2-(4-甲氧基苯基)-N-(4-(吡啶-4-基)噻唑-2-基)乙酰胺

• 常用名: 2-(4-甲氧基苯基)-N-(4-(吡啶-4-基)噻唑-2-基)乙酰胺
• 英文名: ROCK1-IN-1
• CAS号: 692869-38-8
• 分子量: 325.38
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₇H₁₅N₃O₂S
• 熔点: N/A
• 闪点: N/A

用途

ROCK1-IN-1是一种ROCK1抑制剂,Ki值为540 nM。ROCK1-IN-1可用于高血压、青光眼和勃起功能障碍的研究[1]。

名称

• 中文名: 2-(4-甲氧基苯基)-N-(4-(吡啶-4-基)噻唑-2-基)乙酰胺
• 英文名: 2-(4-Methoxyphenyl)-N-(4-(pyridin-4-yl)thiazol-2-yl)acetamide

生物活性

• 描述: ROCK1-IN-1是一种ROCK1抑制剂,Ki值为540 nM。ROCK1-IN-1可用于高血压、青光眼和勃起功能障碍的研究[1]。
• 相关类别:
  研究领域 >> 心血管疾病
  信号通路 >> 细胞周期/DNA损伤 >> 岩石
  信号通路 >> 干细胞及 Wnt 通路 >> 岩石
  信号通路 >> TGF-beta/Smad 信号通路 >> 岩石
• 参考文献:

  [1]. Green J, et al. Design, Synthesis, and Structure-Activity Relationships of Pyridine-Based Rho Kinase (ROCK) Inhibitors. J Med Chem. 2015 Jun 25;58(12):5028-37.

物理化学性质

• 分子式: C₁₇H₁₅N₃O₂S
• 分子量: 325.38
• InChIKey: ALHMHPNOEONPMW-UHFFFAOYSA-N
• SMILES: COc1ccc(CC(=O)Nc2nc(-c3ccncc3)cs2)cc1
• 储存条件: 室温， 密封， 干燥

靶点实验

查看更多实验

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实验名称：QFRET-based biochemical primary high throughput screening assay to identify exosite i... 来源：The Scripps Research Institute Molecular Screening Center 靶标：disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens] External Id：ADAM17_INH_QFRET_1536_1X%INH PRUN

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify ago... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_AG_FLUO8_1536_1X%ACT PRUN

实验名称：uHTS identification of small molecule activators of the adaptive arm of the Unfolded ... 来源：Burnham Center for Chemical Genomics 靶标：N/A External Id：BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay

实验名称：High throughput fluorescence intensity-based biochemical assay to screen for small mo... 来源：University of Pittsburgh Molecular Library Screening Center 靶标：furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens] External Id：MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.

实验名称：Fluorescence polarization to screen for inhibitor that competite the binding of FadD2... 来源：Broad Institute 靶标：FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) External Id：2147-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect... 来源：Broad Institute 靶标：N/A External Id：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity

实验名称：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify pos... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_PAM_FLUO8_1536_1X%ACT PRUN

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英文别名

• MFCD06338963