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AZD1208

    
99.1%

AZD1208

MedMol
S81232 一键复制产品信息
1204144-28-4
C21H21N3O2S
379.48
货号 规格 价格 上海 北京 武汉 南京 购买数量
S81232-2mg
99.1% ¥100.00 5 - - -
S81232-5mg
99.1% ¥170.00 6 - - -
S81232-10mg
99.1% ¥320.00 6 - - -
S81232-25mg
99.1% ¥430.00 6 - - -
S81232-50mg
≥99% ¥620.00 货期:2-3天 - - -
S81232-100mg
≥99% ¥860.00 货期:2-3天 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

AZD1208 is a novel, orally bioavailable, highly selective PIM kinase inhibitor with single nanomolar potency against all three PIM kinases.

产品描述: AZD1208 is a novel, orally bioavailable, highly selective PIM kinase inhibitor with single nanomolar potency against all three PIM kinases.
靶点: Apoptosis;Autophagy;Pim;Apoptosis; Pim; Autophagy
体内研究: AZD1208在培养的MOLM-16细胞中引起细胞周期停滞和细胞凋亡。 这伴随着BAD,4EBP1和p70S6K磷酸化的剂量依赖性降低。 另外,AZD1208导致有效抑制来自骨髓抽吸物的原代AML细胞的集落生长并下调Pim靶标的磷酸化
细胞实验: AZD1208 is dissolved in DMSO. MOLM-16 cells, purchased from DSMZ and cultured in RPMI containing 10% fetal bovine serum (FBS) and 1% L-glutamine, are plated at 20,000 cells per well in 96 well plates overnight. Cells are treated for 72 hours with compound or control vehicle (dimethyl sulfoxide) and cell viability is measured after the addition of Cell Titer-Blue for 4 hours at 37?C and reading of fluorescence on a Tecan Infinite? 200. The GI50 is determined by calculating growth at each dose relative to vehicle treated cells and cell viability at the time of treatment.
参考文献: 1.Erika Keeton, et al. 53rd ASH Annual Meeting (2011) Abstract nr 1540
溶解性: DMSO:7.6  mg/mL  (20  mM)),with  gentle  warming
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.635 ml 13.176 ml 26.352 ml
5 mM 0.527 ml 2.635 ml 5.27 ml
10 mM 0.264 ml 1.318 ml 2.635 ml
50 mM 0.053 ml 0.264 ml 0.527 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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