SLIGRL-NH2 产品活性：SLIGRL-NH2 (Protease-Activated Receptor-2 Activating Peptide) 是一种蛋白酶激活受体-2 (PAR-2) 激动剂。 产品来源： https://www.medchemexpress.cn/Protease-Activated_Receptor-2_Activating_Peptide.html 研究领域：GPCR/G Protein 作用靶点：Protease Activated Receptor (PAR) In Vitro: SLIGRL-NH2 is an agonist of PAR-2 and MrgprC11. SLIGRL-NH2 causes an L-NAME-inhibited relaxation. Based on SLIGRL-NH2 causing a concentration-dependent relaxation with an EC50 of 10 μM in endothelium-free preparations in the presence of perivascular adipose tissue (PVAT) , 20 μM is used as a suitable ‘test’ concentration of peptide in subsequent experiments designed to evaluate the effects of potential inhibitors of ADRF release/action. In the endothelium-free aorta preparations, SLIGRL-NH2 causes a concentration-dependent relaxation in preparations only in the presence of PVAT [+PVAT, -ENDO (endothelium)]. 相关产品：Bioactive Compound Library Plus | Peptide Library | Vorapaxar | TRAP-6 | Trypsin | AZ3451 | PAR-4 Agonist Peptide, amide TFA | 2-Furoyl-LIGRLO-amide | SCH79797 | GB-88 | Protease-Activated Receptor-2, amide | BMS-986120 | GB-110 hydrochloride | AZ8838 | I-191 | AC-55541 | FSLLRY-NH2 TFA | Parmodulin 2 | ENMD-1068 hydrochloride | PZ-128 | TFLLR-NH2(TFA) | Atopaxar | PAR-4 Agonist Peptide, amide | PAR-2-IN-1 | Protease-Activated Receptor-4 | PAR-2 (1-6) (human) | tcY-NH2 TFA | VKGILS-NH2 | Protease-Activated Receptor-1, PAR-1 Agonist TFA 品牌介绍: MCE (MedChemExpress) 拥有数百种全球独家化合物，我们致力于为全球科研客户提供最新最全的高品质小分子活性化合物；10,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域；设有专业的实验中心和严格的质控、验证体系；提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告，确保产品的高纯度、高品质；产品的生物活性多经各国客户实验验证；Nature, Cell, Science 等多种顶级期刊及制药专利收录了MCE客户的科研成果；专业团队跟踪最新的制药及生命科学研究进展，为您提供全球最新的活性化合物；与世界各大制药公司及知名科研机构建立了长期的合作。