Activin and Inhibin

KU 59403 is a potent ATM inhibitor, with IC 50 values of 3 nM, 9.1 μM and 10 μM for ATM , DNA-PK and PI3K , respectivelyIn VitroKU 59403 (1 μM) enhances VP-16 (1 μM) cytotoxicity to a similar extent in HCT116 and HCT116-N7 cells, and in the p53

KU 59403 is a potent ATM inhibitor, with IC 50 values of 3 nM, 9.1 μM and 10 μM for ATM , DNA-PK and PI3K , respectivelyIn VitroKU 59403 (1 μM) enhances VP-16 (1 μM) cytotoxicity to a similar extent in HCT116 and HCT116-N7 cells, and in the p53

Kushenol A (Leachianone E) is isolated from the root of Sophora flavescent . Kushenol A is a non-competitive tyrosinase inhibitor to block the conversion of L-tyrosine to L-DOPA, shows IC 50 and K i values of 1.1 μM and 0.4 μM, respectively

Kushenol A (Leachianone E) is isolated from the root of Sophora flavescent . Kushenol A is a non-competitive tyrosinase inhibitor to block the conversion of L-tyrosine to L-DOPA, shows IC 50 and K i values of 1.1 μM and 0.4 μM, respectively

Kushenol A (Leachianone E) is isolated from the root of Sophora flavescent . Kushenol A is a non-competitive tyrosinase inhibitor to block the conversion of L-tyrosine to L-DOPA, shows IC 50 and K i values of 1.1 μM and 0.4 μM, respectively

Kushenol E is a class of flavonoids isolated from Sophora flavescens and is a non-competitive indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor with an IC 50 of 7.7 µM and a K i of 9.5 µM, has anti-tumor activity.Form:Solid.

Kushenol E is a class of flavonoids isolated from Sophora flavescens and is a non-competitive indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor with an IC 50 of 7.7 µM and a K i of 9.5 µM, has anti-tumor activity.Form:Solid.

Kuwanon G is a flavonoid isolated from Morus alba , acts as a bombesin receptor antagonist, with potential antimicrobial activity.Form:Solid.

KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2In VitroKW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE 2 in mouse osteoblastic cells. KW-8232 possesses anti-viral activity

KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2In VitroKW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE 2 in mouse osteoblastic cells. KW-8232 possesses anti-viral activity

KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2In VitroKW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE 2 in mouse osteoblastic cells. KW-8232 possesses anti-viral activity

KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2In VitroKW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE 2 in mouse osteoblastic cells. KW-8232 possesses anti-viral activity