THZ 531
CAS No. 1702809-17-3
THZ 531 ( THZ531 )
产品货号. M12601 CAS No. 1702809-17-3
THZ 531 (THZ531) 是一种一流的选择性 CDK12 和 CDK13 共价抑制剂,IC50 分别为 158 nM 和 69 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥672 | 有现货 |
|
| 5MG | ¥915 | 有现货 |
|
| 10MG | ¥1256 | 有现货 |
|
| 25MG | ¥2811 | 有现货 |
|
| 50MG | ¥4026 | 有现货 |
|
| 100MG | ¥5856 | 有现货 |
|
| 500MG | ¥12069 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称THZ 531
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述THZ 531 (THZ531) 是一种一流的选择性 CDK12 和 CDK13 共价抑制剂,IC50 分别为 158 nM 和 69 nM。
-
产品描述THZ 531 (THZ531) is a first-in-class, selective CDK12 and CDK13 covalent inhibitor with IC50 of 158 nM and 69 nM, respectively; dispalys 50-fold selectivity over CDK7 and CDK9 (IC50 of 8.5 and 10.5 uM, respectively), and shows no appreciable inhibitory effect on ERK1; irreversiblely inhibits Jurkat cell proliferation with an IC50 of 50 nM, induces apoptosis in a dose- and time-dependent manner with low doses (<350 nM); selectively reduced Ser2 phosphorylation levels without appreciable effect on CTD pSer5/pSer7 levels, causes a loss of gene expression with concurrent loss of elongating and hyperphosphorylated RNA polymerase II, inhibits DDR and transcription factor gene expression.
-
体外实验The results from Kinase assays demonstrate that THZ531 potently inhibits CDK12 and CDK13 with IC50s of 158 nM and 69 nM, respectively; whereas inhibition of CDK7 and CDK9 is more than 50-fold weaker with IC50s of 8.5 and 10.5 μM, respectively. THZ531 treatment leads to a dramatic and irreversible decrease in Jurkat cell proliferation with an IC50 of 50 nM. FACS cell cycle analysis following treatment with escalating doses of THZ531 displays a dose and time-dependent increase in the number of cells exhibiting sub-G1 content. At 50 nM THZ531, no increase in the percentage of apoptotic cells is observed over DMSO control for the time course of the experiment. Higher doses of THZ531 leads to pronounced Annexin V signal with 30 to 40% annexin V-positively stained cells by 72 hrs. A dramatic reduction in elongating Pol II following THZ531 treatment is also observed.
-
体内实验——
-
同义词THZ531
-
通路Angiogenesis
-
靶点CDK
-
受体CDK12,CDK13
-
研究领域Other Indications
-
适应症——
化学信息
-
CAS Number1702809-17-3
-
分子量558.083
-
分子式C30H32ClN7O2
-
纯度>98% (HPLC)
-
溶解度DMSO: Soluble ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESO=C(NC1=CC=C(C(N2C[C@H](NC3=NC=C(Cl)C(C4=CNC5=C4C=CC=C5)=N3)CCC2)=O)C=C1)/C=C/CN(C)C
-
化学全称(R,E)-N-(4-(3-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)piperidine-1-carbonyl)phenyl)-4-(dimethylamino)but-2-enamide
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Zhang T, et al. Nat Chem Biol. 2016 Oct;12(10):876-84.
2. Paculová H, et al. Cell Div. 2017 Oct 27;12:7. doi: 10.1186/s13008-017-0033-x.
3. Iniguez AB, et al. Cancer Cell. 2018 Jan 17. pii: S1535-6108(17)30561-5.
产品手册
关联产品
-
Bohemine
Bohemine 是一种细胞周期蛋白依赖性激酶抑制剂。
-
Kenpaullone
Kenpaullone (9-Bromopaullone,NSC-664704) 是一种有效的 CDK1/cyclin B 抑制剂,IC50 为 0.4 uM,还抑制 CDK2/cyclin A (IC50=0.68 uM)、CDK2/cyclin E (IC50-7.5 uM) 和 CDK5 /p25 (IC50=0.85 uM)。
-
NU-6027
NU-6027 (NU6027) 是 CDK1 和 CDK2 的 ATP 竞争性抑制剂,Ki 分别为 2.5 uM 和 1.3 uM。
021-51111890
购物车()
sales@molnova.cn

