耗材描述
GSK-25
产品活性:GSK-25 是一种有效的、选择性的,具有口服活性的 ROCK1 抑制剂 (IC50=7 nM)。GSK-25 对 31 种激酶以及 RSK1 和 p70S6K 保持良好的选择性 (RSK1: IC50=398 nM, p70S6K: IC50=1 μM)。GSK-25 可抑制 P450 (CYP2C9、CYP2D6、CYP3A4的IC50 分别为2.5、5.2、2.5 μM)。
产品来源: https://www.medchemexpress.cn/gsk-25.html
研究领域:Cell Cycle/DNA Damage | Stem Cell/Wnt | Cytoskeleton | TGF-beta/Smad | MAPK/ERK Pathway
作用靶点:ROCK | Ribosomal S6 Kinase (RSK)
In Vivo: GSK-25 (Rat aorta IC50=256 nM) is profiled in a spontaneously hypertensive rat (SHR) model of hypertension. At 30 mg/kg (p.o.), GSK-25 induces a 25 mmHg (t=3 hours) drop in blood pressure.?
GSK-25 has promising oral bioavailability (49% in male Sprague-Dawley rats and 19% in monkey), good half-life (1.8 hours in rat and 2.2 hours in monkey).
相关产品:Covalent Screening Library Plus | Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Immunology/Inflammation Compound Library | Kinase Inhibitor Library | MAPK Compound Library | Stem Cell Signaling Compound Library | TGF-beta/Smad Compound Library | Anti-Aging Compound Library | Covalent Screening Library | Reprogramming Compound Library | Oxygen Sensing Compound Library | Anti-Cardiovascular Disease Compound Library | Cytoskeleton Compound Library | Orally Active Compound Library | Glutamine Metabolism Compound Library | Anti-Cancer Metabolism Compound Library | Anti-Obesity Compound Library | Targeted Diversity Library | Cancer Stem Cells Compound Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Highly Selective Inhibitors Library | Serine/Threonine Kinase Inhibitor Library | Extracellular Vesicles (EVs) Compound Library | Multi-Target Compound Library | Bioactive Compound Library Max | Y-27632 | Chroman 1 | Fasudil Hydrochloride | Belumosudil | BI-D1870 | Thiazovivin | Narciclasine | PF-4708671 | Carnosol | Afuresertib | GSK269962A | H-1152 dihydrochloride | GSK429286A | Quercitrin | Ripasudil | SM1-71 | LY-2584702 tosylate salt | LJH685 | Y-33075 | CCG-222740 | SL 0101-1 | AT13148 | Pentanoic acid | Sodium Salicylate | AT7867 | LJI308 | ROCK inhibitor-2 | M2698
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