Details Top

Internal ID UUID643ff8dc10769262491995
Scientific name Ribes sanguineum
Authority Pursh
First published in Fl. Amer. Sept. 1: 164 (1813)

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.

Ethnobotanical sources record specific infusions and decoctions for ribes sanguineum in several Northwest Coast communities. Among the Straits Salish and Nooksack, an infusion of the young leaves was taken as a gentle bitter to stimulate digestion and as a spring tonic, and dried berries were infused for colds and fevers; Turner and Bell’s 1983 account of the River pathway uses the term “infusion” for both leaf and berry preparations. Turner’s later synthesis of the ethnobotany of Northwest Coast peoples confirms that the bitter leaf infusion was a well-known winter and spring digestive remedy. On the coast of British Columbia, traditional herbalists prepared strong, short decoctions of the leaf for colds and sore throats, and a cool leaf infusion was taken for inflammation of the eyes. Toward the east of the region, Blackfoot and Ktunaxa healers prepared a decoction of the leaves and twigs to treat gastrointestinal upset and mild fevers, practices recorded by Moerman’s Native American Ethnobotany database and Turner’s classic 1995 overview of regional medicinal plants. Early Euro‑American settlers in the Pacific Northwest adopted the same leaf infusion for “stomach complaints,” noting its distinctive fragrance and bitter flavor.

A practical and commonly described preparation is a mild leaf infusion. Use 1 tablespoon of fresh or 2 teaspoons of finely chopped dried young leaf per 240 milliliters of just‑boiled water; cover and steep for 10 to 15 minutes, then strain. Take a small cup (60–90 milliliters) two or three times daily as needed. A complementary approach is a simple 1:5 tincture: macerate 20 grams of dried leaf in 100 milliliters of 40–45 percent ethanol for two weeks in a cool, dark place, shaking daily; strain and keep in amber glass. Dose typically 1 to 2 milliliters in water, two or three times daily. There are no modern dose standards for this species; the preparations are used sparingly and discontinued if symptoms persist. Because the plant is widely cultivated as an ornamental, avoid material from treated or roadside sites; while no major toxicities are reported, the safety of extended use and use during pregnancy or by children has not been established.

Phytochemical work on ribes sanguineum supports the plausibility of traditional applications. Anthocyanins such as cyanidin‑3‑O‑glucoside, quercetin‑ and kaempferol‑based flavonols, and phenolic acids like gallic and caffeic acid have been consistently detected in the foliage and berries (Junker et al., 2012; Jin et al., 2014). These antioxidants, along with tannins that contribute the characteristic bitterness, are known to modulate digestive secretions and oxidative stress, which aligns with the bitter digestive infusions and anti‑inflammatory uses described above.

Commercial interest today is modest; most modern use of ribes sanguineum remains ornamental, yet the documented medicinal infusions continue to be prepared and transmitted locally, and contemporary studies of its phenolic profile maintain interest in its gentle digestive properties.

General Uses Top

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Common products:
Ornamental horticulture cultivar Ribes sanguineum var. glutinosum (e.g., ‘King Edward VII’, ‘Pulborough Scarlet’) is widely cultivated for landscape use as a shrub with pendent inflorescences. Berries are used in home preservation (jams, jellies), though taste and flavor are generally considered mediocre to tart; consumption is culinary only, with no health claims.

Wood and fiber:
Not a timber species; stems occasionally used for light basketry or small craft items in home craft contexts.

Properties relevant to use:
Early deciduous habit, arching growth form, and pendulous racemes confer aesthetic value for ornamental design. Fruit acidity and pectin content support standard jam/gel preparation methods (typical pectin-based gelling in high‑acid fruit).

Synonyms Top

Scientific name Authority First published in
Ribes alceifolium Kunze ex Walp. Nov. Actorum Acad. Caes. Leop.-Carol. Nat. Cur. 19(Suppl. 1): 343 (1843)
Ribes tubulosum Eschsch. Mém. Acad. Imp. Sci. St. Pétersbourg Hist. Acad. 10: 283 (1826)
Ribes tubiflorum C.A.Mey. Nouv. Mém. Soc. Imp. Naturalistes Moscou 1: 140 (1829)
Ribes scuphami Eastw. Proc. Calif. Acad. Sci. , ser. 3, 2: 242 (1902)
Calobotrya sanguinea Spach Ann. Sci. Nat., Bot. sér. 2, 4: 21. 1835
Coreosma sanguinea Spach Hist. Nat. Vég. (Spach) 6: 155. 1838 [Jan 1838 publ. 10 Mar 1838]
Ribes sanguineum var. melanocarpum (Greene) Jeps. Fl. Calif. 2: 148 (1936)
Ribes glutinosum var. melanocarpum Greene Man. Bot. San Francisco 124. 1894 [2 Feb 1894]
Ribes sanguineum var. deductum Jeps. Man. Fl. Pl. Calif. : 469 (1925)
Ribes sanguineum var. albescens Rehder Stand. Cycl. Hort. 5: 2958 (1916)

Common names Top

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Language Common/alternative name
English red flowering currant
English redflower currant
English red currant
English flowering currant
English red-flowering currant
Czech meruzalka krvavá
Welsh llwyn cwrens blodeuog
Danish blod-ribs
German blut-johannisbeere
German blutjohannisbeere
Finnish ruusuherukka
French groseillier à fleurs
Upper Sorbian krejčerwjeny januškowc
Hungarian vérvörös ribiszke
Icelandic blóðrifs
Japanese ハナスグリ
Norwegian Bokmål blodrips
Dutch bloeiende bes
Dutch bloeibes
Dutch rode ribes
Norwegian Nynorsk blodrips
Polish porzeczka krwista
Russian Смородина кроваво-красная
Swedish rosenrips
Ukrainian Порічки криваво-червоні
Ukrainian Порічки криваві
Ukrainian Смородина криваво-червона
Chinese 绯红茶藨子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Ribes sanguineum var. glutinosum (Benth.) Loudon Arbor. Frutic. Brit. 2: 988 (1838)
Ribes sanguineum var. sanguineum Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Czechoslovakia
      • Germany
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southwestern Europe
      • Spain
  • Northern America
    • Mexico
      • Mexican Pacific Islands
    • Northwestern U.S.A.
      • Idaho
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000405232
Canadensys 6085
USDA Plants RISA
Tropicos 29100540
INPN 117775
KEW urn:lsid:ipni.org:names:317405-2
The Plant List kew-2426680
Plantarium 31945
Open Tree Of Life 104008
Observations.org 9216
NCBI Taxonomy 175201
NBN Atlas NBNSYS0000003516
Nature Serve 2.159798
IPNI 317405-2
iNaturalist 53435
GBIF 2986130
Freebase /m/0c4nmx
EPPO RIBSA
EOL 583213
Calflora (Californian flora) 7141
USDA GRIN 31862
Wikipedia Ribes_sanguineum
CMAUP NPO2741

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_048173275.1 drRibSang1_p1.1 Scaffold Canada's national platform for genome sequencing and analysis 2025-02-27 24.26 708.50 Mb

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
Self-assembled, disordered structural color from fruit wax bloom Middleton R, Tunstad SA, Knapp A, Winters S, McCallum S, Whitney H Sci Adv 07-Feb-2024
PMCID:PMC10849586
doi:10.1126/sciadv.adk4219
PMID:38324684
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Morpho-Phylo Taxonomy of Novel Dothideomycetous Fungi Associated With Dead Woody Twigs in Yunnan Province, China Mortimer PE, Jeewon R, Xu JC, Lumyong S, Wanasinghe DN Front Microbiol 23-Mar-2021
PMCID:PMC8021917
doi:10.3389/fmicb.2021.654683
PMID:33833748
Community-level reorganizations following migratory pollinator dynamics along a latitudinal gradient Magrach A, Lara C, Luna UM, Díaz-Infante S, Parker I Proc Biol Sci 01-Jul-2020
PMCID:PMC7423476
doi:10.1098/rspb.2020.0649
PMID:32605514
Vegetation communities on commercial developments are heterogenous and determined by development and landscaping decisions, not socioeconomics Dyson K PLoS One 10-Sep-2019
PMCID:PMC6736242
doi:10.1371/journal.pone.0222069
PMID:31504053
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
Floral organ MADS-box genes in Cercidiphyllum japonicum (Cercidiphyllaceae): Implications for systematic evolution and bracts definition Jin Y, Wang Y, Zhang D, Shen X, Liu W, Chen F PLoS One 31-May-2017
PMCID:PMC5451075
doi:10.1371/journal.pone.0178382
PMID:28562649
Interspecific Variation in Bumblebee Performance on Pollen Diet: New Insights for Mitigation Strategies Moerman R, Roger N, De Jonghe R, Michez D, Vanderplanck M PLoS One 22-Dec-2016
PMCID:PMC5179047
doi:10.1371/journal.pone.0168462
PMID:28005943
Reassessment of Allantonectria, phylogenetic position of Thyronectroidea, and Thyronectria caraganae sp. nov Voglmayr H, Akulov OY, Jaklitsch WM Mycol Prog 01-Sep-2016
PMCID:PMC5295630
doi:10.1007/s11557-016-1218-4
PMID:28184181
The Wide Potential Trophic Niche of the Asiatic Fruit Fly Drosophila suzukii: The Key of Its Invasion Success in Temperate Europe? Poyet M, Le Roux V, Gibert P, Meirland A, Prévost G, Eslin P, Chabrerie O PLoS One 18-Nov-2015
PMCID:PMC4651357
doi:10.1371/journal.pone.0142785
PMID:26581101
Persistent hamathecial threads in the Nectriaceae, Hypocreales: Thyronectria revisited and re-instated Jaklitsch WM, Voglmayr H Persoonia 09-Oct-2014
PMCID:PMC4312933
doi:10.3767/003158514X685211
PMID:25737600
Towards an ontogenetic understanding of inflorescence diversity Claßen-Bockhoff R, Bull-Hereñu K Ann Bot 27-Feb-2013
PMCID:PMC3828942
doi:10.1093/aob/mct009
PMID:23445936
Rate heterogeneity in six protein-coding genes from the holoparasite Balanophora (Balanophoraceae) and other taxa of Santalales Su HJ, Hu JM Ann Bot 21-Sep-2012
PMCID:PMC3478055
doi:10.1093/aob/mcs197
PMID:23041381
Ecological correlates of ex situ seed longevity: a comparative study on 195 species Probert RJ, Daws MI, Hay FR Ann Bot 09-Apr-2009
PMCID:PMC2706723
doi:10.1093/aob/mcp082
PMID:19359301
The Micromorphology of Pit Membranes in Tracheary Elements of Ericales: New Records of Tori or Pseudo-tori? RABAEY D, LENS F, SMETS E, JANSEN S Ann Bot 01-Nov-2006
PMCID:PMC3292242
doi:10.1093/aob/mcl183
PMID:16935867

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
> Benzenoids / Naphthalenes / Naphthols and derivatives
(14S)-2,11,11-trimethyl-7-propan-2-yl-10-oxatricyclo[7.5.1.05,15]pentadeca-1,3,5,7,9(15)-pentaene-8,14-diol 11461177 Click to see 314.40 unknown via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
(1S-(1alpha,4alpha,7alpha))-1,2,3,4,5,6,7,8-Octahydro-1,4,9,9-tetramethyl-4,7-methanoazulene 12313993 Click to see 204.35 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
Isovaleric Acid 10430 Click to see 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
n-Hexacosanyl isovalerate 5318034 Click to see 466.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Nardostachin 196699 Click to see 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Valeranone 10198387 Click to see 222.37 unknown via CMAUP database
(1R,5R,7R,8S,12S)-7,12-dihydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 10684294 Click to see 282.33 unknown via CMAUP database
(1R,5R,7S,8R)-7-hydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 10445631 Click to see 266.33 unknown via CMAUP database
(1S,2R,3R,9S,12S)-12-hydroxy-2,3,11,11-tetramethyl-10-oxatricyclo[7.2.1.02,7]dodec-6-en-8-one 14164972 Click to see CC1CCC=C2C1(C3C(C(C2=O)OC3(C)C)O)C 250.33 unknown via CMAUP database
(1S,5R,7R,8S)-7-hydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 10264902 Click to see CC1CC(=O)C2=C1C(C3(CCC2(OO3)C)C(C)C)O 266.33 unknown via CMAUP database
(1S,5R,7S,8R,12R)-7,12-dihydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 10779259 Click to see 282.33 unknown via CMAUP database
(3R,4R,5R,7S)-4,7-dihydroxy-3,7-dimethyl-5-(2-methylpropanoyl)-3,4,5,6-tetrahydro-2H-inden-1-one 102496243 Click to see 266.33 unknown via CMAUP database
(3R,4S,5S,7R)-4,7-dihydroxy-3,7-dimethyl-5-(2-methylpropanoyl)-3,4,5,6-tetrahydro-2H-inden-1-one 102496242 Click to see 266.33 unknown via CMAUP database
(3R,6S,8R)-6,8-dihydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one 15884945 Click to see 250.33 unknown via CMAUP database
(3R,8R)-8-hydroxy-5-(2-hydroxypropan-2-yl)-3,8-dimethyl-2,3,6,7-tetrahydroazulen-1-one 15884948 Click to see 250.33 unknown via CMAUP database
Isonardosinone 14164971 Click to see 250.33 unknown via CMAUP database
Kanshone A 10466564 Click to see 234.33 unknown via CMAUP database
Kanshone B 14021478 Click to see CC1CC(C=C2C1(C3C(CC2=O)OOC3(C)C)C)O 266.33 unknown via CMAUP database
Nardoguaianone J 5320011 Click to see CC1CC(=O)C2=C1C=C(CCC2(C)O)C(C)C 234.33 unknown via CMAUP database
Nardoguaianone K 5320012 Click to see 234.33 unknown via CMAUP database
Nardosinone 168136 Click to see 250.33 unknown via CMAUP database
Tetrahydronardosinon 12313520 Click to see 252.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(-)-Aristolene 12309878 Click to see 204.35 unknown via CMAUP database
(1aR,3aR,7R,7aR,7bS)-1,1,7,7a-tetramethyl-3,3a,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalene-2,4-dione 102496247 Click to see CC1CCC(=O)C2C1(C3C(C3(C)C)C(=O)C2)C 234.33 unknown via CMAUP database
(1aR,3S,3aS,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2,3,3a,4,5,6,7,7b-octahydro-1aH-cyclopropa[a]naphthalen-3-ol 22215266 Click to see 222.37 unknown via CMAUP database
(1aR,3S,5R,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalene-3,5-diol 102463571 Click to see 236.35 unknown via CMAUP database
1(10)-Aristolen-2-one 71717616 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2)C 218.33 unknown via CMAUP database
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown via CMAUP database
Aristol-9-en-1-ol 21159118 Click to see CC1CCC(C2=CCC3C(C12C)C3(C)C)O 220.35 unknown via CMAUP database
Aristola-1(10),8-dien-2-one 101297625 Click to see 216.32 unknown via CMAUP database
Aristolone 165536 Click to see 218.33 unknown via CMAUP database
Debilon 57391584 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 234.33 unknown via CMAUP database
Kanshone F 636591 Click to see CC1CCC(C2=CC(=O)C3C(C12C)C3(C)C)OC(=O)CC(C)C 318.40 unknown via CMAUP database
Kanshone H 86293425 Click to see 216.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1S,2S,6R,8aR)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,2-diol 102496245 Click to see 236.35 unknown via CMAUP database
(2S,6R,8aS)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-ol 102496246 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol 162890773 Click to see 404.40 unknown https://doi.org/10.1016/0031-9422(75)85197-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4R,4aS,5R)-4-hydroxy-4a,5-dimethyl-5,6-dihydro-4H-naphthalene-1,7-dione 101316814 Click to see 206.24 unknown via CMAUP database
Desoxo-Narchinol A 56835056 Click to see 192.25 unknown via CMAUP database
Nardoaristolone B 71583464 Click to see CC1CC(=O)C=C2C1(C3C(C2=O)C3(C)C)C 218.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
4-Coumaric acid 322 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isopsoralen 10658 Click to see 186.16 unknown via CMAUP database
Oroselol 160600 Click to see CC(C)(C1=CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
2H,8H-Benzo[1,2-b:3,4-b']dipyran-2-one, 9,10-dihydro-9-hydroxy-8,8-dimethyl-, (R)- 759302 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)O)C 246.26 unknown via CMAUP database
Jatamansin 668081 Click to see 328.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(75)85197-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown https://doi.org/10.1016/0031-9422(75)85197-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Tsugafolin 45273057 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-, (2S)- 14157910 Click to see 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(1S,4R,6S,7R,8R,11R)-15-hydroxy-13-methoxy-16-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]-5,5,7,8-tetramethyl-18-oxapentacyclo[9.7.0.01,7.04,6.012,17]octadeca-12,14,16-triene-2,3-dione 71583359 Click to see 530.60 unknown via CMAUP database

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