Metabolism and pharmacokinetics of covalent tyrosine kinase inhibitors / 药学学报
Acta Pharmaceutica Sinica
; (12): 432-439, 2019.
Article
en Zh
| WPRIM
| ID: wpr-780125
Biblioteca responsable:
WPRO
ABSTRACT
Covalent tyrosine kinase inhibitors (TKIs) can inhibit the signaling pathway of tumor cells by covalent binding with cysteine residues of target proteins, which has the advantages of high potency, extended duration of action and overcoming drug resistance. In this article, we will review the metabolism and pharmacokinetics of some covalent TKIs. Currently, the covalent TKIs approved by US food and drug administration (FDA) are afatinib, neratinib, dacomitinib, osimertinib, ibrutinib and acalabrutinib. Pyrotinib have been approved by National Medical Products Administration (NMPA) to reach the market recently. Covalent TKIs can covalently bind with plasma proteins, especially human serum albumin, thus effected the pharmacokinetics of these drugs.
Texto completo:
1
Banco de datos:
WPRIM
Idioma:
Zh
Año:
2019
Tipo del documento:
Article