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Mimosa tenuiflora

Mimosa tenuiflora - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Mimosa tenuiflora - 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 UUID643fd781727a7030966223
Scientific name Mimosa tenuiflora
Authority (Willd.) Poir.
First published in J.B.A.M.de Lamarck, Encycl., Suppl. 1: 82 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mimosa nigra Huber Bull. Herb. Boissier, sér. 2, 1: 303 (1901)
Acacia tenuiflora Willd. Sp. Pl., ed. 4, 4: 1088 (1806)
Mimosa limana Rizzini Leandra3-4(4-5): 14 (1974)
Mimosa cabrera H.Karst. Fl. Columb.2: 63 (1863)
Mimosa hostilis Benth. Trans. Linn. Soc. London30: 415 (1875)
Acacia hostilis Mart. Reise Bras.1: 555 (1823)
Acacia jurema Mart. Reise Bras.2: 788 (1828)
Mimosa apodocarpa var. hostilis Hassl. Repert. Spec. Nov. Regni Veg.9: 1 (1910)

Common names Top

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Language Common/alternative name
English tepezcohuite
English jurema
Azerbaijani dəri ağacı
bpy জুরেমা
Czech citlivka stydlivá
Czech mimosa hostilis
Esperanto nigra ĵuremo
Persian میموسا تنویفلورا
Hebrew מימוזה טניפלורה
Italian mimosa hostilis
Japanese ミモザ・テヌイフローラ
Polish mimosa cabrera
Polish mimosa hostilis
Portuguese jurema-preta
Portuguese mimosa hostilis
Romanian arborele pielii
Russian mimosa cabrera
Russian mimosa hostilis
Russian acacia tenuiflora
Russian mimosa limana
Russian acacia hostilis
Chinese 细花含羞草
Chinese 細花含羞草

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Malesia
      • Jawa
      • Malaya
      • Sumatera
    • Papuasia
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
    • Central America
      • El Salvador
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000174654
UNII OC4S1RE0Z1
Tropicos 13036820
KEW urn:lsid:ipni.org:names:508775-1
The Plant List ild-20760
Open Tree Of Life 530242
NCBI Taxonomy 138060
IUCN Red List 144287589
IPNI 508775-1
iNaturalist 287688
GBIF 2969531
Freebase /m/05tsgk
EOL 640925
USDA GRIN 24430
Wikipedia Mimosa_tenuiflora

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
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Plant-Based Films and Hydrogels for Wound Healing Lopes AI, Pintado MM, Tavaria FK Microorganisms 21-Feb-2024
PMCID:PMC10972459
doi:10.3390/microorganisms12030438
PMID:38543489
Advancing burn wound treatment: exploring hydrogel as a transdermal drug delivery system Goh M, Du M, Peng WR, Saw PE, Chen Z Drug Deliv 16-Feb-2024
PMCID:PMC10878343
doi:10.1080/10717544.2023.2300945
PMID:38366562
The Potential of Wood Vinegar to Replace Antimicrobials Used in Animal Husbandry—A Review Gama GS, Pimenta AS, Feijó FM, de Azevedo TK, de Melo RR, de Andrade GS Animals (Basel) 25-Jan-2024
PMCID:PMC10854697
doi:10.3390/ani14030381
PMID:38338024
Green Synthesis of Metal and Metal Oxide Nanoparticles: A Review of the Principles and Biomedical Applications Radulescu DM, Surdu VA, Ficai A, Ficai D, Grumezescu AM, Andronescu E Int J Mol Sci 20-Oct-2023
PMCID:PMC10607471
doi:10.3390/ijms242015397
PMID:37895077
Plant parentage influences the type of timber use by traditional peoples of the Brazilian Caatinga Pedrosa KM, Ramos MB, La Torre-Cuadros MD, Lopes SD PLoS One 17-Oct-2023
PMCID:PMC10581497
doi:10.1371/journal.pone.0286434
PMID:37847702
Effects of Increasing Levels of Total Tannins on Intake, Digestibility, and Balance of Nitrogen, Water, and Energy in Hair Lambs da Silva Aguiar F, Bezerra LR, Cordão MA, Cavalcante IT, de Oliveira JP, do Nascimento RR, de Souza BB, Oliveira RL, Pereira ES, Filho JM Animals (Basel) 02-Aug-2023
PMCID:PMC10416999
doi:10.3390/ani13152497
PMID:37570305
Ulvan/Silver nanoparticle hydrogel films for burn wound dressing Sulastri E, Lesmana R, Zubair MS, Abdelwahab Mohammed AF, Elamin KM, Wathoni N Heliyon 06-Jul-2023
PMCID:PMC10362238
doi:10.1016/j.heliyon.2023.e18044
PMID:37483826
Role of Polyphenols from the Aqueous Extract of Aloysia citrodora in the Inhibition of Aflatoxin B1 Synthesis in Aspergillus flavus Cadenillas LF, Hernandez C, Bailly S, Billerach G, Durrieu V, Bailly JD Molecules 30-Jun-2023
PMCID:PMC10343729
doi:10.3390/molecules28135123
PMID:37446789
Effect of Streptomyces roseolus Cell-Free Supernatants on the Fungal Development, Transcriptome, and Aflatoxin B1 Production of Aspergillus flavus Maud L, Boyer F, Durrieu V, Bornot J, Lippi Y, Naylies C, Lorber S, Puel O, Mathieu F, Snini SP Toxins (Basel) 30-Jun-2023
PMCID:PMC10467112
doi:10.3390/toxins15070428
PMID:37505697
The ethanolic extract of Salvia lachnostachys Benth is not maternotoxic, does not alter reproductive performance, but has teratogenic potential Ortiz HC, das Neves SC, Kassuya CA, Coelho HR, Martins AC, Vilela ML, do Nascimento VA, Karuppusamy A, Stefanello MÉ, Oliveira RJ, da Silva Gomes R BMC Complement Med Ther 04-May-2023
PMCID:PMC10157921
doi:10.1186/s12906-023-03953-6
PMID:37143000
In vitro effects of different levels of quebracho and chestnut tannins on rumen methane production, fermentation parameters, and microbiota Battelli M, Colombini S, Parma P, Galassi G, Crovetto GM, Spanghero M, Pravettoni D, Zanzani SA, Manfredi MT, Rapetti L Front Vet Sci 18-Apr-2023
PMCID:PMC10154982
doi:10.3389/fvets.2023.1178288
PMID:37152691
Comparative Study of the Antibacterial, Biodegradable, and Biocompatibility Properties of Composite and Bi-Layer Films of Chitosan/Gelatin Coated with Silver Particles Valencia-Gómez LE, Reyes-Blas H, Hernández-Paz JF, Rodríguez-González CA, Olivas-Armendáriz I Materials (Basel) 10-Apr-2023
PMCID:PMC10144850
doi:10.3390/ma16083000
PMID:37109836
In Vitro Biological Activity and Lymphoma Cell Growth Inhibition by Selected Mexican Medicinal Plants Rodríguez-Garza NE, Quintanilla-Licea R, Romo-Sáenz CI, Elizondo-Luevano JH, Tamez-Guerra P, Rodríguez-Padilla C, Gomez-Flores R Life (Basel) 06-Apr-2023
PMCID:PMC10143981
doi:10.3390/life13040958
PMID:37109486
Fabrication and desired properties of conductive hydrogel dressings for wound healing Nie L, Wei Q, Li J, Deng Y, He X, Gao X, Ma X, Liu S, Sun Y, Jiang G, Okoro OV, Shavandi A, Jing S RSC Adv 14-Mar-2023
PMCID:PMC10012873
doi:10.1039/d2ra07195a
PMID:36926300

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4R,5R,6S)-2-[(3S)-5-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-6-methyloxane-3,4,5-triol 101427305 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)O)O)O 438.60 unknown https://doi.org/10.1248/CPB.54.1728
(2R,3R,4R,5R,6S)-2-[(3S)-5-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-6-methyloxane-3,4,5-triol 163010040 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)O)O)O 438.60 unknown https://doi.org/10.1248/CPB.54.1728
[(2R,3R,4R,5R,6S)-2-[(3S)-5-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-4,5-dihydroxy-6-methyloxan-3-yl] acetate 101427307 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)O)O 480.70 unknown https://doi.org/10.1248/CPB.54.1728
[(2R,3R,4R,5R,6S)-2-[(3S)-5-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-4,5-dihydroxy-6-methyloxan-3-yl] acetate 163049553 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)O)O 480.70 unknown https://doi.org/10.1248/CPB.54.1728
[(2R,3R,4R,5S,6S)-2-[(3S)-5-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-3-acetyloxy-5-hydroxy-6-methyloxan-4-yl] acetate 101427306 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)OC(=O)C)O 522.70 unknown https://doi.org/10.1248/CPB.54.1728
[(2R,3R,4R,5S,6S)-2-[(3S)-5-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 101427304 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)O)OC(=O)C)O 480.70 unknown https://doi.org/10.1248/CPB.54.1728
[(2R,3R,4R,5S,6S)-2-[(3S)-5-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentoxy]-3-acetyloxy-5-hydroxy-6-methyloxan-4-yl] acetate 162924912 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)OC(=O)C)O 522.70 unknown https://doi.org/10.1248/CPB.54.1728
[2-[5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentoxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 85123163 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)O)OC(=O)C)O 480.70 unknown https://doi.org/10.1248/CPB.54.1728
[2-[5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentoxy]-4,5-dihydroxy-6-methyloxan-3-yl] acetate 163049552 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)O)O 480.70 unknown https://doi.org/10.1248/CPB.54.1728
[3-acetyloxy-2-[5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentoxy]-5-hydroxy-6-methyloxan-4-yl] acetate 162924911 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C)OC(=O)C)O 522.70 unknown https://doi.org/10.1248/CPB.54.1728
2-[5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentoxy]-6-methyloxane-3,4,5-triol 85089020 Click to see CC1C(C(C(C(O1)OCCC(C)CCC2C(=C)CCC3C2(CCCC3(C)C)C)O)O)O 438.60 unknown https://doi.org/10.1248/CPB.54.1728
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R,5R)-4-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162844077 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4C(C(C(OC4OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CCC9(C8CC(CC9)(C)C)C(=O)O)C)C)C)CO)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(CO1)O)O)O)CO)O)O)O)O)O 1323.50 unknown https://doi.org/10.1016/0031-9422(91)83648-5
10-[3-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3-hydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14866240 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4C(C(C(OC4OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CCC9(C8CC(CC9)(C)C)C(=O)O)C)C)C)CO)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(CO1)O)O)O)CO)O)O)O)O)O 1323.50 unknown https://doi.org/10.1016/0031-9422(91)83648-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
campesterol beta-D-glucoside 12895787 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C 562.80 unknown https://doi.org/10.1016/0031-9422(91)83648-5
campesterol-3-O-beta-d-glucoside 12895788 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C 562.80 unknown https://doi.org/10.1016/0378-8741(93)90010-3
ST 28:1;O;Hex 12895785 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C 562.80 unknown https://doi.org/10.1016/0031-9422(91)83648-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1016/0031-9422(91)83648-5
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/0378-8741(93)90010-3
https://doi.org/10.1016/0031-9422(91)83648-5
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Dimethyltryptamine 6089 Click to see CN(C)CCC1=CNC2=CC=CC=C21 188.27 unknown https://doi.org/10.1021/JO01091A032
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenoxy)-6-methoxychromen-4-one 91407427 Click to see COC1=C(C=C(C=C1)OC2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 346.30 unknown https://doi.org/10.1055/S-2004-827154
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenoxy)chromen-4-one 129716130 Click to see COC1=C(C=C(C=C1)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 316.26 unknown https://doi.org/10.1055/S-2004-827154
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenoxy)-6-methoxychromen-4-one 129716140 Click to see COC1=C(C=CC(=C1)OC2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 346.30 unknown https://doi.org/10.1055/S-2004-827154
6-Demethoxycapillarisin 5316511 Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown https://doi.org/10.1055/S-2004-827154
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
5-[(2S,3R,4S)-4-[3-[2-(dimethylamino)ethyl]-1H-indol-2-yl]-3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol 122386737 Click to see CN(C)CCC1=C(NC2=CC=CC=C21)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O 476.50 unknown https://doi.org/10.1055/S-2005-873131
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.54.1728
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,8-Dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 85987351 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=CC(=C3O2)O)O)O 270.24 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2S)-6-hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 101427303 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=CC(=C3OC)O 300.30 unknown https://doi.org/10.1248/CPB.54.1728
6-Hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 162868517 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=CC(=C3OC)O 300.30 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2-Propen-1-one, 1-(2,5-dihydroxyphenyl)-3-(4-hydroxyphenyl)- 3995255 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=CC(=C2)O)O)O 256.25 unknown https://doi.org/10.1248/CPB.54.1728
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/10.1248/CPB.54.1728
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/10.1248/CPB.54.1728

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