SR-3306
目录号: PL02922 纯度: ≥99%
CAS No. :1128096-91-2
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中文名称
SR-3306
中文别名
SR-3306
英文名称
SR-3306
英文别名
SR-3306;n-(4-(3-(6-methylpyridin-3-yl)-1h-1,2,4-triazol-1-yl)phenyl)-4-(3-morpholinophenyl)pyrimidin-2-amine;MLS006012045;BDBM50059654;SB17012;SMR004703567;N-[4-[3-(6-methylpyridin-3-yl)-1,2,4-triazol-1-yl]phenyl]-4-(3-morpholin-4-ylphenyl)pyrimidin-2-amine;CID 57519510
Cas No.
1128096-91-2
分子式
C28H26N8O
分子量
490.56
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
SR-3306 是一种有效的可渗透脑的选择性 JNK 抑制剂。
生物活性
SR-3306 is a selective, potent, highly brain penetrant JNK inhibitor.
性状
Solid
IC50 & Target[1][2]
JNK
体外研究(In Vitro)
The effect of SR-3306 or Tat-Sab on cell viability in response to oxidative stress is measured by an MTT assay. H9c2 cells treated with 100 μM H2O2/FeSO4 are ~40% viable, whereas the addition of 500 nM SR-3306 or 500 nM SR3562 to cells treated with 100 μM H2O2/FeSO4 increases viability to ~90%, and the addition of 10 μM Tat-Sab peptide to cells treated with 100 μM H2O2/FeSO4 increases viability to ~70% compared with 98% viability in untreated cells. Similar results are found for primary human cardiomyocytes . has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Administration of SR-3306 [10 mg/kg/day (s.c.) for 14 days] increases the number of tyrosine hydroxylase immunoreactive (TH) neurons in the SNpc by 6-fold and reduces the loss of the TH terminals in the striatum relative to the corresponding side of 6-OHDA-lesioned rats that receive only vehicle (p<0.05). In addition, SR-3306 [10 mg/kg/day (s.c.) for 14 days] decreases d-amphetamine-induced circling by 87% compared to 6-hydroxydopamine (6-OHDA)-lesioned animals given vehicle. Steady-state brain levels of SR-3306 at day 14 are 347 nM, which is approximately 2-fold higher than the cell-based IC 50 for this compound. Finally, immunohistochemical staining for phospho-c-jun (p-c-jun) reveals that SR-3306 [10 mg/kg/day (s.c.) for 14 days] produces a 2.3-fold reduction of the number of immunoreactive neurons in the substantia nigra pars compacta (SNpc) relative to vehicl
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Crocker CE, et al. JNK Inhibition Protects Dopamine Neurons and Provides Behavioral Improvement in a Rat 6-hydroxydopamine Model of Parkinsons Disease. ACS Chem Neurosci. 2011 Apr 20;2(4):207-212.
[2]. Gao S, et al. Pharmacological Inhibition of c-Jun N-terminal Kinase Reduces Food Intake and Sensitizes Leptins Anorectic Signaling Actions. Sci Rep. 2017 Feb 6;7:41795.
溶解度数据
In Vitro: DMSO : 125 mg/mL (254.81 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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