BQR695
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- CAS号:
- 1513879-21-4
- 英文名:
- BQR695
- 英文别名:
- BQR695;NVP-BQR695;BQR695 - NVP-BQR695;BQR-695 (Synonyms: NVP-BQR695);NVP-BQR-695;NVP-BQR 695;NVP-BQR695;2-((7-(3,4-Dimethoxyphenyl)quinoxalin-2-yl)amino)-N-methylacetamide;Acetamide, 2-[[7-(3,4-dimethoxyphenyl)-2-quinoxalinyl]amino]-N-methyl-;PI4K,PI4 kinases,Parasite,BQR 695,BQR-695,Inhibitor,inhibit,Phosphatidylinositol 4 kinases
- 中文名:
- BQR695
- 中文别名:
- 化合物BQR695;2-((7-(3,4-二甲氧基苯基)喹喔啉-2-基)氨基)-N-甲基乙酰胺
- CBNumber:
- CB73344889
- 分子式:
- C19H20N4O3
- 分子量:
- 352.39
- MOL File:
- 1513879-21-4.mol
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BQR695化学性质
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沸点:
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607.1±55.0 °C(Predicted)
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密度:
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1.250±0.06 g/cm3(Predicted)
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储存条件:
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2-8°C(protect from light)
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溶解度:
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DMSO:60.0(Max Conc. mg/mL);170.27(Max Conc. mM)
Ethanol:3.0(Max Conc. mg/mL);8.51(Max Conc. mM)-
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形态:
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A solid
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酸度系数(pKa):
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15.14±0.46(Predicted)
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BQR695性质、用途与生产工艺
BQR695 (NVP-BQR695)是PI4KIIIβ抑制剂，对人源PI4KIIIβ的IC50值约为90 nM。
| Target | Value |
PI4KIIIβ
()
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~90 nM
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Treatment with 0.5 μM of either KAI407 or BQR695 causes GFP-PH
Osh2
to redistribute to the parasite plasma membrane, consistent with depletion of intracellular PI4P upon inhibition of PfPI4K function. BQR695 shows no evidence of toxicity against mature red blood cells (RBCs), induces a schizont-stage arrest indistinguishable from that observed in imidazopyrazine-treated parasites and exhibits cross-resistance with the imidazopyrazine-resistant lines.
BQR695
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下游产品
| 更新日期 | 产品编号 | 产品名称 | CAS编号 | 包装 | 价格 |
|---|
| 2024/04/30 | HY-18748 | BQR695
BQR-695 | 1513879-21-4 | 5mg | 800元 |
| 2024/04/30 | HY-18748 | BQR695
BQR-695 | 1513879-21-4 | 10mM * 1mLin DMSO | 880元 |
1513879-21-4, BQR695 相关搜索:
- 药靶配体
- 2-((7-(3,4-二甲氧基苯基)喹喔啉-2-基)氨基)-N-甲基乙酰胺
- 化合物BQR695
- 1513879-21-4
- PI4K,PI4 kinases,Parasite,BQR 695,BQR-695,Inhibitor,inhibit,Phosphatidylinositol 4 kinases
- 2-((7-(3,4-Dimethoxyphenyl)quinoxalin-2-yl)amino)-N-methylacetamide
- Acetamide, 2-[[7-(3,4-dimethoxyphenyl)-2-quinoxalinyl]amino]-N-methyl-
- BQR695 - NVP-BQR695
- NVP-BQR-695;NVP-BQR 695;NVP-BQR695
- BQR-695 (Synonyms: NVP-BQR695)
- NVP-BQR695
- BQR695