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Inhibitors of JAK-family kinases: an update on the patent literature 2013-2015, part 2.
Kettle, Jason G; Åstrand, Annika; Catley, Matthew; Grimster, Neil P; Nilsson, Magnus; Su, Qibin; Woessner, Richard.
Afiliação
  • Kettle JG; a AstraZeneca, Oncology iMED, Mereside , Stockport , UK.
  • Åstrand A; b AstraZeneca, Respiratory, Inflammation and Autoimmunity iMED Pepparedsleden 1 , Mölndal , Sweden.
  • Catley M; b AstraZeneca, Respiratory, Inflammation and Autoimmunity iMED Pepparedsleden 1 , Mölndal , Sweden.
  • Grimster NP; c AstraZeneca, Oncology iMED , Waltham , MA , USA.
  • Nilsson M; b AstraZeneca, Respiratory, Inflammation and Autoimmunity iMED Pepparedsleden 1 , Mölndal , Sweden.
  • Su Q; c AstraZeneca, Oncology iMED , Waltham , MA , USA.
  • Woessner R; c AstraZeneca, Oncology iMED , Waltham , MA , USA.
Expert Opin Ther Pat ; 27(2): 145-161, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27774822
ABSTRACT

INTRODUCTION:

Janus kinases (JAKs) are a family of four enzymes; JAK1, JAK2, JAK3 and tyrosine kinase 2 (TYK2) that are critical in cytokine signalling and are strongly linked to both cancer and inflammatory diseases. There are currently two launched JAK inhibitors for the treatment of human conditions tofacitinib for Rheumatoid arthritis (RA) and ruxolitinib for myeloproliferative neoplasms including intermediate or high risk myelofibrosis and polycythemia vera. Areas covered This review covers patents claiming activity against one or more JAK family members in the period 2013-2015 inclusive, and covers 95 patents from 42 applicants, split over two parts. The authors have ordered recent patents according to the primary applicant's name, with part 2 covering J through Z. Expert opinion Inhibition of JAK-family kinases is an area of growing interest, catalysed by the maturity of data on marketed inhibitors ruxolitinib and tofacitinib in late stage clinical trials. Many applicants are pursuing traditional fast-follower strategies around these inhibitors, with a range of chemical strategies adopted. The challenge will be to show sufficient differentiation to the originator compounds, since dose limiting toxicities with such agents appear to be on target and mechanism-related and also considering that such agents may be available as generic compounds by the time follower agents reach market.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Inibidores de Proteínas Quinases / Janus Quinases Limite: Animals / Humans Idioma: En Revista: Expert Opin Ther Pat Assunto da revista: TERAPEUTICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Inibidores de Proteínas Quinases / Janus Quinases Limite: Animals / Humans Idioma: En Revista: Expert Opin Ther Pat Assunto da revista: TERAPEUTICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido
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