688342-78-1
物理化学性质
| 沸点 | 582.0±60.0 °C(Predicted) |
| 密度 | 1.147±0.06 g/cm3(Predicted) |
| 储存条件 | -20°C储存 |
| 溶解度 | DMSO: ≥ 100 mg/mL (233.30 mM) |
| 酸度系数(pKa) | 12.00±0.70(Predicted) |
| 形态 | Solid |
| 颜色 | Off-white to light yellow |
常见问题列表
| Target | Value |
|
RAD52
(Cell-free assay) | 25.8 μM(Ki) |
D-I03 (0-10 μM; on days 1 and 3; Capan-1 and UWB1.289 cells) treatment preferentially suppressed the growth of Capan-1 and UWB1.289 cells in a concentration-dependent manner.
D-I03 inhibits RAD52 foci formation induced by cisplatin in BCR-ABL1-positive BRCA1-deficient 32Dcl3 murine hematopoietic cell line that expresses GFP-RAD52. In the presence of D-I03 (2.5 μM), the fraction of cells with RAD52 foci is decreased, from 38.7% to 171%; at the same time, the fraction of Cisplatin-treated cells without foci is increased from 48.4% to 71.9%. D-I03 does not effect on RAD51 foci induced by Cisplatin. Also, D-I03 alone induce neither RAD51 foci nor RAD52 foci (in BRCA1-deficient cells) indicating low genotoxicity of D-I03.
Cell Proliferation Assay
| Cell Line: | Capan-1 (BRCA2 − ) and UWB1.289 (BRCA1 + ) cells |
| Concentration: | 0 μM, 2.5 μM, 5 μM, or 10 μM |
| Incubation Time: | On days 1 and 3 |
| Result: | Preferentially suppressed the growth of Capan-1 and UWB1.289 cells. |
D-I03 (50 mg/kg/day; intraperitoneal injection; daily; for 7 days;
nu/nu
mice) treatment reduces BRCA1-deficient MDA-MB-436 tumor growth. Talazoparib puls D-I03 does not affect the growth of BRCA1-proficient tumors and does not exert any significant toxicity against normal tissues and organs.
Pharmacokinetic and toxicity studies indicates that maximal tolerated dose of D-I03 is ≥50 mg/kg, and t
1/2
is 23.4 hours, resulting in >1 μM maximal concentration in peripheral blood.
| Animal Model: | Nu/nu mice injected with BRCA1-deficient MDA-MB-436 cells |
| Dosage: | 50 mg/kg/day |
| Administration: | Intraperitoneal injection; daily; for 7 days |
| Result: | Reduced BRCA1-deficient MDA-MB-436 tumor growth. |