SB 242235
(Synonyms: 4-[4-(4-氟苯基)-1-(4-哌啶基)-1H-咪唑-5-基]-2-甲氧基嘧啶) 目录号 : GC37595A p38α MAPK inhibitor
Cas No.:193746-75-7
Sample solution is provided at 25 µL, 10mM.
SB-242235 is an inhibitor of p38α MAPK (IC50 = 0.019 ?M).1 It is selective for p38α MAPK over a panel of 10 kinases, including ERK2, JNK1, EGFR, and C-RAF (IC50s = >10 ?M for all). SB-242235 inhibits IL-1α-induced production of nitric oxide (NO) in bovine articular cartilage explants but not IL-1β-induced production of NO in human articular cartilage explants (IC50s = ~1 and >20 ?M, respectively).2 It inhibits increases in epidermal COX-2 levels and erythema in mice exposed to UVB irradiation when administered at a dose of 100 mg/kg.3 SB-242235 (10, 30, and 60 mg/kg) reduces paw edema in a rat model of adjuvant-induced arthritis.4
1.Adams, J.L., Boehm, J.C., Gallagher, T.F., et al.Pyrimidinylimidazole inhibitors of p38: cyclic N-1 imidazole substituents enhance p38 kinase inhibition and oral activityBioorg. Med. Chem. Lett.11(21)2867-2870(2001) 2.Badger, A.M., Roshak, A.K., Cook, M.N., et al.Differential effects of SB 242235, a selective p38 mitogen-activated protein kinase inhibitor, on IL-1 treated bovine and human cartilage/chondrocyte culturesOsteoarthritis Cartilage8(6)434-443(2000) 3.Kim, A.L., Labasi, J.M., Zhu, Y., et al.Role of p38 MAPK in UVB-induced inflammatory responses in the skin of SKH-1 hairless miceJ. Invest. Dermatol.124(6)1318-1325(2005) 4.Badger, A.M., Griswold, D.E., Kapadia, R., et al.Disease-modifying activity of SB 242235, a selective inhibitor of p38 mitogen-activated protein kinase, in rat adjuvant-induced arthritisArthritis Rheum.43(1)175-183(2000)
Cas No. | 193746-75-7 | SDF | |
别名 | 4-[4-(4-氟苯基)-1-(4-哌啶基)-1H-咪唑-5-基]-2-甲氧基嘧啶 | ||
Canonical SMILES | COC1=NC=CC(C2=C(C3=CC=C(F)C=C3)N=CN2C4CCNCC4)=N1 | ||
分子式 | C19H20FN5O | 分子量 | 353.39 |
溶解度 | DMSO: ≥ 48 mg/mL (135.83 mM) | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 2.8297 mL | 14.1487 mL | 28.2973 mL |
5 mM | 0.5659 mL | 2.8297 mL | 5.6595 mL |
10 mM | 0.283 mL | 1.4149 mL | 2.8297 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
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- Purity: >98.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
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