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Cat.No. Product Name Information Area
T4327 LY2606368 dihydrochloride Prexasertib (LY2606368) is an ATP-competitive CHK1 inhibitor with a Ki value of 0.9 n... Cancer
T4189 4-Oxofenretinide 4-oxo-fenretinide, a recently identified fenretinide metabolite, induces marked G2-M ... Cancer
T4048 Monastrol Monastrol is a potent and cell-permeable inhibitor of the mitotic kinesin Eg5 with an... Others
T4045 Epetraborole hydrochloride Epetraborole, also known as GSK2251052 and AN3365, is a potent and selective leucyl-t... Immunology
T4005 FDI-6 FDI-6 is a potent and specific inhibitor of FOXM1 that blocks DNA binding. FDI-6 bind... Others
T3960 T5601640 T56-LIMKi is a selective inhibitor of LIMK2; inhibits the growth of Panc-1 cells with... Others
T3951 NSC632839 NSC632839 is a nonselective isopeptidase inhibitor, which inhibits USP2, USP7, and SE... Others
T3555 ML364 ML364 is an USP2 inhibitor extracted from patent WO 2016134026 A1, compound example 1... Others
T3811 Ginsenoside K Ginsenoside compound K (C-K) could be a potentially effective anti-colorectal cancer ... Others
T3774 Gracillin Gracillin has anti-tumor activity, can induce cell cycle arrest, oxidative stress, an... Others
T3434 BAY1217389 BAY 1217389 is a potent, and selective inhibitor of the monopolar spindle 1 (MPS1) ki... Cancer
T3686 10074-G5 The c-Myc oncoprotein is overexpressed in many tumors and is essential for maintainin... Others
T3118 Dimethylenastron Dimethylenastron is an Eg5 inhibitor, which arrests cells with monopolar spindles to ... Others
T3120 K858 K858 selectively inhibits Eg5 ATPase activity with an IC50 of 1.3 μM. Others
T6693 TAME Tosyl-L-Arginine Methyl Ester (TAME) is an APC inhibitor. Cancer
T6014 FRAX597 FRAX597 is a potent, ATP-competitive inhibitor of group I PAKs with IC50 of 8 nM, 13 ... Cancer
T2695 TBB TBB(NSC 231634) is a highly selective, ATP/GTP-competitive inhibitor of casein kinase... Cancer
T2628 RI-2 RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA bin... Cancer
T2276 RI-1 RI-1 is a RAD51 inhibitor with IC50 ranging from 5 to 30 _mu_M. Other
T2220 2-Methoxyestradiol 2-Methoxyestradiol (2ME2) is a drug that prevents the formation of new blood vessels ... Cancer
T2197 10-Deacetylbaccatin III 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. Other
T2164 Wiskostatin Wiskott-Aldrich syndrome protein (WASP) and WAVE stimulate actin-related protein (Arp... Other
T1973 PFI-4 PFI-4 is a potent and selective and cell permeable BRPF1 bromodomain inhibitor (IC50 ... Other
T1972 GSK-5959 GSK-5959 is a potent, selective and cell permeable BRPF1 bromodomain inhibitor with I... Other
T1854 MS436 MS436 is a diazobenzene-based small-molecule inhibitor for the BRD4 bromodomains with... Other
T1839 Mps1-IN-2 Mps1-IN-2 is a potent Mps1 kianse inhibitor with IC50 value of 145 nM. Other
T1828 TTP 22 TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/... Other