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PQA-18 是p21激活激酶2(PAK2;IC50 = 10 nM)的有效抑制剂,并作为Ppc-1(产品编号42352)衍生物展现出免疫抑制特性。该化合物能够降低由刀豆A(产品编号14951)刺激的Jurkat T细胞中IL-2的生成(IC50 = 400 nM)。在应用0.1% PQA-18的情况下,NC/Nga小鼠模型显示异位性皮炎的严重程度、血清IgE水平及皮肤厚度有所减轻。此外,0.05%的剂量可有效减少该小鼠模型中皮肤神经纤维的密度。PQA-18(4 mg/kg)还在大鼠小肠移植模型中显著提高了移植物的存活率。
PQA-18 是p21激活激酶2(PAK2;IC50 = 10 nM)的有效抑制剂,并作为Ppc-1(产品编号42352)衍生物展现出免疫抑制特性。该化合物能够降低由刀豆A(产品编号14951)刺激的Jurkat T细胞中IL-2的生成(IC50 = 400 nM)。在应用0.1% PQA-18的情况下,NC/Nga小鼠模型显示异位性皮炎的严重程度、血清IgE水平及皮肤厚度有所减轻。此外,0.05%的剂量可有效减少该小鼠模型中皮肤神经纤维的密度。PQA-18(4 mg/kg)还在大鼠小肠移植模型中显著提高了移植物的存活率。
产品描述 | PQA-18, an inhibitor of p21-activated kinase 2 (PAK2; IC50 = 10 nM), is derived from Ppc-1 (product number 42352) and exhibits immunosuppressive properties. It inhibits IL-2 production in Jurkat T cells induced by Concanavalin A (product number 14951) with an IC50 of 400 nM. Topically applied at 0.1%, PQA-18 reduces the severity of atopic dermatitis, serum IgE levels, and skin thickness in the NC/Nga mouse model. A lower concentration of 0.05% also decreases skin nerve fiber density in NC/Nga mice. Additionally, PQA-18 administered at 4 mg/kg improves graft survival in a rat small intestine transplantation model. |
别名 | Prenylated Quinolinecarboxylic Acid Compound-18 |
分子量 | 409.51798 |
分子式 | C25H31NO4 |
CAS No. | 1604678-82-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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