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Casein Kinase

Casein Kinase

Cat. No. Product Name CAS No. Information
CSN15858 TTP 22   329907-28-0 TTP 22 is a high affinity ATP-competitive casein kinase 2 CK2 inhibitor with IC50Ki of 01 M40 nM showing selectivity for CK2 over JNK3 ROCK1 and MET IC50 10 M
CSN25710 TMCB 905105-89-7 TMCB is a dual-kinase inhibitor of both casein kinase 2 (CK2) and extracellular-signal-regulated kinase 8 (ERK8) with IC50s of 0.50 μM.
CSN19438 TBB   17374-26-4 TBB is a highly selective ATPGTP-competitive inhibitor of casein kinase-2 CK2with IC50s of 09 and 16 M for rat liver and human recombinant CK2 respectively
CSN18028 TA-01 1784751-18-3 TA-01 potently inhibits CK1 CK1and p38 IC50values are 64 68 and 67 nM respectively
CSN17879 SR-3029 1454585-06-8 SR-3029 is a potent and highly specific CK1CK1 inhibitor with the IC50 of 97 nM
CSN26213 PI-828 942289-87-4 PI-828 is a dual PI3K and casein kinase 2 (CK2) inhibitor with IC50s of 173 nM, 149 nM, and 1127 nM for p110α, CK2, and CK2α2 in lipid kinase assay, respectively.
CSN16518 PF-670462 950912-80-8 PF-670462 is a potent and selective inhibitor of CK1 with IC50 of 77 22 nM
CSN22941 PF-4800567 1188296-52-7 PF-4800567 is an inhibitor of casein kinase 1 CK1 with IC50 of 32 nM
CSN22893 3-((3-Chlorophenoxy)methyl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine hydrochloride 1391052-28-0 PF-4800567 HCl is a selective casein kinase 1ε inhibitor with IC50 of 32 nM.
CSN24190 NCC007 2342583-66-6 NCC007 is a dual CK1α and CK1δ inhibitor with IC50 value of 1.8 and 3.6μM, respectively.
CSN11346 LY294002   154447-36-6 LY294002 is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of 0.5 μM/0.57 μM/0.97 μM in cell-free assays. It is an early-stage autophagy inhibitor and also inhibits CK2.
CSN16329 LH846   639052-78-1 LH846 is a selective inhibitor of casein kinase CK 1 with IC50 of 290 nM 13 M and 25 M for CK1 and displays no inhibitory activity at CK2
CSN18054 IC261   186611-52-9 IC261 is an ATP-competitive inhibitor of CK1 with IC50s about 1 M for CK1 and CK1 16 M for CK1
CSN19160 H-89 dihydrochloride   130964-39-5 H 89 2HCl is a potent and selective inhibitor of cyclic AMP-dependent protein kinase (protein kinase A) with IC50 of 48 nM. It also shows weak inhibition on PKG, PKC, CK1, CK2 and others kinases.
CSN19160 H-89 dihydrochloride   130964-39-5 H 89 2HCl is a potent and selective inhibitor of cyclic AMP-dependent protein kinase (protein kinase A) with IC50 of 48 nM. It also shows weak inhibition on PKG, PKC, CK1, CK2 and others kinases.
CSN63435 (E/Z)-GO289 694522-87-7 GO289 is a potent and selective CK2 inhibitor.
CSN26540 CK2/PIM1-IN-1 292640-28-9 for CK2 and PIM1, respectively. CK2/PIM1-IN-1 is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions including inflammation, pain, vascular disorders, pathogenic infections and certain immunological disorders[1].
CSN18468 Emodin 518-82-1 Emodin shows antiproliferative effects in cancer cells that are regulated by different signaling pathways it is a naturally occurring anthraquinone present in the roots and barks of numerous plants
CSN10902 Ellagic acid   476-66-4 Ellagic acid is a potent and cell permeable casein kinase 2 (CK2) inhibitor with Ki of 20 nM, acts as a potent antioxidant and anti-mutagenic.
CSN16246 DMAT 749234-11-5 DMAT is a potent and specific CK2 inhibitor with an IC50 value of 130 nM
CSN13638 D4476 301836-43-1 D4476 is a potent selective and cell-permeant CK1 casein kinase 1 inhibitor with IC50 of 200 nM and 300 nM in a cell-free assay for CK1 from Schizosaccharomyces pombe and CK1 respectively Also acts as an ALK5 inhibitor with IC50 of 500 nM
CSN17673 Silmitasertib sodium salt 1309357-15-0 CX-4945 Sodium is a selective inhibitor of CK2 catalytic subunits with an IC50 value of 1 nmolL.
CSN12957 Silmitasertib   1009820-21-6 CX-4945 is a potent and selective ATP-competitive small molecule protein kinase CK2 inhibitor with a Ki and an IC50 of 038 and 1 nM for recombinant human CK2 respectively
CSN23747 CK1-IN-1 1784751-20-7 CK1-IN-1 is a casein kinase 1 (CK1) inhibitor extracted from patent WO2015119579A1, compound 1c, has IC50s of 15 nM, 16 nM, 73 nM for CK1δ, and CK1ε, p38σ MAPK, respectively[1].
CSN21284 Casein Kinase II Inhibitor IV 863598-09-8 Casein Kinase II Inhibitor IV is a small-molecule inducer of epidermal keratinocyte differentiation
CSN20162 CAM4066 2101206-81-7 CAM4066 is a selective Casein Kinase 2 CK2 inhibitor
CSN27228 BioE-1115 1268863-35-9 BioE-1115 is a highly selective and potent PAS kinase (PASK) inhibitor with an IC50 of ~4 nM. BioE-1115 is also a potent casein kinase 2α inhibitor with an IC50 of ~10 μM .
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