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CAS No. : 68302-57-8
MCE 國(guó)際站:Amlexanox
產(chǎn)品活性:Amlexanox (AA673; Amoxanox; CHX3673) 是特異性的 IKKε 和 TBK1 抑制劑,IC50 值為 1-2 μM。
研究領(lǐng)域:NF-κB
作用靶點(diǎn):IKK
In Vitro: Amlexanox increases phosphorylation of TBK1 on Ser172 in 3T3-L1 adipocytes, and blocks polyinosinic:polycytidylic acid (poly I:C)-stimulated phosphorylation of interferon responsive factor-3 (IRF3), a presumed substrate of IKKε and TBK1.
Amlexanox potently inhibits the release of histamine and leukotrienes from mast cells, basophils and neutrophils in in vitro settings, possibly through increasing intracellular cyclic AMP content in inflammatory cells, a mem-brane-stabilising effect or inhibition of calcium influx.
In primary bone marrow derived macrophages (BMMs), amlexanox inhibits osteoclast formation and bone resorption. At the molecular level, amlexanox suppresses RANKL-induced activation of nuclear factor-κB (NF-κB), mitogen-activated protein kinase (MAPKs), c-Fos and NFATc1. Amlexanox decreases the expression of osteoclast-specific genes, including TRAP, MMP9, Cathepsin K and NFATc1.
In Vivo: Amlexanox (100 mg/kg, p.o.) prevents and reverses diet-induced or genetic obesity, and produces reversible weight loss in obese mice. Amlexanox also causes a significant decrease in adipose tissue mass in these mice, and an increase in circulating adiponectin. Amlexanox (25 mg/kg) significantly improves insulin sensitivity in mice with established DIO, and after four weeks of treatment, amlexanox produces marked improvements in glucose.
Amlexanox before the first application of the paste and at each has been shown to suppress both immediate and evaluation thereafter. A categorical scale is also delayed-type hypersensitivity reactions.
Amlexanox (20 mg/kg) enhances osteoblast differentiation of BMSCs. In ovariectomized (OVX) mouse model, amlexanox prevents OVX-induced bone loss by suppressing osteoclast activity.
相關(guān)產(chǎn)品:Drug Repurposing Compound Library Plus | FDA-Approved Drug Library Plus | FDA-Approved Drug Library Mini | Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | Kinase Inhibitor Library | NF-κB Signaling Compound Library | Stem Cell Signaling Compound Library | FDA-Approved Drug Library | Anti-Aging Compound Library | Drug Repurposing Compound Library | Differentiation Inducing Compound Library | Anti-COVID-19 Compound Library | NMPA-Approved Drug Library | FDA Approved & Pharmacopeial Drug Library | Mitochondria-Targeted Compound Library | Targeted Diversity Library | Anti-Liver Cancer Compound Library | Human Metabolite Library | Anti-Prostate Cancer Compound Library | Withdrawn Drug Compound Library | Off-patent Drug Library | Highly Selective Inhibitors Library | Serine/Threonine Kinase Inhibitor Library | Multi-Target Compound Library | Mitophagy Compound Library | Bioactive Compound Library Max | Protein Kinase Compound Library | BAY 11-7082 | Resveratrol | BX795 | GSK8612 | TPCA-1 | MRT67307 | IMD-0354 | BMS-345541 | IKK 16 | BAY-985 | MLN120B | Vinpocetine | TBK1/IKKε-IN-5 | Tizoxanide | β-1,3-Glucan | ACHP Hydrochloride | Peramivir trihydrate | WS6 | PS-1145 | HOIPIN-1 | TBK1-IN-1 | GS143 | SC-514 | BAY32-5915 | Plantainoside D | Abietic acid | BI605906
熱門產(chǎn)品線:重組蛋白 | 藥物篩選 | 天然產(chǎn)物 | 熒光染料 | PROTAC | 同位素標(biāo)記物
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
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