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Cat.No. Product name Product Description
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
R10228 PHA767491 PHA-767491 is a potent ATP-competitive dual Cdc7/CDK9 inhibitor with IC50 of 10
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
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
R11449 AT7519 AT7519 is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM.
R11461 LY2835219 mesylate LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM
R11502 LEE-011 Ribociclib (LEE011) is an orally available, and highly specific CDK4/6 inhibitor
R11611 KENPAULLONE Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs).
R11620 Ro 3306 RO-3306 is an ATP-competitive, and selective CDK1 inhibitor with Ki of 20 nM, >1
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