Casein Kinase

Casein Kinase

货号 产品名 CAS号 信息
FB08450 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).
FB17153 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.
FB08183 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).
FB04005 TA-01 1784751-18-3 TA-01 potently inhibits CK1ε, CK1δ,and p38α (IC50values are 6.4, 6.8, and 6.7 nM respectively).
FB03250 SR-3029 1454585-06-8 SR-3029 is a potent and highly specific CK1δ/CK1ε inhibitor with the IC50 of 97 nM.
FB00034 PF-670462 950912-80-8 PF-670462 is a potent and selective inhibitor of CK1ε with IC50 of 7.7 ± 2.2 nM.
FB12762 PF-4800567 1188296-52-7 PF-4800567 is an inhibitor of casein kinase 1ε (CK1ε) with IC50 of 32 nM.
FB12164 PF-4800567 HCl 1391052-28-0 PF-4800567 HCl is a selective casein kinase 1ε inhibitor with IC50 of 32 nM.
FB15652 NCC007 2342583-66-6 NCC007 is a dual CK1α and CK1δ inhibitor with IC50 value of 1.8 and 3.6μM, respectively.
FB03874 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.
FB04030 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.
FB06839 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.
FB01273 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.
FB00810 DMAT 749234-11-5 DMAT is a potent and specific CK2 inhibitor with an IC50 value of 130 nM.
FB02998 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.
FB02722 CX-4945 Sodium 1309357-15-0 CX-4945 Sodium is a selective inhibitor of CK2 catalytic subunits with an IC50 value of 1 nmol/L.
FB00163 CX-4945 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.
FB15251 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].
FB11679 Casein Kinase II Inhibitor IV 863598-09-8 Casein Kinase II Inhibitor IV is a small-molecule inducer of epidermal keratinocyte differentiation.
FB11068 CAM4066 2101206-81-7 CAM4066 is a selective Casein Kinase 2α (CK2α) inhibitor.
FB17655 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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