熔点 | 107-111° C |
溶解性 | DMSO: ≥ 56 mg/mL |
存贮条件 | 储存温度-20°C |
应用 | A novel and potent cyclin-dependent kinase inhibitor for Cdk2, Cdk5, Cdk1, and Cdk9 |
产品介绍 | Dinaciclib (SCH727965)是CDK抑制剂,对CDK2,CDK5,CDK1和CDK9的IC50分别为1 nM,1 nM,3 nM和4 nM。 |
备注 | Dinaciclib (SCH727965) is a novel and potent CDK inhibitor for CDK2, CDK5, CDK1 and CDK9 with IC50 of 1 nM, 1 nM, 3 nM and 4 nM, respectively. It also blocks thymidine (dThd) DNA incorporation. Phase 3. |
生化机理 | Dinaciclib(SCH 727965 ) is a pyrazolo[1,5-a]pyrimidine with potential antineoplastic activity. Dinaciclib(SCH 727965 ) selectively inhibits cyclin dependent kinases CDK1, CDK2, CDK5, and CDK9; inhibition of CDK1 and CDK2 may result in cell cycle repression and tumor cell apoptosis. |
别名 | SCH 727965; (2S)-1-(3-乙基-7-(((1-氧代-3-吡啶基)甲基)氨基)吡唑并(1,5-a)嘧啶-5-基)-2-哌啶乙醇;;SCH727965; SCH-727965;(2s)-1-(3-ethyl-7-(((1-oxido-3-pyridinyl)methyl)amino)pyrazolo(1,5-a)pyrimidin-5-yl)-2-piperidineethanol |
Dinaciclib (SCH727965),新型CDK抑制剂
Dinaciclib (SCH727965) (订货以英文为准)
编号:D127362
CAS号:779353-01-4
分子式:C21H28N6O2
分子量:396.49
产品名称 | Dinaciclib (SCH727965) |
中文名称 | Dinaciclib (SCH727965),新型CDK抑制剂 |
CAS号 | 779353-01-4 |
分子式(M.F.) | C21H28N6O2 |
分子量(M.W.) | 396.49 |
储存条件 | -20°C储存 |
技术规格
Background: | The function of this protein remains unknown. |
Applications: | ELISA, WB, IHC |
Name of antibody: | RPUSD2 |
Immunogen: | Fusion protein of human RPUSD2 |
Full name: | RNA pseudouridine synthase domain containing 2 |
Synonyms: | PUS9; C18B11; C15orf19 |
SwissProt: | Q8IZ73 |
ELISA Recommended dilution: | 5000-10000 |
IHC positive control: | Human gastric cancer and Human tonsil |
IHC Recommend dilution: | 150-300 |
WB Predicted band size: | 61 kDa |
WB Positive control: | Hela, 231 and 293T cell lysates |
WB Recommended dilution: | 1000-5000 |
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