Review

Anti-inflammatory activity of natural coumarin compounds from plants of the Indo-Gangetic plain

  • Received: 15 October 2022 Revised: 14 February 2023 Accepted: 05 March 2023 Published: 01 April 2023
  • Natural compounds are a repertoire of organoleptic molecules. This indicates that although they are not a significant source of nutrients, still they exhibit a wide range of medicinal properties through their plethora of anti-inflammatory and immune-modulatory activities. Coumarins, found in a variety of plants from different biodiversity regions, also have been reported to be present in many plants of the Indo-Gangetic plain. Here, we would attempt to enumerate the natural coumarin compounds, their pharmaco-therapeutic potential and their occurrence as well as abundance in the flora of the aforesaid biodiversity region. Coumarins, derived their name from the French word “coumarou” for Tonka bean. First isolated in 1820, coumarin still finds its relevance in the study of implementation of natural compounds in treating neuro-degenerative and cancer-like fatal diseases. Naturally occurring benzopyrones, chemically classified as lactones and coumarin compounds need to be reviewed to develop new era drugs from natural resources. This promises an effective treatment regimen with minimal side effects and also paves the path for a sustainable future with efforts to manage our health problems from the plant products in our immediate environment.

    Citation: Ramkrishna Ghosh, Partha Sarathi Singha, Lakshmi Kanta Das, Debosree Ghosh, Syed Benazir Firdaus. Anti-inflammatory activity of natural coumarin compounds from plants of the Indo-Gangetic plain[J]. AIMS Molecular Science, 2023, 10(2): 79-98. doi: 10.3934/molsci.2023007

    Related Papers:

  • Natural compounds are a repertoire of organoleptic molecules. This indicates that although they are not a significant source of nutrients, still they exhibit a wide range of medicinal properties through their plethora of anti-inflammatory and immune-modulatory activities. Coumarins, found in a variety of plants from different biodiversity regions, also have been reported to be present in many plants of the Indo-Gangetic plain. Here, we would attempt to enumerate the natural coumarin compounds, their pharmaco-therapeutic potential and their occurrence as well as abundance in the flora of the aforesaid biodiversity region. Coumarins, derived their name from the French word “coumarou” for Tonka bean. First isolated in 1820, coumarin still finds its relevance in the study of implementation of natural compounds in treating neuro-degenerative and cancer-like fatal diseases. Naturally occurring benzopyrones, chemically classified as lactones and coumarin compounds need to be reviewed to develop new era drugs from natural resources. This promises an effective treatment regimen with minimal side effects and also paves the path for a sustainable future with efforts to manage our health problems from the plant products in our immediate environment.



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    Acknowledgments



    RG acknowledges the Department of Botany, Govt. General Degree College, Kharagpur II West Bengal, India. Dr. PSS and Dr. LKD acknowledge the Department of Chemistry, Govt. General Degree College, Kharagpur II West Bengal, India. Dr. DG and Dr. SBF acknowledge the Department of Physiology, Govt. General Degree College, Kharagpur II West Bengal, India.

    Conflict of Interests



    We declare no conflicts of interest in the paper.

    [1] Bansal Y, Sethi P, Bansal G (2013) Coumarin: a potential nucleus for anti-inflammatory molecules. Med Chem Res 22: 3049-3060. https://doi.org/10.1007/s00044-012-0321-6
    [2] Musa MA, Cooperwood JS, Khan MO (2008) A review of coumarin derivatives in pharmacotherapy of breast cancer. Curr Med Chem 15: 2664-2679.
    [3] Kontogiorgis CA, Hadjipavlou-Litina DJ (2005) Synthesis and antiinflammatory activity of coumarin derivatives. J Med Chem 48: 6400-6408. https://doi.org/10.1021/jm0580149
    [4] Kirsch G, Abdelwahab AB, Chaimbault P (2016) Natural and Synthetic Coumarins with Effects on Inflammation. Molecules 21: 1322. https://doi.org/10.3390/molecules21101322
    [5] Medzhitov R (2010) Inflammation 2010: new adventures of an old flame. Cell 140: 771-776.
    [6] Nathan C, Ding A (2010) Nonresolving inflammation. Cell 140: 871-882.
    [7] Chen L, Deng H, Cui H, et al. (2017) Inflammatory responses and inflammation-associated diseases in organs. Oncotarget 9: 7204-7218.
    [8] Jabbour HN, Sales KJ, Catalano RD, et al. (2009) Inflammatory pathways in female reproductive health and disease. Reprod 138: 903-919.
    [9] Omoigui S (2007) The biochemical origin of pain: the origin of all pain is inflammation and the inflammatory response. Part 2 of 3-inflammatory profile of pain syndromes. Med Hypotheses 69: 1169-1178.
    [10] Rostom B, Karaky R, Kassab I, et al. (2022) Coumarins derivatives and inflammation: Review of their effects on the inflammatory signaling pathways. Eur J Pharmacol 922: 174867.
    [11] Witaicenis A, Seito LN, da Silveira Chagas A, et al. (2014) Antioxidant and intestinal anti-inflammatory effects of plant-derived coumarin derivatives. Phytomedicine 21: 240-246.
    [12] Fylaktakidou KC, Hadjipavlou-Litina DJ, Litinas KE, et al. (2004) Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities. Curr Pharm Des 10: 3813-3833.
    [13] Narayanaswamy R, Veeraragavan V (2020) Chapter 8-Natural products as antiinflammatory agents, Bioactive Natural Products in Studies.Atta-ur-Rahman, Elsevier 269-306.
    [14] Borges M F, Roleira F M, Milhazes N J, et al. (2009) Simple coumarins: privileged scaffolds in medicinal chemistry. Front Med Chem 4: 23-85. https://doi.org/10.2174/978160805207310904010023
    [15] Coumarin in Cinnamon, Cinnamon-Containing Foods and Licorice Flavoured Foods. Government of Canada (2015). Available from: https://inspection.canada.ca/food-safety-for-industry/food-chemistry-and-microbiology/food-safety-testing-bulletin-and-reports/coumarin/eng/1568641632892/1568641633299.
    [16] Bioactive Natural Products. Studies in Natural Products Chemistry (2000). Available from: https://www.sciencedirect.com/topics/food-science/licorice.
    [17] Tava A (2001) Coumarin-containing grass: volatiles from sweet vernalgrass (Anthoxanthum odoratum L.). J Essent Oil Res 13: 367-370. https://doi.org/10.1080/10412905.2001.9712236
    [18] Sharopov F, Setzer WN (2018) Medicinal plants of Tajikistan. Vegetation of Central Asia and environs. Switzerland: Springer Nature 163-210.
    [19] Sharifi-Rad J, Cruz-Martins N, López-Jornet P, et al. (2021) Natural Coumarins: Exploring the Pharmacological Complexity and Underlying Molecular Mechanisms. Oxid Med Cell Longev 2021: 6492346. https://doi.org/10.1155/2021/6492346
    [20] Garg SS, Gupta J, Sharma S, et al. (2020) An insight into the therapeutic applications of coumarin compounds and their mechanisms of action. Eur J Pharm Sci 152: 105424.
    [21] Matos MJ, Santana L, Uriarte E, et al. (2015) Coumarins-An Important Class of Phytochemicals. Phytochemicals-Isolation, Characterisation and Role in Human Health 25: 533-538.
    [22] Han XL, Wang H, Zhang ZH, et al. (2015) nStudy on Chemical Constituents in Seeds of Datura metel from Xinjiang. Zhong Yao Cai = Zhongyaocai = J Chinese Med Mater (in Chinese) 38: 1646-1648.
    [23] Ding Z, Dai Y, Hao H, et al. (2008) Anti-Inflammatory Effects of Scopoletin and Underlying Mechanisms. Pharm Biol 46: 854-860.
    [24] Chang TN, Deng JS, Chang YC, et al. (2012) Ameliorative Effects of Scopoletin from Crossostephium chinensis against Inflammation Pain and Its Mechanisms in Mice. Evid Based Complement Alternat Med 2012: 595603.
    [25] Debaggio T, Tucker AO (2009) The Encyclopedia of Herbs, A Comprehensive Reference to Herbs of Flavor and Fragrance.Timber Press.
    [26] National Center for Biotechnology Information, PubChem Compound Summary for CID 8417. Scoparone (2022). Availablefrom: https://pubchem.ncbi.nlm.nih.gov/compound/Scoparone.
    [27] Artemisia absinthium. Flora Italiana (2022). Available from: http://luirig.altervista.org/.
    [28] Lu C, Li Y, Hu S, et al. (2018) Scoparone prevents IL-1β-induced inflammatory response in human osteoarthritis chondrocytes through the PI3K/Akt/NF-κB pathway. Biomed Pharmacother 106: 1169-1174.
    [29] Liu B, Deng X, Jiang Q, et al. (2019) Scoparone alleviates inflammation, apoptosis and fibrosis of non-alcoholic steatohepatitis by suppressing the TLR4/NF-κB signaling pathway in mice. Int Immunopharmacol 75: 105797.
    [30] National Center for Biotechnology Information, PubChem Compound Summary for CID 5273569. Fraxetin (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Fraxetin.
    [31] Li J, Lin B, Wang G, et al. (2012) Chemical constituents of Datura stramonium seeds. Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China J Chinese Materia Medica (in Chinese) 37: 319-322.
    [32] Wang Q, Zhuang D, Feng W, et al. (2020) Fraxetin inhibits interleukin-1β-induced apoptosis, inflammation, and matrix degradation in chondrocytes and protects rat cartilage in vivo. Saudi Pharm J 28: 1499-1506.
    [33] Deng S, Ge J, Xia S, et al. (2022) Fraxetin alleviates microglia-mediated neuroinflammation after ischemic stroke. Ann Transl Med 10: 439.
    [34] National Center for Biotechnology Information, PubChem Compound Summary for CID 3047739. Fraxinol (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Fraxinol.
    [35] Mountain Cherry. Flowers of India (2023). Available from: http://www.flowersofindia.net/catalog/slides/Mountain%20Cherry.html.
    [36] Soto-Blanco B (2022) Chapter 12-Herbal glycosides in healthcare. Herbal Biomolecules in Healthcare Applications.Academic Press 239-282.
    [37] Sankara Rao K, Navendu Page, Deepak Kumar Pan India Bouquets (2020). Available from: http://flora-peninsula-indica.ces.iisc.ac.in/pan/plants.php?
    [38] National Center for Biotechnology Information, PubChem Compound Summary for CID 5281426. Umbelliferone (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Umbelliferone.
    [39] Sim MO, Lee HI, Ham JR, et al. (2015) Anti-inflammatory and antioxidant effects of umbelliferone in chronic alcohol-fed rats. Nutr Res Pract 9: 364-369.
    [40] Wang D, Wang X, Tong W, et al. (2019) Umbelliferone Alleviates Lipopolysaccharide-Induced Inflammatory Responses in Acute Lung Injury by Down-Regulating TLR4/MyD88/NF-κB Signaling. Inflammation 42: 440-448.
    [41] Selim YA, Ouf NH (2012) Anti-inflammatory new coumarin from the Ammi majus. L Org Med Chem Lett 2: 1. https://doi.org/10.1186/2191-2858-2-1
    [42] PubChem. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2004-. PubChem Compound Summary for CID 238946, 6-Hydroxy-7-methoxy-4-methyl-2H-chromen-2-one (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/6-Hydroxy-7-methoxy-4-methyl-2H-chromen-2-one.
    [43] El-Haggar R, Al-Wabli RI (2015) Anti-inflammatory screening and molecular modeling of some novel coumarin derivatives. Molecules 20: 5374-5391.
    [44] Quattrocchi U (2012) Ammi majus, CRC World Dictionary of Medicinal and Poisonous Plants: Common Names. Scientific Names, Eponyms, Synonyms, and Etymology (5 Volume Set).CRC Press 244.
    [45] Walliser J (2014) Ammi majus, Attracting Beneficial Bugs to Your Garden: A Natural Approach to Pest Control. Portland, Oregon: Timber Press 114-115.
    [46] Elgamal MHA, Shalaby NMM, Duddeck H, et al. (2013) Coumarins and coumarin glucosides from the fruits of Ammi majus. Phytochemistry 34: 819-823. https://doi.org/10.1016/0031-9422(93)85365-X
    [47] 4-methylumbellione. Merck (2022). Available from: https://www.sigmaaldrich.com/IN/en/product/aldrich/m1381.
    [48] PubChem. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2004-. PubChem Compound Summary for CID 5318565, Isofraxidin, 2023. Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Isofraxidin.
    [49] Yamazaki T, Tokiwa T (2010) Isofraxidin, a coumarin component from Acanthopanax senticosus, inhibits matrix metalloproteinase-7 expression and cell invasion of human hepatoma cells. Bio Pharm Bull 33: 1716-1722.
    [50] Jin J, Yu X, Hu Z, et al. (2018) Isofraxidin targets the TLR4/MD-2 axis to prevent osteoarthritis development. Food Funct 9: 5641-5652.
    [51] Jacqueline N (2006) Chinese Celery. Vegetables and Vegetarian Foods 13: 15-34.
    [52] PubChem. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2004-. PubChem Compound Summary for CID 5281417. Esculin (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Esculin.
    [53] Taxon: Hordeum vulgare L. subsp. spontaneum (K. Koch) Thell. GRIN Taxonomy for Plants. GRIN (2022). Available from: https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=4513.
    [54] Wang YH, Liu YH, He GR, et al. (2015) Esculin improves dyslipidemia, inflammation and renal damage in streptozotocin-induced diabetic rats. BMC Complement Altern Med 15: 402.
    [55] National Center for Biotechnology Information. PubChem Compound Summary for CID 439514. Scopolin (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Scopolin.
    [56] Taxon. Arabidopsis thaliana (L.) Heynh (2022). Available from: http://www.tn-grin.nat.tn/gringlobal/taxon/taxonomydetail?id=3769.
    [57] Döll S, Kuhlmann M, Rutten T, et al. (2018) Accumulation of the coumarin scopolin under abiotic stress conditions is mediated by the Arabidopsis thaliana THO/TREX complex. Plant J 93: 431-444.
    [58] Artemisia minor. EFolra of India (2022). Aviailable from: https://efloraofindia.com/2022/07/23/artemisia-minor/.
    [59] Scopolin. Wikipedia (2022). Available from: https://en.wikipedia.org/wiki/Scopolin.
    [60] Glycosmis pentaphylla (2022). Available from: https://indiabiodiversity.org/species/show/32607.
    [61] Zich FA, Hyland BPM, Whiffen T, et al. (2020) Murraya paniculata. Australian Tropical Rainforest Plants Edition 8 (RFK8). Centre for Australian National Biodiversity Research (CANBR), Australian Government .
    [62] Silván AM, Abad MJ, Bermejo P, et al. (1999) Antiinflammatory activity of coumarins from Santolina oblongifolia. J Nat Prod 59: 1183-1185.
    [63] Pan R, Dai Y, Gao X, et al. (2009) Scopolin isolated from Erycibe obtusifolia Benth stems suppresses adjuvant-induced rat arthritis by inhibiting inflammation and angiogenesis. Int Immunopharmacol 9: 859-869.
    [64] India Biodiversity Portal, 2022. Available from: https://indiabiodiversity.org/species/show/250754#habitat-and-distribution.
    [65] Flacourtia jangomas (Lour.) Raeuschel, Pacific Island Ecosystems at Risk (PIER) (2022). Available from: http://www.hear.org/pier/species/flacourtia_jangomas.htm.
    [66] Ayurvedic Medicinal Plants of Sri Lanka Compendium version 3 (2022). Aailable from: http://www.instituteofayurveda.org/plants/plants_detail.php?i=1188&s=local_name.
    [67] Tuan Anh HL, Kim DC, Ko W, et al. (2017) Anti-inflammatory coumarins from Paramignya trimera. Pharm Biol 55: 1195-1201.
    [68] National Center for Biotechnology Information, PubChem Compound Summary for CID69304032,3′,5,7-Trihydroxy-4-methoxyflavanone (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/3_5_7-Trihydroxy-4-methoxyflavanone.
    [69] 357-trihydroxy-4-methoxyflavone (2022). Available from: https://www.biosynth.com/p/FT66491/491-54-3-357-trihydroxy-4-methoxyflavone.
    [70] Lima JCS, de Oliveira RG, Silva VC, et al. (2018) Anti-inflammatory activity of 4′,6,7-trihydroxy-5-methoxyflavone from Fridericia chica (Bonpl.) L.G.Lohmann. Nat Prod Res 34: 726-730.
    [71] Rahayu D, Setyani D, Dianhar H, et al. (2020) Phenolic Compounds From Indonesian White Turmeric (Curcuma Zedoaria) Rhizomes. Asian J Pharm Clin Res 2020: 194-198.
    [72] Hardigree AA, Epler JL (1978) Comparative mutagenesis of plant flavonoids in microbial systems. Mutat Res/Genet Toxicol 58: 1109-1114.
    [73] Wattenberg LW, Page MA, Leong JL (1968) Induction of increased benzpyrene hydroxylase activity by flavones and related compounds. Cancer Res 28: 934-936.
    [74] 3′,5,7-Trihydroxy-4′-methoxyflavanone. Alfa Aesar (2022). Available from: https://www.alfa.com/en/catalog/B20528/.
    [75] Botanical Survey of India. Government of India, Ministry of Environment, Forest & ClimateChange (2022). Available from: https://efloraindia.bsi.gov.in/eFlora/speciesDesc_PCL.action?species_id=28580.
    [76] National Center for Biotechnology Information. PubChem Compound Summary for CID 10748,7-Methoxycoumarin (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/7-Methoxycoumarin.
    [77] Cheriyan BV, Kadhirvelu P, Nadipelly J, et al. (2017) Anti-nociceptive Effect of 7-methoxy Coumarin from Eupatorium Triplinerve vahl (Asteraceae). Pharmacogn Mag 13: 81-84.
    [78] Gurib-Fakim A, Brendler T (2004) Medicinal and aromatic plants of Indian Ocean Islands: Madagascar, Comoros, Seychelles and Mascarenes.Medpharm GmbH Scientific Publishers.
    [79] National Center for Biotechnology Information. PubChem Compound Summary for CID 1550607, Auraptene (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Auraptene.
    [80] Askari VR, Rahimi VB, Zargarani R, et al. (2021) Anti-oxidant and anti-inflammatory effects of auraptene on phytohemagglutinin (PHA)-induced inflammation in human lymphocytes. Pharmacol Rep 73: 154-162.
    [81] Okuyama S, Morita M, Kaji M, et al. (2015) Auraptene Acts as an Anti-Inflammatory Agent in the Mouse Brain. Molecules 20: 20230-20239. https://doi.org/10.3390/molecules201119691
    [82] La VD, Zhao L, Epifano F, et al. (2013) Anti-inflammatory and wound healing potential of citrus auraptene. J Med Food 16: 961-964.
    [83] National Center for Biotechnology Information. PubChem Compound Summary for CID 31553, Silibinin (2022). Availablefrom: https://pubchem.ncbi.nlm.nih.gov/compound/Silibinin.
    [84] BSBI List (xls). Botanical Society of Britain and Ireland. Archived from the original (xls) on (2022). Available from: https://bsbi.org/.
    [85] Xin W, Xin W, Zhen Z, et al. (2020) Health Benefits of Silybum marianum: Phytochemistry, Pharmacology, and Applications. Agric. Food Chem 68: 11644-11664. https://doi.org/10.1021/acs.jafc.0c04791
    [86] Silibinin. Wikipedia (2022). Available from: https://en.wikipedia.org/wiki/Silibinin.
    [87] Lim R, Morwood CJ, Barker G, et al. (2014) Effect of silibinin in reducing inflammatory pathways in in vitro and in vivo models of infection-induced preterm birth. PLoS One 9: e92505.
    [88] Giorgi VS, Peracoli MT, Peracoli JC, et al. (2012) Silibinin modulates the NF-κb pathway and pro-inflammatory cytokine production by mononuclear cells from preeclamptic women. J Reprod Immunol 95: 67-72.
    [89] Tong WW, Zhang C, Hong T, et al. (2018) Silibinin alleviates inflammation and induces apoptosis in human rheumatoid arthritis fibroblast-like synoviocytes and has a therapeutic effect on arthritis in rats. Sci Rep 8: 3241.
    [90] National Center for Biotechnology InformationPubChem Compound Summary for CID 5319464, Murracarpin (2022). Retrieved September 17, 2022 from https://pubchem.ncbi.nlm.nih.gov/compound/Murracarpin.
    [91] Tian-Shung W, Meei-Jen L, Chang-Sheng K (1989) Coumarins of the flowers of Murraya paniculata. Phytochemistry 28: 293-294.
    [92] Shi WM, Liu HQ, Li LF, et al. The anti-inflammatory activity of a natural occurring coumarin: Murracarpin. By. Medicine Sciences and Bioengineering. 1st Editio, Imprint CRC Press, 6 (2015).
    [93] White Himalayan Rue. Flowers of India (2022). http://www.flowersofindia.net/catalog/slides/White%20Himalayan%20Rue.html.
    [94] Glycosmis pentaphylla. Germplasm Resources Information Network (GRIN). Agricultural Research Service (ARS), United States Department of Agriculture (USDA) (2020) . Available from: https://www.ars-grin.gov/.
    [95] Md Mubarak H, Faiza T, Md M, et al. (2017) 7-Methoxy-8-Prenylated Coumarins from Murraya koenigii (Linn.) Spreng. Dhaka Univ J Pharm Sci 15: 155.
    [96] National Center for Biotechnology InformationPub Chem Compound Summary for CID 181514, Murrangatin, 2022 (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Murrangatin.
    [97] Longhuo W, Li J, Guo X, et al. (2013) Chondroprotective evaluation of two natural coumarins: murrangatin and murracarpin. J Intercult Ethnopharmacol 2: 91-98. https://doi.org/10.5455/jice.20130313082010
    [98] Murraya paniculata (L.) Jack (2022). Available from: https://apps.lucidcentral.org/rainforest/text/entities/murraya_paniculata.htm.
    [99] Long W, Wang M, Luo X, et al. (2018) Murrangatin suppresses angiogenesis induced by tumor cell-derived media and inhibits AKT activation in zebrafish and endothelial cells. Drug Des Devel Ther 12: 3107-3115. https://doi.org/10.2147/DDDT.S145956
    [100] National Center for Biotechnology Information. PubChem Bioassay Record for Bioactivity AID 1204915-SID 312393603, Bioactivity for AID 1204915 - SID 312393603, Source: ChEMBL (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/bioassay/1204915#sid=312393603.
    [101] National Center for Biotechnology InformationPubChem Compound Summary for CID 5280569, Daphnetin, 2022 (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Daphnetin.
    [102] Yu WW, Lu Z, Zhang H, et al. (2014) Anti-inflammatory and protective properties of daphnetin in endotoxin-induced lung injury. J Agric Food Chem 62: 12315-12325.
    [103] Indian Paper Plant. Flowers of India (2022). Available from: http://www.flowersofindia.net/catalog/slides/Indian%20Paper%20Plant.html.
    [104] Kim M, Lee H, Randy A, et al. (2017) Stellera chamaejasme and its constituents induce cutaneous wound healing and anti-inflammatory activities OPEN. Scientific Reports 7. https://doi.org/10.1038/srep42490
    [105] Himalayan Stellera (2022). Available from: https://www.flowersofindia.net/catalog/slides/Himalayan%20Stellera.html.
    [106] Liu Z, Liu J, Zhao K, et al. (2016) Role of Daphnetin in Rat Severe Acute Pancreatitis Through the Regulation of TLR4/NF-[Formula: see text]B Signaling Pathway Activation. Am J Chin Med 44(1): 149-163.
    [107] Murthy HN, Bhat MA, Dalawai D (2019) Bioactive Compounds of Bael (Aegle marmelos (L.) Correa). Bioactive Compounds in Underutilized Fruits and Nuts. Reference Series in Phytochemistry.Springer, Cham. https://doi.org/10.1007/978-3-030-06120-3_35-1
    [108] “M.M.P.N.D.-Sorting Aegle names” (2022). Available from: https://unimelb.edu.au.
    [109] Aegle marmelos (L.) Correa (2023). Available from: https://eol.org/pt-BR/pages/483583/articles.
    [110] Alan Davidson (2014) The Oxford Companion to Food. Illustrated by Soun Vannithone (3rd ed.).Oxford University Press 191.
    [111] Benni JM, Jayanthi MK, Suresha RN (2011) Evaluation of the anti-inflammatory activity of Aegle marmelos (Bilwa) root. Indian J Pharmacol 43: 393-397.
    [112] Yun-Fang H, Si-Wen Q, Li Y, et al. (2021) Marmin from the blossoms of Citrus maxima (Burm.) Merr. exerts lipid-lowering effect via inducing 3T3-L1 preadipocyte apoptosis. Journal of Funct Foods 82: 104513.
    [113] Wang C, Al-Ani MK, Sha Y, et al. (2019) Psoralen Protects Chondrocytes, Exhibits Anti-Inflammatory Effects on Synoviocytes, and Attenuates Monosodium Iodoacetate-Induced Osteoarthritis. Int J Biol Sci 15: 229-238.
    [114] Li H, Xu J, Li, X, et al. (2021) Anti-inflammatory activity of psoralen in human periodontal ligament cells via estrogen receptor signaling pathway. Sci Rep 11: 8754.
    [115] National Center for Biotechnology Information. PubChem Compound Summary for CID6199, Psoralen (2022). Available from: https://pubchem.ncbi.nlm.nih.gov/compound/Psoralen.
    [116] Mirjana L, Martina L, Drago S, et al. (2020) Coumarins in Food and Methods of Their Determination. Foods 9: 645.
    [117] Limoniaacidissima (2023). Avilable from: https://www.scientificlib.com/en/Biology/Plants/Magnoliophyta/LimoniaAcidissima01.html.
    [118] Thada R, Chockalingam S, Dhandapani RK, et al. (2013) Extraction and Quantitation of Coumarin from Cinnamon and its Effect on Enzymatic Browning in Fresh Apple Juice: A Bioinformatics Approach to Illuminate its Antibrowning Activity. J Agric Food Chem 61: 5385-5390.
    [119] Leal LKAM, Ferreira AAG, Bezerra GA, et al. (2000) Antinociceptive, anti-inflammatory and bronchodilator activities of Brazilian medicinal plants containing coumarin: A comparative study. J Ethnopharmacol 70: 151-159. https://doi.org/10.1016/S0378-8741(99)00165-8
    [120] Celeghini RMS, Vilegas JHY, Lanças FM (2001) Extraction and quantitative HPLC analysis of coumarin in hydroalcoholic extracts of Mikania glomerata Spreng. (“guaco”) leaves. J Braz Chem Soc 12: 706-709.
    [121] Maja M, Igor J, Dragica S, et al. (2017) Screening of Six Medicinal Plant Extracts Obtained by Two Conventional Methods and Supercritical CO2 Extraction Targeted on Coumarin Content, 2,2-Diphenyl-1-picrylhydrazyl Radical Scavenging Capacity and Total Phenols Content. Molecules 22: 348.
    [122] Skalicka-Woźniak K, Głowniak K (2012) Pressurized liquid extraction of coumarins from fruits of Heracleum leskowii with application of solvents with different polarity under increasing temperature. Molecules 17: 4133-4141.
    [123] Wang T, Li Q (2022) DES Based Efficient Extraction Method for Bioactive Coumarins from Angelica dahurica (Hoffm.) Benth. & Hook.f. ex Franch. & Sav. Separations 9: 5.
    [124] Arora RK, Kaur N, Bansal Y, et al. (2014) Novel coumarin-benzimidazole derivatives as antioxidants and safer anti-inflammatory agents. Acta Pharm Sin B 4: 368-375.
    [125] Hadjipavlou-Litina JD, Litinas EK, Kontogiorgis C (2007) The Anti-inflammatory Effect of Coumarin and its Derivatives. Anti-Inflamm Anti-Allergy Agents in Med Chem 6: 293-306.
    [126] Debosree G, Elina M, Syed BF, et al. (2012) In vitro studies on the antioxidant potential of the aqueous extract of Curry leaves (Murraya koenigii L.) collected from different parts of the state of West Bengal. Indian J Physiol Allied Sci 66: 77-95.
    [127] Luzia L, Aline S, Glauce V (2017) Justicia pectoralis, a coumarin medicinal plant have potential for the development of antiasthmatic drugs?. Revista Brasileira de Farmacognosia 27. https://doi.org/10.1016/j.bjp.2017.09.005
    [128] Rohini K, Srikumar PS (2014) Therapeutic Role of Coumarins and Coumarin-Related Compounds. J Thermodyn Catal 5: 2. https://doi.org/10.4172/2157-7544.1000130
    [129] Dipteryx odorata (2023). Available from: https://tropical.theferns.info/viewtropical.php?id=Dipteryx+odorata.
    [130] Liao JC, Deng JS, Chiu CS, et al. (2012) Anti-Inflammatory Activities of Cinnamomum cassia Constituents In Vitro and In Vivo. Evid Based Complement Alternat Med 2012: 429320. https://doi.org/10.1155/2012/429320
    [131] Anthoxanthum odoratum (2022). Available from: https://en.wikipedia.org/wiki/Anthoxanthum_odoratum.
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