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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- |
| 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 |
| 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 |
| 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 | Abemaciclib methanesulfonate (LY2835219 methanesulfonate) | LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM |
| 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 |
| R2032672 | PHA767491 | PHA-767491 is a dual Cdc7/Cdk9 inhibitor, with IC50s of 10 nM and 34 nM, respect |
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