Polypharmacology 2022
DOI: 10.1007/978-3-031-04998-9_3
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Polypharmacology in Clinical Applications—Anticancer Polypharmacology

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Cited by 2 publications
(2 citation statements)
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“…In the realm of pharmaceutical interventions, the Food and Drug Administration (FDA) has granted approval to over 300 chemotherapeutic agents, including nivolumab, ipilimumab, pembrolizumab, 5-flurouracil, Olaparib, taxol, vinca alkaloids, and their derivatives, as well as gemcitabine and methotrexate [6][7][8]. Presently, the majority of Pharmaceuticals 2023, 16, 1617 2 of 24 chemotherapeutic treatments focus on single targets within nucleic acids, proteins, and carcinogenic signaling pathways.…”
Section: Introductionmentioning
confidence: 99%
“…In the realm of pharmaceutical interventions, the Food and Drug Administration (FDA) has granted approval to over 300 chemotherapeutic agents, including nivolumab, ipilimumab, pembrolizumab, 5-flurouracil, Olaparib, taxol, vinca alkaloids, and their derivatives, as well as gemcitabine and methotrexate [6][7][8]. Presently, the majority of Pharmaceuticals 2023, 16, 1617 2 of 24 chemotherapeutic treatments focus on single targets within nucleic acids, proteins, and carcinogenic signaling pathways.…”
Section: Introductionmentioning
confidence: 99%
“…Medicinal polypharmacology also stretches far into the very basis of drug design, discovery, and development itself (Anighoro et al, 2014; Proschak et al, 2019). Multitarget agents allow not only for addressing multiple druggable targets of the addressable “diseasome” (Wang & Yang, 2022); they also reach into a network of (yet) undruggable targets by either of two ways: (i) impact on a druggable target which subsequently reaches into a network of undruggable targets by a known or unknown pathway; or (ii) direct interaction with the to this point undruggable target itself (Korcsmaros et al, 2007). Multitarget agents are suitable ligands to de‐orphanize undruggable targets: …”
mentioning
confidence: 99%