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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 (CID-2950007) ML141 is a potent, selective and reversible non-competitive inhibitor of Rho fam
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-
R10139 Roscovitine; Seliciclib Roscovitine (Seliciclib, CYC202) is a potent and selective CDK inhibitor for Cdc
R10189 AT7519 HCl AT7519 HCl is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210
R10219 AZD7762;AZD-7762 AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-
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 BI 2536;BI2536 BI 2536 is a dual PLK1 and BRD4 inhibitor with IC50s of 0.83 and 25 nM, respecti
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 hydrochloride;PD 0332991 hydrochloride Palbociclib (PD-0332991) HCl is a highly selective inhibitor of CDK4/6 with IC50
R10417 EHop016 EHop-016 is a specific Rac GTPase inhibitor with IC50 of 1.1 μM for Rac1 in MDA-
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
R10910 MK-8776 MK-8776 (SCH 900776) is a selective Chk1 inhibitor with IC50 of 3 nM in a cell-f
R11042 HMN214 HMN-214 is a prodrug of HMN-176, which alters the cellular spatial orientation o
R11449 AT7519 AT7519 is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM.
R11461 Abemaciclib methanesulfonate (LY2835219 methanesulfonate) LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM
R11591 GSK-461364; GSK-461364A GSK461364 inhibits purified Plk1 with Ki of 2.2 nM in a cell-free assay. It is m
R11611 KENPAULLONE Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CD
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