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Eranthis cilicica

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401a0cdf1ed556515448
Scientific name Eranthis cilicica
Authority Schott & Kotschy
First published in Oesterr. Bot. Wochenbl. 4: 113 (1854)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Eranthis isaurica C.Simon Bauhinia 7: 5 (1980)

Common names Top

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Language Common/alternative name
Finnish turkintalventähti

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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Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
germination unlikely after dry storage > 6 months; best stored in moist towels at either 4°C or 20°C; grow seedlings at cool temperature

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000670673
Tropicos 100331544
KEW urn:lsid:ipni.org:names:711188-1
The Plant List kew-2791910
Open Tree Of Life 5922989
NCBI Taxonomy 1765017
IPNI 711188-1
iNaturalist 486522
GBIF 3925417
EPPO ETHCI

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
Karyotypes and Physical Mapping of Ribosomal DNA with Oligo-Probes in Eranthis sect. Eranthis (Ranunculaceae) Mitrenina EY, Alekseeva SS, Badaeva ED, Peruzzi L, Artemov GN, Krivenko DA, Pinzani L, Aytaç Z, Çeçen Ö, Baasanmunkh S, Choi HJ, Mesterházy A, Tashev AN, Bancheva S, Lian L, Xiang K, Wang W, Erst AS Plants (Basel) 22-Dec-2023
PMCID:PMC10780877
doi:10.3390/plants13010047
PMID:38202355
Novel Oleanane-Type Triterpene Glycosides from the Saponaria officinalis L. Seeds and Apoptosis-Inducing Activity via Mitochondria Takahashi N, Iguchi T, Kuroda M, Mishima M, Mimaki Y Int J Mol Sci 12-Feb-2022
PMCID:PMC8877789
doi:10.3390/ijms23042047
PMID:35216169
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728
Cycloartane and Oleanane Glycosides from the Tubers of Eranthis cilicica Watanabe K, Mimaki Y, Fukaya H, Matsuo Y Molecules 25-Dec-2018
PMCID:PMC6337325
doi:10.3390/molecules24010069
PMID:30585226
Chapter 6 Cubic Membranes: The Missing Dimension of Cell Membrane Organization Almsherqi ZA, Landh T, Kohlwein SD, Deng Y Int Rev Cell Mol Biol 05-Apr-2009
PMCID:PMC7105030
doi:10.1016/S1937-6448(08)02006-6
PMID:19349040
Chromones from the tubers of Eranthis cilicica and their antioxidant activity. Kuroda M, Uchida S, Watanabe K, Mimaki Y Phytochemistry 01-Jan-2009
doi:10.1016/J.PHYTOCHEM.2008.12.002
PMID:19162283
First Nuclear DNA Amounts in more than 300 Angiosperms ZONNEVELD BJ, LEITCH IJ, BENNETT MD Ann Bot 19-May-2005
PMCID:PMC4246870
doi:10.1093/aob/mci170
PMID:15905300
Eranthisaponins A and B, two new bisdesmosidic triterpene saponins from the tubers of Eranthis cilicica. Watanabe K, Mimaki Y, Sakuma C, Sashida Y J Nat Prod 01-Jun-2003
doi:10.1021/NP030071M
PMID:12828483

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aS,9R,10R,12aR,14bS)-9-(hydroxymethyl)-10-[(2S,3R,4S,5S)-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162922974 Click to see 1853.90 unknown https://doi.org/10.1021/NP030071M
Eranthisaponin A 11062265 Click to see 1545.70 unknown https://doi.org/10.1021/NP030071M
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-Hydroxy-2-(hydroxymethyl)-8-(4-hydroxy-3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74817437 Click to see CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)CO)O)OC3C(C(C(C(O3)CO)O)O)O)CO 454.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-hydroxy-2-(hydroxymethyl)-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 42603922 Click to see CC(=CCC1=C(C=C(C2=C1OC(=CC2=O)CO)O)OC3C(C(C(C(O3)CO)O)O)O)CO 454.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-Hydroxy-8-(4-hydroxy-3-methylbut-2-enyl)-2-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74817436 Click to see 438.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-hydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-2-methyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 42603921 Click to see 438.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2-(hydroxymethyl)-8-(4-hydroxy-3-methylbut-2-enyl)chromen-4-one 74817389 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)CO)CO 292.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5,7-Dihydroxy-2-hydroxymethyl-8-[(2e)-4-hydroxy-3-methylbut-2-enyl]-4h-1-benzopyran-4-one 42603811 Click to see 292.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5,7-Dihydroxy-8-(4-hydroxy-3-methylbut-2-enyl)-2-methylchromen-4-one 91220040 Click to see 276.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5,7-dihydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-2-methylchromen-4-one 102286688 Click to see CC1=CC(=O)C2=C(C=C(C(=C2O1)CC=C(C)CO)O)O 276.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
4-hydroxy-7-[[(2R,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]oxymethyl]furo[3,2-g]chromen-5-one 42603924 Click to see 556.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
4-Hydroxy-7-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]furo[3,2-g]chromen-5-one 74817438 Click to see 556.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
Cimifugin 441960 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)CO)O 306.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
Cimitin 5087850 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)CO)O 306.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
> Organoheterocyclic compounds / Benzoxepines
(9R)-5,9-dihydroxy-9-(hydroxymethyl)-2-methyl-8H-pyrano[2,3-g][1]benzoxepin-4-one 162892319 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OCC(C=C3)(CO)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
(9S)-5,9-dihydroxy-2-methyl-9-[[(2R,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]oxymethyl]-8H-pyrano[2,3-g][1]benzoxepin-4-one 162842172 Click to see 614.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-hydroxy-2-methyl-9-[[(2R,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]oxymethyl]-8,11-dihydropyrano[2,3-g][1]benzoxepin-4-one 14034913 Click to see 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-Hydroxy-2-methyl-9-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxymethyl]-8,11-dihydropyrano[2,3-g][1]benzoxepin-4-one 373656 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OCC(=CC3)COC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5-Hydroxy-2,9-bis(hydroxymethyl)-8,11-dihydro-4H-pyrano[2,3-g][1]benzooxepin-4-one 42603810 Click to see C1C=C(COC2=C1C3=C(C(=C2)O)C(=O)C=C(O3)CO)CO 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5,9-dihydroxy-2-methyl-9-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]-8H-pyrano[2,3-g][1]benzoxepin-4-one 162842171 Click to see 614.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002
5,9-dihydroxy-9-(hydroxymethyl)-2-methyl-8H-pyrano[2,3-g][1]benzoxepin-4-one 42603923 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OCC(C=C3)(CO)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.002

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