Dehydro-ZINC39395747

• 常用名: Dehydro-ZINC39395747
• 英文名: Dehydro-ZINC39395747
• CAS号: 433248-87-4
• 分子量: 291.35
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₂H₉N₃O₂S₂
• 熔点: N/A
• 闪点: N/A

Dehydro-ZINC39395747用途

Dehydro-ZINC39395747 是一种 ZINC39395747 的衍生物。ZINC39395747 是一种有效的细胞色素 b5 还原酶 3 (CYB5R3) 抑制剂,IC50 为 9.14 μM,Kd 为1.11 μM。ZINC39395747 可以增加血管细胞中 NO 的生物利用度。

Dehydro-ZINC39395747名称

• 英文名: Dehydro-ZINC39395747

Dehydro-ZINC39395747生物活性

• 描述: Dehydro-ZINC39395747 是一种 ZINC39395747 的衍生物。ZINC39395747 是一种有效的细胞色素 b5 还原酶 3 (CYB5R3) 抑制剂,IC50 为 9.14 μM,Kd 为1.11 μM。ZINC39395747 可以增加血管细胞中 NO 的生物利用度。
• 相关类别:
  研究领域 >> 其他
  信号通路 >> 其他 >> 其他
• 参考文献:

  [1]. Rahaman MM, et al. Structure Guided Chemical Modifications of Propylthiouracil Reveal Novel Small Molecule Inhibitors of Cytochrome b5 Reductase 3 That Increase Nitric Oxide Bioavailability. J Biol Chem. 2015 Jul 3;290(27):16861-72.

Dehydro-ZINC39395747物理化学性质

• 分子式: C₁₂H₉N₃O₂S₂
• 分子量: 291.35
• InChIKey: ZBZUSIRGXUAECB-UHFFFAOYSA-N
• SMILES: O=c1cc(CSc2nc3ccccc3o2)[nH]c(=S)[nH]1
• 外观性状: 固体
• 储存条件: -20°C

Dehydro-ZINC39395747靶点实验

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实验名称：Inhibitors of CDC25B-CDK2/CyclinA interaction 来源：Center for Chemical Genomics, University of Michigan External Id：MScreen:TargetID_600

实验名称：High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ... 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School External Id：HMS1303

实验名称：A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School External Id：HMS979

实验名称：Cell-based high throughput primary assay to identify activators of GPR151 来源：The Scripps Research Institute Molecular Screening Center 靶标：RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL External Id：GPR151_PHUNTER_AG_LUMI_1536_1X%ACT

实验名称：AlphaScreen-based biochemical high throughput primary assay to identify activators of... 来源：The Scripps Research Institute Molecular Screening Center 靶标：N/A External Id：FBW7_ACT_ALPHA_1536_1X%ACT PRUN

实验名称：AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of... 来源：The Scripps Research Institute Molecular Screening Center External Id：MITF_INH_Alpha_1536_1X%INH PRUN

实验名称：A screen for compounds that inhibit viral RNA polymerase binding and polymerization a... 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School 靶标：Chain A, Poliovirus Polymerase With Gtp External Id：HMS750

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