Iris spuria - Unknown
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Internal ID UUID644027bf04daa659678380
Scientific name Iris spuria
Authority L.
First published in Sp. Pl. : 39 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chamaeiris spuria Medik. Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. 6: 418 (1790)
Iris spathacea J.St.-Hil. Syst. Veg. 1: 468 1817
Limniris spuria Fuss Fl. Transsilv. : 637 (1866)
Xyridion spurium (L.) Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 163 (1869)
Xiphion spurium Alef. Bot. Zeitung (Berlin) 21: 297 (1863)
Iris spuria var. reichenbachiana (Klatt) Dykes Gen. Iris 60. 1913
Iris spuria var. subbarbata (Joó) Baker Handb. Irid. 15. 1892
Iris gueldenstadtiana subsp. subbarbata (Joó) Nyman Consp. Fl. Eur. 702 1882

Common names Top

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Language Common/alternative name
English seashore iris
English blue iris
Spanish spurio
Spanish xiphion nothum
Spanish xyridion carthaliniae
Spanish xyridion demetrii
Spanish xyridion maritimum
Spanish xyridion musulmanicum
Arabic سوسن كاذب
Arabic زهرة السوسن سبوريا
Arabic سوسن سبوريا
Arabic زهره السوسن سبريا
Arabic السوسن الأرجواني
Czech kosatec žlutofialový
Welsh gellesgen las
German wiesen-schwertlilie
German salzwiesen-schwertlilie
German steppen-schwertlilie
German bastard-schwertlilie
Persian زنبق نمکزار
Finnish etelänkurjenmiekka
Upper Sorbian přeměnita škleńčica
Hungarian korcs nőszirom
Hungarian fátyolos nőszirom
Serbian Перуника бастардна
Swedish dansk iris
Swedish dansk svärdslilja
Swedish blå svärdslilja
Vietnamese diên vĩ hoa tím
Chinese 琴瓣鸢尾
Chinese 拟鸢尾

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Iris spuria subsp. carthaliniae (Fomin) B.Mathew Iris : 117 (1981)
Iris spuria subsp. demetrii (Achv. & Mirzoeva) B.Mathew Iris : 117 (1981)
Iris spuria subsp. maritima (Dykes) P.Fourn. Quatre Fl. France 190 1935
Iris spuria subsp. musulmanica (Fomin) Takht. Fl. Erevana , ed. 2: 330 (1972)
Iris spuria subsp. spuria Unknown

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 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
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
    • Northern Europe
      • Denmark
      • Great Britain
      • Sweden
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000783889
USDA Plants IRSP80
Tropicos 16600062
KEW urn:lsid:ipni.org:names:439117-1
The Plant List kew-322411
Missouri Botanical Garden 281088
Open Tree Of Life 1087622
Observations.org 104707
NCBI Taxonomy 93026
NBN Atlas NBNSYS0000002266
Nature Serve 2.150566
IUCN Red List 200242
IPNI 439117-1
iNaturalist 57733
GBIF 5298946
Freebase /m/02wb2ql
EOL 487182
Elurikkus 5254
Calflora (Californian flora) 10016
USDA GRIN 20409
Wikipedia Iris_spuria
CMAUP NPO15902

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
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
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162
Ethanolic extract of Iris songarica rhizome attenuates methotrexate-induced liver and kidney damages in rats Moodi H, Hosseini M, Abedini MR, Hassanzadeh-Taheri M, Hassanzadeh-Taheri M Avicenna J Phytomed 01-Jul-2020
PMCID:PMC7430963
PMID:32850294
Iranian Medicinal Plants: From Ethnomedicine to Actual Studies Buso P, Manfredini S, Reza Ahmadi-Ashtiani H, Sciabica S, Buzzi R, Vertuani S, Baldisserotto A Medicina (Kaunas) 26-Feb-2020
PMCID:PMC7143749
doi:10.3390/medicina56030097
PMID:32110920
QUINONES FROM THE SEEDS OF IRIS SPURIA VAR. HALOPHILA Faten Darwish, Omar Abdallah, Nasr El-Emary, A. Ali Egypts Presidential Specialized Council for Education and Scientific Research 10-Feb-2020
doi:10.21608/BFSA.1995.69678
Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury Subramanya SB, Venkataraman B, Meeran MF, Goyal SN, Patil CR, Ojha S Int J Mol Sci 28-Nov-2018
PMCID:PMC6321362
doi:10.3390/ijms19123776
PMID:30486484
Environmental effects on the maturation of the endodermis and multiseriate exodermis of Iris germanica roots Meyer CJ, Seago JL Jr, Peterson CA Ann Bot 16-Jan-2009
PMCID:PMC2707867
doi:10.1093/aob/mcn255
PMID:19151041
New isoflavone glycosides from Iris spuria L. (Calizona) cultivated in Egypt. Farag SF, Kimura Y, Ito H, Takayasu J, Tokuda H, Hatano T J Nat Med 01-Jan-2009
doi:10.1007/S11418-008-0291-7
PMID:18791667
Flavonoids from Iris spuria (Zeal) cultivated in Egypt. Singab AN Arch Pharm Res 01-Oct-2004
doi:10.1007/BF02975425
PMID:15554258
Isoflavones of Iris spuria Abdul S. Shawl, Vishwapaul, Asif Zaman, Ashok K. Kalla Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80573-7
Irispurinol, A 12a-hydroxyrotenoid from Iris spuria Abdul S. Shawl, N. Mengi, L.N. Misra, Vishwapaul Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80061-X
Flavonoids of Iris spuria Abdul S. Shawl, N. Mengi, M.K. Kaul, Vishwapaul Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80245-0
Iridal glycosides from Iris spuria (Zeal), cultivated in Egypt. Marner FJ, Singab AN, Al-Azizi MM, El-Emary NA, Schäfer M Phytochemistry 01-Jun-2002
doi:10.1016/S0031-9422(02)00110-3
PMID:12031450

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 / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
3,5-Dimethoxytoluene 77844 Click to see CC1=CC(=CC(=C1)OC)OC 152.19 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
alpha-Asarone 636822 Click to see CC=CC1=CC(=C(C=C1OC)OC)OC 208.25 unknown via CMAUP database
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown via CMAUP database
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
gamma-Asarone 636750 Click to see COC1=CC(=C(C=C1CC=C)OC)OC 208.25 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Asarinin 11869417 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
4-[(3R,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 57404419 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 386.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 46917405 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC(=C(C=C5)O)O 342.30 unknown via CMAUP database
5-[(3S,3aS,6R,6aS)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 10089592 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
Pluviatilol 70695727 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Sesaminone 158370 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)C(=O)C4=CC5=C(C=C4)OCO5 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z)-N-(2-methylpropyl)dodeca-2,4,8,10-tetraenamide 70693621 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
alpha-Sanshool 6440935 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
Pellitorine 5318516 Click to see CCCCCC=CC=CC(=O)NCC(C)C 223.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+/-)-Asarinol A 46174001 Click to see CC1=CC(C2C(C1=O)C2(C)C)O 166.22 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(1S,6R)-6-Isopropyl-3-methyl-cyclohex-2-en-1-ol 11367127 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2E)-2-[(2S,3R,4S)-3-[(3E,5R,7E,11S)-11,12-dihydroxy-4,8,12-trimethyl-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-4-hydroxy-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 162955039 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(C(C)(C)O)O 833.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2E)-2-[(2S,3R,4S)-4-hydroxy-3-[(3E,5R,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 162929506 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)O 831.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2E)-2-[(2S,3R,4S)-4-hydroxy-3-[(3E,5R,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl]cyclohexylidene]propanal 163194539 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)C)C)OC4C(C(C(C(O4)CO)O)O)O)CCC(=O)C(C)(C)O 993.10 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2E)-2-[(2S,3R,4S)-4-hydroxy-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3-[(3E,5R,7E)-4,8,12-trimethyl-11-oxo-5,12-bis[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]trideca-3,7-dienyl]cyclohexylidene]propanal 162972674 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)OC4C(C(C(C(O4)CO)O)O)O 993.10 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2E)-2-[(4S)-4-hydroxy-3-[(3E,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 11968624 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)O 831.00 unknown via CMAUP database
(2E)-2-[(4S)-4-hydroxy-3-[(3E,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl]cyclohexylidene]propanal 11968623 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)C)C)OC4C(C(C(C(O4)CO)O)O)O)CCC(=O)C(C)(C)O 993.10 unknown via CMAUP database
(2E)-2-[(4S)-4-hydroxy-3,4-dimethyl-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3-[(3E,7E)-4,8,12-trimethyl-11-oxo-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-12-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]cyclohexylidene]propanal 11968622 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)OC4C(C(C(C(O4)CO)O)O)O 993.10 unknown via CMAUP database
(2Z)-2-[(2R,3S,4S)-3-[(3E,5R,7E,11S)-11,12-dihydroxy-4,8,12-trimethyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-4-hydroxy-3,4-dimethyl-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 162955038 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(C(C)(C)O)O 833.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2Z)-2-[(2S,3R,4S)-4-hydroxy-3-[(3E,5R,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 162929509 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)O 831.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2Z)-2-[(2S,3R,4S)-4-hydroxy-3-[(3E,5R,7E)-12-hydroxy-4,8,12-trimethyl-11-oxo-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl]cyclohexylidene]propanal 163185710 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)C)C)OC4C(C(C(C(O4)CO)O)O)O)CCC(=O)C(C)(C)O 993.10 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
(2Z)-2-[(4S)-3-[(3E,7E)-11,12-dihydroxy-4,8,12-trimethyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-4-hydroxy-3,4-dimethyl-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 11968626 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(C(C)(C)O)O 833.00 unknown via CMAUP database
2-[3-[11,12-Dihydroxy-4,8,12-trimethyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-4-hydroxy-3,4-dimethyl-2-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 73157146 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(C(C)(C)O)O 833.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
2-[4-Hydroxy-3-[12-hydroxy-4,8,12-trimethyl-11-oxo-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]cyclohexylidene]propanal 73157144 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)O 831.00 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
2-[4-Hydroxy-3-[12-hydroxy-4,8,12-trimethyl-11-oxo-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytrideca-3,7-dienyl]-3,4-dimethyl-2-[3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl]cyclohexylidene]propanal 73157143 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)C)C)OC4C(C(C(C(O4)CO)O)O)O)CCC(=O)C(C)(C)O 993.10 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
2-[4-Hydroxy-3,4-dimethyl-2-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-3-[4,8,12-trimethyl-11-oxo-5,12-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]trideca-3,7-dienyl]cyclohexylidene]propanal 73157145 Click to see CC(=CCC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCOC2C(C(C(C(O2)CO)O)O)O)C)C)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)C(C)(C)OC4C(C(C(C(O4)CO)O)O)O 993.10 unknown https://doi.org/10.1016/S0031-9422(02)00110-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
2-Formyl-5-(hydroxymethyl)-1H-pyrrole-1-butyric acid 10198218 Click to see C1=C(N(C(=C1)C=O)CCCC(=O)O)CO 211.21 unknown https://doi.org/10.1007/S11418-008-0291-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Primin 84800 Click to see CCCCCC1=CC(=O)C=C(C1=O)OC 208.25 unknown https://doi.org/10.21608/BFSA.1995.69678
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
1,6,6-Trimethyl-1,3-cycloheptadiene-7-one 85794676 Click to see CC1=CC=CCC(C1=O)(C)C 150.22 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Croweacin 5316141 Click to see COC1=C(C=CC2=C1OCO2)CC=C 192.21 unknown via CMAUP database
Kakuol 596894 Click to see CCC(=O)C1=CC2=C(C=C1O)OCO2 194.18 unknown via CMAUP database
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown via CMAUP database
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
Maesopsin 6-beta-D-glucopyranoside 42607792 Click to see C1=CC(=CC=C1CC2(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1007/S11418-008-0291-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2',5,8-Trihydroxy-7-methoxyflavanone 133556370 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3O)C(=C1)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(88)80245-0
5,8,2'-Trihydroxy-7-methoxyflavanone 14034288 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3O)C(=C1)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(88)80245-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7-Dihydroxy-2',6-dimethoxyisoflavone 5491794 Click to see COC1=CC=CC=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)80573-7
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/10.1007/BF02975425
https://doi.org/10.1007/S11418-008-0291-7
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-methoxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 138911432 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)80573-7
5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162875589 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF02975425
5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154497558 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1007/BF02975425
5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 16126681 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1007/S11418-008-0291-7
5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one 102034325 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC6C(C(C(C(O6)CO)O)O)O 786.70 unknown https://doi.org/10.1007/S11418-008-0291-7
5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162916995 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1007/BF02975425
5,7-dihydroxy-6-methoxy-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one 102034324 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 654.60 unknown https://doi.org/10.1007/S11418-008-0291-7
5,7-dihydroxy-6-methoxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 44133603 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1007/S11418-008-0291-7
https://doi.org/10.1007/BF02975425
5,7-dihydroxy-6-methoxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one 11972472 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S11418-008-0291-7
5,7-Dihydroxy-6-methoxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 163021887 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1007/BF02975425
CID 132993930 132993930 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)80573-7
Genistein 7-O-beta-D-glucoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/S11418-008-0291-7
Iristectorin A 11968629 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)80573-7
Tectoridin 5281810 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1007/BF02975425
Tectorigenin 7-O-gentiobioside 44257343 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S11418-008-0291-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
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/S0031-9422(00)80573-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
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/S0031-9422(00)80573-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
5,2'-Dihydroxy-7,8-dimethoxyisoflavone 14034287 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=CO2)C3=CC=CC=C3O)OC 314.29 unknown https://doi.org/10.1016/0031-9422(88)80245-0
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(6aS,12aR)-9,11,12a-trihydroxy-10-methoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 162904798 Click to see COC1=C(C2=C(C=C1O)OC3COC4=CC=CC=C4C3(C2=O)O)O 330.29 unknown https://doi.org/10.1016/0031-9422(88)80061-X
10,15-Dihydroxy-2,6,8,20-tetraoxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-1(13),3,5(9),10,14,16,18-heptaen-12-one 163106698 Click to see C1C2=C(C3=C(C=CC=C3O1)O)C(=O)C4=C(C5=C(C=C4O2)OCO5)O 326.26 unknown https://doi.org/10.1007/BF02975425
9,11,12a-Trihydroxy-10-methoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 14104356 Click to see COC1=C(C2=C(C=C1O)OC3COC4=CC=CC=C4C3(C2=O)O)O 330.29 unknown https://doi.org/10.1016/0031-9422(88)80061-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown https://doi.org/10.1007/S11418-008-0291-7
Glucosyringic acid 10383888 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1007/S11418-008-0291-7

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