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Dalbergia ecastaphyllum

Dalbergia ecastaphyllum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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)

Description Top

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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)

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

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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

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
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
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
Phenolic Constituents, Antioxidant and Antimicrobial Activity and Clustering Analysis of Propolis Samples Based on PCA from Different Regions of Anatolia Altuntaş Ü, Güzel İ, Özçelik B Molecules 22-Jan-2023
PMCID:PMC9920892
doi:10.3390/molecules28031121
PMID:36770788
Essential Oils and Terpenic Compounds as Potential Hits for Drugs against Amitochondriate Protists Menezes SA, Tasca T Trop Med Infect Dis 05-Jan-2023
PMCID:PMC9865018
doi:10.3390/tropicalmed8010037
PMID:36668944
Natural products and extracts from plants as natural UV filters for sunscreens: A review Li L, Chong L, Huang T, Ma Y, Li Y, Ding H Animal Model Exp Med 19-Dec-2022
PMCID:PMC10272908
doi:10.1002/ame2.12295
PMID:36536536
Potential in vitro anti-periodontopathogenic, anti-Chikungunya activities and in vivo toxicity of Brazilian red propolis Silva NB, de Souza JH, Santiago MB, da Silva Aguiar JR, Martins DO, da Silva RA, de Andrade Santos I, Aldana-Mejía JA, Jardim AC, dos Santos Pedroso R, Ambrósio SR, Veneziani RC, Bastos JK, Pires RH, Martins CH Sci Rep 07-Dec-2022
PMCID:PMC9729292
doi:10.1038/s41598-022-24776-4
PMID:36477635
Propolis, Aloe Vera, Green Tea, Cranberry, Calendula, Myrrha and Salvia Properties against Periodontal Microorganisms Figueiredo LC, Figueiredo NF, da Cruz DF, Baccelli GT, Sarachini GE, Bueno MR, Feres M, Bueno-Silva B Microorganisms 31-Oct-2022
PMCID:PMC9693270
doi:10.3390/microorganisms10112172
PMID:36363764
Molecular and Cellular Mechanisms of Propolis and Its Polyphenolic Compounds against Cancer Oršolić N, Jazvinšćak Jembrek M Int J Mol Sci 09-Sep-2022
PMCID:PMC9499605
doi:10.3390/ijms231810479
PMID:36142391

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 COC(=O)C1=CC=C(C=C1)O 152.15 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Methoxy-4-propenylbenzene 7703 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/0031-9422(73)85033-2
> Lignans, neolignans and related compounds
(1R,2S)-1-(3-Methoxy-4-hydroxyphenyl)-2-[2-methoxy-4-[(E)-3-hydroxy-1-propenyl]phenoxy]-1,3-propanediol 14274760 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown via CMAUP database
2-Methoxy-4-[(1R,2S)-1,3-dihydroxy-2-[2-methoxy-4-(3-hydroxypropyl)phenoxy]propyl]phenol 13893597 Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 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
Tetracosanoic 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
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemacarmanin 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 C=C1CC2C(C(C3C1CC(C3=C)O)OC(=O)C(=C)CO)C(=C)C(=O)O2 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 CC1=CCCC(=CC(C2C(C1)OC(=O)C2=C)OC(=O)C(=C)CO)C=O 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,6abeta,9abeta,9balpha)-Decahydro-8alpha-hydroxy-6,9-bis(methylene)-4beta-[(3-hydroxy-2-methylenepropanoyl)oxy]-3beta-methylazuleno[4,5-b]furan-2(3H)-one 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
11,13-Dihydrodesacylcynaropicrin 12047617 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown via CMAUP database
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown via CMAUP database
Desacylcynaropicrin 13943205 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 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
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Stigmast-5-en-3-yl acetate 521199 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(73)85033-2
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 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
(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
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 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 COC(=O)C1=CNC2=CC=CC=C21 175.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 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 COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O 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 COC1=C(C=C2C(=C1)C(=O)C(C(O2)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(75)83053-6
7-Hydroxy-6-methoxydihydroflavonol 44446832 Click to see COC1=C(C=C2C(=C1)C(=O)C(C(O2)C3=CC=CC=C3)O)O 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 C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 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 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
Mucronulatol 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 COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 271.24 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 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 COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)OC)OC2)O 286.32 unknown https://doi.org/10.1016/0031-9422(75)83053-6
Isosativan 591624 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)OC)OC2)O 286.32 unknown https://doi.org/10.1016/0031-9422(75)83053-6
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
2-(4-hydroxy-2-methoxyphenyl)-4-(4-hydroxyphenyl)-6-(7-methoxy-3,4-dihydro-2H-chromen-3-yl)chromen-7-one 135580489 Click to see COC1=CC2=C(CC(CO2)C3=CC4=C(C=C(OC4=CC3=O)C5=C(C=C(C=C5)O)OC)C6=CC=C(C=C6)O)C=C1 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
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP030008X
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP030008X

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