相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
221671-61-0
- 规格:
10 mM * 1 mL/1 mg/5 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥ |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥2000.0 |
| 规格: | 5 mg | 产品价格: | ¥5000.0 |
MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。
SR 146131
CAS No. : 221671-61-0
MCE 国际站:SR 146131
产品活性:SR 146131是一种有效,有口服活性,选择性的非多肽缩胆囊素1 (cholecystokinin 1)受体激动剂。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:Cholecystokinin Receptor
In Vitro: SR 146131 inhibits in the binding of [125I]-BH-CCK-8S to CCK1sites on 3T3-hCCK1 cell membranes with an IC50 value of 0.56 ± 0.10 nM. At much higher concentrations, SR 146131 also inhibits the binding of radiolabeled CCK to CCK2sites in CHO-hCCK2 membranes with an IC50 of 162 ± 27 nM. SR 146131 is a potent CCK1 agonist on several intracellular events linked to CCK1 receptor activation in various cell types: on [Ca2+]i release and IP1 formation, SR 146131 appears as a full CCK1 receptor agonist in the 3T3-hCCK1 cells, but a partial CCK1receptor agonist on MAPK activation and early gene expression in this cell line. SR 146131 also acts as a partial agonist in the two neuroblastoma cell lines.
In Vivo: SR 146131 completely inhibits gastric and gallbladder emptying in mice (ED50 of 66 and 2.7 μg/kg p.o., respectively). SR 146131 dose dependently reduces food intake in fasted rats (from 0.1 mg/kg p.o.), in nonfasted rats in which food intake has been highly stimulated by the administration of neuropeptide Y (1–36) (from 0.3 mg/kg p.o.), in fasted gerbils (from 0.1 mg/kg p.o.), and in marmosets maintained on a restricted diet (from 3 mg/kg p.o.). SR 146131 (10 mg/kg p.o.) also increases the number of Fos-positive cells in the hypothalamic paraventricular nucleus of rats. Locomotor activity of mice is reduced by orally administered SR 146131 (from 0.3 mg/kg p.o.).
相关产品:Bioactive Compound Library Plus | GPCR/G Protein Compound Library | Neuronal Signaling Compound Library | Endocrinology Compound Library | Neurotransmitter Receptor Compound Library | Anti-Obesity Compound Library | Targeted Diversity Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Highly Selective Activators Library | Ceruletide | Gastrin I, human | Pentagastrin | Devazepide | Sincalide ammonium | Sograzepide | Tetragastrin | L-365260 | Proglumide | Lorglumide sodium salt | Nastorazepide | Loxiglumide | A71623 | Dexloxiglumide | CCK-B Receptor Antagonist 2 | Gastrin I, rat | Lintitript | Mini Gastrin I, human TFA | Anthramycin | AP1153 aptamer sodium | Benzotript | CI-988 | Gastrazole | JNJ-17156516 | JNJ-26070109 | LY288513
热门产品线:重组蛋白 | 化合物库 | 天然产物 | 荧光染料 | PROTAC | 同位素标记物
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Purification of SR Protein Splicing Factors
In recent years, the SR protein family of precursor messenger RNA splicing factors has emerged as a key player in the assembly of the spliceosomal machinery onto pre-mRNA. The SR proteins are essential splicing factors and different family
清道夫受体 (scavenger receptor , SR) 是固有免疫中一类重要的模式识别受体,分为多种类型,主要为SRA和SRB,可能还包括SRC等,其中各自又由不同的分子组成。 注:M。:单核细胞;P1t:血小板;LTA:淋巴毒素。;LDL:低密度脂蛋白。MARCO:带胶原结构的巨噬细胞受体;LOX-1:凝集素样氧化低密度脂蛋白受体;SREC:内 皮细胞表达的清道夫受体。 SPA为三聚体缠绕的糖蛋白跨膜分子,各带有5个不同的结构域。其中胶原样结构
1、目的:为使仪器正常运转,保证结果的可靠性,特制定此操作规程。2、适用范围:化验室3、责任者:化验员应严格遵照该操作规程,QC主管负责监督本规程的实施。4、定义:无5、安全注意事项:无6、操作规程6.1.准备6.1.1.控制水槽水位,使之高于溶出杯中介质的高度。6.1.2.开启溶出仪,自动取样器及打印机电源。6.1.3.排除对试验有影响振动干扰。6.1.4.调节高度:将桨或蓝的底部轻轻置于杯的底部,抬起显示面板,垫上标准垫块P或B(P为转桨法,B为转蓝法),放下显示面板,测桨或蓝的底部距杯底
技术资料暂无技术资料 索取技术资料


















