Signaling pathways
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BA3605 XRK3F2Summary: Inhibitors of structural domains. - BA3606 STO-609Summary: STO-609 is a selective and cell permeable inhibitor with values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively.
- BA3607 THZ-P1-2Summary: THZ-P1-2 is a first-of-its-kind, selective inhibitor.
- BA3608 SBP-7455Summary: SBP-7455 is a potent, high-affinity, orally active dual autophagy inhibitor with 13 nM and 476 nM in ADP-Glo analysis, respectively.
- BA3610 EACCSummary: EACC is a reversible autophagy inhibitor that blocks autophagic flux.
- BA3611 eIF4A3-IN-2Summary: eIF4A3-IN-2 is a highly selective.
- BA3612 TrifaroteneSummary: Trifarotene (CD5789) is a potent and selective agonist.
- BA3613 NL-1Summary: NL-1 is an inhibitor with anti-leukemic effects.
- BA3614 ArglabinSummary: Arglabin ((+)-Arglabin), a natural product isolated from Artemisia leucocephala, is an NLRP3 inflammatory vesicle inhibitor.
- BA3615 SertindoleSummary: Sertindole (Lu23-174) is an antagonist.