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PD 198306

SKU: orb1306133

描述

PD 198306 is a selective MEK inhibitor exhibiting antihyperalgesic properties. It effectively attenuates the Streptozocin-induced elevation of active ERK1 levels, making it a useful research tool for studying MAPK/ERK signaling in diabetic neuropathy models both in vitro and in vivo.

研究领域

Signal Transduction

图片与验证

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关键属性

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CAS 号212631-61-3
MW476.23
纯度99.75% (May vary between batches)
分子式C18H16F3IN2O2
SMILESN(C1=C(C(NOCC2CC2)=O)C=C(F)C(F)=C1F)C3=C(C)C=C(I)C=C3
靶点MEK
溶解性DMSO:45 mg/mL (94.49 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:5 mg/mL (10.5 mM)

生物活性

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体内
In male Sprague Dawley rats bearing neuropathic pain, PD 198306 (1-30 μg/10 μL; i.t.) dose-dependently blocks static allodynia in both the chronic constriction injury and the streptozocin models.
体外
PD 198306 (10 μM) reduces Tha-Crimson replication by 30% at 18 h and 50% at 36 h. PD 198306 (10  μM) significantly inhibits Tha-GFP replication by 25%.

储存与操作

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储存-20°C
有效期12 months from date of receipt.
免责声明For research use only

别名

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rabies, phosphatases, phosphate, screening, RNA, antihyperalgesic, drug, inhibit, Inhibitor, kinases, neuropathic, Mitogen-activated protein kinase kinase, mitogen-activated protein, PD 198306, PD198306, PD-198306, pain, ERK, inositol, interference, MAPK, MAP2K, MAPKK, MEK
质量保证

质量保证

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关键属性

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暂无计算属性。

实验方案信息

可选规格

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1 mg
¥ 1,300.00
5 mg
¥ 2,470.00
1 ml x 10 mM (in DMSO)
¥ 2,730.00
10 mg
¥ 3,120.00
25 mg
¥ 5,070.00
50 mg
¥ 7,020.00
100 mg
¥ 9,490.00
500 mg
¥ 18,200.00
发货Usually dispatched within 5-10 working days
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