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Our FAS in vivo tool compound BI 99179 is characterised by high potency, good selectivity and significant peripheral and central exposure upon oral administration in rats.
BI 665915 demonstrates nanomolar FLAP binding potency and is a molecule suitable for testing biological hypotheses in vitro and also in vivo.
BI 653048 is a “dissociated” GR agonist (displaying different transcriptional regulatory profiles between gene transrepression and transactivation) with selectivity for other nuclear receptors (MR, PR) and good drug-like properties.
BI-1388 is a nanomolar to picomolar inhibitor of Hepatitis C Virus (HCV) NS3 protease activity and of viral replication for various HCV genotypes and for resistant mutants D168V and R155K.
BI-1230 is a single digit nanomolar inhibitor of Hepatitis C Virus (HCV) NS3 protease activity and of viral replication. BI-1230 was shown to be highly selective against other serine/cysteine proteases and to be suitable for in vivo studies.