7 Results for "

CHK-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "CHK-IN-1" in MCE Product Catalog:

Cat. No.: HY-U00345
CAS No.: 1278405-51-8
Research Areas:  

Cancer

CHK-IN-1 is an inhibitor of CHK1 and CHK2, with anti-proliferative activities.
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9
9 Publications Verification
Cat. No.: HY-13925
CAS No.: 185039-89-8
Purity:  99.46%
Target:  

Wee1 Apoptosis

Research Areas:  

Cancer

PD0166285, a substrate of P-gp, is a WEE1 inhibitor and a weak Myt1 inhibitor with IC50 values of 24 and 72 nM, respectively. PD0166285 exhibits an IC50 of 3.433 μM for Chk1 .
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1
1 Cited Publications
Cat. No.: HY-114302
CAS No.: 2100864-57-9
Purity:  99.89%
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

CCB02 is a selective CPAP-tubulin interaction inhibitor, binding to tubulin and competing for the CPAP binding site of β-tubulin, with an IC50 of 689 nM, and shows potent anti-tumor activity. CCB02 shows no inhibition on the cell cycle- and centrosome-related kinases, or the phosphorylation status of Aurora A, Plk1, Plk2, CDK2, and CHK1 .
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Cat. No.: HY-155195
CAS No.: 2991054-23-8
Purity:  98.00%
Target:  

FLT3

Research Areas:  

Cancer

FLT3/CHK-IN-1 (Compound 18) is a dual inhibitor of FLT3/CHK1. FLT3/CHK-IN-1 is more than 1700 times more selective to c-KI T and greatly reduces hERG affinity with an IC50 value of 58.4 μM. FLT3/CHK-IN-1 inhibits tumor growth in mouse xenotransplantation models inoculated with MV-4-11 cells [1].
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Cat. No.: HY-P10574
Research Areas:  

Cancer

Phosphorylated CHKtide is a synthetic peptide substrate derived from CDC25C, which is phosphorylated by CHK1/CHK2 in one of the DNA repair pathways. Phosphorylated CHKtide is used in the assays of cell cycle checkpoint kinases 1 and 2 (CHK1/CHK2) and salt-inducible kinases (SIKs) [1].
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Cat. No.: HY-13925A
CAS No.: 212391-63-4
Target:  

Wee1 Apoptosis

Research Areas:  

Cancer

PD0166285 dihydrochloride, a substrate of P-gp, is a WEE1 inhibitor and a weak Myt1 inhibitor with IC50 values of 24 and 72 nM, respectively. PD0166285 dihydrochloride exhibits an IC50 of 3.433 μM for Chk1 .
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Cat. No.: HY-119699
CAS No.: 1093793-10-2
Research Areas:  

Cancer

PV1115 is a potent and highly selective Chk2 inhibitor with an IC50 of 0.14 nM, 66000 nM, >100000 nM for Chk2, Chk1 and RSK2, respectively. PV1115 is situated within the ATP-binding pocket of Chk2 .
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