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| 目录号 | 产品名称 | 产品描述 |
| 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 hydrochloride 是一种有效的，选择性的，ATP 竞争性的 Cdc7 抑制剂，IC50 值为 3.4 nM，同时对 CK2 和 PIM1 |
| R10090 | AZD5438 | AZD-5438 是有效的 CDK1/2/9 抑制剂，IC50 值分别为 16 nM/6 nM/20 nM；对GSK3β，CDK5，CDK6的抑制作用较弱。&n |
| 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 是一种有效的，高度选择性的 PLK1 抑制剂，IC50 和 Kd 值分别为 3 nM 和 0.09 nM，对 PLK2 和 PLK3 几乎没作用。 |
| R10271 | BI 2536;BI2536 | BI 2536 是 PLK1 和 BRD4 的双抑制剂，IC50 分别为 0.83 和 25 nM。BI-2536 抑制 IFNB (IFN-β，干扰素 β) |
| 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 |
| 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 |
| R10910 | MK-8776 | MK-8776 (SCH 900776) is a selective Chk1 inhibitor with IC50 of 3 nM in a cell-f |
