GSK2830371 50mg | Purity Not Available
Selleck Chemicals
GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM.
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GSK2830371 200mg | Purity Not Available
Selleck Chemicals
GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM.
More Information Supplier PageLedipasvir (GS5885) 5mg | Purity Not Available
Selleck Chemicals
Ledipasvir (GS5885) is a HCV NS5A polymerase inhibitor, used for the treatment of hepatitis C virus infection.
More Information Supplier PageAGK2 100mg | Purity Not Available
Selleck Chemicals
AGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 μM that minimally affects either SIRT1 or SIRT3 at 10-fold higher levels.
More Information Supplier PageAGK2 25mg | Purity Not Available
Selleck Chemicals
AGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 μM that minimally affects either SIRT1 or SIRT3 at 10-fold higher levels.
More Information Supplier PageGSK-LSD1 2HCl 100mg | Purity Not Available
Selleck Chemicals
GSK-LSD1 2HCl is an irreversible, and selective LSD1 inhibitor with IC50 of 16 nM, > 1000 fold selective over other closely related FAD utilizing enzymes (i.e. LSD2, MAO-A, MAO-B).
More Information Supplier PageGSK-LSD1 2HCl 25mg | Purity Not Available
Selleck Chemicals
GSK-LSD1 2HCl is an irreversible, and selective LSD1 inhibitor with IC50 of 16 nM, > 1000 fold selective over other closely related FAD utilizing enzymes (i.e. LSD2, MAO-A, MAO-B).
More Information Supplier PageGSK-LSD1 2HCl 5mg | Purity Not Available
Selleck Chemicals
GSK-LSD1 2HCl is an irreversible, and selective LSD1 inhibitor with IC50 of 16 nM, > 1000 fold selective over other closely related FAD utilizing enzymes (i.e. LSD2, MAO-A, MAO-B).
More Information Supplier PageXL413 5mg | Purity Not Available
Selleck Chemicals
XL413 is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor with IC50 of 3.4 nM, showing 63-, 12- and 35-fold selectivity over CK2, Pim-1 and pMCM2, respectively.
More Information Supplier PageXL413 25mg | Purity Not Available
Selleck Chemicals
XL413 is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor with IC50 of 3.4 nM, showing 63-, 12- and 35-fold selectivity over CK2, Pim-1 and pMCM2, respectively.
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