CAS NO: | 147076-36-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Laflunimus (HR325) is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726. Laflunimus is an orally active inhibitor ofdihydroorotate dehydrogenase(DHODH). Laflunimus suppresses immunoglobulin (Ig) secretion, with IC50values of 2.5 and 2 μM forIgMandIgG, respectively. Laflunimus also is aprostaglandin endoperoxide H synthase (PGHS) -1and-2inhibitor[1][2]. |
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体外研究 (In Vitro) |
Ig secretion from mouse splenocytes was induced by lipopolysaccharide (LPS) for 5 days. Laflunimus inhibited the secretion of IgM and IgG with IC50values of 2.5 and 2 μM , respectively. Adding Uridine (50 μ M) increased these values to 70 and 60 μ M, respectively. Laflunimus inhibits LPS-induced kappa light-chain cell surface expression on 70Z/3 cells, a property also reversed by uridine[1].
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体内研究 (In Vivo) |
HR325 (50 mg/kg; p.o.; days 14-18 after being injected with SRBC) inhibits the secondary anti-sheep red blood cell (SRBC) antibody response with ID50values of 38 mg/kg[1].
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分子量 |
310.27 |
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性状 |
Solid |
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Formula |
C15H13F3N2O2 |
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CAS 号 |
147076-36-6 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 50 mg/mL(161.15 mM;Need ultrasonic)
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In Vivo:
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