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• 产品描述： SGC707 is a potent, selective, and non-competitive PRMT3 (protein arginine methyltransferase 3) inhibitor (IC50=31 nM, Kd=53 nM).

• 靶点： PRMT3:31 nM (IC50)

• 体外研究： SGC707 (0-10 μM; 6 h) binds to PRMT3 in both HEK293 and A549 cells. Cell Viability Assay Cell Line: HEK293 and A549 cells Concentration: 0-10 μM Incubation Time: 6 hours Result: Stabilized PRMT3 in both HEK293 and A549 cells with EC50 values of 1.3 μM and 1.6 μM, respectively.

• 体内研究： SGC707 (intraperitoneal injection; 10 mg/kg; 3 times per week; 3 w) treatment reduces hepatic steatosis and plasma triglyceride levels and induces pruritus in Western-type diet-fed LDL receptor knockout mice. Animal Model: Western-type diet-fed LDL (lipoprotein) receptor knockout mice Dosage: 10 mg/kg Administration: Intraperitoneal injection; 10 mg/kg; 3 times per week; 3 weeks Result: Exhibited 50% lower liver triglyceride stores as well as 32% lower plasma triglyceride levels.

• 参考文献：
  1. Kaniskan HÜ, et al. A potent, selective and cell-active allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3). Angew Chem Int Ed Engl. 2015 Apr 20;54(17):5166-70. 2. de Jong LM, et al. PRMT3 inhibitor SGC707 reduces triglyceride levels and induces pruritus in Western-type diet-fed LDL receptor knockout mice. Sci Rep. 2022 Jan 10;12(1):483.

• 溶解性： soluble  in  DMSO

• 保存条件： -20℃

• 配置溶液浓度参考：
  

  	1mg	5mg	10mg
  1 mM	3.352 ml	16.759 ml	33.519 ml
  5 mM	0.67 ml	3.352 ml	6.704 ml
  10 mM	0.335 ml	1.676 ml	3.352 ml
  50 mM	0.067 ml	0.335 ml	0.67 ml

• 注意：部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

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本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系，公式为：

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子量 (g/mol)

• pg ng μg mg g kg =
  fM pM nM μM mM M *
  nL μL mL L *