N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
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- CAS號:
- 116686-15-8
- 英文名:
- FK-3311
- 英文別名:
- FK-3311;CS-1073;FK-3311; FK3311;COX-2 Inhibitor V;FK 3311, 10 mM in DMSO;COX-2 Inhibitor V, FK3311;COX,Cyclooxygenase,Inhibitor,inhibit,FK 3311,FK3311;N-[4-Acetyl-2-(2,4-difluorophenoxy)phenyl]methanesulfonamide;Methanesulfonamide, N-[4-acetyl-2-(2,4-difluorophenoxy)phenyl]-;N-[4-Acetyl-2-(2,4-difluorophenoxy)phenyl]-methanesulfonamide FK3311
- 中文名:
- N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
- 中文別名:
- 化合物FK 3311;FK 3311,環(huán)氧合酶2(COX-2)抑制劑;化合物FK 3311,10 MM DMSO 溶液;N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
- CBNumber:
- CB91247805
- 分子式:
- C15H13F2NO4S
- 分子量:
- 341.33
- MOL File:
- 116686-15-8.mol
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N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺化學(xué)性質(zhì)
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沸點:
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431.3±55.0 °C(Predicted)
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密度:
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1.419±0.06 g/cm3(Predicted)
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儲存條件:
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Store at RT
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溶解度:
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Soluble in DMSO
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形態(tài):
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White solid
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酸度系數(shù)(pKa):
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6.82±0.10(Predicted)
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顏色:
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Light yellow to yellow
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N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺性質(zhì)、用途與生產(chǎn)工藝
FK-3311 (COX-2 Inhibitor V)是選擇性的、細(xì)胞可滲透的、口服 cyclooxygenase-2 (COX-2) 抑制劑，具有抗炎作用。FK-3311 可通過顯著抑制 TxA2 來對肝熱性缺血再灌注損傷起到保護作用。
| Target | Value |
COX-2
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TxA2
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Cyclooxygenase (COX) is an intracellular enzyme that converts arachidonic acid into prostaglandin (PG)G2 and PGH2.
The racemic mixtures and the (R)- and (S)-isomers of the 2 metabolites were inactive in the PGE2 test. IC50 values were more than 100 uM for (2 and 5), compared to 1.6 uM for FK 3311 (COX-2 Inhibitor V). Antiinflammatory activity was assessed by inhibition of adjuvant-induced arthritis, and analgesic activity was determined in the acetic acid-induced writhing assay. Following p.o. administration of 10 mg/kg, racemic (2) and its optical isomers showed activity comparable to FK-3311 (76% inhibition) in the adjuvant arthritis test, whereas racemic (5) showed very weak activity, and (R)- and (S)-(5) were not tested. With regard to analgesic effects, FK-3311 and racemic (2) showed 81 and 62% inhibitions, respectively, at a dose of 100 mg/kg p.o. The (R)- and (S)-isomers of (2) and racemic (5) all showed 46% inhibition of writhing syndrome. (R)- and (S)-(5) were less active showing 16 and 20% inhibitions, respectively.
L-PVR, CO, PaO(2), and WDR were significantly better in the FK group than in the control group. Histological tissue edema was mild, and PMN infiltration was significantly reduced in the FK group compared to the control group. The serum TxB(2) levels were significantly lower in the FK group than in the control group, while 6-keto-PGF(1alpha) levels were not significantly reduced. Two-day survival rate was significantly better in the FK group than in the control group.
Survival rate was significantly better and serum GOT levels 30 min after reperfusion were significantly lower in the FK high-dose group compared to the other two groups. Four hours after reperfusion, GPT levels and liver tissue flow were significantly better in the FK high-dose group compared to the control. Both 30 min and 4 hr after reperfusion, serum TxB(2) levels were significantly lower in the FK high-dose group compared to the control.
N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
上下游產(chǎn)品信息
上游原料
下游產(chǎn)品
| 更新日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS編號 | 包裝 | 價格 |
|---|
| 2024/11/08 | HY-14445 | FK 3311 | | 5 mg | 656元 |
| 2024/11/08 | HY-14445 | N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
FK 3311 | 116686-15-8 | 10mg | 1050元 |
N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
生產(chǎn)廠家
116686-15-8, N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺 相關(guān)搜索:
- 藥靶配體
- 抑制劑
- 化合物FK 3311,10 MM DMSO 溶液
- FK 3311,環(huán)氧合酶2(COX-2)抑制劑
- 化合物FK 3311
- N-[4-乙?；?2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺
- 116686-15-8
- FK 3311, 10 mM in DMSO
- COX,Cyclooxygenase,Inhibitor,inhibit,FK 3311,FK3311
- Methanesulfonamide, N-[4-acetyl-2-(2,4-difluorophenoxy)phenyl]-
- COX-2 Inhibitor V
- FK-3311; FK3311
- CS-1073
- COX-2 Inhibitor V, FK3311
- N-[4-Acetyl-2-(2,4-difluorophenoxy)phenyl]-methanesulfonamide FK3311
- N-[4-Acetyl-2-(2,4-difluorophenoxy)phenyl]methanesulfonamide
- FK-3311