Bioactivity | ATR-IN-29 is a potent and orally active ATR kinase inhibitor with an IC50 value of 1 nM. ATR-IN-29 shows antiproliferative activity[1]. |
Invitro | ATR-IN-29 (compound 1) (4 days) 显示抗增殖活性,对 A549、HCC1806、HCT116、OVCAR-3、NCI-H460 细胞的 IC50 值分别为 156.70、38.81、22.48、181.60、19.02 nM[1]。 |
In Vivo | ATR-IN-29 (10 mg/kg;口服;一次) 在 CD-1 (ICR) 小鼠中显示出良好的药代动力学参数,t1/2 为 1.64 h,Cmax 为 9343 ng/mL,AUC0-t 为 98507 ng·h/mL,AUC0-inf 为 98517 ng·h/mL。 |
Name | ATR-IN-29 |
CAS | 2761193-67-1 |
Formula | C19H22N8O |
Molar Mass | 378.43 |
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]. Sui Xiong Cai, et al. Substituted imidazo[1,5-b]pyridazine compounds as kinase inhibitors and use thereof. WO2022135560A1. |