Bioactivity | Nav1.8-IN-9 (Example 16) is an orally active, potent Nav1.8 inhibitor with an IC50 of 0.084 nM. Nav1.8-IN-9 has the potential for widespread pain research[1]. |
In Vivo | Nav1.8-IN-9 (Example 16;30 mg/kg;单次口服) 在 1 小时、2 小时、4 小时均可抑制大鼠术后疼痛模型诱发的机械超敏反应[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
CAS | 2966089-14-3 |
Formula | C22H20F4N4O3S |
Molar Mass | 496.48 |
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]. Ting Liu, et al. Aromatic paracyclic Nav1.8 inhibitors and their applications. CN116462662A. |