生物活性 | |||
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描述 | Olsalazine is a potent inhibitor of macrophage chemotaxis towards leukotriene B4 (LTB4) with an IC50 value of 0.39 mM. It also reduces the synthesis of various hydroxyeicosatetraenoic acids (HETEs), including 5-HETE, 11-HETE, 12-HETE, and 15-HETE in polymorphonuclear leukocytes (PMNL) and mononuclear cells (MNL). Olsalazine is researched primarily for its potential in treating ulcerative colitis due to its anti-inflammatory properties[1].[2]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.31mL 0.66mL 0.33mL |
16.54mL 3.31mL 1.65mL |
33.09mL 6.62mL 3.31mL |
参考文献 |
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