Chemical Name:(E)-2-Cyano-3-(3,4-dihydrophenyl)-N-(phenylmethyl)-2-pr
openamide
Biological Activity:
Selective inhibitor of EGF receptor tyrosine kinase (IC50
values are 2 and 13.5 μM for EGFR and Her2-neu
respectively). Inhibitor of Jak2, Jak3/STAT, Jak3/AP-1 and Jak3/MAPK pathways.
Gazitet al (1991) Tyrphostins. 2. Heterocyclic and α-substituted benzylidenemalononitrile tyrphostins as potent
inhibitors of EGF receptor and ErbB2/neu tyrosine kinases. J.Med.Chem. 34
1896. Meydanet al (1996) Inhbition of acute
lymphoblastic leukaemia by a JAK-2 inhibitor. Nature 379 645.
Wang et al (1999) JAK3, STAT, and MAPK signaling pathways as novel molecular
targets for the tyrphostin AG-490 regulation of IL-2-mediated T cell response.
J.Immunol. 162 3897.