PROTAC TTK degrader-1 是一种有效的TTK(苏氨酸酪氨酸激酶)PROTAC降解剂,在 COLO-205 和 HCT-116 细胞中的DC50值分别为 1.7 和 5.8 nM。PROTAC TTK degrader-1 在 COLO-205 人结直肠癌细胞异种移植小鼠模型中显示出靶向降解和抗癌效果。
生物活性 | PROTACTTK degrader-1 is a potentTTK(threonine tyrosine kinase)PROTACdegrader, withDC50values of 1.7 and 5.8 nM in COLO-205 and HCT-116 cell, respectively.PROTACTTK degrader-1 exhibits target degradation and anticancer efficacy in a xenograft mouse model of COLO-205 human colorectalcancercells[1]. |
IC50& Target | DC50: 1.7 nM (TTK) in COLO-205, 5.8 nM (TTK) in HCT-116[1] |
体外研究 (In Vitro) | PROTAC TTK degrader-1 (compound 8e) (0-10 μM, 96 h) inhibits cancer cell proliferation[1]. PROTAC TTK degrader-1 (5 and 50 nM, 6 h) induces degradation of TTK protein in a dose-dependent manner[1].
Cell Proliferation Assay Cell Line: | COLO-205 and HCT-116 cells[1] | Concentration: | 0-10 μM | Incubation Time: | 96 h | Result: | Inhibited the growth of COLO-205 cancer cells with an IC50of 0.1 μM. |
Western Blot Analysis Cell Line: | COLO-205, HCT-116 LOVO, HCT-8, and HCT-29 human colon cancer cell lines[1] | Concentration: | 5, 50 nM | Incubation Time: | 6 h | Result: | Induced degradation of TTK protein in a dose-dependent manner. |
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体内研究 (In Vivo) | PROTAC TTK degrader-1 (10 mg/kg, IP, single) demonstrates reasonable pharmacokinetics profiles[1]. PROTAC TTK degrader-1 (10, 20 mg/kg, IP, once daily for 16 days) significantly reduces the TTK protein levels, and exhibits tumor-growth inhibition[1]. Pharmacokinetic Parameters of PROTAC TTK degrader-1 in male SD rats[1].
| 8e | AUC (ng/mL*h) | 2235 | T1/2(h) | 4.3 |
Animal Model: | Male SD rats[1] | Dosage: | 10 mg/kg, dissolved in mixed solvents (5% 20 mg/mL DMSO stock, 30% PG, 30% PEG400, and 35% Saline) | Administration: | IP, single (Pharmacokinetic Analysis) | Result: | Demonstrated reasonable pharmacokinetics profiles. |
Animal Model: | Male CB17-SCID mice (bearing COLO-205 tumor xenografts)[1] | Dosage: | 10, 20 mg/kg | Administration: | IP, once daily for 16 days | Result: | Significantly reduced the TTK protein levels in animal tumor tissues, exhibited tumor-growth inhibition value of 46.0% upon 20 mg/kg dosing, did not cause a significant body weight loss of the animal. |
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运输条件 | Room temperature in continental US; may vary elsewhere. |
储存方式 | Please store the product under the recommended conditions in the Certificate of Analysis. |