| 名称 | AM966 |
| 描述 | AM966, a excellent affinity, specific, oral LPA1(IC50=17 nM) antagonist, suppresses LPA-stimulated intracellular calcium release. |
| 细胞实验 | AM966 (Chem Scene, Monmouth Junction, NJ, USA) is dissolved in DMSO and stored, and then diluted with appropriate media (DMSO 0.5%) before use.CHO-K1 cells are grown to 80% confluency in 12-well plates, serum-starved for 24 h and incubated in serum-free medium with AM966. After 21 h, [3H]thymidine (0.5 μCi/well) is added and the incubation is continued for 3 h. The medium is then removed, and the cells are placed on ice and washed twice with 1 mL of ice-cold PBS containing 5% trichloroacetic acid. Cells are solubilized and [3H]thymidine incorporation is determined by liquid scintillation counting. Assays are performed in triplicate. |
| 动物实验 | In fasted mice, received AM966 (10 mg/kg), which is prepared in water, by oral gavage. |
| 体外活性 | Pre-treatment with AM966 (100 nM) completely blocks ERK1/2 phosphorylation induced by either amitriptyline or mianserin. LPA-induced ERK1/2 activation is completely blocked by AM966 (100 nM), which selectively antagonizes LPA1 over LPA2-5, with an IC50 value of 3.8±0.4 nM. AM966 inhibits LPA1-mediated chemotaxis of human A2058 melanoma cells (IC50=138±43 nM), IMR-90 human lung fibroblasts (IC50=182±86 nM) and CHO mLPA1 cells (IC50=469±54 nM). |
| 体内活性 | In a 3-day bleomycin model, AM966 (30 mg/kg, BID) reduces vascular leakage, inflammation and lung injury and inflammation. |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | 10% DMSO+90% Saline : < 10 mg/mL (20.37 mM), Lower concentrations may be soluble, but exact solubility limit is unknown. DMSO : 125 mg/mL (254.62 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 10 mg/mL (20.37 mM), Solution. 10% DMSO+90% Corn Oil : 2 mg/mL (4.07 mM), Sonication is recommended.
|
| 关键字 | Lysophospholipid Receptor | LPLReceptor | LPL Receptor | LPL | LPAReceptor | LPA1 | LPA Receptor | Inhibitor | inhibit | AM-966 | AM966 | AM 966 |
| 相关产品 | Poloxamer 407 | Sphingosine-1-phosphate | S1PR1 modulator 1 | Siponimod | LX-2931 | Tyloxapol | SLP9101555 | Ki16198 | CAY10444 | CYM5181 | CYM50374 | ASP-4058 |
| 相关库 | 抑制剂库 | 抗癌活性化合物库 | 经典已知活性库 | 已知活性化合物库 | ReFRAME 相关化合物库 | 高选择性抑制剂库 | NO PAINS 化合物库 | GPCR靶点分子库 | 免疫/炎症分子化合物库 | 膜蛋白靶向化合物库 | 口服活性化合物库 | 表型筛选靶点鉴定库 |