ZHU Peng-ju, HOU Xu-ben, FANG Hao. Progress of lymphoid-specific tyrosine phosphatase inhibitorsJ. Acta Pharmaceutica Sinica, 2017,52(5): 699-705. doi: 10.16438/j.0513-4870.2017-0084
Citation: ZHU Peng-ju, HOU Xu-ben, FANG Hao. Progress of lymphoid-specific tyrosine phosphatase inhibitorsJ. Acta Pharmaceutica Sinica, 2017,52(5): 699-705. doi: 10.16438/j.0513-4870.2017-0084

Progress of lymphoid-specific tyrosine phosphatase inhibitors

  • Lymphoid-specific tyrosine phosphatase (LYP) is a phosphatase that is encoded by protein tyrosine phosphatase non-receptor type 22 and is mainly distributed in lymphoid. In psychological condition, LYP inhibits T-cell receptor (TCR) signaling in association with C-terminal kinase (CSK). While in pathological condition, mutant LYP dissociates with CSK, which augments the inhibition of TCR signaling and leads to autoimmune diseases. Consequently, LYP is now considered as a new target of type I diabetes, rheumatic arthritis and Graves disease and some other autoimmune disorders. This review mainly focuses on the development of LYP inhibitors in their structures and activities.
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