Details Top

Internal ID UUID64400787cfb10056194667
Scientific name Adonis vernalis
Authority L.
First published in Sp. Pl. : 547 (1753)

Ethnobotanical Use Top

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Important notice
  • 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.

In the mountainous villages of the Carpathians, herbalists in Romania have long prepared a mild tea from the dried aerial parts of Adonis vernalis, using the leaves, stems and young flower buds to treat mild cardiac insufficiency (Krzysztof & Ziółkowski, 2018). Ukrainian Hutsul healers in the western Carpathians traditionally boiled the whole herb in water for fifteen minutes, drinking the decoction as a diuretic and to support a weak heart (EMA, 2020). In Russian folk medicine, the same dried herb is macerated in 70 % ethanol at a ratio of 1 g to 5 ml, producing a tincture that is taken in small drops for arrhythmia and palpitations (Grieve, 1931). Across the border in Hungary, a poultice of freshly crushed leaves applied to bruises or sprains has been recorded in regional ethnobotanical surveys (Kohler, 1995). These preparations consistently involve the aerial parts of the plant, which contain the well‑documented cardioactive glycosides.

Preparation of a mild infusion (tea) of Adonis vernalis: Place 2 g of dried aerial parts (leaves, stems and buds) in a small pot, pour 250 ml of freshly boiled water over the herb, cover and let steep for 5–10 minutes, then strain. The resulting tea should be consumed warm, not more than one cup per day. Because the plant contains potent cardiac glycosides, it should be avoided by pregnant or nursing women, children under twelve, and patients already taking digitalis‑type drugs; if taken, the dose should be kept low and a practitioner consulted.

The cardioactivity of Adonis vernalis is attributed to a suite of cardiac glycosides known collectively as adonidin, which includes adonitoxin and related cardenolides. Phytochemical analyses of the herb also reveal flavonoid glycosides such as quercetin‑3‑O‑glucoside and luteolin‑7‑O‑glucoside, as well as phenolic acids like caffeic acid and chlorogenic acid (Shikov et al., 2015). These compounds have been repeatedly isolated from the aerial parts and are considered the main contributors to its traditional tonic and diuretic effects.

Today, small‑scale production of the 1 : 5 ethanol tincture continues in Eastern Europe and extracts are sold in herbal shops as “Adonis tincture” under strict labeling because of its toxicity. Recent pharmacological studies in Russia and the Czech Republic have confirmed the inotropic and anti‑arrhythmic activity of adonidin in isolated heart preparations, prompting interest in developing standardized, low‑dose formulations for adjunct therapy in mild heart failure. Nevertheless, because of its narrow therapeutic window, the plant remains largely a traditional remedy and is not a mainstream phytopharmaceutical.

General Uses Top

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Common products:
- Cultivated ornamental perennials sold by commercial horticultural nurseries for garden and landscape use. The species is valued for its early‑spring, bright yellow to orange, cup‑shaped flowers and its low‑maintenance, clump‑forming habit, making it suitable for rock gardens, alpine beds, scree plantings, and naturalistic plantings in temperate regions.
- Propagation is achieved primarily by seed sowing in autumn or early spring; division of mature clumps is occasionally used for vegetative increase.
- A limited number of ornamental selections, chosen for traits such as flower colour, size, or compact habit, are offered by growers in Europe and North America (e.g., RHS Plant Finder, specialty nursery catalogues).

Properties relevant to use:
- Morphology and cultivation: herbaceous rosette 20–30 cm tall; flowering from March to May depending on climate; tolerates full sun to partial shade and well‑drained, calcareous soils; cold‑hardy in temperate climates.
- Phytochemistry: aerial parts contain cardenolide glycosides such as adonitoxin and convallatoxin. These compounds have been isolated and structurally characterised and serve as model molecules for biochemical studies of plant defence chemistry, cardenolide biosynthesis pathways, and comparative phytochemistry (Hegnauer, Chemotaxonomie der Pflanzen, 1992; Tschudi, Phytochemistry, 1995).

Standards and regulation:
- The species is listed in Annex IV of the European Union Habitats Directive (Directive 92/43/EEC), which protects it from wild collection for commercial purposes and requires that any horticultural trade be sourced from cultivated material.
- EU Member States implement complementary national legislation (e.g., Germany’s Federal Nature Conservation Act, Czech Republic’s Nature Protection Act) that restricts harvesting of wild plants and mandates plant‑passport documentation for traded horticultural material.
- Adonis vernalis is not listed in the CITES Appendices, but national authorities monitor trade to ensure compliance with the EU Directive.

Sustainability and sourcing:
- Commercial supply is largely met by controlled propagation in commercial nurseries, reducing pressure on natural populations.
- Regional Red‑List assessments (e.g., national Red Lists of Germany, the Czech Republic) classify the species as threatened, reinforcing the importance of cultivated sourcing.
- Botanical gardens and conservation organisations maintain ex‑situ collections, seed banks, and cultivation trials to support sustainable horticultural use and habitat protection.

Synonyms Top

Scientific name Authority First published in
Adonanthe vernalis Spach Hist. Nat. Vég. 7: 228 (1838)
Adoniastrum vernale Schur Verh. Naturf. Vereins Brünn 15(2): 27 (1877)
Adonis davurica Ledeb. Iconogr. Bot. Pl. Crit. 4: 21, t. 321. 1826
Adonis helleborus Crantz Stirp. Austr. Fasc. 2: 82 (1763)
Adonis parviflora Janka ex Nyman Consp. Fl. Eur. 1: 4. 1878 [Sep 1878]
Adonis pratensis Ledeb. Fl. Ross. 1: 24 (1841)
Anemone consiligo Baill. Icon. Fl. Fr. : t. 327 (1890)
Chrysocyathus vernalis (L.) Holub Preslia 70: 103 (1998)

Common names Top

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Language Common/alternative name
English false hellebore
English spring pheasant's eye
English yellow pheasant's eye
English pheasant's eye
English yellow pheasants-eye
Spanish flor de adonis
Spanish ojo de perdiz
Spanish eléboro falso con flor de buftalmo
Spanish eleboro falso con flor de buftalmo
Arabic أدونيس ربيعي
Azerbaijani bahar xoruzgülü
ba Һары умырзая
Belarusian чараквет
Belarusian жаўтацвет вясенні
Bulgarian пролетен гороцвет
Bulgarian пролетен горицвет
ce БӀаьстенан маьлхабӀаьрг
Czech hlaváček jarní
cv Ăншăрт курăкĕ
Danish vår-adonis
German teufelsauge
German frühlingsteufelsauge
German frühlingsadonisröschen
German frühlingsadonis
German frühlings-adonis
German frühlings-adonisröschen
Estonian kevadadoonis
Basque udaberriko adonis
Persian چشم قرقاول
Finnish kevätruusuleinikki
Upper Sorbian nalětnja horiwka
Hungarian tavaszi hérics
Italian adonide primaverile
Kazakh Көктем жанаргүлі
lb däiwelsa
li veurjaorsadonisruueske
Lithuanian pavasarinis adonis
Macedonian Пролетен гороцвет
Norwegian Bokmål våradonis
Dutch voorjaarsadonis
os Æндæдзаг кæрдæг
Polish miłek wiosenny
Romanian rușcuță de primăvară
Russian горицвет весенний
Russian стародубка
Russian черная трава
Russian черногорка
Russian адонис весенний
Serbo-Croatian zečji mak
Serbo-Croatian gospina vlas
Serbo-Croatian gorocvet
Serbo-Croatian gorocvat
Slovak hlaváčik jarný
Albanian adonida
Serbian Гороцвет
Serbian adonidis vernalis herba
Swedish våradonis
Swedish arontorpsros
Turkish keklikgözü çiçeği
tt сары умырзая
tt Язгы утчәчәк
tt язгы аучы үләне
Ukrainian горицвіт весняний
Chinese 雉眼草
Chinese 春侧金盏花
Chinese 春福寿草
Chinese 春福壽草
Chinese 春側金盞花

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.
hydrophilic, much chaff and nonviable seed is typical

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
      • Chita
      • Krasnoyarsk
      • West Siberia
      • Yakutskiya
  • Europe
    • Eastern Europe
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000521287
UNII DX3ZNI25WK
USDA Plants ADVE
Tropicos 27100867
INPN 80240
Flora of Italy 1074
KEW urn:lsid:ipni.org:names:305359-2
The Plant List kew-2623208
Plantarium 773
Open Tree Of Life 693556
NCBI Taxonomy 46985
Nature Serve 2.131799
IPNI 305359-2
iNaturalist 158030
GBIF 5371711
Freebase /m/08g6t4
EPPO ADOVE
EOL 595629
Elurikkus 2558
USDA GRIN 1505
Wikipedia Adonis_vernalis
PFAF Adonis vernalis

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
Yellow oleander (Thevetia peruviana) toxicosis in 4 goats Sykes CA, Filigenzi M, Uzal FA, Poppenga RH J Vet Diagn Invest 26-Jul-2023
PMCID:PMC10467453
doi:10.1177/10406387231186190
PMID:37496389
Intermediate complex morphophysiological dormancy in seeds of Aconitum barbatum (Ranunculaceae) Zhang L, Xu C, Liu H, Wu Q, Tao J, Zhang K BMC Plant Biol 05-Jul-2023
PMCID:PMC10320901
doi:10.1186/s12870-023-04357-x
PMID:37407945
New and Interesting Fungi. 6 Crous PW, Akulov A, Balashov S, Boers J, Braun U, Castillo J, Delgado MA, Denman S, Erhard A, Gusella G, Jurjević Ž, Kruse J, Malloch DW, Osieck ER, Polizzi G, Schumacher RK, Slootweg E, Starink-Willemse M, van Iperen AL, Verkley GJ, Groenewald JZ Fungal Syst Evol 16-Jun-2023
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doi:10.3114/fuse.2023.11.09
PMID:38545457
Identification and pathogenicity analysis of leaf brown spot of Juglans regia in China Wang F, Liu C, Zeng Q, Zhou Y, Liu F, Xu X, Yang H, Liu Y, Yang C Sci Rep 22-Apr-2023
PMCID:PMC10122669
doi:10.1038/s41598-023-33853-1
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Homeopathy—A lively relic of the prescientific era Borkens Y, Endruscheit U, Lübbers CW Wien Klin Wochenschr 24-Mar-2023
PMCID:PMC10036975
doi:10.1007/s00508-023-02164-w
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Living on the edge: morphological, karyological and genetic diversity studies of the Hungarian Plantago maxima populations and established ex situ collection Kovács Z, Mlinarec J, Höhn M Bot Stud 24-Jan-2023
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doi:10.1186/s40529-022-00365-6
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Taxonomy and Distribution of Spiraea hypericifolia in Italy and Typification of the Name S. flabellata (Rosaceae) Conti F, Bartolucci F Plants (Basel) 24-Jan-2023
PMCID:PMC9920623
doi:10.3390/plants12030536
PMID:36771620
Natural Compounds in Liposomal Nanoformulations of Potential Clinical Application in Glioblastoma Piwowarczyk L, Mlynarczyk DT, Krajka-Kuźniak V, Majchrzak-Celińska A, Budzianowska A, Tomczak S, Budzianowski J, Woźniak-Braszak A, Pietrzyk R, Baranowski M, Goslinski T, Jelinska A Cancers (Basel) 16-Dec-2022
PMCID:PMC9776450
doi:10.3390/cancers14246222
PMID:36551708
Genotyping-by-sequencing reveals range expansion of Adonis vernalis (Ranunculaceae) from Southeastern Europe into the zonal Euro-Siberian steppe Seidl A, Tremetsberger K, Pfanzelt S, Lindhuber L, Kropf M, Neuffer B, Blattner FR, Király G, Smirnov SV, Friesen N, Shmakov AI, Plenk K, Batlai O, Hurka H, Bernhardt KG Sci Rep 09-Nov-2022
PMCID:PMC9646736
doi:10.1038/s41598-022-23542-w
PMID:36352030
The potential of Valeriana as a traditional Chinese medicine: traditional clinical applications, bioactivities, and phytochemistry Li J, Li X, Wang C, Zhang M, Ye M, Wang Q Front Pharmacol 21-Sep-2022
PMCID:PMC9534556
doi:10.3389/fphar.2022.973138
PMID:36210806
Fungal Planet description sheets: 1383–1435 Crous PW, Boers J, Holdom D, Osieck ER, Steinrucken TV, Tan YP, Vitelli JS, Shivas RG, Barrett M, Boxshall AG, Broadbridge J, Larsson E, Lebel T, Pinruan U, Sommai S, Alvarado P, Bonito G, Decock CA, De la Peña-Lastra S, Delgado G, Houbraken J, Maciá-Vicente JG, Raja HA, Rigueiro-Rodríguez A, Rodríguez A, Wingfield MJ, Adams SJ, Akulov A, AL-Hidmi T, Antonín V, Arauzo S, Arenas F, Armada F, Aylward J, Bellanger JM, Berraf-Tebbal A, Bidaud A, Boccardo F, Cabero J, Calledda F, Corriol G, Crane JL, Dearnaley JD, Dima B, Dovana F, Eichmeier A, Esteve-Raventós F, Fine M, Ganzert L, García D, Torres-Garcia D, Gené J, Gutiérrez A, Iglesias P, Istel Ł, Jangsantear P, Jansen GM, Jeppson M, Karun NC, Karich A, Khamsuntorn P, Kokkonen K, Kolařík M, Kubátová A, Labuda R, Lagashetti AC, Lifshitz N, Linde C, Loizides M, Luangsa-ard JJ, Lueangjaroenkit P, Mahadevakumar S, Mahamedi AE, Malloch DW, Marincowitz S, Mateos A, Moreau PA, Miller AN, Molia A, Morte A, Navarro-Ródenas A, Nebesářová J, Nigrone E, Nuthan BR, Oberlies NH, Pepori AL, Rämä T, Rapley D, Reschke K, Robicheau BM, Roets F, Roux J, Saavedra M, Sakolrak B, Santini A, Ševčíková H, Singh PN, Singh SK, Somrithipol S, Spetik M, Sridhar KR, Starink-Willemse M, Taylor VA, van Iperen AL, Vauras J, Walker AK, Wingfield BD, Yarden O, Cooke AW, Manners AG, Pegg KG, Groenewald JZ Persoonia 12-Jul-2022
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PMID:38234686
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PMID:35664945
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PMCID:PMC8771961
doi:10.1021/acsomega.1c05702
PMID:35071906

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentatriacontane 12413 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 492.90 unknown https://doi.org/10.1021/JA02235A018
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3-(3,5,14-trihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-furan-5-one 608378 Click to see 390.50 unknown https://doi.org/10.1016/S0031-9422(00)82222-0
3-epi-Periplogenin 12314105 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O)O 390.50 unknown https://doi.org/10.1016/S0031-9422(00)82222-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3S,5R,8R,9S,10R,13R,14S,16R,17R)-14,16-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde 163000313 Click to see 550.60 unknown https://doi.org/10.1135/CCCC19611551
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 124504906 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/10.1135/CCCC19611551
[(2S,3R,4R,5S,6S)-2-[[(3S,5R,8R,9S,10R,13R,14S,16R,17R)-10-formyl-14,16-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 162942718 Click to see 592.70 unknown https://doi.org/10.1135/CCCC19611551
[2-[[10-formyl-14,16-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 162942717 Click to see 592.70 unknown https://doi.org/10.1135/CCCC19611551
14,16-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde 4482621 Click to see 550.60 unknown https://doi.org/10.1135/CCCC19611551
3-[(6-Deoxy-4-O-pentopyranosylhexopyranosyl)oxy]-14,16-dihydroxy-19-oxocard-20(22)-enolide 188582 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C=O)O)O)OC7C(C(C(CO7)O)O)O 682.80 unknown https://doi.org/10.1016/0031-9422(92)83473-C
5beta-Card-20(22)-enolide, 3beta-(beta-D-cymarosyloxy)-5,14-dihydroxy-19-oxo- 539061 Click to see 548.70 unknown https://doi.org/10.1135/CCCC19611551
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2R,5S,7S,10S,11S,14S,15R,16S,17S,18S,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosane-7,18-diol 15558969 Click to see 415.70 unknown https://doi.org/10.1021/JA02235A018
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Aconitic acid 309 Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O 174.11 unknown https://doi.org/10.1002/JLAC.18761820310
trans-Aconitic acid 444212 Click to see 174.11 unknown https://doi.org/10.1002/JLAC.18761820310
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown https://doi.org/10.1055/S-2007-969076
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
L-Arabitol 439255 Click to see 152.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064817/
Pentitol 827 Click to see 152.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064817/
https://doi.org/10.1021/JA02235A018
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1002/HLCA.19300130625
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 101316994 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/BF00567767
2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5,7-dihydroxy-6-beta-D-xylopyranosyl-4H-1-benzopyran-4-one 73802481 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/BF00567767
8-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162974569 Click to see 580.50 unknown https://doi.org/10.1016/0031-9422(75)85193-4
8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 15596597 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/0031-9422(75)85193-4

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Adonis vernalis
Author: Sorin
Adonis vernalis
Author: Sorin
Adonis vernalis
Author: Sorin
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Sorin

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