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PD 98059
  • 品牌:Chemstan
  • 产地:中国
  • 货号:LC-01
  • cas:167869-21-8
  • 价格: ¥800/支
  • 发布日期: 2019-11-06
  • 更新日期: 2025-09-25
产品详请
产地 中国
品牌 Chemstan
货号 LC-01
用途 中间体
包装规格 20mg
纯度 98%%
CAS编号 167869-21-8
是否进口

联合知名大学科研院所及企业开发药食两用植物标准品和天然植物有效单体,主打中药对照品/标准品/天然植物有效单体,小分子化合物库,药物杂质。所有产品仅用作科学研究,我们不为任何个人用途提供产品和服务。


Fields of Application : 
PD 98059 is a selective inhibitor of MEK and blocker of MAPK

CAS Number:167869-21-8
Purity:

>98%

Molecular Weight:267.28
Molecular Formula:C16H13NO3

Quality Control: HPLC、NMR、 LC/MS(Please contact us to get the QC report)

Synonyms:PD-98059,PD98059
Chemical Name:;2-(2-AMINO-3-METHOXYPHENYL)-4H-1-BENZOPYRAN-4-ONE;2-(2-AMINO-3-METHOXY-PHENYL)CHROMEN-4-ONE;2'-AMINO-3'-METHOXYFLAVONE
Storage:2 years -20°C Powder, 2 weeks4°C in DMSO,6 months-80°C in DMSO

Note: Products for research use only, not for human use

Description:
PD 98059 is a potent, selective and reversible cell permeable inhibitor of MEK-1 (MAPKK1 or MAPKs ) that binds to the inactive Form of MEK-1 blocking MEK-1 activation leading to inhibition of phosphorylation and the activation of MAP kinase. In PC12 pheochromocytoma cells at an IC50= 2 μM, it produced complete blockage of any increase in MAPK activity produced by nerve growth factor. It has been shown to enhance self-renewal of embryonic stem cells and has been used to unravel the role of the MAPK cascade in biological systems. The compound has been reported to induce GSTA2 (glutathione S-transferase A2) production in H4IIE cells. PD 98059 has also been shown to enhance insulin-mediated increase in glutathione levels as well as, independent of MEK1 inhibition, elevate primary cultured rat hepatocyte glutathione levels.For the detailed information of PD 98059, the solubility of PD 98059 in water, the solubility of PD 98059 in DMSO, the solubility of PD 98059 in PBS buffer, the animal experiment (test) of PD 98059, the cell expriment (test) of PD 98059, the in vivo, in vitro and clinical trial test of PD 98059, the EC50, IC50,and Affinity of PD 98059.

References: 
COC1=CC=CC(=C1N)C2=CC(=O)C3=CC=CC=C3O2


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