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Merck
CN

SML1538

Sigma-Aldrich

NMDI14

≥97% (HPLC)

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别名:
2-{[(6,7-二甲基-3-氧代-1,2,3,4-四氢-2-喹喔啉基)乙酰基]氨基} -4,5-二甲基-3-噻吩甲酸乙酯, 4,5-二甲基-2-[[2-(1,2,3,4-四氢-6,7-二甲基-3-氧代-2-喹喔啉基)乙酰基]氨基]-3-噻吩甲酸乙酯
经验公式(希尔记法):
C21H25N3O4S
分子量:
415.51
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

检测方案

≥97% (HPLC)

形式

powder

颜色

white to beige

溶解性

DMSO: 0.2 mg/mL, clear (warmed)

储存温度

2-8°C

应用

NMDI14作为mRNA无义介导降解(NMD)抑制剂的应用:
  • 研究其对分化心肌细胞的影响
  • 研究其对斑马鱼pdzk1基因敲除胚胎的影响
  • 分析其对结直肠癌细胞凋亡的影响

生化/生理作用

NMDI14 是一种有效的无意义介导 RNA 衰变(NMD)抑制剂。 NMDI14 靶向 SMG7 蛋白的口袋,并破坏 SMG7-UPF1 相互作用。 NMDI14 可恢复具有提前终止密码子(PTC)突变的 p53 的细胞中的全长 p53 蛋白活性。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Michael Bordonaro et al.
Journal of Cancer, 10(2), 287-292 (2019-02-06)
Deregulated Wnt signaling initiates most cases of colorectal cancer (CRC). Butyrate, a product of dietary fiber, hyperactivates Wnt signaling, resulting in induction of CRC cell apoptosis, which may in part explain the protective action of fiber. Nonsense mediated decay (NMD)
Greg H P Ngo et al.
Nature communications, 12(1), 3849-3849 (2021-06-24)
DNA-RNA hybrid structures have been detected at the vicinity of DNA double-strand breaks (DSBs) occurring within transcriptional active regions of the genome. The induction of DNA-RNA hybrids strongly affects the repair of these DSBs, but the nature of these structures
Xinyun Chen et al.
Nature communications, 12(1), 89-89 (2021-01-06)
The RNA-binding protein QKI belongs to the hnRNP K-homology domain protein family, a well-known regulator of pre-mRNA alternative splicing and is associated with several neurodevelopmental disorders. Qki is found highly expressed in developing and adult hearts. By employing the human
Jiaheng Xie et al.
Investigative ophthalmology & visual science, 62(3), 29-29 (2021-03-23)
The human PDZK1 gene is located in a genomic susceptibility region for neurodevelopmental disorders. A genome-wide association study identified links between PDZK1 polymorphisms and altered visual contrast sensitivity, an endophenotype for schizophrenia and autism spectrum disorder. The PDZK1 protein is

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