CAS NO: | 1338934-20-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | MKC9989 is aHydroxy aryl aldehydes(HAA) inhibitor and also inhibitsIRE1αwith anIC50of 0.23 to 44 μM. | ||||||||||||||||
IC50& Target | IC50: 0.23 to 44 μM (IRE1α)[1] | ||||||||||||||||
体外研究 (In Vitro) | At 10 μM concentration, MKC9989 completely inhibits both basal and thapsigargin induced splicing of XBP1 mRNA. These effects are observed even in cells pre-treated with thapsigargin, indicating that MKC9989 can fully reverse the onset of XPB1 splicing after the UPR is initiated. In parallel analysis, MKC9989, significantly stabilizes the RIDD target CD59 mRNA when co-administered with thapsigargin relative to thapsigargin treatment alone and modestly increases levels of CD59 mRNA in non-stressed cells, the latter likely reflects the inhibition of baseline RIDD activity. In contrast to effects on XBP1 splicing, MKC9989 moderately stabilizes CD59 levels when administered 2 hour post treatment with thapsigargin. Finally, the potency of MKC9989 against the splicing of XBP1 mRNA (EC50=0.33 μM) is comparable to its potency against RNA cleavage in vitro[1]. | ||||||||||||||||
分子量 | 336.34 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H20O7 | ||||||||||||||||
CAS 号 | 1338934-20-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 50 mg/mL(148.66 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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以下溶剂前显示的百
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