Tyrosine Kinases as New Molecular Targets in Treatment of Inflammatory Disorders and Leukemia

Title: Tyrosine Kinases as New Molecular Targets in Treatment of Inflammatory Disorders and Leukemia

Volume: 10 Issue: 10

Author(s): Fatih M. Uckun and Chen Mao

Affiliation:

Keywords: structure-based drug design, ptk, sar, btk, jak3, computational chemistry, inflammation, leukemia

Abstract: Many protein tyrosine kinases (PTK), including Janus kinase 3 (JAK3) and Bruton ’ s tyrosine kinase (BTK), have been recently identified as potential drug targets to treat diverse diseases including inflammation and cancer. The wealth of structural information currently available for protein kinase-inhibitor complexes facilitates the structure-based design of novel kinase inhibitors. In this report, we discuss the structural basis of protein kinase inhibitor design and the common binding features of small molecule kinase inhibitors including pyridinyl imidazoles, purines, oxindoles, anilinoquinazolines and isoquinalines. The structural features of targeted kinase proteins and their inhibitor complexes are discussed with respect to their structure-and-activity relationships (SAR). We present a structural comparison of kinase inhibitors with a special emphasis on inhibitors of JAK3 and BTK.

Cite this article as:

Uckun M. Fatih and Mao Chen, Tyrosine Kinases as New Molecular Targets in Treatment of Inflammatory Disorders and Leukemia, Current Pharmaceutical Design 2004; 10 (10) . https://dx.doi.org/10.2174/1381612043452677