![]() ISPA-28结构式
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常用名 | ISPA-28 | 英文名 | ISPA-28 |
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CAS号 | 1006335-39-2 | 分子量 | 408.454 | |
密度 | 1.4±0.1 g/cm3 | 沸点 | N/A | |
分子式 | C21H24N6O3 | 熔点 | N/A | |
MSDS | 美版 | 闪点 | N/A |
ISPA-28用途ISPA-28 是特异性的疟原虫表面阴离子通道 (PSAC) 拮抗剂。ISPA-28 直接可逆的与CLAG3 结合。 |
英文名 | N-(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-3-(1-ethyl-3-methyl-1H-pyrazol-4-yl)-4,5-dihydro-1,2-oxazole-5-carboxamide |
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英文别名 | 更多 |
描述 | ISPA-28 是特异性的疟原虫表面阴离子通道 (PSAC) 拮抗剂。ISPA-28 直接可逆的与CLAG3 结合。 |
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相关类别 | |
体外研究 | ISPA-28仅作为Dd2通道的抑制剂有效(Dd2和HB3通道的K0.5值分别为56 nM和43μM)[2]。 |
参考文献 |
[1]. Sanjay A Desai, et al. Ion and Nutrient Uptake by Malaria Parasite-Infected Erythrocytes. |
密度 | 1.4±0.1 g/cm3 |
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分子式 | C21H24N6O3 |
分子量 | 408.454 |
精确质量 | 408.190979 |
LogP | 0.18 |
折射率 | 1.672 |
危险品运输编码 | NONH for all modes of transport |
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An epigenetic antimalarial resistance mechanism involving parasite genes linked to nutrient uptake.
J. Biol. Chem. 288(27) , 19429-40, (2013) Acquired antimalarial drug resistance produces treatment failures and has led to periods of global disease resurgence. In Plasmodium falciparum, resistance is known to arise through genome-level chang... |
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Malaria parasite mutants with altered erythrocyte permeability: a new drug resistance mechanism and important molecular tool.
Future Microbiol. 5(1) , 81-97, (2010) Erythrocytes infected with plasmodia, including those that cause human malaria, have increased permeability to a diverse collection of organic and inorganic solutes. While these increases have been kn... |
5-Isoxazolecarboxamide, N-(2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)-3-(1-ethyl-3-methyl-1H-pyrazol-4-yl)-4,5-dihydro- |
N-(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-3-(1-ethyl-3-methyl-1H-pyrazol-4-yl)-4,5-dihydro-1,2-oxazole-5-carboxamide |
MFCD08106635 |