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Home > Products > Cell Cycle
Cat.No. Product name Product Description
R10022 GSK429286A GSK429286A is a selective inhibitor of ROCK1 and ROCK2 with IC50 of 14 nM and 63
R10029 ML141 ML141 is a potent, selective and reversible non-competitive inhibitor of Rho fam
R10051 PF-477736 PF-477736 is a selective, potent and ATP-competitive Chk1 inhibitor with Ki of 0
R10083 XL413 Hydrochloride XL413 (BMS-863233) is a potent and selective cell division cycle 7 homolog (CDC7
R10090 AZD5438 AZD5438 is a potent inhibitor of CDK1/2/9 with IC50 of 16 nM/6 nM/20 nM in cell-
R10117 PD0332991 Palbociclib (PD-0332991) HCl is a highly selective inhibitor of CDK4/6 with IC50
R10139 Roscovitine; Seliciclib Roscovitine (Seliciclib, CYC202) is a potent and selective CDK inhibitor for Cdc
R10170 SCH727965 Dinaciclib (SCH727965) is a novel and potent CDK inhibitor for CDK2, CDK5, CDK1
R10189 AT7519 HCl AT7519 HCl is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210
R10219 AZD7762 AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-
R10228 PHA767491 PHA-767491 is a potent ATP-competitive dual Cdc7/CDK9 inhibitor with IC50 of 10
R10252 MK1775 MK-1775 is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM in a cell-f
R10264 RO3280 RO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with
R10271 BI2536 BI2536 is a potent Plk1 inhibitor with IC50 of 0.83 nM in a cell-free assay. It
R10314 PD0332991; PD0332991; Palbociclib Palbociclib (PD0332991) Isethionate is a highly selective inhibitor of CDK4/6 wi
R10341 BS-181 hydrochloride BS-181 HCl is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more t
R10377 Palbociclib; PD0332991HCl Palbociclib (PD-0332991) HCl is a highly selective inhibitor of CDK4/6 with IC50
R10413 10058-F4 10058-F4 is a c-Myc inhibitor that specificallly inhibits the c-Myc-Max interact
R10417 EHop016 EHop-016 is a specific Rac GTPase inhibitor with IC50 of 1.1 μM for Rac1 in MDA-
R10596 RKI-1447 RKI-1447 is a potent inhibitor of ROCK1 and ROCK2, with IC50 of 14.5 nM and 6.2
R10616 ZCL278 ZCL278 is a selective Cdc42 GTPase inhibitor with Kd of 11.4 μM.
R10701 CCG1423 CCG-1423 is a specific RhoA pathway inhibitor, which inhibits SRF-mediated trans
R10707 PURVALANOLA Purvalanol A is a potent, and cell-permeable CDK inhibitor with IC50 of 4 nM, 70
R10729 BML-277 BML-277 (Chk2 Inhibitor II) is a Chk2 (checkpoint kinase 2) inhibitor.
R10755 BPR1J-097 BPR1J-097 is a novel small molecule FLT-3 inhibitor(IC50=11±7 nM) with promising
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