5-溴-2-（4-氟苯基）-3-（4-甲基磺酰基苯基）噻吩
5-溴-2-（4-氟苯基）-3-（4-甲基磺酰基苯基）噻吩
5-溴-2-（4-氟苯基）-3-（4-甲基磺酰基苯基）噻吩 性质
| 储存条件 | 2-8°C |
|---|---|
| 溶解度 | DMF：54 mg/ml； DMF:PBS (pH 7.2) (1:1)：0.5 mg/ml； DMSO：15 mg/ml；乙醇：7 mg/ml |
| 形态 | 白色至类白色固体。 |
| 颜色 | 白色至米白色 |
5-溴-2-（4-氟苯基）-3-（4-甲基磺酰基苯基）噻吩 用途与合成方法
|
hCOX-2 10 nM (IC 50 ) |
hCOX-1 800 nM (IC 50 ) |
DuP-697 (0-100 nM; 24 hours; HT29 cells) treatment shows antiproliferative with an IC
50
value of 42.8 nM.
DuP-697 (25-100 nM; 72 hours; HT29 cells) treatment causes concentration dependent apoptosis in HT29 cells. The percentage of UR (apoptosis portion) area increases gradually according to the concentration of DuP-697 from 7% in control group to 52% in 100 nM DuP-697.
DuP-697 in 100, 10 and 1 nM concentrations cause antiangiogenic effect. Antiangiogenic scores of DuP-697 are 1.2, 0.8 and 0.5, respectively.
Cell Proliferation Assay
| Cell Line: | HT29 cells |
| Concentration: | 0 nM, 12.5 nM, 25 nM, 50 nM, 100 nM |
| Incubation Time: | 24 hours |
| Result: | Exhibited decreasing CI values in a concentration dependent manner. Showed statistically significant cytotoxic effect. |
Apoptosis Analysis
| Cell Line: | HT29 cells |
| Concentration: | 25 nM, 50 nM, 100 nM |
| Incubation Time: | 72 hours |
| Result: | Caused concentration dependent apoptosis in HT29 cells. |
DuP-697 is a potent inhibitor of paw swelling in nonestablished and established adjuvant arthritis in rats (ED
50
= 0.03 and 0.18 mg/kg/day, respectively). DuP-697 has no effect on phenylquinone writhing in rats (ED
50
greater than 100 mg/kg), but is analgetic against inflammation-related pain in the Randall-Selitto assay (ED
50
= 3.5 mg/kg) and is a very potent antipyretic agent (ED
50
= 0.05 mg/kg). DuP-697 (5 mg/kg i.v.) does not alter renal blood flow or the renal vascular response to angiotensin II in furosemide-pretreated, volume-depleted rats.
DuP-697 is a moderate inhibitor of bull seminal vesicle prostaglandin (PG) synthesis (IC
50
of 24 μM) and a potent inhibitor of rat brain PG synthesis (IC
50
of 4.5 μM) but was ineffective against rat kidney PG synthesis (IC
50
of 75 μM).
5-溴-2-（4-氟苯基）-3-（4-甲基磺酰基苯基）噻吩 价格(试剂级)
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2024-11-08 | HY-103387 | 1 mg | 450 | ||
| 2024-11-08 | HY-103387 | 5 mg | 990 |
