| CAS: | 600734-06-3 | ||||||
| 分子式: | C22H26ClN3O4 | ||||||
| 分子量: | 431.91 | ||||||
| 中文名称: |
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| 英文名称: |
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| 用途: | Bay 65-1942 hydrochloride 是一种 ATP 竞争性的选择性 IKKβ 抑制剂。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||
| B878267 | MACKLIN | Bay 65-1942 hydrochloride | ≥99% | 1525元/2mg; 2642元/5mg; | 展开 | ||||||||||||||||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||||||||||||||||
| SML2098 | Sigma-Aldrich | KINK-1 hydrochloride | ≥98% (HPLC) | 1677元/5 MG; 6777.37元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||
产品说明 生化/生理作用 KINK-1 (Kinase Inhibitor of NF-ΚB-1; Bay 65-1942; CmpdA; Compound A) is an ATP-competitive, IKKβ-selective IΚB kinase (IKK) inhibitor (Ki against ATP = 2 nM/IKKβ and 135 nM/IKKα) that potently inhibits IKKβ-catalyzed GST-IΚBα(1–54) phosphorylation (IC50 = 4 nM, 200 nM ATP) without affecting (IC50 >10μM) IKK3 or 27 other kinases, lipases, phosphatases, caspases, and MMPs. KINK-1 effectively inhibits NF-ΚB activation and cytokines production in various human and murine cultures (IC50 from 18 to 502 nM) and is efficacious against LPS-induced plasma TNF-α production in mice and rats in vivo (EC50 = 9.1 and 6.6 mg/kg p.o., repectively) with good pharmacokinetic profile and oral availability. KINK-1 is also shown to effectively inhibit OVA-induced lung inflammation in a rat model of asthma (ED50 <0.3 mg/kg p.o.) without adverse effects to the animals. 基本信息
产品性质
安全信息
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