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AGU654 (Compound 44) 是一种效力强的mPGES-1选择性抑制剂,对mPGES-1的IC50值为2.9 nM。通过抑制mPGES-1,AGU654 阻断COX-1/2将花生四烯酸转化为前列腺素E2 (PGE2) 的通路,从而有效缓解炎症、疼痛及发热。在活化的人单核细胞衍生巨噬细胞和人全血模型中,AGU654 能选择性抑制细菌外毒素诱导的PGE2生成,同时不影响其他前列腺素的产生。在豚鼠模型中,它显著减轻了发热、炎症和炎症性疼痛,展现出显著的抗炎、镇痛和退热功效。AGU654 有潜力成为研究炎症性疾病和疼痛的新方法。
AGU654 (Compound 44) 是一种效力强的mPGES-1选择性抑制剂,对mPGES-1的IC50值为2.9 nM。通过抑制mPGES-1,AGU654 阻断COX-1/2将花生四烯酸转化为前列腺素E2 (PGE2) 的通路,从而有效缓解炎症、疼痛及发热。在活化的人单核细胞衍生巨噬细胞和人全血模型中,AGU654 能选择性抑制细菌外毒素诱导的PGE2生成,同时不影响其他前列腺素的产生。在豚鼠模型中,它显著减轻了发热、炎症和炎症性疼痛,展现出显著的抗炎、镇痛和退热功效。AGU654 有潜力成为研究炎症性疾病和疼痛的新方法。
产品描述 | AGU654 (Compound 44) is a selective mPGES-1 inhibitor with an IC50 value of 2.9 nM against mPGES-1. By inhibiting mPGES-1, AGU654 interrupts the pathway where COX-1/2 converts arachidonic acid to prostaglandin E2 (PGE2), effectively reducing inflammatory responses, pain, and fever symptoms. In models using activated human monocyte-derived macrophages and whole blood, AGU654 selectively inhibits PGE2 production induced by bacterial endotoxins, while preserving the production of other prostaglandins. In guinea pig models, AGU654 significantly alleviates fever, inflammation, and inflammatory pain, demonstrating excellent anti-inflammatory, analgesic, and antipyretic effects. AGU654 holds promise as a new approach for researching inflammatory diseases and pain. |
分子量 | 580.91 |
分子式 | C27H19ClF6N4O2 |
CAS No. | 3038861-74-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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