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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 |
