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DOI: 10.1055/a-2690-9342
Exploring Chalcone Derivatives Against Alzheimer’s Disease: Biological Activity and Structure–Activity Relationships
Authors

Abstract
Chalcone is a versatile scaffold that has gained attention for its potential in developing treatments for Alzheimer’s disease (AD). This review highlights recent progress in the design and evaluation of chalcone hybrids and derivatives with anti-Alzheimer activity, particularly against key enzymes such as acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and monoamine oxidases (MAO-A and MAO-B). Many of these compounds show promising inhibition, suggesting their potential to improve cholinergic transmission and reduce neurodegeneration. Structure–activity relationship (SAR) studies reveal that substitution patterns on aromatic rings strongly influence activity. Oxindole-based chalcone analogues (5) were good AChE inhibitors, while chalcone–rivastigmine hybrids (11) were excellent BChE inhibitors. For MAO-B, 4-aminochalcone–rivastigmine hybrids (10) and morpholine-based chalcone hybrids (20) were potent inhibitors. Molecular docking studies further explain how these molecules interact with target enzymes, supporting their biological relevance. The combination of pharmacophores with the chalcone core has also improved selectivity and potency. Overall, the findings summarized in this review suggest that chalcone-based compounds are promising candidates for further development as anti-Alzheimer agents. With their multitarget potential and ease of structural modification, chalcones represent a valuable pharmacophore for addressing the complex pathology of AD. Future work focusing on rational design and computational tools may enable the discovery of effective therapies.
Declaration of generative AI in scientific writing
The authors declare that they have not used any AI tool in scientific writing.
Publication History
Received: 24 July 2025
Accepted after revision: 26 August 2025
Accepted Manuscript online:
26 August 2025
Article published online:
23 September 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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References
- 1 Magalingam KB, Radhakrishnan A, Ping NS, Haleagrahara N. Biomed Res Int 2018; 2018 (01) 3740461
- 2 Javaid SF, Giebel C, Khan MA, Hashim MJ. F1000Res 2021; 10: 425
- 3 Global Status Report on the Public Health Response to Dementia. 2021
- 4 Wimo A, Seeher K, Cataldi R. et al. Alzheimers Dement 2023; 19 (07) 2865-2873
- 5 Association As. 2019 Alzheimer’s disease facts and figures. Alzheimers Dement 2019; 15 (03) 321-387
- 6 Tatulian SA. Drug Discovery Today 2022; 27 (04) 1027-1043
- 7 Van Cauwenberghe C, Van Broeckhoven C, Sleegers K. Genet Med 2016; 18 (05) 421-430
- 8 Brück CC, Wolters FJ, Ikram MA, de Kok IM. Alzheimers Dement 2023; 19 (10) 4532-4541
- 9 Chen S, Cao Z, Nandi A. et al. Lancet Glob Health 2024; 12 (09) e1534-e1543
- 10 Atri A. Med Clin North Am 2019; 103 (02) 263-293
- 11 Reisberg B, Gordon B, McCarthy M, Ferris SH. Alzheimer’s Dement: Dilemmas Clin Res 1985; 19-39
- 12 Husain MM, Garrett RK. Neuroimag Clin 2005; 15 (04) 767-777
- 13 Gupta UJ, Jacobsen J, Haider MA, Mushtaq S. IGI Global 2024; 303-325
- 14 Zarit SH, Talley RC. Caregiving for Alzheimer’s Disease and Related Disorders. Springer; 2012
- 15 DeTure MA, Dickson DW. Mol Neurodegener 2019; 14 (01) 32
- 16 Gallardo G, Holtzman DM. Tau Biol 2020; 187-203
- 17 Moloney CM, Lowe VJ, Murray ME. Alzheimers Dement 2021; 17 (09) 1554-1574
- 18 Ashford JW. J Alzheimer’s Dis 2019; 68 (01) 77-83
- 19 Shankar GM, Walsh DM. Mol Neurodegener 2009; 4: 1-13
- 20 Tönnies E, Trushina E. J Alzheimer’s Dis 2017; 57 (04) 1105-1121
- 21 Jasim HA, Nahar L, Jasim MA, Moore SA, Ritchie KJ, Sarker SD. Biomolecules 2021; 11 (08) 1203
- 22 Yazdan SK, Sagar GV, Shaik AB. J Chem Pharm Res 2015; 7 (11) 829-842
- 23 Gomes MN, Muratov EN, Pereira M. et al. Molecules 2017; 22 (08) 1210
- 24 Zhuang C, Zhang W, Sheng C, Zhang W, Xing C, Miao Z. Chem Rev 2017; 117 (12) 7762-7810
- 25 Singh UP, Pathak M, Dubey V, Bhat HR, Gahtori P, Singh RK. Chem Biol Drug Des 2012; 80 (04) 572-583
- 26 Zhang X, Rakesh K, Bukhari SNA, Balakrishna M, Manukumar H, Qin H-L. Bioorg Chem 2018; 80: 86-93
- 27 DeToma AS, Krishnamoorthy J, Nam Y. et al. Chem Sci 2014; 5 (12) 4851
- 28 Šimić G, Babić Leko M, Wray S. et al. Biomolecules 2016; 6 (01) 6
- 29 Mathew B, Parambi DG, Sivasankarapillai VS. et al. CNS Neurol Disord-Drug Targets-CNS Neurol Disord 2019; 18 (06) 432-445
- 30 Simunkova M, Alwasel SH, Alhazza IM. et al. Arch Toxicol 2019; 93 (09) 2491-2513
- 31 Perry G, Taddeo MA, Nunomura A. et al. Comp Biochem Physiol C 2002; 133 (04) 507-513
- 32 Buccellato FR, D’Anca M, Fenoglio C, Scarpini E, Galimberti D. Antioxidants 2021; 10 (09) 1353
- 33 Salehi B, Quispe C, Chamkhi I. et al. Front Pharmacol 2021; 11: 592654
- 34 Adelusi TI, Akinbolaji GR, Yin X, Ayinde KS, Olaoba OT. Eur J Pharmacol 2021; 891: 173695
- 35 Bhatia R, Chakrabarti SS, Kaur U, Parashar G, Banerjee A, Rawal RK. Curr Alzheimer Res 2021; 18 (10) 802-830
- 36 Alarcón-Espósito J, Mallea M, Rodríguez-Lavado J. Curr Neuropharmacol 2021; 19 (06) 832-867
- 37 Rani H. Curr Bioact Compd 2024; 20 (01) 80-99
- 38 Sharma D, Dhobi M, Lather V, Pandita D. Naunyn Schmiedeberg’s Arch Pharmacol 2024; 397 (12) 9503-9519
- 39 Malaník M. Phytochem Rev 2025; 1-19
- 40 Ali Z, Hawwal M, Ahmed MM. et al. Nat Prod Res 2021; 36 (01) 200-206
- 41 El-Saber Batiha G, Magdy Beshbishy A, El-Mleeh A, Abdel-Daim M, Prasad Devkota H. Biomolecules 2020; 10 (03) 352
- 42 Souza JM, de Carvalho ÉA, Candido ACB. et al. Science 2020; 7: 527
- 43 Li Z, Li B, Chen Z. et al. J Med Virol 2023; 95 (08) e29059
- 44 Park HG, Bak EJ, Woo G-H. et al. J Nutr Biochem 2012; 23 (07) 759-767
- 45 Wang Y, Su C, Zhang B. et al. Evid Based Complement Alternat Med 2021; 2021 (01) 6851798
- 46 Abu N, Ho WY, Yeap SK. et al. Cancer Cell Int 2013; 13: 1-7
- 47 Golmei P, Kasna S, Kumar S. Health Sci Rev 2024; 100197
- 48 Padmavathi G, Roy NK, Bordoloi D. et al. Phytomedicine 2017; 25: 118-127
- 49 Elkhalifa D, Al-Hashimi I, Al Moustafa A-E, Khalil A. J Drug Target 2021; 29 (04) 403-419
- 50 Asif M. Chem Int 2016; 2 (01) 1-18
- 51 Wang K-L, Yu Y-C, Hsia S-M. Cancers 2021; 13 (01) 115
- 52 Zhang B, Lai Y, Li Y. et al. Eur J Pharmacol 2018; 821: 57-67
- 53 Chen M, Theander TG, Christensen SB, Hviid L, Zhai L, Kharazmi A. Antimicrob Agents Chemother 1994; 38 (07) 1470-1475
- 54 Li J, Zheng L, Yan M. et al. Oncol Lett 2020; 19 (01) 379-387
- 55 Feldman M, Tanabe S, Epifano F, Genovese S, Curini M, Grenier D. J Nat Prod 2011; 74 (01) 26-31
- 56 Chen W, Song J, Guo P, Wen Z. J Mol Struct THEOCHEM 2006; 763 (1/3) 161-164
- 57 Cheng Z-J, Kuo S-C, Chan S-C, Ko F-N, Teng C-M. Metabolism 1998; 1392 (2/3) 291-299
- 58 Kuete V, Sandjo LP. Chin J Integr Med 2012; 18 (07) 543-547
- 59 Wang M, Lin L, Lu J-J, Chen X. Pharmacol Res 2021; 165: 105483
- 60 Gao X, Jiang Y, Xu Q. et al. Foods 2021; 10 (09) 2036
- 61 Sumiyoshi M, Taniguchi M, Baba K, Kimura Y. Phytomedicine 2015; 22 (7/8) 759-767
- 62 Tabata K, Motani K, Takayanagi N. et al. Biol Pharm Bull 2005; 28 (08) 1404-1407
- 63 Mizar P, Arya R, Kim T. et al. J Med Chem 2018; 61 (23) 10473-10487
- 64 Hseu Y-C, Chiang Y-C, Vudhya Gowrisankar Y. et al. Cancers 2020; 12 (10) 2936
- 65 Rampa A, Bartolini M, Pruccoli L. et al. Molecules 2018; 23 (08) 1902
- 66 Sahu KN, Balbhadra S, Choudhary J, Kohli VD. Curr Med Chem 2012; 19 (02) 209-225
- 67 Goyal K, Kaur R, Goyal A, Awasthi R. J Appl Pharm Sci 2021; 11 (01) 001-014
- 68 Hasan AH, Shakya S, Hussain FH. et al. J Biomol Struct Dyn 2023; 41 (21) 11450-11462
- 69 Tian C, Qiang X, Song Q. et al. Bioorg Chem 2020; 94: 103477
- 70 Islam MS, Al-Majid AM, Sholkamy EN. et al. J Mol Struct 2022; 1269: 133843
- 71 Al-ghulikah HA, Mughal EU, Elkaeed EB. et al. J Mol Struct 2023; 1275: 134658
- 72 Taha M, Sadia H, Rahim F. et al. J Mol Struct 2023; 1285: 135530
- 73 Bai P, Wang K, Zhang P. et al. Eur J Med Chem 2019; 183: 111737
- 74 Sang Z, Wang K, Shi J, Liu W, Tan Z. Eur J Med Chem 2019; 178: 726-739
- 75 Sang Z, Wang K, Zhang P, Shi J, Liu W, Tan Z. Eur J Med Chem 2019; 180: 238-252
- 76 Sang Z, Song Q, Cao Z, Deng Y, Tan Z, Zhang L. Eur J Med Chem 2021; 216: 113310
- 77 Xiao G, Li Y, Qiang X. et al. Bioorg Med Chem 2017; 25 (03) 1030-1041
- 78 Wang L, Wang Y, Tian Y. et al. Bioorg Med Chem 2017; 25 (01) 360-371
- 79 Cao Z, Yang J, Xu R. et al. Bioorg Med Chem 2018; 26 (05) 1102-1115
- 80 Gürdere MB, Budak Y, Kocyigit UM, Taslimi P, Tüzün B, Ceylan M. In Silico Pharmacol 2021; 9 (01) 34
- 81 Al-Maqtari HM, Hasan AH, Suleiman M. et al. ACS Omega 2024; 9 (30) 32901-32919
- 82 Sang Z, Song Q, Cao Z, Deng Y, Zhang L. J Enzyme Inhib Med Chem 2022; 37 (01) 69-85
- 83 Al-Mosawi S, Al-Hazam H, Abbas A, Nasif Z, Saeed B, Al-Masoudi N. Russ J Bioorg Chem 2022; 48 (04) 801-808
- 84 Kang L, Gao X-H, Liu H-R. et al. Mol Divers 2018; 22: 893-906
- 85 Sasidharan R, Eom BH, Heo JH. et al. J Enzyme Inhib Med Chem 2021; 36 (01) 188-197
- 86 Keçeci Sarıkaya M, Yıldırım Ş, Kocyigit U, Ceylan M, Yırtıcı Ü, Eyüpoğlu V. Silico Anal Chem Biodivers 2025; 22: e202402777
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