CAS NO: | 1589527-65-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | KIRA6 is an advanced small-moleculeIRE1αRNase kinase inhibitor with anIC50of 0.6 μM[2]. KIRA6 can trigger anapoptoticresponse[1]. | ||||||||||||||||||||||||||||||||
IC50& Target | IC50: 0.6 μM (IRE1α RNase kinase)[2] | ||||||||||||||||||||||||||||||||
体外研究 (In Vitro) | KIRA6 (1nM-100μM) bounds to the cytoplasmic domain of KIT with a Kdvalue of 10.8 μM[1].KIRA6 (10-1000 nM; 72 hours) strongly compromises the viability of the KIT-dependent cell line HMC-1.1 at the low nM concentration, in a manner that coincided with KIT blockade[1].KIRA6 (10-1000 nM; 1 hour) reduces signaling output of KIT, including the phosphorylation of KIT as well as its downstream signaling modules, PSTAT5 and phosphorylated ERK1/2[1].KIRA6 (1 μM; 0-48 hours) inhibits Ins1 mRNA decay from IRE1α hyperactivation at a dose-dependent manner[2].KIRA6 (0.1-10μM; 72 hours) dose-dependently reduces 1NM-PP1 potentiation of Ins1 apoptosis during ER stress in a dose-dependent manner[2]. Cell Viability Assay[1]
Western Blot Analysis[1]
RT-PCR[2]
Apoptosis Analysis[2]
| ||||||||||||||||||||||||||||||||
体内研究 (In Vivo) | KIRA6 (intraperitoneal injection; 5 mg/kg; 37 days) shows significant amelioration of random glucose levels over several weeks compared to vehicle, both fed ad lib[2].KIRA6 (intraperitoneal injection; 5 mg/kg; 21 or 18 days postinjections) increases both plasma insulin and C-peptide levels, remains insulin-positive islet areas at high level after stopping injections in the Akita Mouse[2].
| ||||||||||||||||||||||||||||||||
分子量 | 518.53 | ||||||||||||||||||||||||||||||||
性状 | Solid | ||||||||||||||||||||||||||||||||
Formula | C28H25F3N6O | ||||||||||||||||||||||||||||||||
CAS 号 | 1589527-65-0 | ||||||||||||||||||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||||||||||||||||||
储存方式 |
| ||||||||||||||||||||||||||||||||
溶解性数据 | In Vitro: DMSO : 25 mg/mL(48.21 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
|