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Casein Kinase
货号 | 产品名 | CAS号 | 信息 |
---|---|---|---|
CSN15858 | TTP 22 | 329907-28-0 | TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/Ki of 0.1 μM/40 nM, showing selectivity for CK2 over JNK3, ROCK1, and MET (IC50> 10 μM). |
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, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2)with IC50s of 0.9 and 1.6 μM for rat liver and human recombinant CK2 respectively). |
CSN18028 | TA-01 | 1784751-18-3 | TA-01 potently inhibits CK1ε, CK1δ,and p38α (IC50values are 6.4, 6.8, and 6.7 nM respectively). |
CSN17879 | SR-3029 | 1454585-06-8 | SR-3029 is a potent and highly specific CK1δ/CK1ε 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 2HCl | 950912-80-8 | PF-670462 is a potent and selective inhibitor of CK1ε with IC50 of 7.7 ± 2.2 nM. |
CSN22941 | PF-4800567 | 1188296-52-7 | PF-4800567 is an inhibitor of casein kinase 1ε (CK1ε) 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) 1δ with IC50 of 290 nM, 1.3 μM and 2.5 μM for CK1δ, ε and α, displays no inhibitory activity at CK2. |
CSN18054 | IC261 | 186611-52-9 | IC261 is an ATP-competitive inhibitor of CK1 with IC50s about 1 μM for CK1δ and CK1ε, 16 μM for CK1α. |
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 CK1δ, 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 nmol/L. |
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 0.38 and 1 nM for recombinant human CK2α, 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 2α (CK2α) 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 . |