Signaling pathways
- BA3237 8-AminoadenosineSummary: 8-Aminoadenosine (8-NH2-Ado) is an RNA-directed nucleoside analog that reduces cellular ATP levels and inhibits synthesis.
- BA3238 T-1-PMPASummary: T-1-PMPA is a potent inhibitor.
- BA3239 NAE-IN-M22Summary: NAE-IN-M22 is a potent, selective and reversible activase inhibitor with potency in the micromolar range.
- BA3240 DPBQSummary: DPBQ activates and triggers apoptosis in a polyploid-specific manner, but does not inhibit topoisomerases or bind DNA.
- BA3241 UCM-1336Summary: UCM-1336 is an effective inhibitor.
- BA3242 IMM-01Summary: IMM-01 is a mammalian clear (mDia)-related formin agonist.
- BA3243 SF1126Summary: SF1126 is a dual pan-inhibitor with antitumor and antiangiogenic activities.
- BA3244 Thalidomide-NH-C2-PEG3-OHSummary: Thalidomide-NH-C2-PEG3-OH is an E3 ligaseligand-linker coupling (E3ligaseligand-linkerconjugate) comprising a Thalidomide-based ligand and 1 linker.
- BA3245 Thalidomide-NH-C4-NH-BocSummary: Thalidomide-NH-C4-NH-Boc is a synthetic.
- BA3246 FD223Summary: FD223 is a potent and selective inhibitor of phosphatidylinositol 3-kinase delta.