| Bioactivity | NLRP3-IN-15 is a potent and selective NLRP3 inflammasome inhibitor. NLRP3-IN-15 inhibits IL-1β release with an IC50 of 0.114 μM. NLRP3-IN-15 can be used for the research of inflammation[1]. |
| Invitro | NLRP3-IN-15 (化合物 12a) 抑制 IL-1β 释放,IC50 为 0.114 μM (ELISA 测定) [1]。NLRP3-IN-15 (2 μM,3 小时) 抑制小鼠腹膜巨噬细胞 (PM) 中 IL-1β (p17) 和 caspase-1 (p20) 的分泌[1]。NLRP3-IN-15 通过抑制 ASC 寡聚化来抑制 NLRP3 炎性体复合物的形成[1]。NLRP3-IN-15 在人和小鼠肝微粒体中表现出代谢稳定性 (T1/2: 693 min; Clint: 2.0 μL/min/mg)[1]. Western Blot Analysis[1] Cell Line: |
| In Vivo | NLRP3-IN-15 (化合物 5j) (50 mg/kg;i.p.) 在败血症小鼠模型中表现出抗炎作用[1]。 Animal Model: |
| Name | NLRP3-IN-15 |
| CAS | 2767369-71-9 |
| Formula | C22H19NO4 |
| Molar Mass | 361.39 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Li J, et al. Scaffold Hybrid of the Natural Product Tanshinone I with Piperidine for the Discovery of a Potent NLRP3 Inflammasome Inhibitor. J Med Chem. 2023 Feb 23;66(4):2946-2963. |