Rule of five violations among the FDA-approved small molecule protein kinase inhibitors

Because genetic alterations including mutations, overexpression, translocations, and dysregulation of protein kinases are involved in the pathogenesis of many illnesses, this enzyme family is the target of many drug discovery programs in the pharmaceutical industry. Overall, the US FDA has approved...

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Main Author: Robert Roskoski, Jr (Author)
Format: Book
Published: Elsevier, 2023-05-01T00:00:00Z.
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100 1 0 |a Robert Roskoski, Jr.  |e author 
245 0 0 |a Rule of five violations among the FDA-approved small molecule protein kinase inhibitors 
260 |b Elsevier,   |c 2023-05-01T00:00:00Z. 
500 |a 1096-1186 
500 |a 10.1016/j.phrs.2023.106774 
520 |a Because genetic alterations including mutations, overexpression, translocations, and dysregulation of protein kinases are involved in the pathogenesis of many illnesses, this enzyme family is the target of many drug discovery programs in the pharmaceutical industry. Overall, the US FDA has approved 74 small molecule protein kinase inhibitors, nearly all of which are orally effective. Of the 74 approved drugs, thirty-nine block receptor protein-tyrosine kinases, nineteen target nonreceptor protein-tyrosine kinases, twelve are directed against protein-serine/threonine protein kinases, and four target dual specificity protein kinases. The data indicate that 65 of these medicinals are approved for the management of neoplasms (51 against solid tumors such as breast, colon, and lung cancers, eight against nonsolid tumors such as leukemia, and six against both types of tumors). Nine of the FDA-approved kinase inhibitors form covalent bonds with their target enzymes and they are accordingly classified as TCIs (targeted covalent inhibitors). Medicinal chemists have examined the physicochemical properties of drugs that are orally effective. Lipinski's rule of five (Ro5) is a computational procedure that is used to estimate solubility, membrane permeability, and pharmacological effectiveness in the drug-discovery setting. It relies on four parameters including molecular weight, number of hydrogen bond donors and acceptors, and the Log of the partition coefficient. Other important descriptors include the lipophilic efficiency, the polar surface area, and the number of rotatable bonds and aromatic rings. We tabulated these and other properties of the FDA-approved kinase inhibitors. Of the 74 approved drugs, 30 fail to comply with the rule of five. 
546 |a EN 
690 |a Hydrogen-bond 
690 |a Lipinski rule of five 
690 |a Lipophilic efficiency 
690 |a Orally bioavailable 
690 |a Partition coefficient 
690 |a Polar surface area 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Pharmacological Research, Vol 191, Iss , Pp 106774- (2023) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1043661823001305 
787 0 |n https://doaj.org/toc/1096-1186 
856 4 1 |u https://doaj.org/article/dc98d3078f1b4bef841fad25cdca6d3c  |z Connect to this object online.