AT-7519 hydrochloride
CAS No. 902135-91-5
AT-7519 hydrochloride ( AT 7519 Hydrochloride | AT7519 Hydrochloride )
产品货号. M16486 CAS No. 902135-91-5
一种有效的 CDK2 抑制剂,IC50 为 47 nM;还抑制 CDK1/4/5,IC50 为 190/67/18 nM,并对某些激酶(Aurora A、IR 激酶、MEK、PDK1、c-Abl,IC50>10 uM)表现出选择性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥392 | 有现货 |
|
| 10MG | ¥629 | 有现货 |
|
| 25MG | ¥1228 | 有现货 |
|
| 50MG | ¥1972 | 有现货 |
|
| 100MG | ¥3042 | 有现货 |
|
| 500MG | ¥6836 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥432 | 有现货 |
|
生物学信息
-
产品名称AT-7519 hydrochloride
-
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
-
产品简述一种有效的 CDK2 抑制剂,IC50 为 47 nM;还抑制 CDK1/4/5,IC50 为 190/67/18 nM,并对某些激酶(Aurora A、IR 激酶、MEK、PDK1、c-Abl,IC50>10 uM)表现出选择性。
-
产品描述A potent CDK2 inhibitor with IC50 of 47 nM; also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM); has antiproliferative activity against HCT116 cells with IC50 of 82 nM; exhibits good profile against cytochrome P450 isoforms (<30% inhibition at 10 uM for 1A2, 2D6, 3A4, 2C9, 2C19).Blood Cancer Phase 2 Clinical(In Vitro):AT7519 (0-4 μM) results in dose-dependent cytotoxicity with IC50s ranging from 0.5 to 2 μM in MM cells, and this induced cytotoxicity is associated with GSK-3β activation independent of transcriptional inhibition. AT7519 overcomes proliferative advantage conferred by cytokines and the protective effect of BMSC. AT7519 (0.5 μM) induces apoptosis of MM cells in a time-dependent manner. Moreover, AT7519 (0.5 μM) inhibits phosphorylation of RNA polymerase II CTD and partially inhibits RNA synthesis in MM.1S cells. AT7519 (250 nM) inhibits cell cycle progression in human tumor cell lines. AT7519 also induces apoptosis of human tumor cell lines. AT7519 (100-700 nM) induces apoptosis in leukemia cell lines. AT7519 also inhibits transcription in human tumor cell lines. Furthermore, AT7519 inhibits RNA polymerase II and reduces antiapoptotic protein levels.(In Vivo):AT7519 inhibits tumor growth in a human MM xenograft mouse model. AT7519 (4.6 and 9.1 mg/kg/dose) inhibits the growth of early-stage HCT116 tumor xenografts. AT7519 (10 mg/kg, i.p.) also inhibits the target CDKs in HCT116 tumor-bearing BALB/c nude mice.
-
体外实验——
-
体内实验——
-
同义词AT 7519 Hydrochloride | AT7519 Hydrochloride
-
通路Cell Cycle/DNA Damage
-
靶点CDK
-
受体CDK2/CyclinA|CDK4/CyclinD1|CDK5/p35|CDK9/CyclinT|GSK-3β
-
研究领域Cancer
-
适应症Blood cancer
化学信息
-
CAS Number902135-91-5
-
分子量418.7054
-
分子式C16H18Cl3N5O2
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILESCl.CC1=C(C(=O)NC2=C(NN=C2)C(=O)NC2CCNCC2)C(Cl)=CC=C1
-
化学全称1H-Pyrazole-3-carboxamide, 4-[(2,6-dichlorobenzoyl)amino]-N-4-piperidinyl-, hydrochloride (1:1)
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. Wyatt PG, et al. J Med Chem. 2008 Aug 28;51(16):4986-99.
2. Squires MS, et al. Mol Cancer Ther. 2009 Feb;8(2):324-32.
3. Dolman ME, et al. Clin Cancer Res. 2015 Nov 15;21(22):5100-9.
021-51111890
购物车()
sales@molnova.cn

