hDHODH-IN-2结构式
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常用名 | hDHODH-IN-2 | 英文名 | hDHODH-IN-2 |
|---|---|---|---|---|
| CAS号 | 183946-00-1 | 分子量 | 304.34 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H16N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
hDHODH-IN-2用途hDHODH-IN-2 是一种 Leflunomide 活性代谢物的类似物。hDHODH-IN-2 是一种人二氢乳清酸脱氢酶 hDHODH 抑制剂,具有抗炎活性。 |
| 英文名 | hDHODH-IN-2 |
|---|
| 描述 | hDHODH-IN-2 是一种 Leflunomide 活性代谢物的类似物。hDHODH-IN-2 是一种人二氢乳清酸脱氢酶 hDHODH 抑制剂,具有抗炎活性。 |
|---|---|
| 相关类别 | |
| 体外研究 | 在自组织分子场分析(SOMFA)中,hDHODH-IN-2(化合物42)对大鼠和小鼠DHODH的log 1/IC50分别为5.83和5.80。 |
| 参考文献 |
| 分子式 | C19H16N2O2 |
|---|---|
| 分子量 | 304.34 |
| InChIKey | CAGGGMPTWTUYHZ-ZCXUNETKSA-N |
| SMILES | N#CC(C(=O)Nc1ccc(-c2ccccc2)cc1)=C(O)C1CC1 |
| 储存条件 | 2-8°C,密封,干燥 |
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实验名称:In vivo ability to inhibit delayed type hypersensitivity in rat at a concentration of...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL794678
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实验名称:Inhibition of ubiquinone binding site of human dihydroorotate dehydrogenase
来源:ChEMBL
靶标:Dihydroorotate dehydrogenase (quinone), mitochondrial
External Id:CHEMBL984852
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实验名称:Inhibition of ubiquinone binding site of Plasmodium falciparum dihydroorotate dehydro...
来源:ChEMBL
靶标:Dihydroorotate dehydrogenase (quinone), mitochondrial
External Id:CHEMBL984851
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实验名称:In vivo ability to inhibit delayed type hypersensitivity in mouse at a concentration ...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL741842
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实验名称:Inhibitory concentration tested on enzyme dihydroorotate dehydrogenase in mouse
来源:ChEMBL
靶标:Dihydroorotate dehydrogenase (quinone), mitochondrial
External Id:CHEMBL666232
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实验名称:Inhibitory concentration tested against enzyme dihydroorotate dehydrogenase in rat
来源:ChEMBL
靶标:Dihydroorotate dehydrogenase (quinone), mitochondrial
External Id:CHEMBL666233
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