1. Cell Cycle/DNA Damage Stem Cell/Wnt
  2. Casein Kinase
  3. SR-4133

SR-4133 is a potent and highly CK1ε selective inhibitor with an IC50 of 58 nM. SR-4133 binds to the ATP-binding site of CK1ε. SR-4133 displays nanomolar growth inhibition of bladder cancer cells, and inhibits the phosphorylation of 4E-BP1.

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SR-4133

SR-4133 Estructura química

No. CAS : 2999645-23-5

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Descripciòn

SR-4133 is a potent and highly CK1ε selective inhibitor with an IC50 of 58 nM. SR-4133 binds to the ATP-binding site of CK1ε. SR-4133 displays nanomolar growth inhibition of bladder cancer cells, and inhibits the phosphorylation of 4E-BP1[1].

IC50 & Target

CK1ε

58 nM (IC50)

CK1γ2

10 μM (IC50)

Cellular Effect
Cell Line Type Value Description References
5637 EC50
314 nM
Compound: SR-4133
Antiproliferative activity against human 5637 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
Antiproliferative activity against human 5637 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
[PMID: 37204207]
T-24 EC50
265 nM
Compound: SR-4133
Antiproliferative activity against human T24 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
Antiproliferative activity against human T24 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
[PMID: 37204207]
U2OS EC50
373 nM
Compound: SR-4133
Antiproliferative activity against human U2OS cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
Antiproliferative activity against human U2OS cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
[PMID: 37204207]
UMUC3 EC50
540 nM
Compound: SR-4133
Antiproliferative activity against human UMUC3 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
Antiproliferative activity against human UMUC3 cells assessed as reduction in cell proliferation incubated for 72 hrs by Cell Titer Glo assay
[PMID: 37204207]
In Vitro

SR-4133 (200-600 nM, 72 h) inhibits cancer cells growth significantly with EC50s of 265 nM (T24), 314 nM (5637), 540 nM (UM-UC-3 EC), 373 nM (U2-OS EC)[1].
SR-4133 (1 μM, 24 h) inhibits the phosphorylation of 4E-BP1 in T24 cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: T24, 5637, UM-UC-3, U2-OS
Concentration: 265 nM, 314 nM, 540 nM, 373 nM
Incubation Time: 72 h
Result: Inhibited cell growth with EC50s of 265 nM (T24), 314 nM (5637), 540 nM (UM-UC-3 EC), 373 nM (U2-OS EC).

Western Blot Analysis[1]

Cell Line: T24
Concentration: 1 μM
Incubation Time: 24 h
Result: Blocked the phosphorylation of T37/46, S65, and T70 of 4E-BP1.
Peso molecular

512.51

Fòrmula

C27H22F2N8O

No. CAS
SMILES

FC1=C(F)C2=C(NC(CNC3=NC(N4CCOCC4)=NC5=C3N=CN5C6=CC(C=CC=C7)=C7C=C6)=N2)C=C1

Envío

Room temperature in continental US; may vary elsewhere.

Almacenamiento

Please store the product under the recommended conditions in the Certificate of Analysis.

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Referencias
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Inquiry Information

Nombre del producto:
SR-4133
Cat. No.:
HY-149292
Cantidad:
MCE Japan Authorized Agent: