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Cat.No. Product Name Information Area
T4598 BMS-5 BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, res... Cancer
T4600 BMS-3

BMS-3 is a potent LIMK inhibitor with IC50s of 5 nM and 6 nM for LIMK1 and LIMK2, ...

T4327 LY2606368 dihydrochloride Prexasertib (LY2606368) is an ATP-competitive CHK1 inhibitor (Ki: 0.9 nmol/L). in the... 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. Others
T4045 Epetraborole hydrochloride Epetraborole hydrochloride is a potent and selective leucyl-tRNA synthetase inhibitor... Immunology
T4005 FDI-6 FDI-6 is an effective and selective inhibitor of FOXM1 that blocks DNA binding. FDI-6... Others
T3960 T5601640 T56-LIMKi is a selective inhibitor of LIMK2. Others
T3951 NSC632839 NSC632839 is a nonselective isopeptidase inhibitor, which inhibits USP2 (EC50: 45±4 μ... Others
T3555 ML364 ML364 is an inhibitor of ubiquitin specific peptidase 2 (USP2) and can be used for th... Others
T3811 Ginsenoside K Ginsenoside C-K is a bacterial metabolite of G-Rb1 exhibiting anti-inflammatory effe... Others
T3774 Gracillin Gracillin can induce cell cycle arrest, oxidative stress, and apoptosis in HL60 cells... Others
T3434 BAY1217389 BAY 1217389 is an effective and selective inhibitor of the monopolar spindle 1 (MPS1)... Cancer
T3686 10074-G5 10074-G5 is an inhibitor of c-Myc-Max dimerization.
T3118 Dimethylenastron Dimethylenastron, an Eg5 inhibitor, arrests cells with monopolar spindles to which al... Others
T3120 K858 K858 is a selective mitotic kinesin Eg5 inhibitor which acts in an ATP-noncompetitive... Others
T6693 TAME Tosyl-L-Arginine Methyl Ester (TAME) is an APC inhibitor. Cancer
T6014 FRAX597 FRAX597 is an effective, ATP-competitive inhibitor of group I PAKs, and for PAK1(IC50... 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 (IC50: 5-30 μM). Other
T2220 2-Methoxyestradiol 2-Methoxyestradiol is an orally bioavailable estradiol metabolite with potential anti...
T2197 10-Deacetylbaccatin III 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations with anti-ca... Other
T2164 Wiskostatin Wiskostatin is a selective inhibitor of N-WASP, a ubiquitously expressed member of th... Other
T1973 PFI-4 PFI-4 is a potent and selective and cell-permeable BRPF1 bromodomain inhibitor. Other
T1972 GSK-5959 GSK-5959 is an effective, specific and cell permeable BRPF1 bromodomain inhibitor (IC... Other
T1854 MS436 MS436 is a selective, small-molecule inhibitor for the BRD4 bromodomains. Other
T1839 Mps1-IN-2 Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor. Other
T1828 TTP 22 TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/... Other