19 Results for "

casein kinase 1ε

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "casein kinase 1ε" in MCE Product Catalog:

8
8 Publications Verification
Cat. No.: HY-15490
CAS No.: 950912-80-8
Purity:  99.96%
Target:  

Casein Kinase

Research Areas:  

Cancer

PF-670462 dihydrochloride is a potent and selective inhibitor of casein kinase (CK1ε and CK1δ), with IC50s of 7.7 nM and 14 nM, respectively.
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5
5 Cited Publications
Cat. No.: HY-12279
CAS No.: 1532533-67-7
Purity:  98.94%
Synonyms: TGR-1202; RP5264
Target:  

PI3K Casein Kinase

Research Areas:  

Cancer

Umbralisib (TGR-1202) is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK1ε) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib can be used for haematological malignancies reseach [1] .
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5
5 Cited Publications
Cat. No.: HY-12279C
CAS No.: 1532533-78-0
Purity:  99.04%
Synonyms: TGR-1202 hydrochloride; RP5264 hydrochloride
Target:  

PI3K Casein Kinase

Research Areas:  

Cancer

Umbralisib (TGR-1202) hydrochloride is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK1ε) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib hydrochloride exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib hydrochloride can be used for haematological malignancies reseach [1] .
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2
2 Cited Publications
Cat. No.: HY-12879
CAS No.: 686772-17-8
Purity:  99.81%
IWP-4 is a Wnt inhibitor with an IC50 of 25 nM. IWP-4 specifically inhibits casein kinase 1δ/ε (CK1δ/ε), with an IC50 of 1.06 μM against wild-type CK1δ, 1.02 μM against the CK1δ kinase domain, and 7.07 μM against CK; it shows enhanced inhibitory activity against the M82F CK1δ mutant (IC50 = 0.14 μM). IWP-4 is applicable to research related to cancer, Alzheimer's disease (AD), and heart failure [1] .
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1
1 Cited Publications
Cat. No.: HY-111820
CAS No.: 1784751-20-7
Purity:  99.19%
Target:  

Casein Kinase p38 MAPK

Research Areas:  

Cardiovascular Disease

CK1-IN-1 (Compound 1c) is a casein kinase 1 (CK1) inhibitor with IC50 values of 15 nM and 16 nM for CK1δ and CK, respectively. CK1-IN-1 inhibits p38α MAPK with an IC50 of 73 nM. CK1-IN-1 can be used to study cardiomyogenesis [1].
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Cat. No.: HY-148233S
CAS No.: 2765264-50-2
JNJ-6204 is a dual inhibitor for CSNK1D (Casein Kinase 1 Delta) and CSNK1E (Casein Kinase 1 Epsilon) (CSNK1D IC50=2.3 nM; CSNK1E IC50=137 nM). JNJ-6204 shows good brain exposure [1] .
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Cat. No.: HY-171278
CAS No.: 1095750-94-9
Target:  

Casein Kinase

Research Areas:  

Metabolic Disease Cancer

Casein kinase 1δ-IN-28 (Compound 4) is the inhibitor for CK1ε with an IC50 of 0.0146 μM. Casein kinase 1δ-IN-28 exhibits a metabolite rate in human liver microsomes of 52% [1].
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Cat. No.: HY-171277
CAS No.: 1095706-65-2
Target:  

Casein Kinase p38 MAPK

Research Areas:  

Cancer

Casein kinase 1δ-IN-27 (Compound 8) is the inhibitor for casein kinase 1 that inhibits CK1α, CK1δ, CK1ε, and p38α with IC50s of 22, 16.5, 9.41 and 14.8 nM, respectively. Casein kinase 1δ-IN-27 inhibits the DUX4 expression with an IC50 of 10 nM [1].
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Cat. No.: HY-12279A
CAS No.: 1532533-72-4
Synonyms: TGR-1202 tosylate; RP5264 tosylate
Target:  

PI3K Casein Kinase

Research Areas:  

Cancer

Umbralisib (TGR-1202) tosylate is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK1ε) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib tosylate exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib tosylate can be used for haematological malignancies reseach [1] .
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Cat. No.: HY-12279B
CAS No.: 1532533-75-7
Synonyms: TGR-1202 sulfate; RP-5264 sulfate
Target:  

PI3K Casein Kinase

Research Areas:  

Cancer

Umbralisib (TGR-1202) sulfate is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK1ε) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib sulfate exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib sulfate can be used for haematological malignancies reseach [1] .
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Cat. No.: HY-171279
CAS No.: 1177418-39-1
Research Areas:  

Inflammation/Immunology

Casein kinase 1δ-IN-29 (Compound 18) is the inhibitor for p38α and casein kinase 1 that inhibits p38α, CK1δ and CK1ε with IC50 of 0.041 µM, 0.005 µM and 0.447 µM, respectively. Casein kinase 1δ-IN-29 arrests cell cycle at subG1 phase, induces apoptosis in cell AC1-M88 [1].
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Cat. No.: HY-12279CR
CAS No.: 1532533-78-0
Synonyms: TGR-1202 hydrochloride (Standard); RP5264 hydrochloride (Standard)
Research Areas:  

Cancer

Umbralisib (hydrochloride) (Standard) is the analytical standard of Umbralisib (hydrochloride). This product is intended for research and analytical applications. Umbralisib (TGR-1202) hydrochloride is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib hydrochloride exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib hydrochloride can be used for haematological malignancies reseach [1] .
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Cat. No.: HY-12279R
CAS No.: 1532533-67-7
Synonyms: TGR-1202 (Standard); RP5264 (Standard)
Research Areas:  

Cancer

Umbralisib (Standard) is the analytical standard of Umbralisib. This product is intended for research and analytical applications. Umbralisib (TGR-1202) is an orally active, potent and selective dual PI3Kδ and casein kinase-1-ε (CK) inhibitor, with EC50 of 22.2 nM and 6.0 μM, respectively. Umbralisib exhibits unique immunomodulatory effects on chronic lymphocytic leukemia (CLL) T cells. Umbralisib can be used for haematological malignancies reseach [1] .
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Cat. No.: HY-123859
CAS No.: 1454584-91-8
SR-2890 is a highly selective, ATP-competitive inhibitor of casein kinase CK1δ and CK1ε, with IC50 values ​​of 4 nM and 44 nM, respectively, and a Ki of 14 nM for CK1δ. SR-2890 exhibits antiproliferative effects. SR-2890 blocks the serine/threonine kinase activity of CK1δ and weakly inhibits a few off-target kinases such as FLT3, CDK4. SR-2890 has an oral bioavailability of 10% and a blood-brain barrier penetration rate of <1%. SR-2890 demonstrates stable in vitro metabolism and favorable in vivo pharmacokinetic properties, effectively inhibiting the growth of human A375 melanoma cells. SR-2890 can be used in melanoma research and is also a useful compound for studying CK1δ/ε-related diseases such as Alzheimer's disease [1].
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Cat. No.: HY-P72152
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1E; Non-Specific Serine/Threonine Protein kinase; casein kinase 1 Epsilon; Alternative Protein CSNK1E; CKIepsilon; casein kinase 1, Epsilon; HCKIE; CKI-Epsilon; CKIE; CKIe; casein kinase I Isoform Epsilon
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P705796
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1E; Non-Specific Serine/Threonine Protein kinase; casein kinase 1 Epsilon; Alternative Protein CSNK1E; CKIepsilon; casein kinase 1, Epsilon; HCKIE; CKI-Epsilon; CKIE; CKIe; casein kinase I Isoform Epsilon
Species:  
Human
Source:  
sf9 insect cells
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Cat. No.: HY-P702666
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1E; Non-Specific Serine/Threonine Protein kinase; casein kinase 1 Epsilon; Alternative Protein CSNK1E; CKIepsilon; casein kinase 1, Epsilon; HCKIE; CKI-Epsilon; CKIE; CKIe; casein kinase I Isoform Epsilon
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-111820R
CAS No.: 1784751-20-7
CK1-IN-1 (Standard) is the analytical standard of CK1-IN-1 (HY-111820). This product is intended for research and analytical applications. CK1-IN-1 (Compound 1c) is a casein Kinase 1 (CK1) inhibitor with IC50 values of 15 nM and 16 nM for CK1δ and CK, respectively. CK1-IN-1 inhibits p38α MAPK with an IC50 of 73 nM. CK1-IN-1 can be used to study cardiomyogenesis [1].
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Cat. No.: HY-12879G
CAS No.: 686772-17-8
IWP-4 (GMP) is the GMP-grade form of IWP-4 (HY-12879). IWP-4 is a Wnt inhibitor with an IC50 of 25 nM. IWP-4 specifically inhibits casein kinase 1δ/ε (CK1δ/ε), with an IC50 of 1.06 μM against wild-type CK1δ, 1.02 μM against the CK1δ kinase domain, and 7.07 μM against CK; it shows enhanced inhibitory activity against the M82F CK1δ mutant (IC50 = 0.14 μM). IWP-4 is applicable to research related to cancer, Alzheimer's disease (AD), and heart failure [1] .
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