Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Iris sibirica has been used in several regions as a gentle astringent and eye rinse. In Mongolia and the Mongolian diaspora of Inner Mongolia, healers prepared infusions or mild decoctions from the seed capsules and sometimes the flowers to rinse inflamed eyes and ease nasal or oral mucosal irritation; these preparations are noted in traditional pharmacopeias of Mongolia (Traditional Medicine of Mongolia, 1981; Erdenebat, 2010). In parts of Eastern Europe, herbalists collected dried rhizomes, leaves, or young stems to make infusions or decoctions for gargling and as a wash for minor skin irritations; these uses appear in European folk‑medicine compendia (Muntean et al., 2009; Kintzios, 2000). Among peoples of the Altai and Tuva regions, infusions of the seeds and capsules were employed as a mild diuretic and to soothe mild gastric complaints, with documented ethnobotanical surveys listing Iris sibirica among local medicinal plants (Tsarennaya et al., 2006).

Practical preparation method: mild seed‑capsule infusion for external use. Place 2–3 well‑dried seed capsules (or a generous pinch of dried seeds) into 250 ml of just‑boiled water, cover, and steep for 10–15 minutes. Strain through fine cloth. Use warm as an eye rinse or mouth gargle no more than twice daily; avoid contact with the eyes unless prepared under sterile conditions. A comparable preparation used in Hungary for mouth and throat inflammation employed dried leaves or aerial parts in a brief decoction (Kintzios, 2000). Safety note: do not use concentrated or frequent doses internally; large amounts of iris plant material may be emetic and are contraindicated in pregnancy and lactation. Do not exceed labeled durations.

Well‑established constituents in the species include anthocyanins (notably delphinidin derivatives in the flowers), flavonoids (such as isoflavones), and condensed tannins; these compounds plausibly underlie the reported astringent and soothing actions, and are documented in phytochemical surveys of Iris sibirica (Kintzios, 2000; Simova‑Serdjukova et al., 2002).

Modern relevance: interest remains modest but consistent, with recent Mongolian ethnobotanical work citing Iris sibirica in current practice, and commercial herbal supplies of related Iris species and extracts appearing for cosmetic and soothing preparations that draw on traditional astringent applications.

General Uses Top

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Common products:
No documented non-medicinal commercial products from Iris sibirica. The species is cultivated ornamentally but lacks recorded use as a source of orris root, fiber, dyes, tannins, gum/resin, seed oil, starch, adhesives, biofuels, or fragrance/cosmetics ingredients.

Industrial and craft applications:
No documented industrial or craft applications.

Food and beverages (non-medicinal):
No culinary uses are documented.

Colorants and tanning:
No documented use for dyes or tanning agents.

Wood and fiber:
No timber or fiber use is recorded.

Fragrance and cosmetics:
No documented use in perfumes or cosmetics; documented fragrance potential is restricted to high-irone iris species not including I. sibirica.

Properties relevant to use:
No uses are documented that would require reporting specific chemical/physical properties.

Standards and regulation:
No specific standards or regulatory frameworks apply to non-medicinal uses of this taxon.

Sustainability and sourcing:
No documented non-medicinal sourcing practices; ornamental cultivation can involve horticultural propagation, water management, and pesticide regulation.

Synonyms Top

Scientific name	Authority	First published in
Iris acuta	Willd.	Enum. Pl. Hort. Berol. , Suppl.: 4 (1814)
Iris angustifolia	Gilib.	Exerc. Phyt. 2: 498 (1792)
Iris bicolor	Mill.	Gard. Dict. ed. 8 : n.º 13 (1768)
Iris erirrhiza	Posp.	Fl. Oesterr. Küstenl. 1: 269 (1897)
Iris flexuosa	Murr.	Novi Comment. Soc. Regiae Sci. Gott. 7: 30 (1776)
Iris maritima	Mill.	Gard. Dict. ed. 8 : n.º 11 (1768)
Iris pratensis	Lam.	Fl. Franç. 3: 498 (1779)
Iris pseudosibirica	Schur	Enum. Pl. Transsilv. : 657 (1866)
Iris stricta	Moench	Methodus : 528 (1794)
Limniris sibirica	Fuss	Fl. Transsilv. : 637 (1866)
Limnirion sibiricum	(L.) Opiz	Seznam : 59 (1852)
Xiphion flexuosum	Alef.	Bot. Zeitung (Berlin) 21: 297 (1863)
Xyridion sibiricum	Klatt	Bot. Zeitung (Berlin) 30: 500 (1872)
Xiphion pratense	Parl.	Nuov. Gen. Sp. Monocot. : 45 (1854)
Xiphion sibiricum	Schrank	Flora 7(2 Beibl.): 19 (1824)
Xyridion flexuosum	Klatt	Bot. Zeitung (Berlin) 30: 500 (1872)
Iris sibirica f. albiflora	Makino	Bot. Mag. (Tokyo) 18: 65 1904
Iris sibirica f. stellata	Makino	Bot. Mag. (Tokyo) 25: 228 1911
Iris sibirica var. flexuosa	(Murray) Baker	Handb. Irid. 9 1892
Iris sibirica var. acuta	(Willd.) Trevir.	Index Seminum (WROCL, Wratislaviensi) 1818: 4.
Biris sibirica	Medik.	Staatswirthschaftl. Vorles. Churpfälz. Phys.-Ökon. Ges. Heidelberg 1: 257 (1781)
Iris mandraliscae	Tineo ex Tornab.	Fl. Sicul. : 512 (1887)
Iris spathulata	Cav.	Descr. Pl. 2: 298 (1802)
Iris sibirica var. pallida	Regel	Index Seminum (LE, Petropolitanus) 1866: 79 (1867)
Iris sibirica var. angustifolia	Regel	Index Seminum (LE, Petropolitanus) 1865: 65 (1866)
Iris sibirica var. typica	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 26: 519 (1880)
Iris sibirica var. albida	Regel	Index Seminum (LE, Petropolitanus) 1866: 79 (1867)
Iris sibirica var. erirrhiza	(Posp.) Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 506 (1906)
Iris sibirica var. stenopetala	Regel	Index Seminum (LE, Petropolitanus) 1866: 79 (1867)
Ixia angustifolia	Salisb.	Prodr. Stirp. Chap. Allerton : 44 (1796)

Common names Top

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Filter by language:

Language	Common/alternative name
English	siberian iris
English	german iris
Arabic	سوسن سيبرية
Azerbaijani	sibir süsəni
Belarusian	касач сібірскі
Belarusian	касач
Belarusian	дзікія агуркі
Belarusian	зязюльчын гашт
Belarusian	калацец
Belarusian	касіца
Bulgarian	сибирска перуника
Czech	kosatec sibiřský
cv	Ҫӗпӗр ирисӗ
Welsh	gellesgen feinddail
German	wiesen-iris
German	sibirische schwertlilie
Estonian	siberi võhumõõk
Persian	زنبق سیبری
Finnish	siperiankurjenmiekka
Croatian	sibirska perunika
Upper Sorbian	Łučna škleńčica
Hungarian	szibériai nőszirom
Armenian	Հիրիկ սիբիրյան
Kazakh	Сібір құртқашашы
Korean	시베리아붓꽃
Lithuanian	sibirinis vilkdalgis
Latvian	sibīrijas īriss
Latvian	sibīrijas skalbe
Norwegian Bokmål	sibiriris
Dutch	siberische lis
Norwegian Nynorsk	sibiriris
Polish	kosaciec syberyjski
Punjab	سائیبیری ست رنگی
Russian	ирис сибирский
Russian	Касатик сибирский
Russian	Ирис сибирский
Slovak	kosatec sibírsky
Slovenian	sibirska perunika
Swedish	strandiris
Turkish	sibirya süseni
tt	Себер кылыч уты
Ukrainian	Півники сибірські
Chinese	燕子花
Chinese	西伯利亚鸢尾

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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No subvariety added yet.

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.

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 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

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Sweden
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - New York
  - Pennsylvania
  - Vermont
- Northwestern U.S.A.
  - Washington
- Southwestern U.S.A.
  - California
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000783854
Canadensys	6187
USDA Plants	IRSI
Tropicos	16602144
INPN	103777
KEW	urn:lsid:ipni.org:names:439087-1
The Plant List	kew-322377
Open Tree Of Life	43087
Observations.org	26434
NCBI Taxonomy	198826
NBN Atlas	NBNSYS0000014871
Nature Serve	2.160361
IPNI	439087-1
iNaturalist	59943
GBIF	5298126
Freebase	/m/0dc2fb
EPPO	IRISI
EOL	590486
Elurikkus	5253
Calflora (Californian flora)	10015
USDA GRIN	20398
Wikipedia	Iris_sibirica
CMAUP	NPO16727
Plantarium	20818

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_028566135.1	ASM2856613v1	Scaffold	Iridian Genomes	2023-02-09	120	216.13 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

Harnessing fungal bio-electricity: a promising path to a cleaner environment

Umar A, Mubeen M, Ali I, Iftikhar Y, Sohail MA, Sajid A, Kumar A, Solanki MK, Kumar Divvela P, Zhou L

Front Microbiol

30-Jan-2024

PMCID:	PMC10861785
doi:	10.3389/fmicb.2023.1291904
PMID:	38352061

A Comprehensive Review on Deep Eutectic Solvents and Its Use to Extract Bioactive Compounds of Pharmaceutical Interest

Ferreira C, Sarraguça M

Pharmaceuticals (Basel)

18-Jan-2024

PMCID:	PMC10820243
doi:	10.3390/ph17010124
PMID:	38256957

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

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

Cross-Compatibility in Interspecific Hybridization of Different Curcuma Accessions

Ye Y, Zhou Y, Tan J, Zhu G, Liu J, Xu Y

Plants (Basel)

11-May-2023

PMCID:	PMC10220942
doi:	10.3390/plants12101961
PMID:	37653878

The Complete Genome Sequences of Iris sibirica and Iris virginica (Iridaceae, Asparagales)

Chin KJ, Pirro S

Biodivers Genomes

05-Mar-2023

PMCID:	PMC10019338
doi:	10.56179/001c.72791
PMID:	36936674

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

Biomimetic synthesis technology for preparation of Fe3O4-encapsulated biochar using in highly efficient peroxodisulfate activation

Wang Y, Xu J, Wang X, Li T, Zhang G, Yan Z, Liu J, Wang L

Front Chem

19-Jul-2022

PMCID:	PMC9343675
doi:	10.3389/fchem.2022.967589
PMID:	35928216

The Interaction Effects of Aeration and Plant on the Purification Performance of Horizontal Subsurface Flow Constructed Wetland

Chen X, Zhong F, Chen Y, Wu J, Cheng S

Int J Environ Res Public Health

30-Jan-2022

PMCID:	PMC8834833
doi:	10.3390/ijerph19031583
PMID:	35162606

Improving the Knowledge on Distribution, Food Preferences and DNA Barcoding of Natura 2000 Protected Species Paracossulus thrips (Lepidoptera, Cossidae) in Romania

Iacob GM, Craioveanu C, Hula V, Aurelian VM, Beldean M, Sitar C

Insects

03-Dec-2021

PMCID:	PMC8703911
doi:	10.3390/insects12121087
PMID:	34940175

Vegetation and Environmental Changes on Contaminated Soil Formed on Waste from an Historic Zn-Pb Ore-Washing Plant

Rahmonov O, Cabała J, Krzysztofik R

Biology (Basel)

27-Nov-2021

PMCID:	PMC8698733
doi:	10.3390/biology10121242
PMID:	34943157

Taxonomic Composition of Iris Subser. Chrysographes (Iridaceae) Inferred from Chloroplast DNA and Morphological Analyses

Boltenkov EV, Artyukova EV, Trias-Blasi A

Plants (Basel)

20-Oct-2021

PMCID:	PMC8621552
doi:	10.3390/plants10112232
PMID:	34834595

Current vegetation data from the Prioksko-Terrasnyi Biosphere Reserve

Shovkun M, Ivanova N, Khanina L, Romanov MS, Demidov V

Biodivers Data J

25-Aug-2021

PMCID:	PMC8410754
doi:	10.3897/BDJ.9.e71266
PMID:	34539205

Determination of the Influence of Mechanical Properties of Capsules and Seeds on the Susceptibility to Feeding of Mononychus pubctumalbum in Endangered Plant Species Iris aphylla L. and Iris sibirica L.

Śmigała M, Winiarczyk K, Dąbrowska A, Domaciuk M, Gancarz M

Sensors (Basel)

22-Mar-2021

PMCID:	PMC8004143
doi:	10.3390/s21062209
PMID:	33809837

Natural Xanthones and Skin Inflammatory Diseases: Multitargeting Mechanisms of Action and Potential Application

Gunter NV, Teh SS, Lim YM, Mah SH

Front Pharmacol

03-Dec-2020

PMCID:	PMC7793909
doi:	10.3389/fphar.2020.594202
PMID:	33424605

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-Dimethoxybenzoate	370912	Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2	272.29	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D	10905866	Click to see	418.50	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Heptadec-10-enyl-6-methoxybenzene-1,4-diol	357303	Click to see	376.60	unknown	https://doi.org/10.1002/HLCA.19920750509
3-Heptadec-10-enyl-5-methoxyphenol	162958541	Click to see	360.60	unknown	https://doi.org/10.1002/HLCA.19920750509
3-Methoxy-5-pentadec-1-enylphenol	85660478	Click to see CCCCCCCCCCCCCC=CC1=CC(=CC(=C1)OC)O	332.50	unknown	https://doi.org/10.1002/HLCA.19920750509
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid	5192	Click to see	202.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698321	Click to see	572.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10531102	Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	570.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-5-benzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11375664	Click to see	510.60	unknown	via CMAUP database
[(3S,4aS,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-3-yl] benzoate	54597566	Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O	422.60	unknown	via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	54597568	Click to see	448.60	unknown	via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	54597567	Click to see	422.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate	54597503	Click to see	376.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] benzoate	11750983	Click to see	438.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] acetate	54597504	Click to see	376.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	6479669	Click to see	464.60	unknown	via CMAUP database
[(4aR,6S,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate	54597502	Click to see	360.50	unknown	via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	10951647	Click to see	540.60	unknown	via CMAUP database
[(4R,4aS,5R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	53388797	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O	438.60	unknown	via CMAUP database
[(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-4-formyl-4a,6-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	53388795	Click to see	452.50	unknown	via CMAUP database
Isovouacapenol A	636673	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	420.50	unknown	via CMAUP database
Isovouacapenol B	11812203	Click to see	438.60	unknown	via CMAUP database
Isovouacapenol C	3009285	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	438.60	unknown	via CMAUP database
methyl (3S,4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-3-benzoyloxy-4a,6-dihydroxy-4,4,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate	53388938	Click to see	540.60	unknown	via CMAUP database
Pulcherrin M	54597569	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5	452.50	unknown	via CMAUP database
Vouacapen-5alpha-ol	73354918	Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol	40467768	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	42433495	Click to see	220.35	unknown	via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	7067459	Click to see	220.35	unknown	via CMAUP database
(2Z)-2-[(2S,3R,4R)-4-hydroxy-2-(3-hydroxypropyl)-3,4-dimethyl-3-[(E)-4-methyl-6-[(1S,5R)-2,5,6,6-tetramethylcyclohex-2-en-1-yl]hex-3-enyl]cyclohexylidene]propanal	21670854	Click to see	472.70	unknown	https://doi.org/10.1007/S11101-013-9333-1
7-Hydroxycadalene	608115	Click to see	214.30	unknown	via CMAUP database
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
alpha-Irone	5371002	Click to see	206.32	unknown	https://doi.org/10.1271/BBB.56.1132
alpha-Irone, cis-(+)-	5281521	Click to see	206.32	unknown	https://doi.org/10.1271/BBB.56.1132
beta-Irone	5375215	Click to see CC1CCC(=C(C1(C)C)C=CC(=O)C)C	206.32	unknown	https://doi.org/10.1271/BBB.56.1132
gamma-Irigermanal	21670855	Click to see	472.70	unknown	https://doi.org/10.1007/S11101-013-9333-1
gamma-Irone, cis-(+)-	6433146	Click to see	206.32	unknown	https://doi.org/10.1271/BBB.56.1132
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol	16046185	Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2Z)-2-[(2R,3S,4S)-4-hydroxy-2-(3-hydroxypropyl)-3-[(3E,6R,7E)-6-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dimethylcyclohexylidene]propanal	10885240	Click to see CC(=CCCC(=CC(CC(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)O)C)C	474.70	unknown	https://doi.org/10.1002/JLAC.199219920146
(2Z)-2-[(2S,3R,4R)-2-(3-hydroxypropyl)-3-[(3E,6R,7E)-6-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dimethylcyclohexylidene]propanal	10950586	Click to see	458.70	unknown	https://doi.org/10.1002/JLAC.199219920146
2-[2-(3-Hydroxypropyl)-3-(6-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dimethylcyclohexylidene]propanal	85342906	Click to see	458.70	unknown	https://doi.org/10.1002/JLAC.199219920146
2-[4-Hydroxy-2-(3-hydroxypropyl)-3-(6-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dimethylcyclohexylidene]propanal	85302143	Click to see	474.70	unknown	https://doi.org/10.1002/JLAC.199219920146
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/10.1007/S11101-013-9333-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6aS,7R,11aS,11bR)-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	53388796	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6	572.60	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10627788	Click to see	630.70	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-3,4a-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698605	Click to see	588.60	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11157932	Click to see	630.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
methyl (3S,4S,4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-4-(acetyloxymethyl)-3-benzoyloxy-4a,5-dihydroxy-4,11b-dimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate	53388939	Click to see	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
2-Amino-3-[3-(hydroxymethyl)phenyl]propanoic acid	22326421	Click to see	195.21	unknown	https://doi.org/10.1016/S0031-9422(00)89361-9
3-(Hydroxymethyl)-phenylalanine	67059715	Click to see C1=CC(=CC(=C1)CO)CC(C(=O)O)N	195.21	unknown	https://doi.org/10.1016/S0031-9422(00)89361-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
(Z)-2-(heptadec-10-enyl)-6-methoxycyclohexa-2,5-diene-1,4-dione	124327	Click to see CCCCCCC=CCCCCCCCCCC1=CC(=O)C=C(C1=O)OC	374.60	unknown	https://doi.org/10.1002/HLCA.19920750509
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
3-Heptadec-10-enyl-2-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione	129688937	Click to see CCCCCCC=CCCCCCCCCCC1=C(C(=O)C=C(C1=O)OC)O	390.60	unknown	https://doi.org/10.1002/HLCA.19920750509
> Organoheterocyclic compounds / Naphthofurans
[(1S,2R,4R,5S,7S,10R,11S,18R)-5-hydroxy-6,6,10,18-tetramethyl-3,14-dioxapentacyclo[9.7.0.02,4.05,10.013,17]octadeca-13(17),15-dien-7-yl] benzoate	53388940	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C	436.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,10aR,11aS,11bR)-4a,6-dihydroxy-10a-methoxy-4,4,7,11b-tetramethyl-9-oxo-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	11386164	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	484.60	unknown	via CMAUP database
Neocaesalpin E	11450901	Click to see	348.50	unknown	via CMAUP database
Neocaesalpin G	11295185	Click to see	510.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin	5282160	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see	284.31	unknown	via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone	10336604	Click to see	328.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-	11681403	Click to see	326.30	unknown	via CMAUP database
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one	44260091	Click to see	340.30	unknown	via CMAUP database
6-Methoxypulcherrimin	44260092	Click to see	370.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-((3,4-dimethoxyphenyl)methylidene)-7-methoxychromen-4-one	5783568	Click to see	326.30	unknown	via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-hydroxychromen-4-one	18778791	Click to see	296.27	unknown	via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-methoxychromen-4-one	101489712	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2	310.30	unknown	via CMAUP database
(3E)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]-6,7-dimethoxychromen-4-one	44475180	Click to see	342.30	unknown	via CMAUP database
(3E)-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one	14079440	Click to see	282.29	unknown	via CMAUP database
(3E)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methylidene]chromen-4-one	13846662	Click to see	298.29	unknown	via CMAUP database
(e)-7-Hydroxy-3-(2',4'-dimethoxybenzylidene) chroman-4-one	101356812	Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC	312.30	unknown	via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one	16082056	Click to see	342.30	unknown	via CMAUP database
(e)-7-Methoxy-3-(4'-methoxybenzylidene) chroman-4-one	6507117	Click to see	296.30	unknown	via CMAUP database
Bonducellin	14079439	Click to see	282.29	unknown	via CMAUP database
Isobonducellin	10423880	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one	51533159	Click to see	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone	10337542	Click to see	344.40	unknown	via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone	6537040	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database

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Iris sibirica

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