839564
doi:	10.3762/bjoc.15.252
PMID:	31728173

The composition of the aphid fauna (Insecta, Hemiptera) of the Royal Botanic Gardens, Kew

Wieczorek K, Fulcher TK, Chłond D

Sci Rep

10-Jul-2019

PMCID:	PMC6620339
doi:	10.1038/s41598-019-46441-z
PMID:	31292495

Composition of Iridals, Unusual Triterpenoids from Sword-Lilies, and the Seasonal Dependence of Their Content in Various Parts of Different Iris Species

Franz-Josef Marner, Bianca Kerp

Walter de Gruyter GmbH

02-Aug-2018

doi:	10.1515/ZNC-1992-1-205

Isolation and Structure Determination of the Precursors of a-and y-Irone and Homologous Compounds from Iris pallida and Iris florentina

W. Krick, F.-J. Marner, L. Jaenicke

Walter de Gruyter GmbH

02-Aug-2018

doi:	10.1515/ZNC-1983-3-404

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
> Benzenoids / Benzene and substituted derivatives / Terphenyls / P-terphenyls
[4-(3-Acetyloxybutanoyloxy)-2,5-dihydroxy-3,6-bis(4-hydroxyphenyl)phenyl] 3-acetyloxybutanoate	56674261	Click to see CC(CC(=O)OC1=C(C(=C(C(=C1C2=CC=C(C=C2)O)O)OC(=O)CC(C)OC(=O)C)C3=CC=C(C=C3)O)O)OC(=O)C	582.60	unknown	https://doi.org/10.1002/FFJ.2730080505 https://doi.org/10.1002/(SICI)1099-1565(199601)7:1<37::AID-PCA281>3.0.CO;2-9 https://doi.org/10.1515/ZNC-1992-1-205 https://doi.org/10.1515/ZNC-1983-3-404
> Benzenoids / Phenanthrenes and derivatives
6-Oxopristimerol	11754914	Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C	480.60	unknown	via CMAUP database
Zeylasterone	13945472	Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C(=O)O)O)O)C)C)(C)C(=O)OC	510.60	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Anhydrosecoisolariciresinol	9974771	Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O	344.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Vierol	101297703	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO	306.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
(2S)-2-[(1S,2S,5R,8S)-2-hydroxy-8-(3-hydroxypropyl)-2-methyl-1-[(3E,5E)-4-methyl-6-[(1R,5S)-2,5,6,6-tetramethylcyclohex-2-en-1-yl]hexa-3,5-dienyl]-6-oxabicyclo[3.2.1]octan-5-yl]propanal	163098212	Click to see CC1CC=C(C(C1(C)C)C=CC(=CCCC23COC(C2CCCO)(CCC3(C)O)C(C)C=O)C)C	486.70	unknown	https://doi.org/10.1002/HLCA.19910740838
2-[2-Hydroxy-8-(3-hydroxypropyl)-2-methyl-1-[4-methyl-6-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)hexa-3,5-dienyl]-6-oxabicyclo[3.2.1]octan-5-yl]propanal	73801295	Click to see CC1CC=C(C(C1(C)C)C=CC(=CCCC23COC(C2CCCO)(CCC3(C)O)C(C)C=O)C)C	486.70	unknown	https://doi.org/10.1002/HLCA.19910740838
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2Z)-2-[(2R,3S,4S)-4-hydroxy-2-(3-hydroxypropyl)-3,4-dimethyl-3-[(E)-4-methyl-6-[(1R,5S)-2,5,6,6-tetramethylcyclohex-2-en-1-yl]hex-3-enyl]cyclohexylidene]propanal	57523217	Click to see CC1CC=C(C(C1(C)C)CCC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)C)C)C	472.70	unknown	https://doi.org/10.1515/ZNC-1983-3-404 https://doi.org/10.1002/(SICI)1099-1565(199601)7:1<37::AID-PCA281>3.0.CO;2-9 https://doi.org/10.1515/ZNC-1992-1-205
(2Z)-2-[(2R,3S,4S)-4-hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[(3E,5E)-4-methyl-6-[(1S,3R)-2,2,3-trimethyl-6-methylidenecyclohexyl]hexa-3,5-dienyl]cyclohexylidene]propanal	162883021	Click to see CC1CCC(=C)C(C1(C)C)C=CC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C	486.70	unknown	https://doi.org/10.1002/HLCA.19900730223
(2Z)-2-[(2R,3S,4S)-4-hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[(3E,5E)-4-methyl-6-[(1S,5R)-2,5,6,6-tetramethylcyclohex-2-en-1-yl]hexa-3,5-dienyl]cyclohexylidene]propanal	163187575	Click to see CC1CC=C(C(C1(C)C)C=CC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C)C	486.70	unknown	https://doi.org/10.1002/HLCA.19900730223
(Z)-alpha-Irone	6431140	Click to see CC1CC=C(C(C1(C)C)C=CC(=O)C)C	206.32	unknown	https://doi.org/10.1002/FFJ.2730080505
2-[4-Hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[4-methyl-6-(2,2,3-trimethyl-6-methylidenecyclohexyl)hexa-3,5-dienyl]cyclohexylidene]propanal	162883020	Click to see CC1CCC(=C)C(C1(C)C)C=CC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C	486.70	unknown	https://doi.org/10.1002/HLCA.19900730223
2-[4-Hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[4-methyl-6-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)hexa-3,5-dienyl]cyclohexylidene]propanal	3751	Click to see CC1CC=C(C(C1(C)C)C=CC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C)C	486.70	unknown	https://doi.org/10.1002/HLCA.19900730223
Iriflorental	102446705	Click to see CC1CCC(=C)C(C1(C)C)C=CC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)CO)C	486.70	unknown	https://doi.org/10.1002/FFJ.2730080505 https://doi.org/10.1002/(SICI)1099-1565(199601)7:1<37::AID-PCA281>3.0.CO;2-9
trans-alpha-Irone	6431141	Click to see CC1CC=C(C(C1(C)C)C=CC(=O)C)C	206.32	unknown	https://doi.org/10.1002/FFJ.2730080505
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2Z)-2-[(2R,3S,4S)-4-hydroxy-2-(3-hydroxypropyl)-3,4-dimethyl-3-[(3E,5E,7E)-4,8,12-trimethyltrideca-3,5,7,11-tetraenyl]cyclohexylidene]propanal	15742332	Click to see CC(=CCCC(=CC=CC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)C)C	456.70	unknown	https://doi.org/10.1002/HLCA.19910740838
(2Z)-2-[(2R,3S,4S)-4-hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[(3E,5E,7E)-4,8,12-trimethyltrideca-3,5,7,11-tetraenyl]cyclohexylidene]propanal	15742333	Click to see CC(=CCCC(=CC=CC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)CO)C)C)C	472.70	unknown	https://doi.org/10.1002/HLCA.19910740838
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/10.1016/0031-9422(93)85451-V https://doi.org/10.1002/HLCA.19900730223
2-[4-Hydroxy-2-(3-hydroxypropyl)-3,4-dimethyl-3-(4,8,12-trimethyltrideca-3,5,7,11-tetraenyl)cyclohexylidene]propanal	162965953	Click to see CC(=CCCC(=CC=CC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)C)C	456.70	unknown	https://doi.org/10.1002/HLCA.19910740838
2-[4-Hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-(4,8,12-trimethyltrideca-3,5,7,11-tetraenyl)cyclohexylidene]propanal	85447068	Click to see CC(=CCCC(=CC=CC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)CO)C)C)C	472.70	unknown	https://doi.org/10.1002/HLCA.19910740838
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/10.1016/0031-9422(93)85451-V https://doi.org/10.1515/ZNC-1992-1-205 https://doi.org/10.1002/(SICI)1099-1565(199601)7:1<37::AID-PCA281>3.0.CO;2-9
Isoiridogermanal	44559084	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-1983-3-404 https://doi.org/10.1002/HLCA.19900730223
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-D:B-Friedoolean-5-ene-3beta,29-diol	13918509	Click to see CC1(C(CCC2C1=CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)O)C	442.70	unknown	via CMAUP database
20(29)-Lupene-1beta,3beta-diol	488250	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
3alpha,16beta-Dihydroxylupa-12-ene	44179020	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
3alpha,16beta,28-Trihydroxylupa-20(29)-ene	44178931	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO	458.70	unknown	via CMAUP database
3beta-Hydroperoxy-7beta,25-epoxy-D:B-friedooleanane-5-ene	101481671	Click to see CC1(CCC2(CCC3(C4C5C=C6C(C4(CCC3(C2C1)C)CO5)CCC(C6(C)C)OO)C)C)C	456.70	unknown	via CMAUP database
3beta,16beta-Dihydroxylupa-12-ene	44178932	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
Calenduladiol	461835	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Glochidiol	13969554	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Paniculatadiol	101286253	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C	442.70	unknown	via CMAUP database
Pristimerin	159516	Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O	464.60	unknown	via CMAUP database
Resinone	101316848	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2O)C)C)(C)C)C)C	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
16beta-Hydroxy-3,4-secolupane-20(29)-ene-3-oic acid	44179021	Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC(C4(C3C(CC4)C(=C)C)C)O)C)C	458.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Fucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(93)85451-V
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dimethoxyacetophenone	14328	Click to see CC(=O)C1=CC(=C(C=C1)OC)OC	180.20	unknown	https://doi.org/10.1002/HLCA.19490320643
Acetovanillone	2214	Click to see CC(=O)C1=CC(=C(C=C1)O)OC	166.17	unknown	https://doi.org/10.1002/HLCA.19490320426
> Organoheterocyclic compounds / Benzofurans
Isololiolide	11019783	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> 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/10.1002/JPS.2600640504

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Iris pallida

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