OG-L002 25mg | Purity Not Available
Selleck Chemicals
OG-L002 is a potent and specific LSD1 inhibitor with IC50 of 20 nM in a cell-free assay, exhibiting 36- and 69-fold selectivity over MAO-B and MAO-A, respectively.
More Information Supplier PageSearch Results
AGI-6780 10mg | Purity Not Available
Selleck Chemicals
AGI-6780 is a potent and selective inhibitor of IDH2 R140Q mutant with IC50 of 23 nM.
More Information Supplier PageErastin 50mg | Purity Not Available
Selleck Chemicals
Erastin is a ferroptosis activator by acting on mitochondrial VDAC, exhibiting selectivity for tumor cells bearing oncogenic RAS. Solutions are unstable and should be fresh-prepared.
More Information Supplier PageFer-1 (Ferrostatin-1) 5mg | Purity Not Available
Selleck Chemicals
Fer-1 (Ferrostatin-1) is a potent and selective inhibitor of ferroptosis with EC50 of 60 nM.
More Information Supplier PageKPT-276 10mg | Purity Not Available
Selleck Chemicals
KPT-276 50mg | Purity Not Available
Selleck Chemicals
Selinexor (KPT-330) 5mg | Purity Not Available
Selleck Chemicals
Selinexor (KPT-330, ATG-010) is an orally bioavailable selective CRM1 inhibitor. Phase 2.
More Information Supplier PageSelinexor (KPT-330) 50mg | Purity Not Available
Selleck Chemicals
Selinexor (KPT-330, ATG-010) is an orally bioavailable selective CRM1 inhibitor. Phase 2.
More Information Supplier PageGSK650394 25mg | Purity Not Available
Selleck Chemicals
GSK650394 is a serum- and glucocorticoid-regulated kinase-1 inhibitor with IC50 of 62 nM and 103 nM for SGK1 and SGK2, respectively.
More Information Supplier PageBisindolylmaleimide I (GF109203X) 10mg | Purity Not Available
Selleck Chemicals
Bisindolylmaleimide I (GF109203X, GO 6850) is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ in cell-free assays, respectively, showing more than 3000-fold selectivity for PKC as compared to EGFR, PDGFR and insulin receptor.
More Information Supplier Page