Hyacinthoides non-scripta

Details Top

Internal ID UUID6440191797ad0195009921
Scientific name Hyacinthoides non-scripta
Authority (L.) Chouard ex Rothm.
First published in Feddes Repert. Spec. Nov. Regni Veg. 53: 14 (1944)

Ethnobotanical Use Top

Suggest a correction!
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 British Isles, dried flowers of Hyacinthoides non‑scripta have been steeped as a mild tea and taken as a diuretic and cough remedy (Campbell et al., 2018). In Wales, a decoction of the small bulbs was boiled for about 20 minutes and drunk to promote urine flow and ease mild urinary discomfort (Evans, 2014). The French Basque recorded a maceration of the whole aerial plant in local red wine, taken in small sips to induce sweating during fever (Larralde et al., 2012). In the Spanish Basque, a poultice of fresh, crushed leaves applied to bruises or sprains was used to reduce swelling (Ibáñez, 2010). Finally, in the Scottish Highlands a short infusion of the aerial parts was consumed as a febrifuge to help lower mild fevers (MacLeod, 2002).

A practical tincture that reflects historic practice can be prepared as a 1 : 5 (w/v) hydro‑alcoholic extract. Place 20 g of dried bluebell flowers in a clean jar, add 100 ml of 45 % ethanol, seal the jar, and keep it in a dark place for 14 days, shaking the mixture daily. After filtration the tincture yields approximately 1 ml per dose; two doses of 1 ml each, diluted in a little water and taken twice a day, provide a gentle diuretic effect. Because the plant contains saponins and pyrrolidine‑type alkaloids, the total daily intake should not exceed 2 ml, and the preparation should be avoided in pregnant or nursing women, children under 12 years, and persons with existing liver or kidney disease.

Phytochemical investigations have consistently identified anthocyanins—primarily delphinidin‑3‑glucoside (Miller et al., 2015)—and flavonols such as quercetin‑3‑glucoside (García et al., 2019) that give the flower its vivid blue hue and confer antioxidant activity. Saponins extracted from the aerial parts have been shown to promote mild diuresis (Rogers et al., 2017), a profile that plausibly underlies the traditional tea‑ and decoction‑based uses. Recent research focuses on the antioxidant capacity of the anthocyanin fraction for potential functional‑food applications, yet commercial exploitation is limited by the plant’s protected status in the United Kingdom and by its inherent toxicity, so the species continues to be harvested only in small, non‑commercial amounts by a handful of rural practitioners.

General Uses Top

Suggest a correction!

Common products:
- Ornamental bulbs sold by horticulture retailers for garden planting.
- Cut‑flower stems harvested from cultivated plants for seasonal floral arrangements.
- Landscape plantings for naturalistic displays in parks, woodland edges, and private gardens, used in mass plantings to achieve seasonal colour.

Properties relevant to use:
- Hyacinthoides non‑scripta produces large, fleshy bulbs that store starch and reserve carbohydrates; bulbs can be lifted, stored at low temperature (≈4 °C) and forced to flower under controlled conditions, enabling reliable commercial propagation and cut‑flower production.
- The species exhibits a clear early‑spring blooming period (April–May in the UK), producing stems typically 20–30 cm high; the height and blue‑violet colour of the flowers are prized attributes for decorative arrangements.
- Bulb size and firmness are key commercial criteria; bulbs ≥ 2 cm diameter are considered marketable, and the absence of rot or fungal infection is a prerequisite for horticultural quality.
- The relatively short stem length and sturdy inflorescence provide a long vase life for cut‑flower arrangements, typically lasting 7–10 days in water.

Standards and regulation:
- Within the European Union, the marketing of vegetative propagating material is governed by the EU Plant Reproductive Material legislation (e.g., Council Directive 1999/57/EC, Commission Directive 2008/62/EC), which requires that bulbs be certified for health, trueness to type, and proper labeling before sale.
- The International Flower Bulb Association (IFBA) publishes grade standards for bluebell bulbs that specify minimum diameter, disease‑free status, and uniform colour; producers typically adhere to these standards for trade.
- In the United Kingdom, the plant is protected under the Wildlife and Countryside Act 1981, prohibiting the uprooting or digging up of wild specimens without a licence; commercial sourcing therefore relies on cultivated bulbs and seed‑propagated material from licensed nurseries.
- UK Plant Health Regulations (as amended 2019) require phytosanitary certification for the movement of bulb material to prevent the introduction of quarantine pests.

Sustainability and sourcing:
- The primary production method is vegetative propagation of bulbs in specialist nurseries, which reduces pressure on wild populations and allows traceability to the original seed source.
- Sustainable practices include rotating nursery beds, using certified disease‑free mother stock, and adhering to EU/UK phytosanitary rules to prevent the spread of pests such as nematodes and fungal pathogens.
- Certification schemes such as the EU Organic Regulation and the UK Soil Association’s “Organic” label can be applied to bluebell bulb production, offering market differentiation for growers adhering to reduced‑input cultivation.

Synonyms Top

Scientific name Authority First published in
Hyacinthus campanulatus Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Hyacinthus cernuus L. Sp. Pl. : 317 (1753)
Hyacinthus non-scriptus L. Sp. Pl. : 316 (1753)
Hyacinthus nutans (Sm.) Gray Nat. Arr. Brit. Pl. 2: 177 (1821 publ. 1822)
Hyacinthus pratensis Lam. Fl. Franç. 3: 271 (1779)
Hylomenes non-scripta (L.) Salisb. Gen. Pl. : 26 (1866)
Lagocodes cernua (L.) Raf. Fl. Tellur. 2: 25 (1837)
Lagocodes belgica Raf. Autik. Bot. : 124 (1840)
Lagocodes nutans (Sm.) Raf. Fl. Tellur. 2: 25 (1837)
Scilla cernua (L.) Salisb. Prodr. Stirp. Chap. Allerton : 242 (1796)
Scilla festalis Salisb. Prodr. Stirp. Chap. Allerton : 242 (1796)
Syncodium nutans (Sm.) Raf. Fl. Tellur. 2: 22 (1837)
Scilla nutans Sm. Engl. Bot. : t. 377 (1796)
Usteria non-scripta (L.) Chouard Bull. Soc. Bot. France 81: 625, in obs. 1934
Usteria secunda Medik. Ann. Bot. (Usteri) 2: 12. 1791
Usteria hyacinthiflora Medik. Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. vi. Phys. (1790) 480.
Agraphis cernua (L.) Rchb. Fl. Germ. Excurs. : 105 (1830)
Agraphis nutans (Sm.) Link Handbuch 1: 166 (1829)
Endymion cernuus Dumort. Fl. Belg. : 140 (1827)
Endymion lacaillei Corb. Nouv. Fl. Normandie : 574 (1894)
Endymion non-scriptus (L.) Garcke Fl. N. Mitt.-Deutschland : 322 (1849)
Endymion nutans (Sm.) Dumort. Fl. Belg. : 140 (1827)
Hyacinthoides non-scripta var. cernua (L.) P.Silva Fl. Veg. Serra da Estrela , ed. 3: 13 (1999)
Scilla non-scripta subsp. cernua (L.) K.Richt. Pl. Eur. 1: 221. 1890 (1890)
Scilla nonscripta (L.) Hoffmanns. & Link Neue Schriften Ges. Naturf. Freunde Berlin 4: 19 (1803)
Hyacinthoides non-scripta (L.) Chouard Bull. Soc. Bot. France 81(7–8): 625 1934

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English scilla nutans sm.
English wild hyacinth
English common bluebell
English fairy flower
English wood bell
English english bluebell
English bluebell
Spanish scilla nutans
Spanish endymion lacaillei
Spanish hyacinthoides non-scripta var. cernua
Spanish hyacinthus cernuus
Spanish hyacinthus nutans
Spanish lagocodes cernua
Spanish hyacinthus pratensis
Spanish endymion non-scriptus
Spanish endymion nutans
Spanish usteria secunda
Spanish scilla festalis
Spanish hyacinthus campanulatus
Arabic صفير غير سكريبتا
co endymion non-scriptus
Czech hyacintovec britský
Welsh clychau'r gog
Welsh croeso haf
Danish endymion non-scriptus
Danish almindelig klokkeskilla
German englisches hasenglöckchen
German waldhyazinthe
German atlantisches hasenglöckchen
German eigentliches hasenglöckchen
Esperanto arbarhiacinto
Persian زنگولهآبی
Finnish englanninsinililja
French endymion penché
French jacinthe sauvage
French petite jacinthe
French scille penchée
French jacinthe des bois
fy wylde hyasint
Irish coinnle corra
Upper Sorbian jasna česnička
Japanese イングリッシュ・ブルーベル
Cornish bleujen an gog
lb bësch-hyazinth
Macedonian непишано сино ѕвонче
Malayalam ഹയാസിന്തോയിഡ്സ് നോൺ-സ്ക്രിപ്റ്റ
Norwegian Bokmål klokkeblåstjerne
Dutch boshyacint
Dutch wilde hyacint
Norwegian Nynorsk klokkeblåstjerne
Slovenian kimasta neprava hijacinta
Swedish engelsk klockhyacint
Chinese 蓝铃花
Chinese 蓝海葱
Chinese 无斑蓝铃花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds directly at 4°C.
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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Germany
      • Netherlands
    • Northern Europe
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Italy
      • Romania
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Northern America
    • Northeastern U.S.A.
      • Indiana
      • New York
      • Ohio
      • Pennsylvania
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Kentucky
      • Virginia
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000664295
UNII 5F658PFU56
Canadensys 2732
USDA Plants HYNO
Tropicos 18405712
INPN 103057
Flora of Italy 6875
KEW urn:lsid:ipni.org:names:971733-1
The Plant List kew-278557
Missouri Botanical Garden 282392
Open Tree Of Life 268365
NCBI Taxonomy 81762
NBN Atlas NBNSYS0000002185
Nature Serve 2.134494
IPNI 971733-1
iNaturalist 56132
GBIF 5304283
Freebase /m/013zv4
EPPO HCJNS
USDA GRIN 405254
Wikipedia Hyacinthoides_non-scripta

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
Application of metabolomics and molecular networking in investigating the chemical profile and antitrypanosomal activity of British bluebells (Hyacinthoides non-scripta). Raheem DJ, Tawfike AF, Abdelmohsen UR, Edrada-Ebel R, Fitzsimmons-Thoss V Sci Rep 22-Feb-2019
PMCID:PMC6385288
doi:10.1038/S41598-019-38940-W
PMID:30796274
Identification of malonated anthocyanins in the liliaceae and labiatae Kosaku Takeda, Jeffrey B. Harborne, Ron Self Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80089-9
Polyhydroxylated pyrrolidine and pyrrolizidine alkaloids from Hyancinthoides non-scripta and Scilla campanulata. Kato A, Adachi I, Miyauchi M, Ikeda K, Komae T, Kizu H, Kameda Y, Watson AA, Nash RJ, Wormald MR, Fleet GW, Asano N Carbohydr Res 31-Mar-1999
doi:10.1016/S0008-6215(99)00043-9
PMID:10515698

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Eleostearic acid 93077 Click to see 278.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Nucleosides, nucleotides, and analogues / 5-deoxyribonucleosides / 5-deoxy-5-thionucleosides
5'-Methylthioadenosine 439176 Click to see 297.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
Xanthosine 64959 Click to see 284.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
5-Methyluridine 445408 Click to see 258.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
Uridine 6029 Click to see 244.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleotides / Pyrimidine ribonucleotides / Pyrimidine ribonucleoside monophosphates
Uridine Monophosphate 6030 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O 324.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Arginine and derivatives
DL-Arginine 232 Click to see 174.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Ergothioneine 5351619 Click to see 229.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
DL-Tyrosine 1153 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Glu-Gly 6427052 Click to see C(CC(=O)O)C(C(=O)NCC(=O)O)N 204.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
L-Valyl-L-proline 9837272 Click to see 214.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
Valylleucine 6993118 Click to see 230.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid 311 Click to see 192.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
Isocitric Acid 1198 Click to see 192.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Hydroxyisobutyric acid 11671 Click to see CC(C)(C(=O)O)O 104.10 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3,4-trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 71446712 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,5R)-2-[(1S)-2-[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxyethyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 100989165 Click to see 325.31 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
(2R,3R,4S,5R)-2-[(2S)-2-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-2-hydroxyethoxy]oxane-3,4,5-triol 15489823 Click to see C1C(C(C(C(O1)OCC(C2C(C(C(N2)CO)O)O)O)O)O)O 325.31 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
2-[2-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxyethyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 162973393 Click to see C1C(C(C(O1)OCC(C2C(C(C(N2)CO)O)O)O)O)(CO)O 325.31 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses / Gluconolactones
delta-Gluconolactone 7027 Click to see 178.14 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
2,3-Dihydroxybutanedioic Acid 875 Click to see 150.09 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,2,6,8-Tetrahydroxyxanthone 5281658 Click to see 260.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Dithiolanes / Lipoic acids and derivatives
alpha Lipoic acid 864 Click to see 206.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Dl-Tryptophan 1148 Click to see 204.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Serotonin 5202 Click to see C1=CC2=C(C=C1O)C(=CN2)CCN 176.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Dehydroascorbate (bicyclic 835 Click to see 174.11 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol 8369 Click to see 126.11 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Organoheterocyclic compounds / Pyrrolidines
1,4-Dideoxy-1,4-imino-d-arabinitol 451991 Click to see C1C(C(C(N1)CO)O)O 133.15 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
2-(3,6-Dihydroxyheptyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol 85280839 Click to see 263.33 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
2-(Hydroxymethyl)pyrrolidine-3,4-diol 1335 Click to see 133.15 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
2(R), 4(R)-dihydroxypyrrolidine 1472 Click to see 163.17 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
> Organoheterocyclic compounds / Pyrrolizidines
(1S,2S,3S,5R,6R,7R,8S)-3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,6,7-tetrol 53494067 Click to see 219.23 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,6,7-tetrol 73316637 Click to see CC1C(C(C2N1C(C(C2O)O)CO)O)O 219.23 unknown https://doi.org/10.1016/S0008-6215(99)00043-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
5-O-Caffeoylshikimic acid 5281762 Click to see 336.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
Malonylawobanin 5281258 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 859.70 unknown https://doi.org/10.1016/0031-9422(86)80089-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see 286.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385288/

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.