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Merck
CN

A8129

阿卡地新

别名:

5-氨基咪唑-4-羧酰胺-1-β-D-呋喃甲苷, N1-(β-D-核糖呋喃甲酰)-5-氨基咪唑-4-羧酰胺, 阿卡地新

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关于此项目

经验公式(希尔记法):
C9H14N4O5
化学文摘社编号:
分子量:
258.23
EC Number:
220-097-5
UNSPSC Code:
12352204
MDL number:
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SMILES string

NC(=O)c1ncn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c1N

InChI

1S/C9H14N4O5/c10-7-4(8(11)17)12-2-13(7)9-6(16)5(15)3(1-14)18-9/h2-3,5-6,9,14-16H,1,10H2,(H2,11,17)/t3-,5-,6-,9-/m1/s1

InChI key

RTRQQBHATOEIAF-UUOKFMHZSA-N

Biochem/physiol Actions

AICAR是AMP活化蛋白激酶(AMPK)的细胞渗透激活剂。
阿卡地新是AMP活化蛋白激酶(AMPK)的细胞渗透性激活剂,是一种代谢主调节因子,在能量利用率降低时被激活(高细胞AMP:ATP比值),用于抑制合成代谢过程。在体内,药物激活AMPK与AICAR可模拟运动和触发胰岛素无关的骨骼肌葡萄糖摄取。


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The increase in monocyte chemoattractant protein-1 (MCP-1) and the decrease in adiponectin production from hypertrophic adipocytes are associated with adipose tissue inflammation and its metabolic complications. The aim of this study was to determine whether 5-aminoimidazole-4-carboxamide 1-β-D-ribofuranoside (AICAR), an adenosine
Elena Y Kochetkova et al.
Aging, 9(11), 2352-2375 (2017-11-16)
The Ras-Raf-MEK-ERK pathway plays a central role in tumorigenesis and is a target for anticancer therapy. The successful strategy based on the activation of cell death in Ras-expressing cells is associated with the suppression of kinases involved in Ras pathway.
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Developmental cell, 51(1), 113-128 (2019-08-27)
Employing inducible genetically engineered and orthotopic mouse models, we demonstrate a key role for transcriptional regulator Yap in maintenance of Kras-mutant pancreatic tumors. Integrated transcriptional and metabolomics analysis reveals that Yap transcribes Myc and cooperates with Myc to maintain global