Signaling pathways
- BA2856 MI-1061Summary: MI-1061 is a potent, orally bioavailable, chemically stable (MDM2-p53 interactions) inhibitor.
- BA2857 CurzereneSummary: Curzerene is a sesquiterpene, isolated from the rhizome of Gaertn, which has anticancer activity.
- BA2858 MC4033Summary: MC4033 is a selective, reversible inhibitor of lysine acetyltransferase 8.
- BA2859 BJE6-106Summary: BJE6-106 (B106) is a potent and selective inhibitor.
- BA2861 InecalcitolSummary: Inecalcitol (TX522), a unique vitamin D3 analog, is an orally active vitamin D receptor agonist.
- BA2862 ForodesineSummary: Forodesine (BCX-1777) is a potent, orally active purine nucleoside phosphorylase inhibitor with values ranging from 0.48 to 1.57 nM in humans, mice, rats, monkeys and dogs.
- BA2863 WDR5-IN-1Summary: WDR5-IN-1 is a potent and selective WD repeat structural domain 5 inhibitor.
- BA2864 AlofanibSummary: Alofanib (RPT835) is a potent and selective variant inhibitor of fibroblast growth factor receptor 2.
- BA2865 KY-05009Summary: KY-05009 is an ATP-competitive inhibitor.
- BA2866 DihydrokaempferolSummary: Could be a good candidate for new anti-arthritic drugs.