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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 PageBisindolylmaleimide I (GF109203X) 1mg | 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 PageBisindolylmaleimide IX (Ro 31-8220) Mesylate 50mg | Purity Not Available
Selleck Chemicals
Bisindolylmaleimide IX (Ro 31-8220 Mesylate) is a pan-PKC inhibitor with IC50 of 5 nM, 24 nM, 14 nM, 27 nM, and 24 nM for PKC-α, PKC-βI, PKC-βII, PKC-γ, and PKC-ε, respectively, and also shows potent inhibition against MAPKAP-K1b, MSK1, GSK3β and S6K1.
More Information Supplier PageBisindolylmaleimide IX (Ro 31-8220) Mesylate 10mg | Purity Not Available
Selleck Chemicals
Bisindolylmaleimide IX (Ro 31-8220 Mesylate) is a pan-PKC inhibitor with IC50 of 5 nM, 24 nM, 14 nM, 27 nM, and 24 nM for PKC-α, PKC-βI, PKC-βII, PKC-γ, and PKC-ε, respectively, and also shows potent inhibition against MAPKAP-K1b, MSK1, GSK3β and S6K1.
More Information Supplier PageCNX-2006 25mg | Purity Not Available
Selleck Chemicals
CNX-2006 is a novel irreversible mutant-selective EGFR inhibitor with IC50 of < 20 nM, with very weak inhibition at wild-type EGFR.
More Information Supplier PageCNX-2006 5mg | Purity Not Available
Selleck Chemicals
CNX-2006 is a novel irreversible mutant-selective EGFR inhibitor with IC50 of < 20 nM, with very weak inhibition at wild-type EGFR.
More Information Supplier Page