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Functional interrogation and therapeutic targeting of protein tyrosine phosphatases.
Krabill, Aaron D; Zhang, Zhong-Yin.
Afiliação
  • Krabill AD; Department of Medicinal Chemistry and Molecular Pharmacology, Department of Chemistry, and Institute for Drug Discovery, Purdue University, West Lafayette, IN 47907, U.S.A.
  • Zhang ZY; Department of Medicinal Chemistry and Molecular Pharmacology, Department of Chemistry, and Institute for Drug Discovery, Purdue University, West Lafayette, IN 47907, U.S.A.
Biochem Soc Trans ; 49(4): 1723-1734, 2021 08 27.
Article em En | MEDLINE | ID: mdl-34431504
ABSTRACT
Protein tyrosine phosphatases (PTPs) counteract the enzymatic activity of protein tyrosine kinases to modulate levels of both normal and disease-associated protein tyrosine phosphorylation. Aberrant activity of PTPs has been linked to the progression of many disease states, yet no PTP inhibitors are currently clinically available. PTPs are without a doubt a difficult drug target. Despite this, many selective, potent, and bioavailable PTP inhibitors have been described, suggesting PTPs should once again be looked at as viable therapeutic targets. Herein, we summarize recently discovered PTP inhibitors and their use in the functional interrogation of PTPs in disease states. In addition, an overview of the therapeutic targeting of PTPs is described using SHP2 as a representative target.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Fosfatases / Inibidores Enzimáticos Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Fosfatases / Inibidores Enzimáticos Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article