54
4
7
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T23090 | CK2-IN-1 | Others | |
CK2 inhibitor | |||
T35557 | CK2 inhibitor 2 | Casein Kinase | |
CK2 Inhibitor 2, characterized as a potent, selective, and orally active inhibitor of CK2, demonstrates an impressive IC50 value of 0.66 nM. It exhibits high selectivity towards Clk2 with an IC50 of 32.69 nM in compariso... | |||
T10827 | CK2/ERK8-IN-1 | TMCB | Apoptosis , ERK , Casein Kinase , Pim , DYRK |
CK2/ERK8-IN-1 (TMCB) is a dual inhibitor of casein kinase 2 (CK2) (Ki: 0.25 µM) and ERK8 (IC50s: 0.50 μM) with pro-apoptotic efficacy. CK2/ERK8-IN-1 also binds to PIM1, DYRK1A, and HIPK2 (Kis: 8.65 µM, 11.9 µM, and 15.25... | |||
T40131 | SGC-CK2-1 | SGC-CK2-1 | |
SGC-CK2-1 is an ATP-competitive chemical compound that acts as a highly potent and cell-active CK2 inhibitor. It demonstrates excellent selectivity towards both isoforms of human CK2, with IC50 values of 36 nM for CK2α a... | |||
T73375 | CK2-IN-4 | Casein Kinase | |
CK2-IN-4 is a protein kinase (CK2) inhibitor with an IC50 value of 8.6 µM. CK2-IN-4 has potential anticancer ah and anti-inflammatory activity for the study of viral infections and glomerulonephritis diseases. | |||
T7390 | DMAT | Casein kinase II Inhibitor,CK2 Inhibitor | Casein Kinase |
DMAT (Casein kinase II Inhibitor) is a potent and specific inhibitor of CK2(IC50 value of 130 nM). | |||
T10828 | CK2/PIM1-IN-1 | Others | |
CK2/PIM1-IN-1 is an inhibitor of CK2 and PIM1 (IC50s: 3.787 μM and 4.327 μM). It is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions. | |||
T61629 | CK2 inhibitor 3 | ||
CK2 inhibitor 3 is a highly potent inhibitor of protein kinase CK2, exhibiting an IC50 value of 280 nM. It effectively inhibits the intracellular activity of CK2 and displays a notable impact on the viability of tumor ce... | |||
T78599 | CK2-IN-9 | ||
CK2-IN-9, a potent and selective CK2 kinase inhibitor, exhibits an inhibitory concentration (IC50) of 3 nM against its target enzyme and hampers Wnt reporter activity with an IC50 of 75 nM. In rats, it demonstrates low e... | |||
T62862 | CK2-IN-3 | ||
CK2-IN-3 is a potent and selective CK2 inhibitor (Kd: 12 nM) with IC50 values of 1.51 μM for CK2α and 7.64 μM for CK2α'. CK2-IN-3 can be used in cancer research. | |||
T73380 | CK2-IN-6 | ||
CK2-IN-6, a powerful inhibitor of protein kinase CK2, shows promise for research in cancer, along with conditions related to kinases such as inflammation, pain, and specific immune diseases. | |||
T63991 | BRD4/CK2-IN-1 | ||
BRD4/CK2-IN-1 is the first potent, orally active dual-target inhibitor of BRD4/CK2 (bromodomain-containing protein 4/casein kinase 2), acting on both BRD4 (IC50: 180 nM) and CK2 (IC50: 230 nM). In triple-negative breast ... | |||
T73269 | CK2α-IN-1 | Casein Kinase | |
CK2α-IN-1 is a selective non-ATP-competitive CK2α inhibitor with an IC50 of 7.0 µM and a Ki of 1.6 µM.CK2α-IN-1 exhibits potential anticancer activity and can be used in cancer research. | |||
T12747 | ROCK2-IN-2 | ROCK | |
ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM). | |||
T72695 | UCK2 Inhibitor-1 | ||
UCK2 Inhibitor-1 is a non-competitive UCK2 inhibitor with an IC 50 of 4.7 µM . | |||
T81261 | ROCK2-IN-7 | ROCK | |
ROCK2 inhibitor is a chemical compound associated with the therapeutic management of psoriasis. It exhibits its efficacy in targeting ROCK2 enzymes within HaCaT cells and has demonstrated beneficial effects in a psoriasi... | |||
T73117 | ROCK2-IN-5 | ||
ROCK2-IN-5, a compound integrating structural elements from the Rho kinase inhibitor fasudil and the NRF2 inducers caffeic and ferulic acids, exhibits a favorable multitarget profile and tolerability. It shows potential ... | |||
T79832 | ROCK2-IN-6 | ROCK | |
ROCK2-IN-6 (Comp A) is a selective inhibitor of ROCK2, applicable in the study and treatment of ROCK-mediated, autoimmune, and inflammatory diseases [1]. | |||
T73194 | DOCK2-IN-1 | ||
DOCK2-IN-1, an analogue of CPYPP, effectively inhibits DOCK2 (IC50 = 19.1 μM) by reversibly binding to its DHR-2 domain, thereby hindering its catalytic function. This compound obstructs the activation of Rac in lymphocy... | |||
T17727 | CCK2R Ligand-Linker Conjugates 1 | Others | |
CCK2R Ligand-Linker Conjugate 1 is a hydrophilic peptide linker that conjugates to the cytotoxic antimicrotubule agents Desacetyl Vinblastine Hydrazide (DAVBH) and Tubulysin B Hydrazide (TubBH) as ligand-linker conjugate... | |||
T29161 | STOCK2S-26016 | WNK IN B,WNK-IN-B,Compound B | |
WNK-IN-B is an inhibitor of Wnk signalling. WNK-IN-B is a cell-permeable diaminoacridine derivative that targets the CCT domain of SPAK and OSR1 via reversible binding. WNK-IN-B selectively suppress hypotonic shock-induc... | |||
T72696 | UCK2 Inhibitor-3 | ||
UCK2 Inhibitor-3 is a non-competitive inhibitor targeting uridine-cytidine kinase 2 (UCK2), a key enzyme in the pyrimidine salvage pathway, with an IC50 value of 16.6 μM. Notably, UCK2 can partially substitute for dihydr... | |||
T68498 | UCK2 Inhibitor-2 | ||
UCK2 Inhibitor-2, a non-competitive inhibitor of uridine-cytidine kinase 2 (UCK2), exhibits an IC50 of 3.8 µM and effectively suppresses uridine salvage within cells. | |||
T78205 | ROCK2-IN-6 hydrochloride | ROCK | |
ROCK2-IN-6 hydrochloride (Comp A) serves as a selective inhibitor of ROCK2, applicable for research into ROCK-mediated diseases, autoimmune disorders, and inflammation [1]. | |||
T2259 | Silmitasertib | CX-4945 | Casein Kinase , Autophagy |
Silmitasertib (CX-4945) is a potent, orally bioavailable inhibitor of casein kinase 2 (CK2; Ki: 0.38 nM). | |||
T1828 | TTP 22 | Casein Kinase | |
TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/Ki of 0.1 uM/40 nM, and shows selectivity >250-fold for CK2 over JNK3, ROCK1, and MET(IC50> 10 uM). | |||
T2695 | TBB | Casein Kinase II Inhibitor I,NSC 231634,4,5,6,7-tetrabromobenzotriazole | GSK-3 , Casein Kinase , CDK |
TBB (NSC-231634)(NSC-231634) is a highly selective, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2). | |||
T60067 | WAY-297174 | Casein Kinase | |
WAY-297174 is a human protein kinase CK2 inhibitor with IC50 of > 33 μM. | |||
T21915 | TBCA | Casein Kinase II Inhibitor III, TBCA | Casein Kinase |
TBCA (Casein Kinase II Inhibitor III, TBCA) is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases. | |||
T6735 | XL413 hydrochloride | BMS-863233 Hydrochloride,XL413,BMS-863233 | cholecystokinin , Casein Kinase , Pim , CDK |
XL413 hydrochloride (BMS-863233 Hydrochloride) is a potent, selective and ATP competitive inhibitor of Cdc7, with an IC 50 of 3.4 nM. XL413 hydrochloride also exhibits potent effect with IC 50 s of 215, 42 nM on CK2, PIM... | |||
T71339 | BMS-863233 HCl | XL413 hydrochloride | Casein Kinase , Pim , CDK |
BMS-863233 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.BMS-863233 HCl inhibited CK2 and PIM1 with IC50 values of 215 and 42 nM, respectively.BMS-863233 HCl showed an EC50 value of... | |||
T15024 | Silmitasertib sodium salt | CX-4945 sodium salt | Casein Kinase , Autophagy |
Silmitasertib sodium salt (CX-4945 sodium salt) is a potent and orally bioavailable, highly selective inhibitor of CK2(IC50 of 1 nM, CK2α). | |||
T6745 | 5-Iodotubercidin | 5-ITu,NSC 113939 | Adenosine Receptor |
5-Iodotubercidin (NSC-113939) is a potent adenosine kinase inhibitor with IC50 of 26 nM. It inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC. | |||
T2008 | LY294002 | LY 294002,NSC 697286,SF 1101 | Apoptosis , DNA-PK , Casein Kinase , PI3K , Autophagy |
LY294002 (SF 1101) is a broad-spectrum inhibitor of PI3K, inhibiting PI3Kα, PI3Kδ, and PI3Kβ (IC50=0.5/0.57/0.97 μM). LY294002 is also an inhibitor of DNA-PK (IC50=1.4 μM) and an inhibitor of CK2 (IC50=98 nM). LY294002 ... | |||
T1877 | LH846 | LH-846,LH 846 | Casein Kinase |
LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 uM for CK1δ, ε and α); exhibits no inhibitory activity at CK2. | |||
T6458 | CYC-116 | VEGFR , FLT , CDK , S6 Kinase , Aurora Kinase | |
CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM, is less potent to VEGFR2 (Ki of 44 nM), with 50-fold greater potency than CDKs, not active against PKA, Akt/PKB, PKC, no effect on GSK-3α/β, CK2, Plk1 ... | |||
T9356 | (E/Z)-GO289 | Casein Kinase | |
(E/Z)-GO289, which strongly lengthened circadian period, is a potent and selective inhibitor of CK2. (E/Z)-GO289 exhibited cell type-dependent inhibition of cancer cell growth that correlated with cellular clock function... | |||
T3352 | XL413 | cholecystokinin , Casein Kinase , Pim , CDK | |
XL-413 is an orally bioavailable cell division cycle 7 homolog (CDC7) kinase inhibitor with potential antineoplastic activity. XL-413 binds to and inhibits the activity of CDC7, which may result in the inhibition of DNA ... | |||
T15469 | Hematein | Hydroxybrasilein | Wnt/beta-catenin , Akt |
Hematein inhibits Akt/PKB Ser129 phosphorylation, the Wnt/TCF pathway, and increases apoptosis in lung cancer cells. Hematein is an oxidation product of hematoxylin acted as a dye and it also is an allosteric casein kina... | |||
T23461 | TMCB | Others | |
CK2 and ERK8 inhibitor | |||
T20791 | Quinalizarin | ||
Quinalizarin, the most selective CK2 inhibitor, is superior to CX-4945 which is the first-in-class CK2 inhibitor. | |||
T24832 | SRPIN-803 | SRPIN803 | |
SRPIN-803 is a selective dual SRPK1 and CK2 inhibitor. | |||
T69307 | IQA | ||
IQA is a casein kinase 2 (CK2) inhibitor. | |||
T71190 | FLC26 | ||
FLC26 is a CK2 inhibitor with IC50 = 9 nM | |||
T76475 | Casein Kinase II Substrate | ||
Casein Kinase II Substrate, a peptide substrate, is selectively phosphorylated by casein kinase II (CK2) [1]. | |||
T76411 | Casein Kinase 2 Substrate Peptide | ||
Casein Kinase 2 Substrate Peptide, a widely recognized CK2 substrate, is synthesized with its C-terminus conjugated to 5-[(2-aminoethyl)amino]naphthalene-1-sulfonic acid (EDANS). This peptide serves as a tool for determi... | |||
T21642 | 4,5,6,7-Tetrabromobenzimidazole | ||
4,5,6,7-Tetrabromobenzimidazole is a selective and ATP-competitive inhibitor of protein kinase CK2 [1]. | |||
T71627 | CX-5011 | Casein Kinase | |
CX-5011, a CK2 inhibitor, induces Rac1 activation and promotes apoptosis, effectively causing cancer cell death [1] [2]. | |||
T16528 | PI-828 | LY 294002, 4gamma-NH2 | Casein Kinase , PI3K |
PI-828 is a phosphatidylinositol 3-kinase (PI3K) inhibitor, which is widely used to study the physiological function of PI3K and also promotes stem cell differentiation into mesoderm. | |||
T79908 | ON 108600 | Casein Kinase | |
ON 108600 is a chemical inhibitor targeting CK2 (Casein Kinase 2), TNIK, and DYRK1, demonstrating IC50 values of 0.016 μM and 0.007 μM for DYRK1A and DYRK1B, 0.028 μM for DYRK2, 0.05 μM and 0.005 μM for CK2α1 and CK2α2, ... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2869 | Emodin | Frangula emodin | SARS-CoV , Casein Kinase , Autophagy |
Emodin (Frangula emodin) is a naturally occurring anthraquinone present in the roots and barks of numerous plants; exerts antiproliferative effects in Y cells that are regulated by different signaling pathways. | |||
T0465 | Ellagic acid | Gallogen,Elagostasine | Hedgehog/Smoothened , Casein Kinase , Reactive Oxygen Species , Topoisomerase , Endogenous Metabolite , PKA , Syk , PKC , Carbonic Anhydrase |
Ellagic acid (Gallogen) is a fused four ring compound isolated from the kino of Eucalyptus maculata Hook and E. Hemipholia F. Muell. Activates Factor XII of the blood clotting system which also causes kinin release; used... | |||
T8305 | Ellagic acid (hydrate) | Ellagic Acid hydrate | Antioxidant , Casein Kinase |
Ellagic acid (hydrate) is a natural antioxidant and acts as a potent and ATP-competitive CK2 inhibitor (IC50:40 nM, Ki: 20 nM). | |||
T16791 | Rottlerin | Mallotoxin,NSC 56346,NSC 94525 | CaMK , Apoptosis , Others , HIV Protease , PKA , PKC , Autophagy |
Rottlerin (NSC-56346) is a natural product purified from Mallotus Philippinensis and is a specific PKC inhibitor (IC50: PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM). Rottlerin causes apoptosis via caspase... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04441 | CK2 alpha/CSNK2A1 Protein, Mouse, Recombinant (His & GST) | Mouse | Baculovirus-Insect Cells |
Casein kinase II subunit alpha, also known as CK II alpha, CSNK2A1 and CK2A1, is a member of the protein kinase superfamily, Ser / Thr protein kinase family and CK2 subfamily. Casein kinase II (CSNK2A1) is a serine / thr... | |||
TMPY-04758 | CK2 alpha/CSNK2A1 Protein, Mouse, Recombinant | Mouse | Baculovirus-Insect Cells |
Casein kinase II subunit alpha, also known as CK II alpha, CSNK2A1 and CK2A1, is a member of the protein kinase superfamily, Ser / Thr protein kinase family and CK2 subfamily. Casein kinase II (CSNK2A1) is a serine / thr... | |||
TMPY-04372 | CK2 alpha/CSNK2A1 Protein, Human, Recombinant (GST) | Human | Baculovirus-Insect Cells |
Casein kinase II subunit alpha, also known as CK II alpha, CSNK2A1 and CK2A1, is a member of the protein kinase superfamily, Ser / Thr protein kinase family and CK2 subfamily. Casein kinase II (CSNK2A1) is a serine / thr... | |||
TMPY-04764 | PCK2 Protein, Human, Recombinant (His & GST) | Human | Baculovirus-Insect Cells |
PCK2 promotes tumor initiation by lowering acetyl-CoA level through reducing the mitochondrial tricarboxylic acid (TCA) cycle. The levels of phosphoenolpyruvate carboxykinase isoform 2 (PCK2) are critical for the metabol... | |||
TMPY-04750 | CSNK2A2 Protein, Human, Recombinant | Human | Baculovirus-Insect Cells |
Casein kinase II subunit alpha', also known as CSNK2A2 and CK2A2, is a member of the protein kinase superfamily, Ser/Thr protein kinase family and CK2 subfamily. Casein kinases are operationally defined by their prefer... | |||
TMPY-04393 | CSNK2A2 Protein, Human, Recombinant (His & GST) | Human | Baculovirus-Insect Cells |
Casein kinase II subunit alpha', also known as CSNK2A2 and CK2A2, is a member of the protein kinase superfamily, Ser/Thr protein kinase family and CK2 subfamily. Casein kinases are operationally defined by their prefer... | |||
TMPJ-01307 | PACSIN1 Protein, Human, Recombinant (His) | Human | Human Cells |
Protein Kinase C and Casein Kinase Substrate in Neurons Protein 1 (PACSIN1) belongs to the PACSIN family. PACSIN1 contains one FCH domain and one SH3 domain. PACSIN1 is highly expressed in the brain and at lower leves in... |