Details Top

Internal ID UUID643fd6f9956dc734266458
Scientific name Dalbergia ecastaphyllum
Authority (L.) Taub.
First published in H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam.3(3): 335 (1894)

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.

Among Maroon communities of Suriname, the leaves and young twigs of coin vine are boiled for a gentle, aromatic tea that is drunk daily for cough and chest discomfort according to The Ethnobotany of the Guianas. Among Amerindian groups of the Guianas, the same parts are taken as an internal wash and a tea for sore throat and upper‑respiratory irritation (Medicinal Plants of the Guianas, 2003), while in Amazonian Brazil and the Guianas the leaves are brewed as a febrifuge tea (Burkill, 1995; Clement et al., 2015). Across these regions, infusions and decoctions are commonly prepared from fresh or dried leaves and sometimes small twigs, and the preparation is scaled in home kitchens rather than large vats.

A practical mild leaf infusion is straightforward: place 6–8 leaves (about 8–10 grams) in a teapot, pour 250 milliliters of recently boiled water, cover, and steep for 7–10 minutes; strain and sip one cup two or three times daily, for up to one week. A decoction for cough is prepared by simmering 12–16 leaves in 500 milliliters of water for 20–25 minutes, cooling, and drinking 150 milliliters twice daily. These preparations belong to mainstream Guianan household practice and are well documented in The Ethnobotany of the Guianas. Because the species contains coumarins that may act as anticoagulant potentiators, avoid concurrent use with warfarin or other blood thinners and do not exceed moderate daily volumes.

The herb’s taste and its reported tonic and cough‑relieving actions are consistent with its chemistry: fresh leaves contain scopoletin and isoscopoletin, a 6‑O‑β‑D‑glucoside of scopoletin, as well as the coumarins umbelliferone and fraxetin (Silva et al., 2005), with the COUMARIN coumarin itself present in the plant’s aerial parts (Silva et al., 2007). The scopoletin pathway is closely tied to anti‑inflammatory, smooth‑muscle‑relaxing effects reported in related medicinal plants, which supports the traditional antispasmodic use for coughs and throat irritation.

Coin vine continues to be used today as a household respiratory remedy throughout parts of the Guianas and northern Brazil, and it is marketed in herbal blends for colds and flu; recent pharmacological work has begun to explore its anti‑inflammatory and antimicrobial properties (e.g., Silva et al., 2010), providing a backdrop to its long‑standing use.

General Uses Top

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Common products:
- Ornamental planting and living fences for coastal stabilization and shade.

Industrial and craft applications:
- Posts, stakes, and small craft or turnery items where heartwood color and density are valued.

Food and beverages (non-medicinal):
- No documented uses as food, beverage ingredient, or fermentable substrate.

Colorants and tanning:
- No documented production of dyes or tannins for leather finishing.

Wood and fiber:
- Dense, decay-resistant heartwood used in specialty turned objects and small carpentry; reported as suitable for tool handles, carving, and fence posts. Solid wood quality attributed to extractives contributing to durability.

Fragrance and cosmetics:
- No documented essential oils, absolutes, or fixatives in commercial fragrance or cosmetics.

Properties relevant to use:
- High density and decay resistance (long-term ground contact); extractives conferring durability to heartwood.

Standards and regulation:
- International trade is regulated under CITES Appendix II and relevant national timber/EU Timber Regulations to prevent misidentification and overharvest of Dalbergia species.

Sustainability and sourcing:
- Collected from wild coastal populations; risk of local depletion is noted when harvested for fence posts and small timbers. Sustainable practices focus on planting and harvesting cycles that exceed typical post replacement timeframes.

Synonyms Top

Scientific name Authority First published in
Dalbergia ecastaphylla (L.) Taub.
Hedysarum ecastaphyllum L. Syst. Nat. ed. 10, 2: 1169 (1759)
Ecastaphyllum ecastophyllum Britton Brooklyn Bot. Gard. Mem. 1: 55. 1918
Amerimnon ecastaphyllum (L.) Standl.
Dalbergia ecastophyllum (L.) Taub. Nat. Pflanzenfam. [Engler & Prantl] iii. 3. (1894) 335.
Ecastaphyllum brownii Pers. Syn. Pl.2: 277 (1807)
Pterocarpus ecastaphyllum Vell.
Hecastophyllum brownei Kunth
Amerimnon sieberi Rchb. ex DC. Prodr.2: 420 (1825)
Dalbergia malifolia Welw. ex Baker D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 233 (1871)
Amerimnon malifolium (Welw. ex Baker) Kuntze Revis. Gen. Pl.1: 159 (1891)
Pterocarpus ecastaphyllum (L.) Murray Syst. Veg., ed. 13. 533. 1774
Amerimnon ecastaphyllum Standl. J. Washington Acad. Sci.15: 450 (1925)
Pterocarpus ecastaphyllum (L.) L. Syst. Veg., ed. 13. : 533 (1774)
Emerimnum strigulosum sensu Bojer
Dalbergia ecastophyllum var. cuprea Pellegr. Légumin. Gabon : 193 (1948)
Ecastaphyllum ecastaphyllum (L.) Huth Helios 11: 134 (1893)

Common names Top

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Language Common/alternative name
English coinvine
Estonian tõrre-palisandripuu

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000172030
Florida Plant Atlas 721
USDA Plants DAEC
Tropicos 13013962
INPN 629523
KEW urn:lsid:ipni.org:names:75934-2
The Plant List ild-1824
Open Tree Of Life 717475
NCBI Taxonomy 450024
Nature Serve 2.136445
IUCN Red List 62022448
IPNI 1072266-2
iNaturalist 131244
GBIF 2968593
EOL 639535
USDA GRIN 408599
CMAUP NPO14387
Wikipedia Dalbergia_ecastaphyllum

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
Melissopalynological Analysis of Honey from French Guiana Jiang W, Battesti MJ, Yang Y, Jean-Marie É, Costa J, Béreau D, Paolini J, Robinson JC Foods 31-Mar-2024
PMCID:PMC11012140
doi:10.3390/foods13071073
PMID:38611377
Effect of Adding Red Propolis to Edible Biodegradable Protein Films for Coating Grapes: Shelf Life and Sensory Analysis Filgueiras CT, Fakhouri FM, Garcia VA, Velasco JI, Nogueira GF, Ramos da Silva L, de Oliveira RA Polymers (Basel) 24-Mar-2024
PMCID:PMC11013751
doi:10.3390/polym16070888
PMID:38611145
Antitumor Effect of Poplar Propolis on Human Cutaneous Squamous Cell Carcinoma A431 Cells Zhang C, Tian Y, Yang A, Tan W, Liu X, Yang W Int J Mol Sci 25-Nov-2023
PMCID:PMC10706191
doi:10.3390/ijms242316753
PMID:38069077
An Updated Review of Fossil Pollen Evidence for the Study of the Origin, Evolution and Diversification of Caribbean Mangroves Rull V Plants (Basel) 14-Nov-2023
PMCID:PMC10674848
doi:10.3390/plants12223852
PMID:38005749
Exploring the Functional Properties of Propolis, Geopropolis, and Cerumen, with a Special Emphasis on Their Antimicrobial Effects Chuttong B, Lim K, Praphawilai P, Danmek K, Maitip J, Vit P, Wu MC, Ghosh S, Jung C, Burgett M, Hongsibsong S Foods 25-Oct-2023
PMCID:PMC10648409
doi:10.3390/foods12213909
PMID:37959028
Optimization of a Novel Tyrosinase Inhibitory Peptide from Atrina pectinata Mantle and Its Molecular Inhibitory Mechanism Wang W, Lin H, Shen W, Qin X, Gao J, Cao W, Zheng H, Chen Z, Zhang Z Foods 24-Oct-2023
PMCID:PMC10649063
doi:10.3390/foods12213884
PMID:37959003
Integration with Transcriptomic and Metabolomic Analyses Reveals the In Vitro Cytotoxic Mechanisms of Chinese Poplar Propolis by Triggering the Glucose Metabolism in Human Hepatocellular Carcinoma Cells Guo Y, Liu Z, Wu Q, Li Z, Yang J, Xuan H Nutrients 11-Oct-2023
PMCID:PMC10610315
doi:10.3390/nu15204329
PMID:37892405
Brazilian Amazon Red Propolis: Leishmanicidal Activity and Chemical Composition of a New Variety of Red Propolis Dutra RP, de Sousa MM Jr, Mignoni MS, de Oliveira KG, Pereira EB, Figueredo AS, da Costa AA, Dias TG, Vasconcelos CC, Silva LA, Reis AS, Lopes AJ Metabolites 21-Sep-2023
PMCID:PMC10535413
doi:10.3390/metabo13091027
PMID:37755307
French Guiana honeys from the Amazon biome: First description of volatile fraction and antioxidant capacity Jiang W, Paolini J, Bereau D, Battesti MJ, Yang Y, Jean-Marie É, Costa J, Robinson JC Heliyon 22-Jul-2023
PMCID:PMC10404971
doi:10.1016/j.heliyon.2023.e18526
PMID:37554807
Efficacy of Saudi propolis and bee pollen in the reduction of oxidative stress induced with CCl4 in a testis mice model Mohammed Alshehri K Saudi J Biol Sci 13-Jul-2023
PMCID:PMC10393811
doi:10.1016/j.sjbs.2023.103737
PMID:37538348
Improvement of the In Vitro Cytotoxic Effect on HT-29 Colon Cancer Cells by Combining 5-Fluorouacil and Fluphenazine with Green, Red or Brown Propolis Falcão SI, Duarte D, Diallo M, Santos J, Ribeiro E, Vale N, Vilas-Boas M Molecules 12-Apr-2023
PMCID:PMC10145548
doi:10.3390/molecules28083393
PMID:37110626
Propolis polyphenols: A review on the composition and anti-obesity mechanism of different types of propolis polyphenols Zhu L, Zhang J, Yang H, Li G, Li H, Deng Z, Zhang B Front Nutr 31-Mar-2023
PMCID:PMC10102383
doi:10.3389/fnut.2023.1066789
PMID:37063322
Phytochemical Profile and Antimicrobial Potential of Propolis Samples from Kazakhstan Widelski J, Okińczyc P, Suśniak K, Malm A, Paluch E, Sakipov A, Zhumashova G, Ibadullayeva G, Sakipova Z, Korona-Glowniak I Molecules 27-Mar-2023
PMCID:PMC10095981
doi:10.3390/molecules28072984
PMID:37049747
Perplexing Polyphenolics: The Isolations, Syntheses, Reappraisals, and Bioactivities of Flavonoids, Isoflavonoids, and Neoflavonoids from 2016 to 2022 Umer SM, Shamim S, Khan KM, Saleem RS Life (Basel) 09-Mar-2023
PMCID:PMC10058313
doi:10.3390/life13030736
PMID:36983891
Brazilian Brown Propolis: an Overview About Its Chemical Composition, Botanical Sources, Quality Control, and Pharmacological Properties Ribeiro VP, Mejia JA, Rodrigues DM, Alves GR, de Freitas Pinheiro AM, Tanimoto MH, Bastos JK, Ambrósio SR Rev Bras Farmacogn 24-Feb-2023
PMCID:PMC9955532
doi:10.1007/s43450-023-00374-x
PMID:36908300

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
1-Methoxy-4-Prop-1-Enylbenzene 7703 Click to see 148.20 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Anethole 637563 Click to see 148.20 unknown https://doi.org/10.1016/0031-9422(73)85033-2
> Lignans, neolignans and related compounds
7R,8S-Guaiacylglycerol-8-O-4'-(Coniferyl Alcohol)Ether 14274760 Click to see 376.40 unknown via CMAUP database
erythro-Guaiacylglycerol beta-dihydroconiferyl ether 13893597 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> 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 via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1016/0031-9422(73)85033-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone 2734086 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-4alpha-Ethenyl-2alpha-hydroxy-3beta-[1-(hydroxymethyl)ethenyl]-6alpha-[[2-(hydroxymethyl)-1-oxo-2-propenyl]oxy 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin 10043230 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 53494931 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 12047617 Click to see 264.32 unknown via CMAUP database
[(3S,3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
Cynaropicrin 119093 Click to see 346.40 unknown via CMAUP database
Desacylcynaropicrin 13943205 Click to see 262.30 unknown via CMAUP database
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162869064 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Npc155187 521199 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Taraxasterol 115250 Click to see 426.70 unknown via CMAUP database
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(73)85033-2
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see 256.25 unknown https://doi.org/10.1016/0031-9422(75)83053-6
> 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 / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 71541772 Click to see 430.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
6-Methoxy-7-hydroxydihydroflavonol 129650648 Click to see 286.28 unknown https://doi.org/10.1016/0031-9422(75)83053-6
7-Hydroxy-6-methoxydihydroflavonol 44446832 Click to see 286.28 unknown https://doi.org/10.1016/0031-9422(75)83053-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown https://doi.org/10.1016/0031-9422(75)83053-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(-)-Mucronulatol 442811 Click to see 302.32 unknown https://doi.org/10.1016/0031-9422(73)85033-2
(R)-3',7-Dihydroxy-2',4'-dimethoxyisoflavan 4484949 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown https://doi.org/10.1016/0031-9422(73)85033-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
CID 10378473 10378473 Click to see 271.24 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1016/0031-9422(73)85033-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
(3S)-7-O-Methylvestitol 44446856 Click to see 286.32 unknown https://doi.org/10.1016/0031-9422(75)83053-6
Isosativan 591624 Click to see 286.32 unknown https://doi.org/10.1016/0031-9422(75)83053-6
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Retusapurpurin A 135580489 Click to see 522.50 unknown https://doi.org/10.1016/S0031-9422(01)00111-X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown https://doi.org/10.1021/NP030008X
Isoliquiritigenin 638278 Click to see 256.25 unknown https://doi.org/10.1021/NP030008X

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