Cyclin-Dependent Kinases(细胞周期蛋白依赖性激酶)
Cyclin-dependent kinases is a group of serine/threonine kinases. It is activated by binding to cyclin and participates in the regulation of cell cycle.
Products for Cyclin-Dependent Kinases
- Cat.No. 产品名称 Information
- GC50175 CGP 74514 dihydrochloride Potent cdk1 inhibitor
- GC15841 Alsterpaullone A dual CDK and GSK3 inhibitor
- GC16520 Olomoucine An inhibitor of cyclin-dependent kinases
- GC15215 Iso-Olomoucine An inactive stereoisomer of olomoucine
- GC14294 Cdk1/2 Inhibitor III A cell-permeable inhibitor of Cdk1 and Cdk2
- GC11564 Cdk4/6 Inhibitor IV A cell-permeable inhibitor of Cdk4/6
- GC15607 ON123300 A multi-kinase inhibitor
- GC14002 Bohemine A Cdk inhibitor
- GC15173 PD 0332991 (Palbociclib) PD 0332991 (Palbociclib) (PD 0332991) 是一种具有口服活性的选择性 CDK4 和 CDK6 抑制剂,IC50 值分别为 11 和 16 nM。 PD 0332991 (Palbociclib) 具有有效的抗增殖活性,可诱导癌细胞的细胞周期停滞,可用于 HR 阳性和 HER2 阴性乳腺癌和肝细胞癌的研究。
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GC18051
CCT251545 analogue, Compound 51
Potent, Selective, orally bioavailable CDK 8/19 Inhibitor
- GC16420 THZ531 An inhibitor of Cdk12 and Cdk13
- GC14230 K03861 K03861 (K03861) 是一种 II 型 CDK2 抑制剂,Kd 为 8.2 nM。 K03861 (K03861) 通过与活化细胞周期蛋白的结合竞争抑制 CDK2 活性。
- GC16545 GX-674 GX-674 是一种有效的、状态依赖性、异构体选择性电压门控钠通道 1.7 (Nav1.7) 拮抗剂,在 -40 mV 时的 IC50 为 0.1 nM。
- GC13511 THZ2 A Cdk7 inhibitor
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GC12826
AZD-5597
Potent CDK inhibitor
- GC14707 Purvalanol A A selective inhibitor of cyclin-dependent kinases
- GC12348 Ro 3306 An inhibitor of Cdk1
- GC11971 LY2857785 A Cdk9 inhibitor
- GC17067 LDC000067 A Cdk9 inhibitor
- GC11944 PF 4800567 hydrochloride A selective CK1ε inhibitor
- GC16413 TMCB A dual inhibitor of CK2 and ERK8
- GC16429 (R)-DRF053 dihydrochloride cdk/CK1 inhibitor,potent and ATP-competitive
- GC17150 Ryuvidine An inhibitor of SETD8
- GC12886 NSC 625987 A Cdk4/cyclin D1 complex inhibitor
- GC11410 Aminopurvalanol A A selective CDK inhibitor
- GC11634 NSC 693868 A selective inhibitor of Cdk1 and Cdk5
- GC13100 [Ala92]-p16 (84-103) inhibitor of cyclin-dependent kinase-4 (cdk4)/cyclin D1
- GC13649 Arcyriaflavin A A CDK4 and CAMKII inhibitor
- GC14182 Kenpaullone A inhibitor of cyclin-dependent kinase and GSK3β
- GC12642 THZ1 Hydrochloride A covalent Cdk7 inhibitor
- GC14162 ML167 A selective Clk4 inhibitor
- GC10840 THZ1 A covalent Cdk7 inhibitor
- GC15377 LEE011 succinate A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
- GC15922 LEE011 hydrochloride A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
- GC11785 CDK4 inhibitor An antiproliferative cyclin D1/Cdk4 inhibitor
- GC14974 AMG 925 A dual inhibitor of FLT3 and Cdk4
- GC16000 WHI-P180 A multi-kinase inhibitor
- GC17400 R547 A selective Cdk inhibitor
- GC10842 LEE011 A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor
- GC16425 Flavopiridol hydrochloride An inhibitor of cyclin-dependent kinases
- GC11835 Deferasirox An iron chelator with anticancer activity
- GC16268 Purvalanol B A CDK inhibitor
- GC17648 Dinaciclib(SCH727965) A CDK inhibitor
- GC12865 BMS265246 A cell-permeable inhibitor of Cdk1 and Cdk2
- GC15588 PHA-848125 An inhibitor of Cdks
- GC15421 Palbociclib (PD0332991) Isethionate Palbociclib (PD 0332991) isethionate 是一种具有口服活性的选择性 CDK4 和 CDK6 抑制剂,IC50 值分别为 11 和 16 nM。 Palbociclib (PD0332991) Isethionate 具有有效的抗增殖活性,可诱导癌细胞的细胞周期停滞,可用于 HR 阳性和 HER2 阴性乳腺癌和肝细胞癌的研究。
- GC12438 AZD-5438 A potent inhibitor of CDKs
- GC17935 PD 0332991 (Palbociclib) HCl A selective cyclin D kinase 4/6 inhibitor
- GC16822 LY2835219 A dual inhibitor of CDK4 and CDK6
- GC15963 Nu 6027 A CDK and ATR inhibitor