Iris sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Iris sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Iris sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644027be3bf17118276003
Scientific name Iris sibirica
Authority L.
First published in Sp. Pl. : 39 (1753)

Description Top

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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)

Common names Top

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Language Common/alternative name
English siberian iris
English german iris
Arabic سوسن سيبرية
Belarusian касач сібірскі
Bulgarian сибирска перуника
Czech kosatec sibiřský
cv Ҫӗпӗр ирисӗ
Welsh gellesgen feinddail
German sibirische schwertlilie
German wiesen-iris
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 skalbe
Latvian sibīrijas īriss
Norwegian Bokmål sibiriris
Norwegian Nynorsk sibiriris
Polish kosaciec syberyjski
Punjab سائیبیری ست رنگی
Russian ирис сибирский
Russian Ирис сибирский
Slovak kosatec sibírsky
Swedish strandiris
Turkish sibirya süseni
Ukrainian Півники сибірські
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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Forms (abbr. f.) Top

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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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Turkey
  • Europe
    • 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
    • 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

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
Name Level Submitter Released Coverage Size
GCA_028566135.1 ASM2856613v1 Scaffold Iridian Genomes 2023-02-09 120.0x 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!
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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 CC1=C2CC(C3(C(CCCC3(C2=CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 418.50 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Heptadec-10-enyl-6-methoxybenzene-1,4-diol 357303 Click to see CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)O 376.60 unknown https://doi.org/10.1002/HLCA.19920750509
3-Heptadec-10-enyl-5-methoxyphenol 162958541 Click to see CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)O 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 C(CCCCC(=O)O)CCCC(=O)O 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 CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 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
[(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 CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 464.60 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 CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)COC(=O)C6=CC=CC=C6 540.60 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 CC1(CCCC2(C1(C(CC3C2CC4=C(C3(C)O)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 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
Pulcharrin G 11750983 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)O)O)(C)C)C 438.60 unknown via CMAUP database
Pulcherrimin F 11375664 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)C 510.60 unknown via CMAUP database
Pulcherrin D 54597502 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(CC2OC(=O)C)O)(C)C)C 360.50 unknown via CMAUP database
Pulcherrin E 54597503 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)O)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin F 54597504 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin H 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
Pulcherrin I 54597567 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 422.60 unknown via CMAUP database
Pulcherrin J 54597568 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C=CC5=CC=CC=C5 448.60 unknown via CMAUP database
Pulcherrin K 53388795 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C=O)C 452.50 unknown via CMAUP database
Pulcherrin L 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
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
Pulcherrin O 53388938 Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1(C(C(CC4)OC(=O)C5=CC=CC=C5)(C)C)O)C)O 540.60 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
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-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 CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 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 CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 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 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/10.1007/S11101-013-9333-1
3-Buten-2-one, 4-(2,5,6,6-tetramethyl-2-cyclohexen-1-yl)- 5281521 Click to see CC1CC=C(C(C1(C)C)C=CC(=O)C)C 206.32 unknown https://doi.org/10.1271/BBB.56.1132
7-Hydroxycadalene 608115 Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O 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 CC1CC=C(C(C1(C)C)C=CC(=O)C)C 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 CC1CCC(=C)C(C1(C)C)CCC(=CCCC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)C)C 472.70 unknown https://doi.org/10.1007/S11101-013-9333-1
gamma-Irone 6433146 Click to see CC1CCC(=C)C(C1(C)C)C=CC(=O)C 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 CC1CCC(=C(C)C=O)C(C1(C)CCC=C(C)CC(C=C(C)CCC=C(C)C)O)CCCO 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 CC1CCC(=C(C)C=O)C(C1(C)CCC=C(C)CC(C=C(C)CCC=C(C)C)O)CCCO 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 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
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,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 CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)OC(=O)C)C 630.70 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 CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)OC(=O)C6=CC=CC=C6)C 630.70 unknown via CMAUP database
(8beta,10beta,14alpha)-6beta,7beta-Bis(benzoyloxy)-3beta,5alpha-dihydroxy-12,16-epoxycassa-12,15-dien-19-oic acid 10698605 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)O)C 588.60 unknown via CMAUP database
Pulcherrin N 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
Pulcherrin P 53388939 Click to see CC(=O)OCC1(C(CCC2(C1(C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)OC(=O)C)O)O)C)OC(=O)C5=CC=CC=C5)C 598.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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
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
> 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 C1=CC(=CC(=C1)CO)CC(C(=O)O)N 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
Neocaesalpin E 11450901 Click to see CC1C2CCC3(C(CCCC3(C2CC4(C1=CC(=O)O4)OC)C)(C)C)O 348.50 unknown via CMAUP database
Neocaesalpin F 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 G 11295185 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 510.60 unknown via CMAUP database
Pulcherrin Q 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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin 5282160 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 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 COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC4=C(C=C3)OCO4)C(=C1)OC 328.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4 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 COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O)OC 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-(2,4-Dimethoxybenzylidene)-7-hydroxychroman-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
(3E)-3-(4-Methoxybenzylidene)-7-methoxychroman-4-one 6507117 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)OC 296.30 unknown via CMAUP database
(3E)-3-[(3,4-dimethoxyphenyl)methylidene]-7-methoxychromen-4-one 5783568 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC(=C(C=C3)OC)OC)CO2 326.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see COC1=CC(=CC(=C1OC)OC)C=C2COC3=C(C2=O)C=CC(=C3)O 342.30 unknown via CMAUP database
3-(4-Hydroxybenzylidene)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one 14079440 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC=C(C=C3)O)CO2 282.29 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 18778791 Click to see C1C(=CC2=CC3=C(C=C2)OCO3)C(=O)C4=C(O1)C=C(C=C4)O 296.27 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-methoxy-2,3-dihydro-4H-1-benzopyran-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
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-6,7-dimethoxy-2,3-dihydro-4H-1-benzopyran-4-one 44475180 Click to see COC1=C(C=C(C=C1)C=C2COC3=CC(=C(C=C3C2=O)OC)OC)O 342.30 unknown via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 13846662 Click to see COC1=C(C=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)O 298.29 unknown via CMAUP database
Bonducellin 14079439 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 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 COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC(=C3)O 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 COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O 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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