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 About 7 results found for searched term "CHK1-IN-7" (0.133 seconds)

Cat.No.  Name Target
M41445 CHK1-IN-7 Checkpoint
CHK1-IN-7 is a potent human CHK1 inhibitor.
M1764 PF-477736 Checkpoint
PF-0044736
PF-477736 is a selective checkpoint kinase 1 (Chk1) inhibitor with Ki values of 0.49 nM and 47 nM for CHK1 and CHK2 respectively.
M2324 Rabusertib (LY2603618) Checkpoint
Rabusertib ; IC-83
Rabusertib (LY2603618) is an effective and selective Chk1 inhibitor with an IC50 of 7 nM.
M9208 PD0166285 Checkpoint
PD166285
PD0166285 is a potent Wee1 inhibitor and Chk1 inhibitor with IC50s of 24 nM and 72 nM, respectively.
M13620 CCT244747 Checkpoint
CCT244747 is a potent, orally bioavailable and highly selective CHK1 inhibitor, with an IC50 of 7.7 nM; CCT244747 also abrogates G2 checkpoint with an IC50 of 29 nM.
M27916 GDC0575 hydrochloride Checkpoint
ARRY-575 hydrochloride; RG7741 hydrochloride
GDC0575 (ARRY-575) hydrochloride is a highly-selective and orally active Chk1 (IC50=1.2 nM) inhibitor. GDC0575 (ARRY-575) hydrochloride can be used for colitis-associated cancer (CAC) and colitis research.
M45307 Multi-kinase-IN-6 Casein Kinase
Multi-kinase-IN-6 is a multikinase inhibitor that shows good enzyme inhibitory activity against TrkA, ALK2, c-KIT, EGFR, PIM1, CK2α, CHK1 and CDK2. In addition, Multi-kinase-IN-6 also showed antiproliferative activity against MCF7, HCT116 and EKVX, with IC50 values of 3.36 μM, 1.40 μM and 3.49 μM, respectively, and showed good apoptotic activity in MCF7 and HCT116 cells with cell-cycle arrest in G1/S and G1 phases. phase, with good apoptosis effect.



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