Adonis amurensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Adonis amurensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID64400783009f8499103126
Scientific name Adonis amurensis
Authority Regel & Radde
First published in Bull. Soc. Imp. Naturalistes Moscou 34(II): 35 (1862)

Description Top

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Synonyms Top

Scientific name Authority First published in
Adonanthe amurensis (Regel & Radde) Chrtek & Slavíková Preslia 50: 24 (1978)
Adonis amurensis var. angustiloba A.I.Baranov & Skvortsov Zap. Kharbin. Obshch. Estestvoisp. Etnogr. 12: 35. 1954
Adonis amurensis var. parviflora Nakai
Adonis amurensis var. puberula Honda Bot. Mag. (Tokyo) 52: 49 1939
Adonis amurensis var. uniflora Makino Bot. Mag. (Tokyo) 8: 97 1894
Adonis barthei Franch. Bull. Annuel Soc. Philom. Paris , sér. 8, 6: 89 (1894)
Adonis vernalis var. amurensis (Regel & Radde) Regel & Radde Bull. Soc. Bot. France 51: 132 1904
Chrysocyathus amurensis (Regel & Radde) Holub Preslia 70: 102 (1998)
Adonis amurensis var. yezoensis Kudô Hokk.-Yak.-Shokub.-Zui 44 1922

Common names Top

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Language Common/alternative name
Arabic أدونيس آموري
Azerbaijani amur xoruzgülü
Czech hlaváček amurský
German amur-adonisröschen
Persian آدونیس آمورنسیس
Finnish amurinruusuleinikki
French adonide de l'amour
Upper Sorbian amurowa horiwka
Japanese 北見福寿草
Japanese キタミフクジュソウ
Korean 복수초
Polish miłek amurski
Russian Адонис амурский
Slovak hlaváčik amurský
Chinese 側金盞花
Chinese 冰凉花
Chinese 福寿草
Chinese 顶冰花
Chinese 福壽草
Chinese 侧金盏花(冰凉花)
Chinese 侧金盏花

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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.
much chaff and nonviable seed is typical; short viability; very poor germination; does not need chilling if seed is fresh. Seedlings will probably die if transplanted, so wait till they have got some size and transplant while dormant.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000521126
UNII F2563E84RC
Tropicos 27100020
KEW urn:lsid:ipni.org:names:708061-1
The Plant List kew-2623058
Open Tree Of Life 243850
Observations.org 113960
NCBI Taxonomy 196574
IPNI 708061-1
iNaturalist 437861
GBIF 7277921
Freebase /m/0nbgs85
EPPO ADOAM
EOL 2873427
Elurikkus 581865
USDA GRIN 1503
Wikipedia Adonis_amurensis
PFAF Adonis amurensis

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
Dynamic transcriptome analysis provides molecular insights into underground floral differentiation in Adonis Amurensis Regel & Radde Xin H, Zhang L, Wang H, Zhu X BMC Genom Data 21-Mar-2024
PMCID:PMC10956236
doi:10.1186/s12863-024-01220-2
PMID:38515034
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
Comparative plastome genomics and phylogenetic relationships of the genus Trollius Li J, Du Y, Xie L, Jin X, Zhang Z, Yang M Front Plant Sci 17-Nov-2023
PMCID:PMC10690957
doi:10.3389/fpls.2023.1293091
PMID:38046610
Astaxanthin: Past, Present, and Future Nishida Y, Berg PC, Shakersain B, Hecht K, Takikawa A, Tao R, Kakuta Y, Uragami C, Hashimoto H, Misawa N, Maoka T Mar Drugs 28-Sep-2023
PMCID:PMC10608541
doi:10.3390/md21100514
PMID:37888449
Beyond NPK: Mineral Nutrient-Mediated Modulation in Orchestrating Flowering Time Jun SE, Shim JS, Park HJ Plants (Basel) 18-Sep-2023
PMCID:PMC10535918
doi:10.3390/plants12183299
PMID:37765463
Complete chloroplast genome of Adonis pseudoamurensis W.T.Wang (Ranunculaceae) Zhang XY, Zhang ZL, Zhang LQ, Zhang LF, Zhu JY, Xue CS Mitochondrial DNA B Resour 15-Sep-2023
PMCID:PMC10506428
doi:10.1080/23802359.2023.2256493
PMID:37727834
How to deal with frenemy NRF2: Targeting NRF2 for chemoprevention and cancer therapy Tang YC, Chuang YJ, Chang HH, Juang SH, Yen GC, Chang JY, Kuo CC J Food Drug Anal 31-Aug-2023
PMCID:PMC10629913
doi:10.38212/2224-6614.3463
PMID:39666284
Genome-Wide Identification and Expression Analysis of C3H Zinc Finger Family in Potato (Solanum tuberosum L.) Deng Z, Yang Z, Liu X, Dai X, Zhang J, Deng K Int J Mol Sci 17-Aug-2023
PMCID:PMC10454627
doi:10.3390/ijms241612888
PMID:37629069
Expanding the Repertoire of the Plant-Infecting Ophioviruses through Metatranscriptomics Data Debat H, Garcia ML, Bejerman N Viruses 25-Mar-2023
PMCID:PMC10144540
doi:10.3390/v15040840
PMID:37112821
Phytochemicals and Regulation of NF-kB in Inflammatory Bowel Diseases: An Overview of In Vitro and In Vivo Effects Laurindo LF, dos Santos AR, de Carvalho AC, Bechara MD, Guiguer EL, Goulart RD, Vargas Sinatora R, Araújo AC, Barbalho SM Metabolites 07-Jan-2023
PMCID:PMC9862976
doi:10.3390/metabo13010096
PMID:36677021
Comparative Transcriptome Analysis of CCCH Family in Roles of Flower Opening and Abiotic Stress in Osmanthus fragrans Ye Y, Cao S, Shen L, Wang Y, Zhong S, Yang L, Xiao Z, Fang Q, Zhao H, Dong B Int J Mol Sci 06-Dec-2022
PMCID:PMC9735588
doi:10.3390/ijms232315363
PMID:36499688
Astaxanthin Protection against Neuronal Excitotoxicity via Glutamate Receptor Inhibition and Improvement of Mitochondrial Function Kandy SK, Nimonkar MM, Dash SS, Mehta B, Markandeya YS Mar Drugs 18-Oct-2022
PMCID:PMC9605357
doi:10.3390/md20100645
PMID:36286468
Analysis of Floral Organ Development and Sex Determination in Schisandra chinensis by Scanning Electron Microscopy and RNA-Sequencing Liu X, Zhang L, Yang S Life (Basel) 18-Aug-2022
PMCID:PMC9410518
doi:10.3390/life12081260
PMID:36013439
AaZFP3, a Novel CCCH-Type Zinc Finger Protein from Adonis amurensis, Promotes Early Flowering in Arabidopsis by Regulating the Expression of Flowering-Related Genes Wang M, Zhang H, Dai S, Feng S, Gong S, Wang J, Zhou A Int J Mol Sci 25-Jul-2022
PMCID:PMC9332444
doi:10.3390/ijms23158166
PMID:35897742
Characterization of Phytohormones and Transcriptomic Profiling of the Female and Male Inflorescence Development in Manchurian Walnut (Juglans mandshurica Maxim.) Li X, Han R, Cai K, Guo R, Pei X, Zhao X Int J Mol Sci 13-May-2022
PMCID:PMC9143237
doi:10.3390/ijms23105433
PMID:35628244

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 / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(3S,8R,9R,10R,17S)-17-acetyl-3-hydroxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one 162883828 Click to see CC(=O)C1CCC2=C1C(=O)CC3C2CC=C4C3(CCC(C4)O)C 314.40 unknown https://doi.org/10.1007/BF01900226
17-acetyl-3-hydroxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one 78384929 Click to see CC(=O)C1CCC2=C1C(=O)CC3C2CC=C4C3(CCC(C4)O)C 314.40 unknown https://doi.org/10.1007/BF01900226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 129628835 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)CO)OC)O 550.70 unknown https://doi.org/10.1002/PTR.1184
CID 6708764 6708764 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)O 548.70 unknown https://doi.org/10.1002/PTR.1184
Cymarine 441853 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)O 548.70 unknown https://doi.org/10.1002/PTR.1184
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,6S)-6-[(2R,3R,4S,6S)-6-[(2R,3R,4S,6S)-6-[(2R,3R,4R,6S)-6-[(2R,3R,4R,6R)-6-[[(3S,8R,9S,10R,12S,13S,14S,17R)-12,14-dihydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162881866 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4CC=C3C2)O)C(C)O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1233.50 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
(3S,8R,9S,10R,17S)-17-acetyl-17-hydroxy-3-[(2R,4R,5R,6R)-4-methoxy-5-[(2S,4R,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-1,2,3,4,7,8,9,11-octahydrocyclopenta[a]phenanthren-12-one 162912770 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)C=CC5(C(=O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1211.40 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
(3S,8R,9S,10R,17S)-17-acetyl-3-[(2R,4R,5R,6R)-4-methoxy-5-[(2S,4R,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one 44818335 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)CCC5C(=O)C)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1197.40 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate 44817974 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CC=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 1063.20 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate 44817802 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CC=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 1063.20 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] pyridine-3-carboxylate 44817975 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CN=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 1064.20 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
[17-acetyl-8,14-dihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate 75076495 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CC=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 1063.20 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
[17-acetyl-8,14-dihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] pyridine-3-carboxylate 75076568 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CN=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 1064.20 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[(3S,8S,9R,10R,12R,13S,14R,17S)-8,12,14-trihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 44818334 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 959.10 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[(3S,8S,9S,10R,11R,13R,14R,17S)-8,11,14-trihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 44818153 Click to see CC1C(C(CC(O1)OC2CCC3(C4C(CC5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 959.10 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[8,11,14-trihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 75076640 Click to see CC1C(C(CC(O1)OC2CCC3(C4C(CC5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 959.10 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[8,12,14-trihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 75076713 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 959.10 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
17-Acetyl-17-hydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-1,2,3,4,7,8,9,11-octahydrocyclopenta[a]phenanthren-12-one 75076837 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)C=CC5(C(=O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1211.40 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
17-acetyl-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one 75076714 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)CCC5C(=O)C)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1197.40 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
2-[6-[6-[6-[6-[6-[[12,14-Dihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 75076780 Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4CC=C3C2)O)C(C)O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC 1233.50 unknown https://doi.org/10.1016/J.STEROIDS.2009.10.008
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/BF00568428

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