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Download our free molecule poster today. Choose a format for print or for digital use.
If you've already used one of our molecules, please leave a review.
BI-9593 is a potent and selective orally bioavailable PHGDH inhibitor. Its high permeability and tolerability render it ideal for in vivo as well as cellular profiling. Its stereoisomer BI-9594 is available as negative control.
With BI-1136, we share an unprecedented, selective orally bioavailable BCL6 degrader with nanomolar potency. The molecule is suitable for in vivo testing in rodents and displays good tolerability.
BI-3231 is potent and selective inhibitor of hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13), a lipid droplet-associated enzyme primarily expressed in hepatocytes and whose exact function and substrates are unknown.
BI-9553 is a potent (EC50 < 30 nM in a qPCR cell-based assay), selective, and well-characterized non-nucleoside cytomegalovirus (CMV) polymerase inhibitor. Its cell activity could be dissociated from cytotoxicity depending on different cell lines.
BI-2800 is a highly potent agonist of beta-3 adrenergic receptors. While bound to the latter, it exhibits long residence time and resistance to antagonist activity.
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