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AS601245 345987-15-7

简要描述:AS601245 345987-15-7
AS601245 is an inhibitor of the c-Jun NH2-terminal kinase (JNK) (hJNK1: IC50=150nM, hJNK2: IC50=220nM and hJNK3: IC50=70 nM), has neuroprotective properties.

  • 产品型号:abs47028003
  • 厂商性质:生产厂家
  • 更新时间:2026-01-12
  • 访  问  量:718

详细介绍

品牌absinCAS345987-15-7
分子式C20H16N6S纯度98%
分子量372.45货号abs47028003
规格1mg供货周期现货
主要用途is an inhibitor of the c-Jun NH2-termin应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

AS601245 345987-15-7

产品描述
描述

AS601245 is an inhibitor of the c-Jun NH2-terminal kinase (JNK) (hJNK1: IC50=150nM, hJNK2: IC50=220nM and hJNK3: IC50=70 nM), has neuroprotective properties.

纯度
98%
储存/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.
基本信息
别名
JNK Inhibitor V
可溶性/溶解性
DMSO ≥35 mg/mL
生物活性
靶点
JNK
In vitro(体外研究)
AS601245 inhibits isolated hJNK3 in an ATP-competitive manner. Selectivity of AS601245 is tested against a large panel of kinases. AS601245 exhibits 10- to 20-fold selectivity over c-src, CDK2, and c-Raf and more than 50- to 100-fold selectivity over a range of Ser/Thr- and Tyr-protein kinases. The effects of AS601245 and Clofibrate alone or in association are analysed on proliferation, apoptosis, differentiation and the gene expression profile of CaCo-2 human colon cancer cells. Reduction of cell proliferation, accompanied by the modulation of p21 expression is observed in HepG2 cells, also. 5 μM Clofibrate, 0.1 μM AS601245, and the combined treatment with the two substances do not cause acute toxicity in HepG2 cells. All treatments reduce cell proliferation starting from 48 hours after the beginning of experiments, and the inhibitory effect reaches the maximum at 72 hours.
In vivo(体内研究)
AS601245 is a potent inhibitor of LPS-induced TNF-α release in mice. Administered orally at 0.3, 1, 3, and 10 mg/kg, AS601245 decreases the TNF-α release in a dose-dependent manner. AS601245 (40, 60, and 80 mg/kg) administered i.p. provides significant protection against the delayed loss of hippocampal CA1 neurons in a gerbil model of transient global ischemia. This effect is mediated by JNK inhibition and therefore by c-Jun expression and phosphorylation. A significant neuroprotective effect of AS601245 administered either by i.p. injection (6, 18, and 60 mg/kg) or as i.v. bolus (1 mg/kg) followed by an i.v. infusion (0.6 mg/kg/h) is also observed in rats after focal cerebral ischemia.
参考文献
参考文献
  • 1. Carboni S, et al. Br J Pharmacol. 2008 Jan;153(1):157-163.

研究领域
研究领域
Immunology
Neuroscience
CancerCancer Metabolism
CancerTumor biomarkers
Drug DiscoverySmall Molecule DrugLead Compound Discovery
AS601245 345987-15-7温馨提示:本产品仅作科研实验使用,不支持临床等研究

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