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Polypharmacology in a Single Drug: Multitarget Drugs
Abstract
Polypharmacology offers a model for the way drug discovery must evolve to develop therapies most suited to treating currently incurable diseases. It is driven by a worldwide demand for safer, more effective, and affordable medicines against the most complex diseases, and by the failures of modern drug discovery to provide these. Polypharmacology can involve combinations and/or multitarget drugs (MTD). Although not mutually exclusive, my premise is that MTDs have inherent advantages over combinations. This review article focuses on MTDs from a medicinal chemistry perspective. I will explore their use in current clinical practice, their likely application in the future, and the challenges to be overcome to achieve this goal. Keywords: Multifactorial diseases, Combination therapy, multitarget drug discovery, network pharmacology, multitargetdirected ligands, designed multiple ligands
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“Both are critical issues in AD: (a) adherence to a complex therapy is unlikely for forgetful AD patients and their caregivers; (b) coexistence of chronic disease, polypharmacy, and impaired organ functions makes geriatric population particularly susceptible to DDIs.49”
From From combinations to multitarget-directed ligands: A continuum in Alzheimer’s disease polypharmacology (2021) · cites this paper as [49]
In the citing paper
“Both are critical issues in AD: (a) adherence to a complex therapy is unlikely for forgetful AD patients and their caregivers; (b) coexistence of chronic disease, polypharmacy, and impaired organ functions makes geriatric population particularly susceptible to DDIs.49”
From From combinations to multitarget-directed ligands: A continuum in Alzheimer’s disease polypharmacology (2021) · cites this paper as [49]
In the citing paper
“Furthermore, the single-molecule pharmacokinetic profile of hybrids, from administration to secretion, may allow to avoid DDI, that occur more frequently in AD patients, because of the coexistence of chronic disease, therapies, and impaired organ functions.49”
From From combinations to multitarget-directed ligands: A continuum in Alzheimer’s disease polypharmacology (2021) · cites this paper as [49]
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Items 101–200 of 223
Lopes, F. B., Aranha, C. M. S. Q., & Fernandes, J. P. S. (2021) · Chemical Biology & Drug Design · doi:10.1111/cbdd.13866 · Cited by 22
“The main approaches to identify DMLs are the random screening of known compounds on selected targets, and the pharmacophore (or framework) combination (Bolognesi, 2013; Morphy & Rankovic, 2009).”
BackgroundSimoni, E., Bartolini, M., Abu, I. F., Blockley, A., Gotti, C., Bottegoni, G., Caporaso, R., Bergamini, C., Andrisano, V., Cavalli, A., et al. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2017-0039 · Cited by 22
Gilberg, E., Stumpfe, D., & Bajorath, J. (2018) · ACS Omega · doi:10.1021/acsomega.7b01849 · Cited by 21
Feldmann, C., & Bajorath, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-87042-z · Cited by 21
Guo, J., Mi, Z., Jiang, X., Zhang, C., Guo, Z., Li, L.-Z., Gu, J., Zhou, T., Bai, R., & Xie, Y. (2020) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2020.104564 · Cited by 21
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Chai, C. L. L., & Mátyus, P. (2015) · Future Medicinal Chemistry · doi:10.4155/fmc.15.167 · Cited by 20
Ladds, M. J. G. W., Popova, G., Fernández, A. P., Kannan, S., van Leeuwen, I. M. M., Håkansson, M., Walse, B., Tholander, F., Bhatia, R., Verma, C. S., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.012056 · Cited by 21
Nozal, V., García‐Rubia, A., Cuevas, E. P., Pérez, C., Tosat‐Bitrián, C., Bartolomé, F. B., Carro, E., Ramírez, D., Palomo, V., & Martı́nez, A. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202106295 · Cited by 20
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Bianco, M. D. C. A. D., Leite, D. I., Branco, F. S. C., Boechat, N., Uliassi, E., Bolognesi, M. L., & Bastos, M. M. (2022) · Molecules · doi:10.3390/molecules27238502 · Cited by 19
“As most of the currently incurable diseases are caused by multiple factors, the concomitant modulation of several targets through polypharmacology is required [2,3].”
BackgroundSelf-citationIntracellular water as a mediator of anticancer drug action
Marques, M. P. M., de Carvalho, A. L. M. B., Mamede, A. P., Rudić, S., Dopplapudi, A., Sakai, V. G., & de Carvalho, L. A. E. B. (2020) · International Reviews in Physical Chemistry · doi:10.1080/0144235x.2020.1700083 · Cited by 18
Rational approaches towards inorganic and organometallic antibacterials
Hess, J. (2021) · Biological Chemistry · doi:10.1515/hsz-2021-0253 · Cited by 19
A Review of the Development of Multitarget Molecules against HIV-TB Coinfection Pathogens
Leite, D. I., Moura, S. D. C. B., da Conceição, A. D. M., Costa, C. C. P., Machado, G. P., Pimentel, L., Branco, F., Moreira, R., Bastos, M., & Boechat, N. (2023) · Molecules · doi:10.3390/molecules28083342 · Cited by 15
“Among the advantages that multitargets can offer concerning FCD, notable pros are more predictable pharmacokinetics, a lower probability of drug‒drug interactions during the development of the formulation, and higher patient tolerance to treatment [65,66].”
BackgroundMultiscale Virtual Screening Optimization for Shotgun Drug Repurposing Using the CANDO Platform
Hudson, M. L., & Samudrala, R. (2021) · Molecules · doi:10.3390/molecules26092581 · Cited by 16
Madapa, S., & Harding, W. W. (2015) · Journal of Natural Products · doi:10.1021/np500893h · Cited by 17
Liu, L., Zou, M., Zeng, K., Ye, X., Wang, R., Wang, W., & Zhang, X. (2021) · Plant Foods for Human Nutrition · doi:10.1007/s11130-020-00874-4 · Cited by 16
“Therefore, it is very important to recognize the multifactorial nature of AD and shift the paradigm of AD drug development from single targets to multiple targets [4, 5].”
BackgroundPerspectives in Designing Multifunctional Molecules in Antipsychotic Drug Discovery
Milelli, A., Turrini, E., Catanzaro, E., Maffei, F., & Fimognari, C. (2016) · Drug Development Research · doi:10.1002/ddr.21334 · Cited by 16
Angelova, V. T., Stoyanov, B. P., & Simeonova, R. (2024) · Molecules · doi:10.3390/molecules29225314 · Cited by 19
Feldmann, C., Yonchev, D., Stumpfe, D., & Bajorath, J. (2020) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.0c00901 · Cited by 15
Toxicological Properties of 7-Methylguanine, and Preliminary Data on its Anticancer Activity
Игоревич, К. К., Fetisov, T. I., Antoshina, E. E., Trukhanova, L. S., Gorkova, T. G., Vlasova, O. A., Александровна, Х. И., Lesovaya, E. A., Kulbachevskaya, N. Y., Shcherbakova, T. A., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.842316 · Cited by 15
“From the point of view of polypharmacology, such a multitarget (PARP1/2, TGT) mechanism of a drug candidate may be promising, if adverse effects are negligible (Bolognesi, 2013; Medina-Franco et al., 2013).”
BackgroundRecent Advances in the Search for Effective Anti-Alzheimer’s Drugs
Ogoś, M., Stary, D., & Bajda, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms26010157 · Cited by 17
Oña, G., & Bouso, J. C. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666191212103330 · Cited by 18
Delogu, G. L., Era, B., Floris, S., et al. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.12.117 · Cited by 15
Liang, Q., Zuo, H., Yang, T., Yin, J., Huang, X., Wang, J., Li, Q., Yin, G., & Zhao, X. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114212 · Cited by 15
Multitarget Anti-Alzheimer Hybrid Compounds
Muñoz‐Torrero, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-101011-2.00006-4 · Cited by 15
Wu, W., Liang, X., Xie, G., Chen, L.-D., Liu, W., Luo, G., Zhang, P., Yu, L., Zheng, X., Ji, H., et al. (2018) · Molecules · doi:10.3390/molecules23102540 · Cited by 15
Biological Activities and ADMET-Related Properties of Novel Set of Cinnamanilides
Kos, J., Bąk, A., Kozik, V., et al. (2020) · Molecules · doi:10.3390/molecules25184121 · Cited by 15
Gu, J., Li, L., Wang, D., et al. (2018) · Annals of Medicine · doi:10.1080/07853890.2018.1453169 · Cited by 14
New Myrtenal–Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
Dragomanova, S., Lazarova, M. I., Munkuev, A. A., Суслов, Е. В., Volcho, K. P., Salakhutdinov, N. F., Bibi, A., Reynisson, J., Tzvetanova, E., Alexandrova, A., et al. (2022) · Molecules · doi:10.3390/molecules27175456 · Cited by 13
Neurodegenerative Drug Discovery: Building on the Past, Looking to the Future
Bolognesi, M. L. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2017-0087 · Cited by 13
Self-citationMathew, G., & Unnikrishnan, M. K. (2015) · Inflammation Research · doi:10.1007/s00011-015-0851-8 · Cited by 13
Wang, J. W., Woodward, D. F., Martos, J. L., Cornell, C. L., Carling, R. W., Kingsley, P. J., & Marnett, L. J. (2015) · The FASEB Journal · doi:10.1096/fj.15-275610 · Cited by 12
“A, B) Samples from monocytes [MC = (1), open bar], and primary human macrophages (MP) with no stimulation [(2), cross-hatched bar], 10 ng/ml LPS [(3), black bar], or 20 ng/ml TNF-a [(4), gray bar] were used for prostanoid receptor mRNA expression by RTqPCR (A) and COX protein expression by Western blot analysis (B) fr…”
BackgroundMethodHoang, N. X., Hoang, V.-H., Luu, T.-T.-T., Luu, H. N., Ngo, T., Hieu, D. V., Long, N. H., Anh, L. V., Ngô, S. T., Nguyen, Y. T. K., et al. (2020) · RSC Advances · doi:10.1039/d0ra09112j · Cited by 12
Kumar, N., Gupta, P., & Bansal, S. (2022) · Letters in Drug Design & Discovery · doi:10.2174/1570180819666220314144219 · Cited by 13
El-Kalyoubi, S. A., Elbaramawi, S. S., Eissa, A. G., Ageeli, E. A., Hobani, Y. H., El-Sharkawy, A. A., Mohamed, H. T., Al-Karmalawy, A. A., & Abulkhair, H. S. (2023) · Future Medicinal Chemistry · doi:10.4155/fmc-2023-0112 · Cited by 13
Gülcan, H. O., & Koşar, M. (2021) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026621666211111153626 · Cited by 12
Kucwaj‐Brysz, K., Ali, W., Kurczab, R., Sudoł-Tałaj, S., Wilczyńska-Zawal, N., Jastrzębska‐Więsek, M., Satała, G., Mordyl, B., Żesławska, E., Olejarz‐Maciej, A., et al. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.105695 · Cited by 14
Acharya, A., Roy, N., Newaskar, V., Rai, A., Ghosh, A., Nagpure, M., Giri, S. K., Sahni, G., & Guchhait, S. K. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117611 · Cited by 12
Rational Approach to an Antiprion Compound with a Multiple Mechanism of Action
Bolognesi, M. L., Bongarzone, S., Aulić, S., Tran, H. N. A., Prati, F., Carloni, P., & Legname, G. (2015) · Future Medicinal Chemistry · doi:10.4155/fmc.15.79 · Cited by 11
Self-citationDesign of Improved Antidiabetic Drugs: A Journey from Single to Multitarget Agents
Tassopoulou, V., Tzara, A., & Kourounakis, A. P. (2022) · ChemMedChem · doi:10.1002/cmdc.202200320 · Cited by 11
Pills of Multi-Target H2S Donating Molecules for Complex Diseases
Corvino, A., Scognamiglio, A., Fiorino, F., Perissutti, E., Santagada, V., Caliendo, G., & Severino, B. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137014 · Cited by 9
Schnitzler, A., Gratz, A., Bollacke, A., et al. (2018) · Pharmaceuticals · doi:10.3390/ph11010023 · Cited by 10
“In addition it emphasizes, that multi-target effects, also named as polypharmacology more recently [65,66], are worth to be considered at early stages of drug discovery and could be subjected to a rational approach.”
BackgroundDowarah, J., Marak, B. N., Lalhruaizela, L., Sran, B. S., & Singh, V. P. (2020) · Crystal Research and Technology · doi:10.1002/crat.202000100 · Cited by 10
Monteiro, P. Q., Schaeffer, E., da Silva, A. J. M., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26052025 · Cited by 9
“Over time, the field of polypharmacology, which encompasses both multitarget and combined chemotherapies, has been growing [19,20].”
Humayun, F., Khan, F., Khan, A., Alshammari, A., Ji, J. H., Farhan, A., Fawad, N., Alam, W., Ali, A., & Wei, D. (2023) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2023.2234481 · Cited by 9
“However, certain complicated diseases cannot be properly treated with a single-target medication (Anighoro et al., 2014; L Bolognesi, 2013).”
BackgroundDias, K. S. T., de Paula, C. T., Riquiel, M. M., do Lago, S. T. L., Costa, K. C. M., Vaz, S. M., Machado, R. P., de Lima, L. M. S., & Viegas, C. (2015) · Revista Virtual de Química · doi:10.5935/1984-6835.20150027 · Cited by 12
Medicinal Chemistry of Hybrids for Neurodegenerative Diseases
Uliassi, E., Prati, F., Bongarzone, S., & Bolognesi, M. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-101011-2.00010-6 · Cited by 10
Self-citationAlbertini, C., Naldi, M., Petralla, S., Strocchi, S., Grifoni, D., Monti, B., Bartolini, M., & Bolognesi, M. L. (2021) · Molecules · doi:10.3390/molecules26041112 · Cited by 9
“Our molecules should offer an alternative to the proposed drug combination, showing pros and cons of a single-molecule conjugate [9].”
BackgroundSelf-citationSharma, A., Cipriano, M. J., Ferrins, L., Hajduk, S. L., & Mensa‐Wilmot, K. (2022) · iScience · doi:10.1016/j.isci.2022.105302 · Cited by 9
“As drugs can bind multiple proteins (Bolognesi, 2013; Hafner et al., 2019), and a single binding pocket on a protein can bind more than one ligand (Cerisier et al., 2019), discovery of physiologic drug targets is not a trivial undertaking (Kubota et al., 2019).”
Therapeutic Approaches to Prion Diseases
Gandini, A., & Bolognesi, M. L. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.06.013 · Cited by 9
Self-citationTang, H., Liang, Y., Yu, M., Cai, S., Ding, K., & Wang, Y. (2023) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2023.117437 · Cited by 9
Some Aspects and Convergence of Human and Veterinary Drug Repositioning
Mag, P., Nemes-Terényi, M., Jerzsele, Á., & Mátyus, P. (2024) · Molecules · doi:10.3390/molecules29184475 · Cited by 12
“Polypharmacology in our context means that the effectiveness of these drugs is due to their ability to influence the pathomechanism of the disease through affecting more than one, even several, pharmacologically relevant targets [46,47].”
BackgroundApplications for Treatment of Neurodegenerative Diseases
Ježek, J., Hlaváček, J., & Šebestı́k, J. (2017) · Progress in drug research · doi:10.1007/978-3-319-63953-6_6 · Cited by 7
El-Atawneh, S., & Goldblum, A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.812745 · Cited by 8
“In the past 2 decades, treating multifactorial illnesses, i.e., infections, cancer, and CNS disorders, shifted towards multitargeting (Csermely et al., 2005; Hopkins et al., 2006; Boran and Iyengar, 2010; L.; Bolognesi, 2013; Bolognesi and Cavalli, 2016; Zhou et al., 2019).”
BackgroundArtificial intelligence systems for the design of magic shotgun drugs
Moreira‐Filho, J. T., da Silva, M. F. B., Borba, J. V. V. B., Filho, A. R. G., Muratov, E. N., Andrade, C. H., Braga, R. C., & Neves, B. J. (2022) · Artificial Intelligence in the Life Sciences · doi:10.1016/j.ailsci.2022.100055 · Cited by 8
Scaling the Andean Shilajit: A Novel Neuroprotective Agent for Alzheimer’s Disease
Andrade, V., Wong-Guerra, M., Cortés, N., Pastor, G., González, A., Calfío, C., Guzmán‐Martínez, L., Navarrete, L. P., Ramos-Escobar, N., Morales, I., et al. (2023) · Pharmaceuticals · doi:10.3390/ph16070960 · Cited by 9
“The use of natural bioactive molecules against AD is a topic that has been researched by several groups [16], as well as ours, suggesting that natural multicomponent formulas have shown efficacy against AD [17,18].”
BackgroundPrediction of Promiscuity Cliffs Using Machine Learning
Blaschke, T., Feldmann, C., & Bajorath, J. (2020) · Molecular Informatics · doi:10.1002/minf.202000196 · Cited by 7
Targeting calciumopathy for neuroprotection: focus on calcium channels Cav1, Orai1 and P2X7
Torres-Rico, M., García-Calvo, V., Gironda-Martínez, A., Pascual-Guerra, J., Garcı́a, A. G., & Maneu, V. (2024) · Cell Calcium · doi:10.1016/j.ceca.2024.102928 · Cited by 8
“The principal underlying drug repurposing lies in the fact that most medicines bind to more than one biological target, showing physio-pharmacological effects beyond the initially conceived one [254].”
BackgroundNozal, V., Fernández-Gómez, P., García‐Rubia, A., Martínez‐González, L., Cuevas, E. P., Carro, E., Palomo, V., & Martı́nez, A. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116626 · Cited by 9
Gali, R., Banothu, J., Salaria, P., et al. (2024) · Journal of Heterocyclic Chemistry · doi:10.1002/jhet.4892 · Cited by 7
Marset, A., Begines, P., López, Ó., et al. (2016) · Future Medicinal Chemistry · doi:10.4155/fmc-2016-0139 · Cited by 7
Prospects of Indole derivatives as methyl transfer inhibitors: antimicrobial resistance managers
Tha, S., Shakya, S., Malla, R., & Aryal, P. (2020) · BMC Pharmacology and Toxicology · doi:10.1186/s40360-020-00402-9 · Cited by 7
Mohamed, A. R., & Kerdawy, A. M. E. (2022) · Chemistry & Biodiversity · doi:10.1002/cbdv.202200328 · Cited by 9
“The signaling pathways’ complexity is well shown in the acquired resistance and the consecutive mutations during the different stages of targeted kinases development.[226,227] Due to the huge genetic changes that result in the resistance mechanisms, several FDAapproved drugs showed no further improvement against certa…”
BackgroundBraun, S., Paskaš, S., Laube, M., George, S., Hofmann, B., Lönnecke, P., Steinhilber, D., Pietzsch, J., Mijatović, S., Maksimović‐Ivanić, D., et al. (2022) · Advanced Therapeutics · doi:10.1002/adtp.202200252 · Cited by 8
Design, synthesis and mechanism studies of dual EZH2/BRD4 inhibitors for cancer therapy
Chen, X., Wang, C., Lu, D., Luo, H., Li, S., Yin, F., Luo, Z., Cui, N., Kong, L., & Wang, X. (2023) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2023.117386 · Cited by 9
Kampasis, D., Uliassi, E., & Bolognesi, M. L. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115621 · Cited by 6
Self-citationMulti-Target-Directed Ligand Approach in Anti-Alzheimer’s Drug Discovery
Patil, V. M., Masand, N., Gautam, V., Kaushik, S., & Wu, D. H. (2023) · Springer eBooks · doi:10.1007/978-981-99-2657-2_13 · Cited by 9
Lamens, A., & Bajorath, J. (2023) · Molecules · doi:10.3390/molecules28020825 · Cited by 6
Kurgina, T. A., Shram, S. I., Kutuzov, M. M., Abramova, T. V., Shcherbakova, T. A., Maltseva, E. A., Poroikov, V., Lavrik, O. I., Švedas, V. K., & Nilov, D. K. (2022) · Biochemistry (Moscow) · doi:10.1134/s0006297922080132 · Cited by 6
“The inhibitory effect of 7mGua on several molecular targets, PARP1 and TGT, may be of interest from the point of view of polypharmacology [39, 40].”
BackgroundComputational Methods in Multitarget Drug Discovery
Bottegoni, G., & Cavalli, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-101011-2.00009-x · Cited by 6
Zhang, Y., Luo, Z., Jiang, Y., Zheng, L. T., Ma, L., Zheng, Y., Zou, M., Kong, L., & Wang, X. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117495 · Cited by 5
Knight, R. A., Gostev, M., Ilisavskii, S., Willis, A. E., Melino, G., & Antonov, A. V. (2014) · Oncotarget · doi:10.18632/oncotarget.1597 · Cited by 5
“Although developed to target a specific protein, most currently efficient anticancer drugs are, in fact, essentially poly-pharmacological: they target multiple off-target proteins which might play important, yet unrecognized, roles in the mechanism of action [11, 13-15].”
The multitarget approach as a green tool in medicinal chemistry
Vlocskó, R. B., Apaydın, S., Török, B., & Török, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822248-5.00016-4 · Cited by 6
Nozal, V., García‐Rubia, A., Cuevas, E. P., Pérez, C., Tosat‐Bitrián, C., Bartolomé, F. B., Carro, E., Ramírez, D., Palomo, V., & Martı́nez, A. (2021) · Angewandte Chemie · doi:10.1002/ange.202106295 · Cited by 6
Fouégué, A. D. T., Mama, D. B., Ghogomu, J. N., Younang, E., & Etoh, M. (2018) · Journal of Chemistry · doi:10.1155/2018/1958047 · Cited by 4
“Moreover, the literature reports the structure-activity relationship of the multitarget antiAlzheimer compounds designed by combining a tacrine and a juglone [15].”
BackgroundBiological Activity Profiles of Multitarget Ligands from X-ray Structures
Feldmann, C., & Bajorath, J. (2020) · Molecules · doi:10.3390/molecules25040794 · Cited by 4
“Multitarget activity of small molecules continues to be a much debated topic in drug discovery [1,2].”
BackgroundGarcía, I. A., Pansa, M. F., Pacciaroni, A. D. V., García, M. E., González, M. L., Oberti, J. C., Bocco, J. L., Carpinella, M. C., Barboza, G. E., Nicotra, V. E., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.593845 · Cited by 4
“Moreover, it was also suggested that molecules with multitarget mechanism of action may possess a safer profile compared to single-target ones (Bolognesi, 2013; Ramsay et al., 2018).”
BackgroundDevelopment of CNS multi-receptor ligands: Modification of known D2 pharmacophores
Etukala, J. R., Zhu, X. Y., Eyunni, S., Onyameh, E. K., Ofori, E., Bricker, B. A., Kang, H. J., Huang, X., Roth, B. L., & Ablordeppey, S. Y. (2016) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2016.06.011 · Cited by 3
Single Molecule Non-cleavable Multiply Active Antibacterials
Bremner, J. B. (2021) · Springer eBooks · doi:10.1007/978-981-16-0999-2_3 · Cited by 3
Multitarget Compounds for Neglected Diseases: A Review
de Sousa, N. F., de Sousa, G. R., de Lima, N. T. R., de Assis, E. B., Aragão, M. C., de Moura, É. P., Gopalsamy, R. G., Scotti, M. T., & Scotti, L. (2024) · Current Drug Targets · doi:10.2174/0113894501298864240627060247 · Cited by 3
Jakubiec, M., Abram, M., Zagaja, M. P., Socała, K., Panic, V., Latacz, G., Mogilski, S., Szafarz, M., Szala‐Rycaj, J., Saunders, J., et al. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00438 · Cited by 3
Strategies of Polypharmacology
Wang, Z., & Yang, B. (2022) · Springer eBooks · doi:10.1007/978-3-031-04998-9_2 · Cited by 4
Halder, A. K., Moura, A. S., & Cordeiro, M. N. D. S. (2018) · Methods in pharmacology and toxicology · doi:10.1007/7653_2018_14 · Cited by 3
Polypharmacology in Drug Discovery
Méndez‐Lucio, O., Naveja, J. J., Vite‐Caritino, H., Prieto-Martínez, F. D., & Medina‐Franco, J. L. (2017) · Methods and principles in medicinal chemistry · doi:10.1002/9783527674381.ch1 · Cited by 4
Bolognesi, M. L., & Rossi, M. (2020) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0028845 · Cited by 3
Self-citationSalarinejad, S., Seyfi, S., Hayashi, S., et al. (2024) · Molecular Diversity · doi:10.1007/s11030-024-10807-x · Cited by 2
Peixoto, J. F., Gonçalves-Oliveira, L. F., Dias-Lopes, G., Souza‐Silva, F., & Alves, C. R. (2024) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760240115 · Cited by 2
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Rashed, J., Majed, A. A., Aufy, M., et al. (2026) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2026.146066 · Cited by 1
Jakubiec, M., Zagaja, M. P., Socała, K., et al. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c02093 · Cited by 1
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Pawar, R. S., & Patravale, V. B. (2020) · ChemistrySelect · doi:10.1002/slct.202004137 · Cited by 1
Shyr, Z. A., Cheng, Y., & Zheng, W. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820472-6.00058-x · Cited by 1
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Alka, T., Sati, B., & Chaudhary, A. (2022) · Medicinal Chemistry · doi:10.2174/1573406418666220815101124 · Cited by 1
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Shakya, A., Bhat, H. R., & Ghosh, S. K. (2019) · Journal of Biologically Active Products from Nature · doi:10.1080/22311866.2019.1684367 · Cited by 1
Acharya, R., & Pattanayak, S. P. (2020) · Indian Journal of Pharmaceutical Education and Research · doi:10.5530/ijper.54.2.27 · Cited by 1
Wang, Z., & Yang, B. (2022) · Springer eBooks · doi:10.1007/978-3-031-04998-9_1 · Cited by 1
Metadata
- Authors
- L. Bolognesi, M.
- Venue
- Current Medicinal Chemistry
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2013-03-01
- Volume
- 20
- Issue
- 13
- Pages
- 1639-1645
- ISSN
- 0929-8673 (ISSN-L)
- OpenAlex
- W2329046360
- Cited by
- 230
- References
- 0
- Citations by year
- 2026: 15 · 2025: 7 · 2024: 23 · 2023: 11 · 2022: 27 · 2021: 23 · 2020: 35 · 2019: 19 · 2018: 12 · 2017: 16 · 2016: 13 · 2015: 13 · 2014: 9 · 2013: 7
- FWCI
- 16.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Medicinal Chemistry (publishedVersion)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Computational Drug Discovery Methods
- Health Sciences › Medicine › Pharmacology (medical) › Cholinesterase and Neurodegenerative Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
- Keywords
- polypharmacology, multi-target drugs, multi-target drug discovery, combination therapy, network pharmacology, multi-target-directed ligands, complex diseases
- MeSH terms
- Animals, Drug Combinations, Drug Resistance, Microbial, Pharmaceutical Preparations, Humans, Drug Discovery
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