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162054-19-5

中文名稱 1-[(4-甲基磺酰基)苯基]-3-三氟甲基-5-(4-氟苯基)吡唑
英文名稱 1-[(4-METHYLSULFONYL)PHENYL]-3-TRIFLUOROMETHYL-5-(4-FLUOROPHENYL)PYRAZOLE
CAS 162054-19-5
分子式 C17H12F4N2O2S
分子量 384.35
MOL 文件 162054-19-5.mol
更新日期 2024/11/05 13:11:12
162054-19-5 結構式 162054-19-5 結構式

基本信息

中文別名
1-[(4-甲基磺?;?苯基]-3-三氟甲基-5-(4-氟苯基)吡唑
5-(4-氟苯基)-1-(4-(甲基磺酰基)苯基)-3-(三氟甲基)-1H-吡唑
英文別名
SC-58125
1-[(4-METHYLSULFONYL)PHENYL]-3-TRIFLUOROMETHYL-5-(4-FLUOROPHENYL)PYRAZOLE
5-(4-Fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-3-(trifluoromethyl)pyrazole
5-(4-Fluoro-phenyl)-1-(4-methanesulfonyl-phenyl)-3-trifluoromethyl-1H-pyrazole
5-(4-Fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-3-(trifluoromethyl)-1H-pyrazole
1H-Pyrazole, 5-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-3-(trifluoromethyl)-

物理化學性質(zhì)

儲存條件Store at +4°C
溶解度二甲基亞砜:≥20mg/mL
形態(tài)粉末
顏色白色至灰白色

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H315-H319-H335
危險品標志T
危險類別碼25
安全說明45-24/25-22
WGK Germany3

常見問題列表

生物活性
SC-58125 是一種有效的和選擇性的環(huán)氧合酶 2 (COX-2) 的抑制劑,IC50 值為 0.04 μM。SC-58125 在體外和體內(nèi)均表現(xiàn)出抗腫瘤活性,還可以抑制炎癥部位的水腫并具有鎮(zhèn)痛作用。
靶點

hCOX-2

0.04 μM (IC 50 )

hCOX-1

>100 μM (IC 50 )

體外研究

SC-58125 (0.001-100 μM) has a high degree of selectivity for the inducible form of COX-2 (IC 50 =1 μM) over the COX-1 (IC 50 >100 μM).
SC-58125 (10 μM; 20-140 s) is time-dependent and is complete by 1 min, with a half-maximal inhibition at 20 s.
SC-58125 (25-100 μM; 3 d) inhibits the in vitro growth of HCA-7 and LLC cells.
SC-58125 (100 μM; 12 h) induces G 2 arrest in LLC cells.
SC-58125 (25-100 μM; 3 d) decreases p34 cdc2 levels in HCA-7 cells.
SC-58125 (100 μM; 24 or 72 h) does not induce apoptosis of HCA-7 and LLC cells.

Cell Proliferation Assay

Cell Line: HCA-7 and LLC cells
Concentration: 0, 25, 50, 100 μM
Incubation Time: 3 days
Result: Reduced the cell number and MTT activity in both cell lines in a dose-dependent manner.

Cell Cycle Analysis

Cell Line: LLC cells
Concentration: 100 μM
Incubation Time: 12 hours
Result: Increased in the number of cells containing 4n DNA content in a dose- and time-dependent manner.
Reduced the number of mitotic figures.

Western Blot Analysis

Cell Line: HCA-7 cells
Concentration: 0, 25, 50, 100 μM
Incubation Time: 3 days
Result: Resulted in a dose-dependent decrease in p34 cdc2 activity with strong inhibition, even at the lowest concentration.
體內(nèi)研究

SC-58125 (10 mg/kg; i.p. every 48 h) inhibits the growth of established colorectal cancer xenografts in mice.
SC-58125 (10 mg/kg; a single i.p.) reduces tumor PGE2 levels in mice.
SC-58125 (10 mg/kg; a single i.p.) does not change the tumor levels of COX-1 and COX-2 protein in mice.

Animal Model: Athymic Sprague-Dawley mice are injected HCA-7 cells
Dosage: 10 mg/kg
Administration: I.p. every 48 h; at the time of tumor implantation or 2 and 4 weeks later
Result: Decreased the tumor growth rates significantly.
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