Falnidamol (BIBX 1382) is an orally active, selective EGFR tyrosine kinase inhibitor with an IC 50 of 3 nM. Falnidamol displays > 1000-fold lower potency against ErbB2 (IC 50 =3.4 μM) and a range of other related tyrosine kinases (IC 50 >10 μM). Falnidamol is a pyrimido-pyrimidine compound and has anti-cancer activity.
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