MI-3 (Menin-MLL Inhibitor) 25mg | Purity Not Available
Selleck Chemicals
MI-3 (Menin-MLL Inhibitor) is a potent menin-MLL interaction inhibitor with IC50 of 648 nM.
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Santacruzamate A (CAY10683) 50mg | Purity Not Available
Selleck Chemicals
Santacruzamate A (CAY10683) is a potent and selective HDAC inhibitor with IC50 of 119 pM for HDAC2, >3600-fold selectivity over other HDACs.
More Information Supplier PageSantacruzamate A (CAY10683) 10mg | Purity Not Available
Selleck Chemicals
Santacruzamate A (CAY10683) is a potent and selective HDAC inhibitor with IC50 of 119 pM for HDAC2, >3600-fold selectivity over other HDACs.
More Information Supplier PageAbscisic Acid (Dormin) 25mg | Purity Not Available
Selleck Chemicals
Abscisic Acid (Dormin, Abscisin II) is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism, and inhibits germination and seedling growth.
More Information Supplier PageAbscisic Acid (Dormin) 5mg | Purity Not Available
Selleck Chemicals
Abscisic Acid (Dormin, Abscisin II) is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism, and inhibits germination and seedling growth.
More Information Supplier PageSplitomicin 50mg | Purity Not Available
Selleck Chemicals
Splitomicin is a selective NAD(+)-dependent histone deacetylase Sir2p inhibitor with IC50 of 60 μM, showing a higher activity in a cell-based assay.
More Information Supplier PageCAY10603 25mg | Purity Not Available
Selleck Chemicals
CAY10603 (BML-281) is a potent and selective HDAC6 inhibitor with IC50 of 2 pM, >200-fold selectivity over other HDACs.
More Information Supplier PageCAY10603 100mg | Purity Not Available
Selleck Chemicals
CAY10603 (BML-281) is a potent and selective HDAC6 inhibitor with IC50 of 2 pM, >200-fold selectivity over other HDACs.
More Information Supplier PageBV-6 5mg | Purity Not Available
Selleck Chemicals
Filgotinib (GLPG0634) 100mg | Purity Not Available
Selleck Chemicals
Filgotinib (GLPG0634) is a selective JAK1 inhibitor with IC50 of 10 nM, 28 nM, 810 nM, and 116 nM for JAK1, JAK2, JAK3, and TYK2, respectively. Phase 2.
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