Mangiferin: A natural miracle bioactive compound against lifestyle related disorders

Bioavailability and bioefficacy of polyphenols in humans. I. Review of 97 bioavailability studies

Manach, C., Williamson, G., Morand, C., Scalbert, A., & Rémésy, C. (2005) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/81.1.230s · Cited by 4,219 · see citing works

[36] Flavonoids as antioxidants: Determination of radical-scavenging efficiencies

Bors, W., Heller, W. E., Michel, C., & Sarán, M. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86128-i · Cited by 1,726 · see citing works

The sugar moiety is a major determinant of the absorption of dietary flavonoid glycosides in man

Hollman, P. C. H., Bijsman, M. N. C. P., van Gameren, Y., Cnossen, E. P. J., de Vries, J. H. M., & Katan, M. (1999) · Free Radical Research · doi:10.1080/10715769900301141 · Cited by 555 · see citing works

Effect of mangiferin on hyperglycemia and atherogenicity in streptozotocin diabetic rats

Muruganandan, S., Srinivasan, K., Gupta, S., Gupta, P. K., & Lal, J. (2005) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2004.12.010 · Cited by 426 · see citing works

Molecular Link Mechanisms between Inflammation and Cancer

Costa, D. B. V., & de Carvalho, J. E. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212802083707 · Cited by 416 · see citing works

Topical and Peripherally Acting Analgesics

Sawynok, J. (2003) · Pharmacological Reviews · doi:10.1124/pr.55.1.1 · Cited by 347 · see citing works

Microwave-assisted extraction of flavonoids from Radix Astragali

Xiao, W., Han, L., & Shi, B. (2008) · Separation and Purification Technology · doi:10.1016/j.seppur.2008.03.025 · Cited by 304 · see citing works

Protective effects of Mangifera indica L. extract, mangiferin and selected antioxidants against TPA-induced biomolecules oxidation and peritoneal macrophage activation in mice

Martı́nez-Sánchez, G., Re, L., Giuliani, A., Sellés, A. J. N., Pérez-Davison, G., & León-Fernández, O. S. (2000) · Pharmacological Research · doi:10.1006/phrs.2000.0727 · Cited by 302 · see citing works

Analgesic and antioxidant activity of mangiferin and its derivatives: The structure activity relationship

Dar, A., Faizi, S., Naqvi, S., Roome, T., Zikr-ur-Rehman, S., Ali, M., Firdous, S., & Moin, S. T. (2005) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.28.596 · Cited by 289 · see citing works

Inhibitory effects of phenolic compounds on CCl4-induced microsomal lipid peroxidation

Cholbi, M. R., Payá, M., & Alcaraz, M. J. (1991) · Cellular and Molecular Life Sciences · doi:10.1007/bf01945426 · Cited by 265 · see citing works

Mangiferin protects the streptozotocin-induced oxidative damage to cardiac and renal tissues in rats

Muruganandan, S., Gupta, S., Kataria, M., Lal, J., & Gupta, P. K. (2002) · Toxicology · doi:10.1016/s0300-483x(02)00069-0 · Cited by 216 · see citing works

Metabolism of chlorogenic acid by human plasma, liver, intestine and gut microflora

Plumb, G. W., García‐Conesa, M., Kroon, P. A., Rhodes, M. J. C., Ridley, S., & Williamson, G. (1999) · Journal of the Science of Food and Agriculture · doi:10.1002/(sici)1097-0010(19990301)79:3 · Cited by 189 · see citing works

Mangiferin attenuates diabetic nephropathy by inhibiting oxidative stress mediated signaling cascade, TNFα related and mitochondrial dependent apoptotic pathways in streptozotocin-induced diabetic rats

Pal, P. B., Sinha, K., & Sil, P. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107220 · Cited by 185 · see citing works

Of the Major Phenolic Acids Formed during Human Microbial Fermentation of Tea, Citrus, and Soy Flavonoid Supplements, Only 3,4-Dihydroxyphenylacetic Acid Has Antiproliferative Activity ,

Gao, K., Xu, A., Krul, C. A. M., Venema, K., Liu, Y., Niu, Y., Lu, J., Bensoussan, L., Seeram, N. P., Heber, D., et al. (2006) · Journal of Nutrition · doi:10.1093/jn/136.1.52 · Cited by 183 · see citing works

Mangiferin exerts hepatoprotective activity against D-galactosamine induced acute toxicity and oxidative/nitrosative stress via Nrf2–NFκB pathways

Das, J., Ghosh, J., Roy, A., & Sil, P. C. (2012) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2012.01.015 · Cited by 173 · see citing works

Neuroprotection by two polyphenols following excitotoxicity and experimental ischemia

Gottlieb, M., Leal‐Campanario, R., Campos‐Esparza, M. R., Sánchez‐Gómez, M. V., Alberdi, E. M., Arranz, A. M., Delgado-Garcia, J. M., Gruart, A., & Matute, C. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.03.017 · Cited by 164 · see citing works

Mangiferin – a Bioactive Xanthonoid, not only from Mango and not just Antioxidant

Matkowski, A., Kuś, P., Goralska, E., & Woźniak, D. (2013) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557511313030011 · Cited by 156 · see citing works

Gallic acid indanone and mangiferin xanthone are strong determinants of immunosuppressive anti-tumour effects of Mangifera indica L. bark in MDA-MB231 breast cancer cells

García-Rivera, D., Delgado, R., Bougarne, N., Haegeman, G., & Vanden Berghe, W. (2011) · Cancer Letters · doi:10.1016/j.canlet.2011.02.011 · Cited by 142 · see citing works

Mangiferin attenuates the symptoms of dextran sulfate sodium-induced colitis in mice via NF-κB and MAPK signaling inactivation

Dou, W., Zhang, J., Ren, G., Ding, L., Sun, A., Deng, C., Wu, X., Wei, X., Mani, S., & Wang, Z. (2014) · International Immunopharmacology · doi:10.1016/j.intimp.2014.08.025 · Cited by 135 · see citing works

Protective effect of mangiferin against lipopolysaccharide-induced depressive and anxiety-like behaviour in mice

Jangra, A., Lukhi, M. M., Sulakhiya, K., Baruah, C. C., & Lahkar, M. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.07.031 · Cited by 122 · see citing works

Iron complexing activity of mangiferin, a naturally occurring glucosylxanthone, inhibits mitochondrial lipid peroxidation induced by Fe2+-citrate

Andreu, G. P., Delgado, R., Velho, J. A., Curti, C., & Vercesi, A. E. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.03.007 · Cited by 122 · see citing works

Salacia root, a unique Ayurvedic medicine, meets multiple targets in diabetes and obesity

Li, Y., Huang, T. H.-W., & Yamahara, J. (2008) · Life Sciences · doi:10.1016/j.lfs.2008.03.005 · Cited by 119 · see citing works

Beneficial effects of mangiferin on hyperlipidemia in high-fat-fed hamsters

Guo, F., Huang, C., Liao, X., Wang, Y., He, Y., Feng, R., Li, Y., & Sun, C. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201100392 · Cited by 118 · see citing works

Mangiferin decreases plasma free fatty acids through promoting its catabolism in liver by activation of AMPK

Niu, Y., Li, S., Na, L., Feng, R., Liu, L., Li, Y., & Sun, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030782 · Cited by 116 · see citing works

Mangiferin – a Bioactive Xanthonoid, not only from Mango and not just Antioxidant

Matkowski, A., Kus, P., Goralska, E., & Wozniak, D. (2013) · Mini Reviews in Medicinal Chemistry · doi:10.2174/138955713804999838 · Cited by 116 · see citing works

Mangiferin decreases inflammation and oxidative damage in rat brain after stress

Márquez, L., García-Bueno, B., Madrigal, J. L. M., & Leza, J. C. (2012) · European Journal of Nutrition · doi:10.1007/s00394-011-0252-x · Cited by 111 · see citing works

Mangiferin inhibits endoplasmic reticulum stress-associated thioredoxin-interacting protein/NLRP3 inflammasome activation with regulation of AMPK in endothelial cells

Song, J., Li, J., Hou, F., Wang, X., & Liu, B. (2015) · Metabolism · doi:10.1016/j.metabol.2014.11.008 · Cited by 109 · see citing works

Anthelminthic and antiallergic activities of <i>Mangifera indica</i> L. stem bark components Vimang and mangiferin

García, D., Escalante, M., Delgado, R., Ubeira, F. M., & Leiro, J. (2003) · Phytotherapy Research · doi:10.1002/ptr.1343 · Cited by 109 · see citing works

Improving permeability and oral absorption of mangiferin by phospholipid complexation

Ma, H., Chen, H., Sun, L., Tong, L., & Zhang, T. (2014) · Fitoterapia · doi:10.1016/j.fitote.2013.10.016 · Cited by 108 · see citing works

Ethnopharmacology of Mangifera indica L. Bark and Pharmacological Studies of its Main C-Glucosylxanthone, Mangiferin

Wauthoz, N., Balde, A. M., Baldé, E. S., Damme, M. V., & Duez, P. (2007) · Cited by 105 · see citing works

Mangiferin exerts antitumor activity in breast cancer cells by regulating matrix metalloproteinases, epithelial to mesenchymal transition, and β-catenin signaling pathway

Li, H., Huang, J., Yang, B. L., Xiang, T., Yin, X., Peng, W., Cheng, W., Wan, J., Luo, F., Li, H., et al. (2013) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2013.05.011 · Cited by 103 · see citing works

Mangiferin ameliorates aluminium chloride-induced cognitive dysfunction via alleviation of hippocampal oxido-nitrosative stress, proinflammatory cytokines and acetylcholinesterase level

Kasbe, P., Jangra, A., & Lahkar, M. (2015) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2015.04.002 · Cited by 98 · see citing works

Mangiferin, a natural xanthone, protects murine liver in Pb(II) induced hepatic damage and cell death via MAP kinase, NF-κB and mitochondria dependent pathways

Pal, P. B., Sinha, K., & Sil, P. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056894 · Cited by 98 · see citing works

Mangiferin inhibits cyclooxygenase-2 expression and prostaglandin E2 production in activated rat microglial cells

Bhatia, H. S., Candelario-Jalil, E., de Oliveira, A. C. P., Olajide, O. A., Martínez-Sánchez, G., & Fiebich, B. L. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.06.017 · Cited by 95 · see citing works

Effects of a natural extract from Mangifera indica L, and its active compound, mangiferin, on energy state and lipid peroxidation of red blood cells

Rodríguez, J., Pierro, D. D., Gioia, M., Monaco, S., Delgado, R., Coletta, M., & Marini, S. (2006) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2006.04.005 · Cited by 93 · see citing works

Mangiferin Attenuate Sepsis-Induced Acute Kidney Injury via Antioxidant and Anti-Inflammatory Effects

He, L., Peng, X., Zhu, J., Chen, X., Liu, H., Tang, C., Dong, Z., Liu, F., & Peng, Y. (2014) · American Journal of Nephrology · doi:10.1159/000369220 · Cited by 92 · see citing works

Mangiferin attenuates MPTP induced dopaminergic neurodegeneration and improves motor impairment, redox balance and Bcl-2/Bax expression in experimental Parkinson’s disease mice

Kavitha, M., Nataraj, J., Essa, M. M., Memon, M. A., & Manivasagam, T. (2013) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2013.09.016 · Cited by 91 · see citing works

Mangiferin prevents diabetic nephropathy progression in streptozotocin‐induced diabetic rats

Li, X., Cui, X., Sun, X., Li, X., Zhu, Q., & Li, W. (2010) · Phytotherapy Research · doi:10.1002/ptr.3045 · Cited by 91 · see citing works

Conformational Differences Between O- and C-Glycosides: Theα-O-Man-(1→1)-β-Gal/α-C-Man-(1→1)-β-Gal Case- A Decisive Demonstration of the Importance of theexo-Anomeric Effect on the Conformation of Glycosides

Asensio, J. L., Cañada, F. J., Cheng, X., Khan, N., Mootoo, D. R., & Jiménez‐Barbero, J. (2000) · Chemistry - A European Journal · doi:10.1002/(sici)1521-3765(20000317)6:6 · Cited by 84 · see citing works

Lemon verbena (Lippia citriodora) polyphenols alleviate obesity-related disturbances in hypertrophic adipocytes through AMPK-dependent mechanisms

Herranz‐López, M., Barrajón‐Catalán, E., Segura‐Carretero, A., Menéndez, J. A., Joven, J., & Micol, V. (2015) · Phytomedicine · doi:10.1016/j.phymed.2015.03.015 · Cited by 83 · see citing works

Modulation of diabetes and dyslipidemia in diabetic insulin-resistant rats by mangiferin: Role of adiponectin and TNF-α

SALEH, S., EL-MARAGHY, N., REDA, E., & BARAKAT, W. (2014) · Anais da Academia Brasileira de Ciências · doi:10.1590/0001-3765201420140212 · Cited by 81 · see citing works

Gastroprotective Effect of Mangiferin, a Xanthonoid from Mangifera indica, against Gastric Injury Induced by Ethanol and Indomethacin in Rodents

Carvalho, A. M., Guedes, M., de Souza, A. Q. L., Trevisan, M. T. S., de Lima, A. K. M. M. N., Santos, F. A., & Rao, V. S. N. (2007) · Planta Medica · doi:10.1055/s-2007-990231 · Cited by 80 · see citing works

Anti-inflammatory effects of mangiferin on sepsis-induced lung injury in mice via up-regulation of heme oxygenase-1

Gong, X., Zhang, L., Jiang, R., Ye, M., Yin, X., & Wan, J. (2012) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2012.09.003 · Cited by 79 · see citing works

Mangiferin ameliorates colitis by inhibiting IRAK1 phosphorylation in NF-κB and MAPK pathways

Jeong, J.-J., Jang, S.-E., Hyam, S. R., Han, M. J., & Kim, D.-H. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.06.013 · Cited by 78 · see citing works

Total Synthesis of Flavocommelin, a Component of the Blue Supramolecular Pigment from Commelina communis, on the Basis of Direct 6-C-Glycosylation of Flavan

Oyama, K., & Kondo, T. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo0494681 · Cited by 78 · see citing works

Suppression of methylglyoxal hyperactivity by mangiferin can prevent diabetes-associated cognitive decline in rats

Liu, Y., Zhu, X., Yang, Q., Lü, Q., Wang, J., Li, H.-P., Wei, Y., Yin, J., & Yin, X. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3061-5 · Cited by 77 · see citing works

Immunotherapeutic effects of mangiferin mediated by the inhibition of oxidative stress to activated lymphocytes, neutrophils and macrophages

Muruganandan, S., Lal, J., & Gupta, P. K. (2005) · Toxicology · doi:10.1016/j.tox.2005.06.008 · Cited by 77 · see citing works

Mangiferin attenuates osteoclastogenesis, bone resorption, and RANKL‐induced activation of NF‐κB and ERK

Ang, E. S. M., Liu, Q., Qi, M., Liu, H. G., Yang, X., Chen, H., Zheng, M., & Xu, J. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22800 · Cited by 76 · see citing works

Mangiferin Ameliorates Scopolamine-Induced Learning Deficits in Mice

Jung, K., Lee, B., Han, S. J., Ryu, J. H., & Kim, D.-H. (2009) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.32.242 · Cited by 75 · see citing works

<i>Mangifera indica</i> L. extract (Vimang) and mangiferin reduce the airway inflammation and Th2 cytokines in murine model of allergic asthma

Rivera, D. G., Hernández, I., Merino, N., Luque, Y., Álvarez, A., Martín, Y., Amador, A., Nuevas, L., & Delgado, R. (2011) · Journal of Pharmacy and Pharmacology · doi:10.1111/j.2042-7158.2011.01328.x · Cited by 74 · see citing works

Mangiferin, a naturally occurring glucoxilxanthone improves long-term object recognition memory in rats

Pardo‐Andreu, G. L., Maurmann, N., Reolon, G. K., de Farias, C. B., Schwartsmann, G., Delgado, R., & Roesler, R. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.03.011 · Cited by 72 · see citing works

Mangiferin in cancer chemoprevention and treatment: pharmacokinetics and molecular targets

Rajendran, P., Rengarajan, T., Nandakumar, N., Divya, H., & Nishigaki, I. (2014) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2014.931431 · Cited by 71 · see citing works

Mangiferin from <i>Salacia chinensis</i> Prevents Oxidative Stress and Protects Pancreatic <b> <i>β</i> </b> -Cells in Streptozotocin-Induced Diabetic Rats

Sellamuthu, P. S., Arulselvan, P., Muniappan, B. P., Fakurazi, S., & Kandasamy, M. (2013) · Journal of Medicinal Food · doi:10.1089/jmf.2012.2480 · Cited by 70 · see citing works

Effect of mangiferin on radiation-induced micronucleus formation in cultured human peripheral blood lymphocytes

Jagetia, G. C., & Venkatesha, V. A. (2005) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20124 · Cited by 70 · see citing works

Mangiferin stimulates carbohydrate oxidation and protects against metabolic disorders induced by high-fat diets

Apontes, P., Liu, Z., Su, K., Benard, O., Youn, D. Y., Li, X., Li, W., Mirza, R. H., Bastie, C. C., Jelicks, L. A., et al. (2014) · Diabetes · doi:10.2337/db14-0006 · Cited by 69 · see citing works

Fe(III) improves antioxidant and cytoprotecting activities of mangiferin

Pardo‐Andreu, G. L., Sánchez-Baldoquín, C., Ávila-González, R., Delgado, R., Naal, Z., & Curti, C. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.07.040 · Cited by 67 · see citing works

Mangiferin induces apoptosis by regulating Bcl-2 and Bax expression in the CNE2 nasopharyngeal carcinoma cell line

Pan, L.-L., Wang, A.-Y., Huang, Y.-Q., Luo, Y., & Ling, M. (2014) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2014.15.17.7065 · Cited by 66 · see citing works

Mangiferin ameliorates 6-hydroxydopamineinduced cytotoxicity and oxidative stress in ketamine model of schizophrenia

Rao, V. S. N., Carvalho, A. C. S., Trevisan, M. T. S., de Andrade, G. M., Júnior, H. V. N., de Moraes, M. O., Iury, H. I. M. H., Morais, T. C., & Santos, F. A. (2012) · Pharmacological Reports · doi:10.1016/s1734-1140(12)70879-4 · Cited by 66 · see citing works

Structure elucidation of in vivo and in vitro metabolites of mangiferin

Liu, H., Wang, K., Tang, Y., Sun, Z., Jian, L., Li, Z., Wu, B., & Huang, C. (2011) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2011.03.012 · Cited by 66 · see citing works

Mangiferin Attenuates Renal Fibrosis Through Down-Regulation of Osteopontin in Diabetic Rats: EFFECTS OF MANGIFERIN ON RENAL FIBROSIS IN DIABETES

Zhu, X., Cheng, Y.-Q., Du, L., Li, Y., Zhang, F., Guo, H., Liu, Y.-W., & Yin, X.-X. (2015) · Phytotherapy Research · doi:10.1002/ptr.5254 · Cited by 66 · see citing works

Synthesis of Mangiferin, Isomangiferin, and Homomangiferin

Wu, Z., Guo, W., Lian, G., & Yu, B. (2010) · The Journal of Organic Chemistry · doi:10.1021/jo100776q · Cited by 66 · see citing works

Mangiferin, a natural occurring glucosyl xanthone, increases susceptibility of rat liver mitochondria to calcium-induced permeability transition

Pardo‐Andreu, G. L., Delgado, R., Velho, J. A., Curti, C., & Vercesi, A. E. (2005) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2005.05.015 · Cited by 66 · see citing works

Mangiferin protects against 1-methyl-4-phenylpyridinium toxicity mediated by oxidative stress in N2A cells

Amazzal, L., Lapôtre, A., Quignon, F., & Bagrel, D. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.03.025 · Cited by 64 · see citing works

Dual mode action of mangiferin in mouse liver under high fat diet

Lim, J., Liu, Z., Apontes, P., Feng, D., Pessin, J. E., Sauve, A. A., Angeletti, R. H., & Chi, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090137 · Cited by 64 · see citing works

Cytoprotective Effect of Mangiferin on Benzo(a)pyrene‐Induced Lung Carcinogenesis in Swiss Albino Mice

Rajendran, P., Ganapathy, E., & Sakthisekaran, D. (2008) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/j.1742-7843.2008.00254.x · Cited by 62 · see citing works

in vitro Modulation of P-glycoprotein, MRP-1 and BCRP Expression by Mangiferin in Doxorubicin-Treated MCF-7 Cells

Louisa, M., Soediro, T. M., & Suyatna, F. D. (2014) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2014.15.4.1639 · Cited by 61 · see citing works

Novel Strategies for Preventing Diabetes and Obesity Complications with Natural Polyphenols

Carpéné, C., Gómez‐Zorita, S., Deleruyelle, S., & Carpene, M. A. (2014) · Current Medicinal Chemistry · doi:10.2174/0929867321666140815124052 · Cited by 61 · see citing works

Mangiferin activates Nrf2-antioxidant response element signaling without reducing the sensitivity to etoposide of human myeloid leukemia cells in vitro

Zhang, B., Zhao, J. J., Li, S., Yang, L., Zeng, L.-L., Chen, Y., & Fang, J. (2013) · Acta Pharmacologica Sinica · doi:10.1038/aps.2013.165 · Cited by 60 · see citing works

Concise Synthesis of Chafurosides A and B

Furuta, T., Nakayama, M., Suzuki, H., Tajimi, H., Inai, M., Nukaya, H., Wakimoto, T., & Kan, T. (2009) · Organic Letters · doi:10.1021/ol900689m · Cited by 60 · see citing works

Untitled work

(2006) · PubMed · Cited by 60 · see citing works

Mangifera indica L: extract (Vimang) and its main polyphenol mangiferin prevent mitochondrial oxidative stress in atherosclerosis-prone hypercholesterolemic mouse

Pardo-Andreu, G. L., Paim, B. A., Castilho, R. F., Velho, J. A., Delgado, R., Vercesi, A. E., & Oliveira, H. C. F. (2008) · Pharmacological Research · doi:10.1016/j.phrs.2008.03.005 · Cited by 58 · see citing works

Mangiferin induces apoptosis by suppressing Bcl-xL and XIAP expressions and nuclear entry of NF-κB in HL-60 cells

Shoji, K., Tsubaki, M., Yamazoe, Y., Satou, T., Itoh, T., Kidera, Y., Tanimori, Y., Yanae, M., Matsuda, H., Taga, A., et al. (2011) · Archives of Pharmacal Research · doi:10.1007/s12272-011-0316-8 · Cited by 57 · see citing works

Soya phospholipid complex of mangiferin enhances its hepatoprotectivity by improving its bioavailability and pharmacokinetics

Bhattacharyya, S., Ahmmed, S. M., Saha, B. P., & Mukherjee, P. K. (2014) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.6422 · Cited by 56 · see citing works

Mangiferin attenuates methylmercury induced cytotoxicity against IMR-32, human neuroblastoma cells by the inhibition of oxidative stress and free radical scavenging potential

Das, S., Rao, B. N., & Rao, B. S. S. (2011) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2011.06.002 · Cited by 51 · see citing works

Mangiferin facilitates islet regeneration and β-cell proliferation through upregulation of cell cycle and β-cell regeneration regulators

Wang, H.-L., Li, C.-Y., Zhang, B., Liu, Y.-D., Lu, B.-M., Shi, Z., An, N., Zhao, L.-K., Zhang, J.-J., Bao, J.-K., et al. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15059016 · Cited by 51 · see citing works

Mangiferin regulates proliferation and apoptosis in glioma cells by induction of microRNA-15b and inhibition of MMP-9 expression

XIAO, J., LIU, L., ZHONG, Z., XIAO, C., & ZHANG, J. (2015) · Oncology Reports · doi:10.3892/or.2015.3919 · Cited by 51 · see citing works

Mangiferin and hesperidin metabolites are absorbed from the gastrointestinal tract of pigs after oral ingestion of a Cyclopia genistoides (honeybush tea) extract

Bock, C., Waldmann, K.-H., & Ternes, W. (2008) · Nutrition Research · doi:10.1016/j.nutres.2008.08.001 · Cited by 50 · see citing works

X-3, a mangiferin derivative, stimulates AMP-activated protein kinase and reduces hyperglycemia and obesity in db/db mice

Han, J., Yi, J., Liang, F., Jiang, B., Xiao, Y., Gao, S., Yang, N., Hu, H., Xie, W.-F., & Chen, W. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.02.008 · Cited by 50 · see citing works

Effect of mangiferin on the development of periodontal disease: Involvement of lipoxin A4, anti-chemotaxic action in leukocyte rolling

Carvalho, R. R., Pellizzon, C. H., Justulin, L. A., Felisbino, S. L., Vilegas, W., Bruni, F. M., Lopes‐Ferreira, M., & Hiruma-Lima, C. A. (2008) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2008.10.041 · Cited by 49 · see citing works

Mangiferin Antagonizes Rotenone: Induced Apoptosis Through Attenuating Mitochondrial Dysfunction and Oxidative Stress in SK-N-SH Neuroblastoma Cells

Kavitha, M., Manivasagam, T., Essa, M. M., Tamilselvam, K., Selvakumar, G. P., Karthikeyan, S., Thenmozhi, J. A., & Subash, S. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1249-7 · Cited by 48 · see citing works

Mangiferin inhibits tumor necrosis factor-α-induced matrix metalloproteinase-9 expression and cellular invasion by suppressing nuclear factor-κB activity

Dilshara, M. G., Kang, C.-H., Choi, Y. H., & Kim, G.-Y. (2015) · BMB Reports · doi:10.5483/bmbrep.2015.48.10.003 · Cited by 47 · see citing works

Inhibition of Matrix Metalloproteinase-1 Induced by Oxidative Stress in Human Keratinocytes by Mangiferin Isolated fromAnemarrhena asphodeloides

Chae, S., Piao, M. J., Kang, K. A., Zhang, R., Kim, K. C., Youn, U. J., Nam, K., Lee, J. H., & Hyun, J. W. (2011) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.110465 · Cited by 46 · see citing works

Mangiferin: A promising therapeutic agent for rheumatoid arthritis treatment

Łuczkiewicz, P., Kokotkiewicz, A., Dampc, A., & Łuczkiewicz, M. (2014) · Medical Hypotheses · doi:10.1016/j.mehy.2014.08.021 · Cited by 44 · see citing works

Potent chemopreventive effect of mangiferin on lung carcinogenesis in experimental Swiss albino mice

Sakthisekaran, D., Rajendran, P., Rengarajan, T., Nishigaki, I., & Ganapathy, E. (2014) · Journal of Cancer Research and Therapeutics · doi:10.4103/0973-1482.137966 · Cited by 44 · see citing works

Efficacy of mangiferin on serum and heart tissue lipids in rats subjected to isoproterenol induced cardiotoxicity

Nair, P. S., & Devi, C. S. S. (2006) · Toxicology · doi:10.1016/j.tox.2006.08.030 · Cited by 44 · see citing works

Peripheral antinociceptive action of mangiferin in mouse models of experimental pain: Role of endogenous opioids, KATP-channels and adenosine

Lopes, S. C., da Silva, A. V. L., Arruda, B. R., Morais, T. C., Rios, J. B., Trevisan, M. T. S., Rao, V. S. N., & Santos, F. A. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.05.016 · Cited by 43 · see citing works

Mangiferin increases Nrf2 protein stability by inhibiting its ubiquitination and degradation in human HL60 myeloid leukemia cells

ZHAO, J., ZHANG, B., LI, S., ZENG, L., CHEN, Y., & FANG, J. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1696 · Cited by 43 · see citing works

Antigenotoxic effect of mangiferin and changes in antioxidant enzyme levels of Swiss albino mice treated with cadmium chloride

Viswanadh, E. K., Rao, B. N., & Rao, B. S. (2010) · Human & Experimental Toxicology · doi:10.1177/0960327110361752 · Cited by 42 · see citing works

On-line purity monitoring in high-speed counter-current chromatography: Application of HSCCC-HPLC-DAD for the preparation of 5-HMF, neomangiferin and mangiferin from Anemarrhena asphodeloides Bunge

Zhou, T., Zhu, Z., Wang, C., Fan, G., Peng, J., Chai, Y., & Wu, Y. (2007) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2007.01.050 · Cited by 42 · see citing works

Mangiferin induces cell cycle arrest at G2/M phase through ATR-Chk1 pathway in HL-60 leukemia cells

Peng, Z. G., Yao, Y. B., Yang, J., Tang, Y. L., & Huang, X. (2015) · Genetics and Molecular Research · doi:10.4238/2015.may.12.2 · Cited by 41 · see citing works

Temperature and solvent dependent NMR studies on mangiferin and complete NMR spectral assignments of its acyl and methyl derivatives

Faizi, S., Zikr‐ur‐Rehman, S., Ali, M. S., & Naz, A. (2006) · Magnetic Resonance in Chemistry · doi:10.1002/mrc.1854 · Cited by 40 · see citing works

Mangiferin, a dietary xanthone protects against mercury‐induced toxicity in HepG2 cells

Agarwala, S., Nageshwar Rao, B., Kaivalya, M., Bhuwania, R., & Rao, B. S. S. (2010) · Environmental Toxicology · doi:10.1002/tox.20620 · Cited by 39 · see citing works

[CML cell line K562 cell apoptosis induced by mangiferin].

Peng, Z., Luo, J., Xia, L.-H., Chen, Y., & Song, S.-J. (2004) · PubMed · Cited by 37 · see citing works

Pharmacological evaluation of mangiferin herbosomes for antioxidant and hepatoprotection potential against ethanol induced hepatic damage

Jain, P. K., Kharya, M. D., & Gajbhiye, A. (2012) · Drug Development and Industrial Pharmacy · doi:10.3109/03639045.2012.738685 · Cited by 36 · see citing works

Mangiferin mitigates diabetic cardiomyopathy in streptozotocin-diabetic rats

Hou, J., Zheng, D., Zhong, G., & Hu, Y. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2013-0090 · Cited by 36 · see citing works

Mangiferin Reduces the Inhibition of Chondrogenic Differentiation by IL-1β in Mesenchymal Stem Cells from Subchondral Bone and Targets Multiple Aspects of the Smad and SOX9 Pathways

Huh, J., Koh, P. S., Seo, B.-K., Park, Y.-C., Baek, Y.-H., Lee, J.-D., & Park, D. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150916025 · Cited by 35 · see citing works

High‐performance liquid chromatographic method for the determination of mangiferin in rat plasma and urine

Wang, H., Ye, G., Tang, Y., Zhu, H., Ma, R., Sun, Z.-L., & Huang, C. (2006) · Biomedical Chromatography · doi:10.1002/bmc.695 · Cited by 35 · see citing works

Antioxidant Activities of Three Dihydrochalcone Glucosides from Leaves of Lithocarpus pachyphyllus

Yang, W., Liu, J., Qin, X.-D., Wu, W.-L., & Chen, Z. (2004) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2004-7-805 · Cited by 33 · see citing works

The effects of mangiferin (Mangifera indica L) in doxorubicin-induced cardiotoxicity in rats

Arozal, W., Suyatna, F., Juniantito, V., Rosdiana, D., Amurugam, S., Aulia, R., Monayo, E., & Siswandi, R. (2014) · Drug Research · doi:10.1055/s-0034-1394457 · Cited by 32 · see citing works

Mangiferin activates the Nrf2-ARE pathway and reduces etoposide-induced DNA damage in human umbilical cord mononuclear blood cells

Zhang, B., Zhao, J. J., Li, S., Linglan, Z., Chen, Y., & Fang, J. (2014) · Pharmaceutical Biology · doi:10.3109/13880209.2014.927890 · Cited by 30 · see citing works

Antidepressant-like effects of a novel 5-HT3 receptor antagonist 6z in acute and chronic murine models of depression

Gupta, D., Radhakrishnan, M., Kurhe, Y., Devadoss, T., Prabhakar, V., & Kanade, P. (2014) · Acta Pharmacologica Sinica · doi:10.1038/aps.2014.89 · Cited by 29 · see citing works

A high-throughput metabolomic approach to explore the regulatory effect of mangiferin on metabolic network disturbances of hyperlipidemia rats

Zhou, C., Li, G., Li, Y., Gong, L., Huang, Y., Shi, Z., Du, S., Li, Y., Wang, M., Yin, J., et al. (2014) · Molecular BioSystems · doi:10.1039/c4mb00421c · Cited by 29 · see citing works

Mangiferin aglycone attenuates radiation‐induced damage on human intestinal epithelial cells

Lei, J., Zhou, C., Hu, H., Hu, L., Zhao, M., Yang, Y., Chuai, Y., Jin, N., & Cai, J. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24138 · Cited by 28 · see citing works

Mangiferin ameliorates the intestinal inflammatory response and the impaired gastrointestinal motility in mouse model of postoperative ileus

Morais, T. C., Arruda, B. R., Magalhães, H. S., Trevisan, M. T. S., Viana, D. D. A., Rao, V. S. N., & Santos, F. A. (2015) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-015-1095-4 · Cited by 26 · see citing works

Anti-hypernociceptive effect of mangiferin in persistent and neuropathic pain models in rats

Garrido‐Suárez, B. B., Garrido, G., Castro-Labrada, M., Merino, N., Valdés, O., Rodeiro, I., Hernández, I., Figueiredo, J. G., Ferreira, S. H., & Delgado, R. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.06.019 · Cited by 25 · see citing works

Mangiferin Regulates Interleukin-6 and Cystathionine-b-Synthase in Lipopolysaccharide-Induced Brain Injury

Fu, Y., Zhang, F., Zhang, L., Liu, H., Zhao, Z., Wen, X., Wu, J. H., Qi, D., Sun, Y., Du, Y., et al. (2014) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-014-0039-8 · Cited by 25 · see citing works

Mangiferin Prevents Guinea Pig Tracheal Contraction via Activation of the Nitric Oxide-Cyclic GMP Pathway

Vieira, A. B., Coelho, L. P., Insuela, D. B. R., Carvalho, V. F., dos Santos, M. H., Silva, P., & Martins, M. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071759 · Cited by 24 · see citing works

Estrogen modulation properties of mangiferin and quercetin and the mangiferin metabolite norathyriol

Wilkinson, A. S., Taing, M., Pierson, J. T., Lin, C.-N., Dietzgen, R. G., Shaw, P. N., Gidley, M. J., Monteith, G. R., & Roberts‐Thomson, S. J. (2015) · Food & Function · doi:10.1039/c5fo00133a · Cited by 23 · see citing works

[The effect of mangiferin on telomerase activity and apoptosis in leukemic K562 cells].

Peng, C., Peng, Z., Yang, J., & Song, S.-J. (2007) · PubMed · Cited by 23 · see citing works

Mangiferin in Leaves of Three Thai Mango (Mangifera indica L.) Varieties

Jutiviboonsuk, A. (2010) · Isan Journal of Pharmaceutical Sciences, IJPS (Isan J Pharm Sci) · doi:10.14456/ijps.2010.28 · Cited by 23 · see citing works

In vitrostudies on mangiferin protection against cadmium-induced human renal endothelial damage and cell death via the MAP kinase and NF-κB pathways

Rajendran, P., Rengarajan, T., Nishigaki, Y., Palaniswami, R., & Nishigaki, I. (2015) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2015.1019137 · Cited by 22 · see citing works

Biotransformation of a C-Glycosylflavone, Abrusin 2-O-.BETA.-D-Apioside, by Human Intestinal Bacteria.

Li, Y., Meselhy, M. R., Wang, L., Ma, C., Nakamura, N., & Hattori, M. (2000) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.48.1239 · Cited by 22 · see citing works

Untitled work

(2010) · PubMed · Cited by 22 · see citing works

Chemopreventive efficacy of mangiferin against benzo(a)pyrene induced lung carcinogenesis in experimental animals

Rajendran, P., Ganapathy, E., Magesh, V., & Sakthisekaran, D. (2008) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2008.05.005 · Cited by 21 · see citing works

Determination of mangiferin in rat eyes and pharmacokinetic study in plasma after oral administration of mangiferin-hydroxypropyl-beta-cyclodextrin inclusion

Zhang, H., Hou, Y., Liu, Y., Yu, X., Li, B., & Cui, H. (2010) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2010.0024 · Cited by 21 · see citing works

Crystalline Structure of Mangiferin, a C‐Glycosyl‐Substituted 9H‐Xanthen‐9‐one Isolated from the Stem Bark of Mangifera indica

Júnior, J. W. D. C., MORAES, L. R. D., dos Santos, M. H., da Silva, G. A., Brigagão, M. R. P. L., Ellena, J., & Doriguetto, A. C. (2008) · Helvetica Chimica Acta · doi:10.1002/hlca.200890005 · Cited by 19 · see citing works

Mangiferin Inhibits Passive Cutaneous Anaphylaxis Reaction and Pruritus in Mice

Lee, B., Trinh, H. T., Bae, E., Jung, K., & Kim, D. (2009) · Planta Medica · doi:10.1055/s-0029-1185773 · Cited by 18 · see citing works

Pharmacokinetic study of mangiferin in rat plasma and retina using high-performance liquid chromatography.

Hou, Y., Fan, S., Zhang, H., Gu, Y., Yu, X., & Li, B. (2010) · PubMed Central · Cited by 14 · see citing works

[Mangiferin promotes uric acid excretion and kidney function improvement and modulates related renal transporters in hyperuricemic mice].

Hu, Q., Zhang, X., Wang, Y., & Kong, L. (2010) · PubMed · Cited by 13 · see citing works

In vitro protective effect of mangiferin against glycated protein-iron chelate induced toxicity in human umbilical vein endothelial cells

Venugopal, R., Sakthiseka, D., Rajkapoor, B., & Nishigaki, I. (2007) · Journal of Biological Sciences · doi:10.3923/jbs.2007.1227.1232 · Cited by 12 · see citing works

Yerba Mate (Ilex Paraguariensis A. St. Hil) and Risk Factors for Cardiovascular Diseases

Pontilho, P. D. M., Teixeira, A. M. N. D. C., BSc, C. Y., Luzia, L. A., Bastos, D. H. M., & Rondó, P. H. D. C. (2015) · Journal of Food and Nutrition Research · doi:10.12691/jfnr-3-3-9 · Cited by 10 · see citing works

[Mangiferin protects rats against chronic bronchitis via regulating NF-kappaB (P65) and IkappaBalpha expression in mononuclear cells].

Zhi-quan, W., Li, Y., Deng, J., & Deng, J. (2014) · PubMed · Cited by 9 · see citing works

Effects of mangiferin on cytokines in rats with chronic bronchitis and expression of macrophage COX-2 in mice

Wang, Q. (2011) · China Journal of Chinese Materia Medica · doi:10.4268/cjcmm20111022 · Cited by 8 · see citing works

Effects of microRNA-139 on myocardial cell injury induced by oxidative stress.

Li, T., Liang, S., Zhang, Y., & Chen, Y. (2015) · PubMed Central · Cited by 8 · see citing works

Heavy metal associated health hazards: An interplay of oxidative stress and signal transduction

Paithankar, J. G., Saini, S., Dwivedi, S., Sharma, A., & Chowdhuri, D. K. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.128350 · Cited by 603 · see citing works

Chemical Composition of Mango (Mangifera indica L.) Fruit: Nutritional and Phytochemical Compounds

Celis, M. E. M., Yahia, E. M., Bedoya, R. A., Landázuri, P., Loango, N., Osma, J. A., Restrepo, B., & Ospina, J. C. G. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01073 · Cited by 539 · see citing works

Nutritional Composition and Bioactive Compounds in Three Different Parts of Mango Fruit

Lebaka, V. R., Wee, Y., Ye, W., & Korivi, M. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18020741 · Cited by 400 · see citing works

Valorization of agro-industrial wastes for biorefinery process and circular bioeconomy: A critical review

Yaashikaa, P. R., Kumar, P. S., & Varjani, S. (2021) · Bioresource Technology · doi:10.1016/j.biortech.2021.126126 · Cited by 360 · see citing works

Mangiferin: A comprehensive review on its extraction, purification and uses in food systems

Castro-Muñoz, R., Cabezas, R., & Plata-Gryl, M. (2024) · Advances in Colloid and Interface Science · doi:10.1016/j.cis.2024.103188 · Cited by 165 · see citing works

A review on coffee leaves: Phytochemicals, bioactivities and applications

Chen, X. (2018) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1546667 · Cited by 138 · see citing works

Mechanisms and therapeutic potential of chinonin in nervous system diseases

Zhang, H., Wang, L., Xue-Qin, W., Deng, L., He, B., & Li, J.-M. (2024) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2024.2371040 · Cited by 137 · see citing works

Effect of feed supplementation with biosynthesized silver nanoparticles using leaf extract of Morus indica L. V1 on Bombyx mori L. (Lepidoptera: Bombycidae)

Some, S., Bulut, O., Biswas, K., Kumar, A., Roy, A., Sen, I. K., Mandal, A., Franco, O. L., İnce, İ. A., Neog, K., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-50906-6 · Cited by 134 · see citing works

An integrated approach for the valorization of mango seed kernel: Efficient extraction solvent selection, phytochemical profiling and antiproliferative activity assessment

Ballesteros-Vivas, D., Álvarez‐Rivera, G., Morantes, S. J., Sánchez‐Camargo, A. D. P., Ibáñez, E., Parada‐Alfonso, F., & Cifuentes, A. (2019) · Food Research International · doi:10.1016/j.foodres.2019.108616 · Cited by 132 · see citing works

Mangiferin prevents myocardial infarction‐induced apoptosis and heart failure in mice by activating the Sirt1/FoxO3a pathway

Chen, L., Li, S., Zhu, J., You, A., Huang, X., Yi, X., & Xue, M. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16329 · Cited by 129 · see citing works

Phytochemical Profile and Antioxidant Capacity of Coffee Plant Organs Compared to Green and Roasted Coffee Beans

Acidri, R., Sawai, Y., Sugimoto, Y., Handa, T., Sasagawa, D., Masunaga, T., Yamamoto, S., & Nishihara, E. (2020) · Antioxidants · doi:10.3390/antiox9020093 · Cited by 120 · see citing works

Mango (Mangifera indicaL.): a magnificent plant with cancer preventive and anticancer therapeutic potential

Mirza, B., Croley, C. R., Ahmad, M., Pumarol, J., Das, N., Sethi, G., & Bishayee, A. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1771678 · Cited by 119 · see citing works

The contribution of mango fruit (Mangifera indica L.) to human nutrition and health

Yahia, E. M., Ornelas‐Paz, J. D. J., Brecht, J. K., García‐Solís, P., & Celis, M. E. M. (2023) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2023.104860 · Cited by 110 · see citing works

From Natural Products to New Synthetic Small Molecules: A Journey through the World of Xanthones

Pinto, M. M. M., Palmeira, A., Fernandes, C., Resende, D. I. S. P., Sousa, E., Cidade, H. M., Tiritan, M. E., Correia‐da‐Silva, M., & Cravo, S. M. M. (2021) · Molecules · doi:10.3390/molecules26020431 · Cited by 100 · see citing works

Effects of phytochemicals against diabetes

Bacanli, M. G., DİLSİZ, S. A., Başaran, N., & Başaran, A. (2019) · Advances in food and nutrition research · doi:10.1016/bs.afnr.2019.02.006 · Cited by 97 · see citing works

A review on valorization of different byproducts of mango (Mangifera indica L.) for functional food and human health

Gupta, A. K., Gurjar, P. S., Beer, K., Pongener, A., Ravi, S., Sıngh, S., Verma, A. K., Singh, A., Thakur, M., Tripathy, S., et al. (2022) · Food Bioscience · doi:10.1016/j.fbio.2022.101783 · Cited by 99 · see citing works

Mangiferin: a review of dietary sources, absorption, metabolism, bioavailability, and safety

Mei, S., Perumal, M., Battino, M., Kitts, D. D., Xiao, J., Ma, H., & Chen, X. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1983767 · Cited by 93 · see citing works

Regulation of immunomodulatory networks by Nrf2-activation in immune cells: Redox control and therapeutic potential in inflammatory diseases

Pant, T., Uche, N., Juric, M., Zielonka, J., & Bai, X. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103077 · Cited by 87 · see citing works

Tropical Fruits and Their Co-Products as Bioactive Compounds and Their Health Effects: A Review

Sáyago‐Ayerdi, S. G., García-Martínez, D. L., Ramírez-Castillo, A. C., Ramírez-Concepción, H. R., & Viuda‐Martos, M. (2021) · Foods · doi:10.3390/foods10081952 · Cited by 82 · see citing works

Phytochemicals and their effective role in the treatment of diabetes mellitus: a short review

Teoh, S. L., & Das, S. (2018) · Phytochemistry Reviews · doi:10.1007/s11101-018-9575-z · Cited by 80 · see citing works

Mango Peels as an Industrial By-Product: A Sustainable Source of Compounds with Antioxidant, Enzymatic, and Antimicrobial Activity

Kučuk, N., Primožič, M., Kotnik, P., Knez, Ž., & Leitgeb, M. (2024) · Foods · doi:10.3390/foods13040553 · Cited by 86 · see citing works

The combinatory effects of natural products and chemotherapy drugs and their mechanisms in breast cancer treatment

Zhang, Y., Li, H., Zhang, J., Zhao, C., Lü, S., Qiao, J., & Han, M. (2019) · Phytochemistry Reviews · doi:10.1007/s11101-019-09628-w · Cited by 76 · see citing works

Bio-molecule functionalized rapid one-pot green synthesis of silver nanoparticles and their efficacy toward the multidrug resistant (MDR) gut bacteria of silkworms ( Bombyx mori )

Some, S., Sarkar, B., Biswas, K., Jana, T. K., Bhattacharjya, D., Dam, P., Mondal, R., Kumar, A., Deb, A. K., Sadat, A., et al. (2020) · RSC Advances · doi:10.1039/d0ra03451g · Cited by 76 · see citing works

Phospholipid complex-loaded self-assembled phytosomal soft nanoparticles: evidence of enhanced solubility, dissolution rate, ex vivo permeability, oral bioavailability, and antioxidant potential of mangiferin

Telange, D. R., Sohail, N. K., Hemke, A. T., Kharkar, P. S., & Pethe, A. M. (2020) · Drug Delivery and Translational Research · doi:10.1007/s13346-020-00822-4 · Cited by 75 · see citing works

Mango Seed Kernel: A Bountiful Source of Nutritional and Bioactive Compounds

Choudhary, P., Devi, T. B., Tushir, S., Kasana, R. C., Dawange, S., & Narsaiah, K. (2022) · Food and Bioprocess Technology · doi:10.1007/s11947-022-02889-y · Cited by 74 · see citing works

Mangifera indica (Mango): A Promising Medicinal Plant for Breast Cancer Therapy and Understanding Its Potential Mechanisms of Action

Yap, K. M., Sekar, M., Seow, L.-J., Gan, S. H., Bonam, S. R., Rani, N. N. I. M., Lum, P. T., Subramaniyan, V., Wu, Y. S., Fuloria, N. K., et al. (2021) · Breast Cancer Targets and Therapy · doi:10.2147/bctt.s316667 · Cited by 81 · see citing works

Mechanism of cadmium-induced nephrotoxicity

Bautista, C. J., Arango, N., Plata, C., Mitre-Aguilar, I. B., Trujillo, J., & Ramírez, V. (2024) · Toxicology · doi:10.1016/j.tox.2024.153726 · Cited by 71 · see citing works

Mangiferin Alleviates Renal Interstitial Fibrosis in Streptozotocin-Induced Diabetic Mice through Regulating the PTEN/PI3K/Akt Signaling Pathway

Song, Y., Liu, W., Tang, K., Zang, J., Li, D., & Gao, H. (2020) · Journal of Diabetes Research · doi:10.1155/2020/9481720 · Cited by 67 · see citing works

Green nanotechnology of MGF-AuNPs for immunomodulatory intervention in prostate cancer therapy

Khoobchandani, M., Khan, A. A., Katti, K. K., Thipe, V. C., Al-Yasiri, A. Y., Mohandoss, D. K. D., Nicholl, M. B., Lugão, A. B., Hans, C. P., & Katti, K. V. (2021) · Scientific Reports · doi:10.1038/s41598-021-96224-8 · Cited by 67 · see citing works

Dietary Antioxidants in Coffee Leaves: Impact of Botanical Origin and Maturity on Chlorogenic Acids and Xanthones

Monteiro, Â. F. A., Colomban, S., Azinheira, H. G., Guerra‐Guimarães, L., Silva, M. D. C., Navarini, L., & Resmini, M. (2019) · Antioxidants · doi:10.3390/antiox9010006 · Cited by 64 · see citing works

Mangiferin nanoemulsions in treatment of inflammatory disorders and skin regeneration

Pleguezuelos-Villa, M., Nácher, A., Hernández, M. J., Busó, M. A. O. V., Ruiz‐Saurí, A., & Dı́ez-Sales, O. (2019) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2019.04.056 · Cited by 61 · see citing works

Mangiferin glycethosomes as a new potential adjuvant for the treatment of psoriasis

Pleguezuelos-Villa, M., Dı́ez-Sales, O., Manca, M. L., Manconi, M., Ruiz‐Saurí, A., Escribano‐Ferrer, E., & Nácher, A. (2019) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2019.118844 · Cited by 61 · see citing works

Innovative Strategies to Treat Skin Wounds with Mangiferin: Fabrication of Transfersomes Modified with Glycols and Mucin

Allaw, M., Pleguezuelos-Villa, M., Manca, M. L., Caddeo, C., Aroffu, M., Nácher, A., Dı́ez-Sales, O., Ruiz‐Saurí, A., Ferrer, E. E., Fadda, A. M., et al. (2020) · Nanomedicine · doi:10.2217/nnm-2020-0116 · Cited by 61 · see citing works

Natural products for the treatment and management of diabetes mellitus in Zimbabwe-a review

Usai, R., Majoni, S., & Rwere, F. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.980819 · Cited by 60 · see citing works

Anti-oxidative effect of mangiferin-chitosan nanoparticles on oxidative stress-induced renal cells

Samadarsi, R., & Dutta, D. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.02.112 · Cited by 57 · see citing works

Utilization of Swertia chirayita Plant Extracts for Management of Diabetes and Associated Disorders: Present Status, Future Prospects and Limitations

Dey, P., Singh, J., Suluvoy, J. K., Dilip, K. J., & Nayak, J. (2020) · Natural Products and Bioprospecting · doi:10.1007/s13659-020-00277-7 · Cited by 61 · see citing works

The management of diabetes mellitus by mangiferin: advances and prospects

Wang, M., Liang, Y., Chen, K., Wang, M., Long, X., Liu, H., Sun, Y., & He, B. (2022) · Nanoscale · doi:10.1039/d1nr06690k · Cited by 56 · see citing works

Mangiferin ameliorates acetaminophen-induced hepatotoxicity through APAP-Cys and JNK modulation

Chowdhury, A., Lu, J., Zhang, R., Jahan, N., Gao, H., Wan, Z., Adelusi, T. I., Yin, X., & Sun, Y. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109097 · Cited by 56 · see citing works

Mangiferin Alleviates Ovalbumin-Induced Allergic Rhinitis via Nrf2/HO-1/NF-κB Signaling Pathways

Piao, C. H., Fan, Y. J., Nguyen, T. V., Song, C. H., & Chai, O. H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103415 · Cited by 56 · see citing works

Obesity‐Associated Diseases Biomarkers Are Differently Modulated in Lean and Obese Individuals and Inversely Correlated to Plasma Polyphenolic Metabolites After 6 Weeks of Mango (Mangifera indica L.) Consumption

Fang, C., Kim, H., Barnes, R. C., Talcott, S. T., & Mertens‐Talcott, S. U. (2018) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201800129 · Cited by 52 · see citing works

Serum Metabolomics of Activity Energy Expenditure and its Relation to Metabolic Syndrome and Obesity

Palmnäs, M. S. A., Kopciuk, K. A., Shaykhutdinov, R. A., Robson, P. J., Mignault, D., RABASA-LHORET, R. P. R., Vogel, H. J., & Csizmadi, I. (2018) · Scientific Reports · doi:10.1038/s41598-018-21585-6 · Cited by 52 · see citing works

Therapeutic potential of mangiferin in the treatment of various neuropsychiatric and neurodegenerative disorders

Walia, V., Chaudhary, S. K., & Kumar Sethiya, N. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2020.104939 · Cited by 51 · see citing works

Natural antioxidants’ effects on endoplasmic reticulum stress-related diseases

Reyes-Fermín, L. M., Aparicio-Trejo, O. E., Avila-Rojas, S. H., Gómez-Sierra, T., Martínez-Klimova, E., & Pedraza-Chaverri, J. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111229 · Cited by 50 · see citing works

Mangiferin exert cardioprotective and anti-apoptotic effects in heart failure induced rats

Jiang, T., Han, F., Gao, G., & Liu, M. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117476 · Cited by 49 · see citing works

Utilisation of Mangifera indica plant extracts and parts in antimicrobial formulations and as a pharmaceutical excipient: a review

Alaiya, M. A., & Odeniyi, M. A. (2023) · Future Journal of Pharmaceutical Sciences · doi:10.1186/s43094-023-00479-z · Cited by 53 · see citing works

The role of inflammation in cadmium nephrotoxicity: NF-κB comes into view

Hassanein, E. H. M., Mohamed, W. R., Ahmed, O. S., Abdel‐Daim, M. M., & Sayed, A. M. M. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120971 · Cited by 48 · see citing works

Medicinal Plants and Bioactive Phytochemical Diversity: A Fountainhead of Potential Drugs Against Human Diseases

Halder, M., & Jha, S. (2023) · Sustainable development and biodiversity · doi:10.1007/978-981-19-9936-9_2 · Cited by 51 · see citing works

Potential of herb-drug / herb interactions between substrates and inhibitors of UGTs derived from herbal medicines

Liu, D., Zhang, L., Duan, L., Wu, J., Hu, M., Liu, Z., & Wang, C. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.104510 · Cited by 47 · see citing works

Mango Peel Pectin: Recovery, Functionality and Sustainable Uses

Wongkaew, M., Chaimongkol, P., Leksawasdi, N., Jantanasakulwong, K., Rachtanapun, P., Seesuriyachan, P., Phimolsiripol, Y., Chaiyaso, T., Ruksiriwanich, W., Jantrawut, P., et al. (2021) · Polymers · doi:10.3390/polym13223898 · Cited by 35 · see citing works

Mangiferin attenuates cisplatin-induced acute kidney injury in rats mediating modulation of MAPK pathway

Sahu, A. K., Verma, V. K., Mutneja, E., Malik, S., Nag, T. C., Dinda, A. K., Arya, D. S., & Bhatia, J. (2018) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-018-3420-y · Cited by 45 · see citing works

A Comprehensive Review of Various Therapeutic Strategies for the Management of Skin Cancer

Dachani, S. R., Kaleem, M., Mujtaba, M. A., Mahajan, N. M., Ali, S. A., Almutairy, A. F., Mahmood, D., Anwer, M. K., Ali, M. D., & Kumar, S. (2024) · ACS Omega · doi:10.1021/acsomega.3c09780 · Cited by 44 · see citing works

Neuroprotective mechanisms of mangiferin in neurodegenerative diseases

Liu, T., Song, Y., & Hu, A. (2021) · Drug Development Research · doi:10.1002/ddr.21783 · Cited by 43 · see citing works

Gold Nanoparticles Synthesized Using Extracts of Cyclopia intermedia, Commonly Known as Honeybush, Amplify the Cytotoxic Effects of Doxorubicin

Aboyewa, J. A., Sibuyi, N. R. S., Meyer, M., & Oguntibeju, O. O. (2021) · Nanomaterials · doi:10.3390/nano11010132 · Cited by 43 · see citing works

Anti-inflammatory and immunomodulatory activity of Mangifera indica L. reveals the modulation of COX-2/mPGES-1 axis and Th17/Treg ratio

Saviano, A., Raucci, F., Casillo, G. M., Mansour, A. A., Piccolo, V., Montesano, C., Smimmo, M., Vellecco, V., Capasso, G., Boscaino, A., et al. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106283 · Cited by 42 · see citing works

A Review of Medicinal Plants with Renoprotective Activity in Diabetic Nephropathy Animal Models

Putra, I. M. W. A., Fakhrudin, N., Nurrochmad, A., & Wahyuono, S. (2023) · Life · doi:10.3390/life13020560 · Cited by 44 · see citing works

In Vitro Anthelmintic Activity of Four Plant-Derived Compounds against Sheep Gastrointestinal Nematodes

Federica, G., Mattellini, M., Fichi, G., Flamini, G., & Perrucci, S. (2018) · Veterinary Sciences · doi:10.3390/vetsci5030078 · Cited by 42 · see citing works

Synthetic Chiral Derivatives of Xanthones: Biological Activities and Enantioselectivity Studies

Fernandes, C., Carraro, M. L., Ribeiro, J., Araújo, J., Tiritan, M. E., & Pinto, M. M. M. (2019) · Molecules · doi:10.3390/molecules24040791 · Cited by 42 · see citing works

Anticancer Potential of Dietary Natural Products: A Comprehensive Review

Ahmad, R., Khan, M. A., Srivastava, A., Gupta, A., Srivastava, A., Jafri, T. R., Siddiqui, Z., Chaubey, S., Khan, T., & Srivastava, A. K. (2019) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520619666191015103712 · Cited by 40 · see citing works

SIRT1/PGC-1α signaling activation by mangiferin attenuates cerebral hypoxia/reoxygenation injury in neuroblastoma cells

Chen, M., Wang, Z., Zhou, W., Lu, C., Ji, T., Yang, W., Jin, Z., Tian, Y., Lei, W., Wu, S., et al. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174236 · Cited by 40 · see citing works

Mangiferin: A promising natural xanthone from Mangifera indica for the control of acyclovir – resistant herpes simplex virus 1 infection

Rechenchoski, D. Z., Agostinho, K. F., Galhardi, L. C. F., Lonni, A. A. S. G., da Silva, J. V. H., de Andrade, F. G., Cunha, A. P., Ricardo, N. M. P. S., Nozawa, C., & Linhares, R. E. C. (2020) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2020.115304 · Cited by 39 · see citing works

Therapeutic potential of mangiferin against kidney disorders and its mechanism of action: A review

Lum, P. T., Sekar, M., Gan, S. H., Jeyabalan, S., Bonam, S. R., Rani, N. N. I. M., Ku-Mahdzir, K.-M., Seow, L.-J., Wu, Y. S., Subramaniyan, V., et al. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2021.11.016 · Cited by 40 · see citing works

Mangifera indica L., By-Products, and Mangiferin on Cardio-Metabolic and Other Health Conditions: A Systematic Review

Minniti, G., Laurindo, L. F., Machado, N. M., Duarte, L. G., Guiguer, E. L., Araujo, A. C., Dias, J. A., Lamas, C. B., Nunes, Y. C., Bechara, M. D., et al. (2023) · Life · doi:10.3390/life13122270 · Cited by 38 · see citing works

Prelusive scale extraction of mangiferin from Mangifera indica leaves: Assessing solvent competency, process optimization, kinetic study and diffusion modelling

Anbalagan, K., Kumar, M. M., Ilango, K., Mohankumar, R., & Priya, R. L. (2019) · Industrial Crops and Products · doi:10.1016/j.indcrop.2019.111703 · Cited by 37 · see citing works

The multifaceted role of mangiferin in health and diseases: a review

Jangra, A., Arora, M. K., Kisku, A., & Sharma, S. (2020) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-020-00471-5 · Cited by 37 · see citing works

In Silico and In Vitro Screening of Natural Compounds as Broad‐Spectrum β ‐Lactamase Inhibitors against Acinetobacter baumannii New Delhi Metallo‐ β ‐lactamase‐1 (NDM‐1)

Vasudevan, A., Kesavan, D. K., Wu, L., Su, Z., Wang, S., Ramasamy, M., Hopper, W., & Xu, H. (2022) · BioMed Research International · doi:10.1155/2022/4230788 · Cited by 36 · see citing works

Mangiferin suppresses allergic asthma symptoms by decreased Th9 and Th17 responses and increased Treg response

Yun, C., Chang, M., Hou, G.-H., Lan, T., Yuan, H., Su, Z., Zhu, D., Liang, W., Li, Q., Zhu, H., et al. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.07.025 · Cited by 36 · see citing works

Adipose tissue as a possible therapeutic target for polyphenols: A case for Cyclopia extracts as anti-obesity nutraceuticals

Jack, B. U., Malherbe, C. J., Mamushi, M., Muller, C. J. F., Joubert, E., Louw, J., & Pheiffer, C. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109439 · Cited by 35 · see citing works

Mangiferin Mitigates Lipopolysaccharide-Induced Lung Injury by Inhibiting NLRP3 Inflammasome Activation

Li, N., Xiong, R., He, R., Liu, B., Wang, B., & Geng, Q. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s304492 · Cited by 34 · see citing works

A Self‐Gelling Powder Directly Co‐Assembled by Natural Small Molecules for Traumatic Brain Injury

Yang, S., Luo, W., Song, X., Chen, Q., Liu, J., Gan, P., Liu, C., Li, T., Xu, G., Zhang, Y., et al. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202401485 · Cited by 34 · see citing works

Mangiferin inhibits cell migration and angiogenesis via PI3K/AKT/mTOR signaling in high glucose‑ and hypoxia‑induced RRCECs

Shi, J., Lv, H., Tang, C., Li, Y., Huang, J., & Zhang, H. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.12112 · Cited by 34 · see citing works

Prospective Evaluation of Mango Fruit Intake on Facial Wrinkles and Erythema in Postmenopausal Women: A Randomized Clinical Pilot Study

Fam, V. W., Holt, R. R., Keen, C. L., Sivamani, R. K., & Hackman, R. M. (2020) · Nutrients · doi:10.3390/nu12113381 · Cited by 35 · see citing works

Pharmacokinetic and metabolomic analyses of Mangiferin calcium salt in rat models of type 2 diabetes and non-alcoholic fatty liver disease

Lin, H., Teng, H., Wu, W., Li, Y., Lv, G., Huang, X., Yan, W., & Lin, Z. (2020) · BMC Pharmacology and Toxicology · doi:10.1186/s40360-020-00438-x · Cited by 32 · see citing works

Response surface optimization of microfluidic formulations of nanobilosomes for enhancement of aqueous solubility, digestive stability, and cellular antioxidant activity of mangiferin

Thiengkaew, P., Thanitwatthanasak, S., Srisala, S., Jittorntrum, B., Chunhabundit, R., & Chitprasert, P. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.129315 · Cited by 32 · see citing works

Mangifera indica L. Leaves as a Potential Food Source of Phenolic Compounds with Biological Activity

Sferrazzo, G., Palmeri, R., Restuccia, C., Parafati, L., Siracusa, L., Spampinato, M., Carota, G., Distefano, A., Di Rosa, M., Tomasello, B., et al. (2022) · Antioxidants · doi:10.3390/antiox11071313 · Cited by 31 · see citing works

Natural products, an important resource for discovery of multitarget drugs and functional food for regulation of hepatic glucose metabolism

Li, J., Yu, H., Wang, S., Wang, W., Chen, Q., Ma, Y., Zhang, Y., & Wang, T. (2018) · Drug Design Development and Therapy · doi:10.2147/dddt.s151860 · Cited by 31 · see citing works

Mechanism of anti-dementia effects of mangiferin in a senescence accelerated mouse (SAMP8) model

Du, Z., Fanshi, F., Lai, Y.-H., Chen, J.-R., Hao, E., Deng, J., & Hsiao, C.-D. (2019) · Bioscience Reports · doi:10.1042/bsr20190488 · Cited by 30 · see citing works

Natural Antidiabetic Agents: Current Evidence and Development Pathways from Medicinal Plants to Clinical use

Uti, D. E., Atangwho, I. J., Alum, E. U., Egba, S. I., Ugwu, O. P.-C., & Ikechukwu, G. C. (2025) · Natural Product Communications · doi:10.1177/1934578x251323393 · Cited by 58 · see citing works

Anti-angiogenic effects of mangiferin and mechanism of action in metastatic melanoma

Delgado-Hernández, R., Hernández-Balmaseda, I., Rodeiro-Guerra, I., Cesar Rodriguez Gonzalez, J., De Wever, O., Logie, E., Declerck, K., Pérez-Novo, C., & Vanden Berghe, W. (2020) · Melanoma Research · doi:10.1097/cmr.0000000000000647 · Cited by 29 · see citing works

Discovery of natural products with metal-binding properties as promising antibacterial agents

Dandawate, P. R., Padhyé, S., Schobert, R., & Biersack, B. (2019) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2019.1593367 · Cited by 29 · see citing works

Chemotherapy-Mediated Neuronal Aberration

Jaiswara, P. K., & Shukla, S. K. (2023) · Pharmaceuticals · doi:10.3390/ph16081165 · Cited by 28 · see citing works

Mangiferin alleviates diabetic pulmonary fibrosis in mice via inhibiting endothelial-mesenchymal transition through AMPK/FoxO3/SIRT3 axis

Fu, T.-L., Li, G.-R., Li, D.-H., He, R.-Y., Liu, B.-H., Xiong, R., Xu, C.-Z., Lu, Z.-L., Song, C.-K., Qiu, H.-L., et al. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01202-7 · Cited by 27 · see citing works

Beyond Antioxidants: How Redox Pathways Shape Cellular Signaling and Disease Outcomes

Sulaiman, A. A., & Katanaev, V. L. (2025) · Antioxidants · doi:10.3390/antiox14091142 · Cited by 28 · see citing works

Trends and Possibilities of the Usage of Medicinal Herbal Extracts in Beverage Production

Suna, S., Tamer, C. E., & Sinir, G. Ö. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816689-5.00013-4 · Cited by 27 · see citing works

A pervasive scientific overview on mangiferin in the prevention and treatment of various diseases with preclinical and clinical updates

Mittal, S., Iqubal, M. K., Iqbal, B., Gupta, M. M., Ali, J., & Baboota, S. (2020) · Journal of Complementary and Integrative Medicine · doi:10.1515/jcim-2019-0250 · Cited by 27 · see citing works

From Nature to Nanotechnology: The Bioactivities of Mangiferin Explored

Al-Madhagi, H. (2025) · Nanotechnology, Science and Applications · doi:10.2147/nsa.s525423 · Cited by 26 · see citing works

Potential enzyme inhibitory properties of extracts and fractions from fruit latex of Ficus carica-based on inhibition of α-amylase and α-glucosidase

Paşayeva, L., Özalp, B., & Fatullayev, H. (2020) · Journal of Food Measurement & Characterization · doi:10.1007/s11694-020-00527-9 · Cited by 26 · see citing works

“Multiomics” Analyses Combined with Systems Pharmacology Reveal the Renoprotection of Mangiferin Monosodium Salt in Rats with Diabetic Nephropathy: Focus on Improvements in Renal Ferroptosis, Renal Inflammation, and Podocyte Insulin Resistance

Zhao, C., Pu, Z., Gao, J., Liu, C., Xing, J., Lang, W., Chen, J., Yuan, C., & Zhou, C. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c05595 · Cited by 26 · see citing works

Phytochemicals as Immunomodulatory Agents in Melanoma

Tabolacci, C., Vita, D. D., Facchiano, A., Bozzuto, G., Beninati, S., Failla, C. M., Martile, M. D., Lintas, C., Mischiati, C., Stringaro, A., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032657 · Cited by 29 · see citing works

Mangiferin alleviates experimental peri-implantitis via suppressing interleukin-6 production and Toll-like receptor 2 signaling pathway

Li, H., Chen, Z., Zhong, X., Li, J., & Li, W. (2019) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-019-1387-3 · Cited by 26 · see citing works

Mangiferin protect oxidative stress against deoxynivalenol induced damages through Nrf2 signalling pathways in endothelial cells

Al‐Saeedi, F. J. (2020) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13432 · Cited by 25 · see citing works

Effects of fresh mango consumption on cardiometabolic risk factors in overweight and obese adults

Rosas, M., Pinneo, S., O'Mealy, C., Tsang, M., Liu, C., Kern, M., Hooshmand, S., & Hong, M. Y. (2022) · Nutrition, Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2021.11.001 · Cited by 25 · see citing works

Selected Plant-Derived Polyphenols as Potential Therapeutic Agents for Peripheral Artery Disease: Molecular Mechanisms, Efficacy and Safety

Froldi, G., & Ragazzi, E. (2022) · Molecules · doi:10.3390/molecules27207110 · Cited by 27 · see citing works

Phospholipid-Based Topical Nano-Hydrogel of Mangiferin: Enhanced Topical Delivery and Improved Dermatokinetics

Alkholifi, F. K., Alam, A., Foudah, A. I., & Yusufoglu, H. S. (2023) · Gels · doi:10.3390/gels9030178 · Cited by 24 · see citing works

Dry amorphisation of mangiferin, a poorly water-soluble compound, using mesoporous silica

Baán, A., Adriaensens, P., Lammens, J., Delgado, R., Berghe, W. V., Pieters, L. A. C., Vervaet, C., & Kiekens, F. (2019) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2019.05.026 · Cited by 24 · see citing works

A Molecular Approach on the Protective Effects of Mangiferin Against Diabetes and Diabetes-related Complications

Aswal, S., Kumar, A., Chauhan, A., Semwal, R. B., Kumar, A., & Semwal, D. K. (2019) · Current Diabetes Reviews · doi:10.2174/1573399815666191004112023 · Cited by 24 · see citing works

Extract of Aquilaria crassna leaves and mangiferin are vasodilators while showing no cytotoxicity

Wisutthathum, S., Kamkaew, N., Inchan, A., Chatturong, U., Paracha, T. U., Ingkaninan, K., Wongwad, E., & Chootip, K. (2018) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2018.09.002 · Cited by 23 · see citing works

Cotton dyeing performance enhancing mechanism of mangiferin enriched bio-waste by transition metals chelation

Islam, M. T., Liman, M. L. R., Roy, M. N., Hossain, M. M., Repon, M. R., & Mamun, M. A. A. (2021) · Journal of the Textile Institute · doi:10.1080/00405000.2021.1892337 · Cited by 23 · see citing works

Supercritical antisolvent fractionation as a tool for enhancing antiproliferative activity of mango seed kernel extracts against colon cancer cells

Ballesteros-Vivas, D., Álvarez‐Rivera, G., Ocampo, A. F. G., Morantes, S. J., Sánchez‐Camargo, A. D. P., Cifuentes, A., Parada‐Alfonso, F., & Ibáñez, E. (2019) · The Journal of Supercritical Fluids · doi:10.1016/j.supflu.2019.104563 · Cited by 23 · see citing works

Allelopathy and allelopathic substances of mango ( Mangifera indica L.)

Kato‐Noguchi, H., & Kurniadie, D. (2020) · Weed Biology and Management · doi:10.1111/wbm.12212 · Cited by 23 · see citing works

Improving Aqueous Solubility of Natural Antioxidant Mangiferin through Glycosylation by Maltogenic Amylase from Parageobacillus galactosidasius DSM 18751

Wu, J., Ding, H., Wang, T., Tsai, Y.-L., Ting, H., & Chang, T. (2021) · Antioxidants · doi:10.3390/antiox10111817 · Cited by 23 · see citing works

Mangiferin: An effective therapeutic agent against several disorders (Review)

Du, S., Liu, H., Lei, T., Xie, X., Wang, H., He, X., Tong, R., & Wang, Y. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9529 · Cited by 139 · see citing works

In-depth analysis of the chemical composition, pharmacological effects, pharmacokinetics, and patent history of mangiferin

Kaurav, M., Kanoujia, J., Gupta, M., Goyal, P., Pant, S., Rai, S., Sahu, K. K., Bhatt, P., & Ghai, R. (2023) · Phytomedicine Plus · doi:10.1016/j.phyplu.2023.100445 · Cited by 27 · see citing works

Perspectives on the potential of Mangiferin as a nutraceutical: a review

Jamwal, D., Saini, P., Tomar, P. C., & Ghosh, A. (2022) · Nutrition & Food Science · doi:10.1108/nfs-01-2022-0013 · Cited by 2 · see citing works

MANGIFERIN FROM MANGIFERA INDICA LINN.: A PHARMACOLOGICAL STUDY

Biswas, M., & Mistry, J. (2020) · Journal of Advanced Scientific Research

Mangiferin and Cancer: Mechanisms of Action

Gold-Smith, F., Fernandez, A., & Bishop, K. (2016) · Nutrients · doi:10.3390/nu8070396 · Cited by 158 · see citing works