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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
- 保质期:
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
- 英文名:
PD-98059,PD98059
- 库存:
现货
- 供应商:
爱必信(上海)生物科技有限公司
- CAS号:
167869-21-8
- 规格:
50mg/10mg/5mg
| 规格: | 50mg | 产品价格: | ¥380.0 |
|---|---|---|---|
| 规格: | 10mg | 产品价格: | ¥173.0 |
| 规格: | 5mg | 产品价格: | ¥139.0 |
| 公告提醒:爱必信所有产品和服务仅用于科学研究,不用于临床应用及其他用途提供产品和服务(也不为任何个人提供产品和服务)!
抑制剂描述: 产品名称:PD 98059 产品别名:见爱必信官网 英文别名:PD 98059 靶点:MEK CAS:167869-21-8 纯度:>98 % 外观:见爱必信官网 保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. 描述:PD98059是一种非ATP竞争性的MEK抑制剂,无细胞试验中IC50为2 μM,特异性抑制MEK-1介导的MAPK激活;不直接抑制ERK1或ERK2。PD98059不会抑制已经被c-Raf磷酸化的 MEK1。 溶解性:DMSO:14 mg/mL warmed (52.37 mM) 体外研究: PD98059 inhibits either basal MEK1 or a partially activated MEK produced by mutation of serine at residues 218 and 222 to glutamate (MEK-2E) with IC50 of 2 μM. PD98059 does not inhibit the MAPK homologues JNK and P38. PD98059 is highly selective against MEK, as it does not inhibit a number of other kinase activities including Raf kinase, cAMP-dependent kinase, protein kinase C, v-Src, epidermal growth factor (EGF) receptor kinase, insulin receptor kinase, PDGF receptor kinase, and phosphatidylinositol 3-kinase. PD98059 inhibits PDGF-stimulated activation of MAPK and thymidine incorporation into 3T3 cells with IC50 of ~10 μM and ~7 μM, respectively. PD98059 potently prevents the activation of MEK1 by Raf or MEK kinase with IC50 of 4 μM, and weakly inhibits the activation of MEK2 by Raf with IC50 of 50 μM. PD98059 does not inhibit the activation of MEK homologues MKK4 and RK kinase that participate in stress and interleukin-1-stimulated kinase cascades in KB and PC12 cells, and the activation of p70 S6 kinase by insulin or epidermal growth factor in Swiss 3T3 cells. PD98059 completely blocks the nerve growth factor (NGF)-induced differentiation of PC12 cells without altering cell viability. PD98059 inhibits the proliferation of RAW264.7 cells in the culture containing RANKL in a dose-dependent manner, resulting in an apparent decrease of TRAP-positive cells. 体内研究:Treatment of mice 30 minutes before focal cerebral ischemia with PD98059 protects against damage, resulting in a decrease in infarct volume. Pretreated with PD98059 (10 mg/kg per i.v. injection) 30 minutes before and then together with hourly cerulein injections for 3 hours significantly ameliorates cerulein-induced acute pancreatitis ipancreatitis on the basis of pancreatic wet weight and histology. Administration of PD98059 (10 mg/kg) in mice 1 hour after carrageenan causes a reduction in all the parameters of inflammation measured. absin,您身边的科研百宝箱 |
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2015 年 12 月,美国前总统吉米 · 卡特在接受了靶向放疗和免疫抗癌新药 Keytruda(PD-1 抑制剂,MSD)治疗后,医生发现,在他的脑部磁共振扫描图像中,此前出现的黑色素瘤(Melanoma)与新生的癌细胞都彻底消失了。这种治疗效果引起了业内的广泛关注,也彰显了 PD-1/PD-L1 免疫疗法在肿瘤治疗中的巨大潜力。PD-1/PD-L1 是什么?1992 年,日本京都大学 Tasuku Honjo 教授首次报道并克隆了 PD-1 基因[1]。1999 年,华人学者陈列平教授报道
宽度:562 px高度:343 px维持原图长宽比:确认自 2011 年第一个免疫检验点 CTLA4 抑制剂伊匹单抗(Ipilimumab)获批上市以来,肿瘤免疫疗法越来越受到重视。特别是近几年陆续获批 PD1/PD-L1 单抗药物在临床治疗中的不断突破,肿瘤免疫治疗已从 1.0 时代进入 2.0 时代。免疫疗法适应症也在不断拓展,从黑色素瘤逐渐延伸到非小细胞肺癌、膀胱癌、头颈癌霍奇金淋巴瘤等癌症的治疗。针对 PD1/PD-L1 免疫检验点的单抗药物无疑是肿瘤免疫治疗中当之无愧的明星,其中 O
上期带大家了解如今大热的 PD-L1免疫疗法,本期文章会对 PD-1 诊断抗体进行详细的分析。PD-1/PD-L1 单克隆抗体药备受瞩目,是目前临床上研究和应用最广泛的免疫检查点抑制剂之一,阻断 PD-1 与 PD-L1 的结合,使 T 细胞恢复肿瘤杀伤活性,在多种肿瘤治疗过程中显示出卓越的疗效[1]。目前 FDA 批准了 2 款 PD-1 抑制剂(Opdivo 和 Keytruda)和 3 款 PD-L1 抑制剂(Tecentriq、Imfinzi、Bavencio)上市。同时,也分别批准










