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Kira8
CAS No. 1630086-20-2
Kira8 ( AMG-18 )
产品货号. M26271 CAS No. 1630086-20-2
Kira8 是一种单选择性 IRE1α 抑制剂,可变构减弱 IRE1α RNase 活性(IC50:5.9 nM)。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1725 | 有现货 |
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10MG | ¥2608 | 有现货 |
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25MG | ¥4836 | 有现货 |
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50MG | ¥6901 | 有现货 |
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100MG | ¥9477 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Kira8
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Kira8 是一种单选择性 IRE1α 抑制剂,可变构减弱 IRE1α RNase 活性(IC50:5.9 nM)。
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产品描述Kira8 is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity (IC50: 5.9 nM).(In Vitro):Kira8 more effectively causes IRE1α-driven apoptosis in INS-1 cells than KIRA6 and also reverses XBP1 splicing promoted by GNF-2. Kira8 blocks IRE1α oligomerization and effectively inhibits IRE1α RNase activity against XBP1 and Ins2 RNAs.(In Vivo):One week of treatment of pre-diabetic NODs mice with Kira8 (50 mg/kg; i.p.; once a day) causes obvious reductions in islet XBP1 splicing and TXNIP mRNAs. It also preserves Ins1/Ins2, BiP, and MANF mRNAs. Male Ins2+/Akita mice are injected i.p. with KIRA8 (50 mg/kg; daily; for 35 days), obviously reduction of hyperglycemia becomes apparent over several weeks.
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体外实验Kira8 blocks IRE1α oligomerization, and potently inhibits IRE1α RNase activity against XBP1 and Ins2 RNAs. Kira8 more potently reduces IRE1α-driven apoptosis in INS-1 cells than KIRA6 and also reverses XBP1 splicing promoted by GNF-2.
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体内实验Male Ins2+/Akita mice are injected i.p. with KIRA8 (50 mg/kg; daily; for 35 days), significant reduction of hyperglycemia become apparent over several weeks. One week treatment of pre-diabetic NODs mice with Kira8 (50 mg/kg; i.p.; once a day) leads to significant reductions in islet XBP1 splicing and TXNIP mRNAs, and preserves Ins1/Ins2, BiP and MANF mRNAs. Animal Model:Male Ins2+/Akita mice Dosage:50 mg/kg Administration:Injected i.p.; daily; for 35 days Result:Significant reduction of hyperglycemia became apparent over several weeks.
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同义词AMG-18
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通路Others
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靶点Other Targets
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受体antiprotozoal
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研究领域——
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适应症——
化学信息
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CAS Number1630086-20-2
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分子量601.12
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分子式C31H29ClN6O3S
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纯度>98% (HPLC)
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溶解度In Vitro:?Ethanol : 76.92 mg/mL (127.96)
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SMILESCc1ccc2c(NS(=O)(=O)c3ccccc3Cl)cccc2c1Oc1ncccc1-c1ccnc(N[C@H]2CCCNC2)n1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Dianzani C, Collino M, Gallicchio M, Di Braccio M, Roma G, Fantozzi R. Effects of anti-inflammatory [1, 2, 4]triazolo[4, 3-a] [1, 8]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study. J Inflamm (Lond). 2006 Mar 28;3:4.
产品手册
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