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Leflunomide-d4
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Leflunomide-d4图片
规格:98%
分子量:274.2
包装与价格:
包装价格(元)
500ug电议
1mg电议

产品介绍
来氟米特-d4 (HWA486-d4) 是氘标记的来氟米特。来氟米特是一种嘧啶合成抑制剂,可抑制二氢乳清酸脱氢酶 (DHODH),并作为一种缓解疾病的抗风湿药物。
货号:ajcx22810
CAS:1189987-23-2
分子式:C12H5D4F3N2O2
分子量:274.2
溶解度:DMSO: soluble,Methanol: soluble
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Leflunomide-d4is intended for use as an internal standard for the quantification of leflunomide by GC- or LC-MS. Leflunomide is a synthetic isoxazol and a prodrug form of A-771726 , a dihydroorotate dehydrogenase inhibitor.1Leflunomide inhibitsde novopyrimidine synthesis to regulate T lymphocyte progression through the cell cycle. It inhibits proliferation and activation of T cells when used at concentrations of 25 and 100 µM, respectively, for naÏve and memory CD4+T cells.2It also reduces the production of Th1 effector cells and increases differentiation of Th2 cellsin vitroand in splenocytes isolated from KLH-immunized mice. Leflunomide (35 mg/kg per day) reduces and prevents inflammation in a proteoglycan-induced mouse model of rheumatoid arthritis.3Formulations containing leflunomide have been used in the treatment of active rheumatoid arthritis.


1.Breedveld, F.C., and Dayer, J.-M.Leflunomide: Mode of action in the treatment of rheumatoid arthritisAnn. Rheum. Dis.59(11)841-849(2000) 2.Dimitrova, P., Skapenko, A., Herrmann, M.L., et al.Restriction of de novo pyrimidine biosynthesis inhibits Th1 cell activation and promotes Th2 cell differentiationJ. Immunol.169(6)3392-3399(2002) 3.Glant, T.T., Mikecz, K., Bartlett, R.R., et al.Immunomodulation of proteoglycan-induced progressive polyarthritis by leflunomideImmunopharmacology23(2)105-116(1992)